Posts tagged: Quot

excruciating heartburn / esophagitis

Question:

Developed after 10 days on Doxycycline as treatment for prostatitis. My gastroenterologist suspects the doxycycline is the cause.  I would tend to agree, but I always took it with a full meal, so can’t quite see how it could have worked its evil on my esophagus.  Anyway, assuming I have doxy induced esophagitis, my doc put me on 30mg prevacid 1x/day, and sucralfate 4x/day.  So far, after only 1 day’s treatment, I am still in agony.  I have slept virtually not at all the past two nights because of the pain, which is still excruciating even when fully upright.  Food or lack of it does little to affect the pain.  Tylenol seems to do nothing as well. Is there any medication I can take to relieve the pain so that I can sleep and let the other medicines do their work?  I’ve heard of a "GI cocktail" that has lidocain in it that is used in ERs.  Is there something similar OTC? TIA for any and all ideas — John.

Response:

In article <95556f1e.0402110805.5b5cc475 > Developed after 10 days on Doxycycline as treatment for prostatitis. > My gastroenterologist suspects the doxycycline is the cause.  I would > tend to agree, but I always took it with a full meal, so can’t quite > see how it could have worked its evil on my esophagus.  Anyway, > assuming I have doxy induced esophagitis, my doc put me on 30mg > prevacid 1x/day, and sucralfate 4x/day.  So far, after only 1 day’s > treatment, I am still in agony.  I have slept virtually not at all the > past two nights because of the pain, which is still excruciating even > when fully upright.  Food or lack of it does little to affect the > pain.  Tylenol seems to do nothing as well. Is there any medication I > can take to relieve the pain so that I can sleep and let the other > medicines do their work?  I’ve heard of a "GI cocktail" that has > lidocain in it that is used in ERs.  Is there something similar OTC? > TIA for any and all ideas — John.

First of all, one can take prevacid 30 mg twice a day.  It is a large dose, but not that infrequently done (I’m doing it for the last month and it’s helped a lot with acid burning my throat till I could barely talk).  If you’re in the US, and using our wonderful insurance plans…..your doctor will have to get special permission for the large dose, but it can be done and it will make a big difference. Also, OTC Gaviscon is different from other antacids in that it creates a barrier of foam so the acid has a harder time refluxing.  If you take too much, the magnesium in it might give you some diahrrea – but again, for a little while, no harm done. In the health food camp:  1 tsp of aloe vera juice (pure) a few times a day.  DGL (deglycerized licorice) tablets chewed 15 minutes before meals. Put some kind of blocks under the head of your bed so that it is at an angle – they usually recommend 6 to 8 inches.   DO NOT USE EXTRA PILLOWS – you need the blocks under the top of the boxspring to create the proper angle. There are other things, such as medicines available in other countries, but not here, but those will take weeks for you to get and you’ll probably be better by then. Hope this helps and that you’re feeling better soon. Louise

Response:

GERD incidence rates for various countries?

Esomeprazole is a medication used to treat gestational acid reflux disease (GERD). Buy esomeprazole tablets and feel better today!

Question:

> Mark, everbody is completely well, right up until the day they get sick… > The mechanism behind TILESR’s is that the LES inappropriately get a signal > to relax. There are several things that can initiate this. Most frequent is > simply a full stomach. There are some foods/substances that can cause this > such as nicotine, alcohol, caffiene, and some spices. There is some > speculation that it can be induced by stress, but this link has not been > demonstrated. > The cause? It just happens. Some people are genetically prone to it. In your > case, I would suspect that GERD runs in the family. > HMc

Thanks again. It seems your suspicions could be correct… I just spoke with my father and found out that he has had GERD for a while. I always remembered him popping a lot of Antacids when I was a kid but I never made the connection. thanks for the insight. Mark

Response:

> It seems your suspicions could be correct… > I just spoke with my father and found out that he has had GERD for a > while. > I always remembered him popping a lot of Antacids when I was a kid but > I never made the connection.

Indeed, like a lot of medical conditions, people may have had problems in your family for years, but it was never diagnosed.  While nobody in my family had ever had heard of "GERD", quite a few of my relatives have had chronic "heartburn." That, and sometimes people don’t talk about their medical problems, even to relatives.  A friend of mine came down with Crohn’s disease, and only after the diagnosis and surgery did she discover that her father and grandfather both had the same disease (although neither of them had required surgery).  And I didn’t find out that red-green colorblindness ran in my mother’s family (or that I had it myself) until I had my medical exam for the Naval Academy, which rather put a damper on things… (yes, you can get quite far in life before you realize that you are red-green colorblind). — Richard W Kaszeta http://www.kaszeta.org/rich

Response:

– Hide quoted text — Show quoted text -> Thanks for the reply. I had not considered the link between obesity > and Gerd as I am not overweight (probably closer to underweight) > So what originally causes the lower esophageal sphincter to not > function correctly? > It seems strange to me that all of a sudden one’s LES can stop working > correctly (as was the case with me…out of the blue one day a year > ago) > In my case, I am not overweight. I am realtively young(23). I do not > smoke or drink. I never eat fast food, or fatty foods. I dont eat > chocolate…or candy…etc The only meats that I eat are chicken and > fish. > but…I have had problems with stress in the past. > Is it possible for stress alone  to cause the LES to not function > correctly?

Mark, everbody is completely well, right up until the day they get sick… The mechanism behind TILESR’s is that the LES inappropriately get a signal to relax. There are several things that can initiate this. Most frequent is simply a full stomach. There are some foods/substances that can cause this such as nicotine, alcohol, caffiene, and some spices. There is some speculation that it can be induced by stress, but this link has not been demonstrated. The cause? It just happens. Some people are genetically prone to it. In your case, I would suspect that GERD runs in the family. HMc

Response:

– Hide quoted text — Show quoted text ->The mechanism behind TILESR’s is that the LES inappropriately get a signal >to relax. There are several things that can initiate this. Most frequent is >simply a full stomach. There are some foods/substances that can cause this >such as nicotine, alcohol, caffiene, and some spices. There is some >speculation that it can be induced by stress, but this link has not been >demonstrated. >The cause? It just happens. Some people are genetically prone to it. In your >case, I would suspect that GERD runs in the family. > A hiatal hernia will exaggerate them, also.

Actually, a hiatus hernia would affect LES resting pressure, but usually wouldn’t contribute to inappropriate LES relaxation. The latter are neurally mediated. Here are the basics: The LES is the barrier between the stomach and esophagus. Reflux occurs when intragastric pressure exceeds intraesophageal pressure, and when that pressure gradient is greater than the pressure of the LES. Therefore, anything that increases that gradient might promote reflux. Also, anything that causes lower pressure in the LES would facilitate reflux (at lower pressure gradients). Obese people (and pregnant people) have higher intrabdominal pressure due to the intrabdominal fat (baby), so that gradient is greater, more likely to exceed the LES pressure and cause reflux. That intrabdominal pressure goes even higher when that person bends over. When lying down, gravity now has no contribution to the pressure gradient. So reflux is more common when lying down, or when bending over. Additionally, some people (fat or thin) have a low LES resting pressure, so that pressure gradient between stomach and esophagus needs to be less for reflux to occur. And, some people have more active transient LES relaxation in response to full stomach, nicotine, alcohol etc. So, you could be a thin person, but have a low LES resting pressure (such as with hiatus hernia), or very active TLESR’s and get bad reflux. It is more common in obese people because of their higher intrabdominal pressure. And, it’s also true that the intrabdominal fat can push upward and aggravate a tendency to hiatus hernia, which in turn can lead to lower LES pressure, which in turn can lead to reflux. So, how do we cure GERD? (CURE, not just treat the symptoms with prilosec). We either have to lower intrabdominal pressure, increase LES pressure, or stop the TLESR’s. Or any combination of the three. If an obese person with GERD loses a lot of weight, their intrabdominal pressure goes down and their GERD will very likely go away. This is one reason why obesity surgery cures GERD. If a person with GERD has a Nissen fundoplication, that will increase the resting LES pressure and splint its relaxations, and GERD is cured. If a person with GERD has a Stretta procedure, that will increase LES pressure, AND it will ablate afferent nerve fibers that contribute to TLESR’s, and the GERD is cured. Medical antisecretory treatment only decreases the amount of acid present in the stomach. It doesn’t stop the reflux. In fact, reflux still occurs, but the refluxate is highly alkaline. This alkaline reflux doesn’t cause symptoms, but still has the capacity to severely damage the esophagus over time (Barrett’s esophagus). Medical treatment may very well not do anything to lower the risk of esophageal cancer. As I have said before, symptom management with antisecretory medication may be entirely appropriate if it   a) controls the symptoms to the patient’s satisfaction, and     b) there is not evidence of  Barrett’s esophagus. HMc

Response:

- Hide quoted text — Show quoted text – > Obesity is a very substantial contributing factor to GERD. Since obesity is > so rampantly epidemic here in the US, it’s not surprising that GERD is too. > Likewise, there is some correlation between lower incidence of GERD and > lower incidence of obesity in countries where the amount and type of food is > less obesity-inducing. > Diet does not cause GERD. GERD is caused by a dysfunctional lower esophageal > sphincter. That dysfunction causing reflux symptoms is exacerbated by the > increased intraabdominal pressure associated with obesity. > So, to the extent that diet contributes to obesity, GERD is indeed > diet -associated, and the classic American diet definitely makes it more > common in the US. > HMc

Thanks for the reply. I had not considered the link between obesity and Gerd as I am not overweight (probably closer to underweight) So what originally causes the lower esophageal sphincter to not function correctly? It seems strange to me that all of a sudden one’s LES can stop working correctly (as was the case with me…out of the blue one day a year ago) In my case, I am not overweight. I am realtively young(23). I do not smoke or drink. I never eat fast food, or fatty foods. I dont eat chocolate…or candy…etc The only meats that I eat are chicken and fish. but…I have had problems with stress in the past. Is it possible for stress alone  to cause the LES to not function correctly? thanks, Mark

Response:

Does anyone have any info on what countries have what incidence rates for GERD (not sure if I am wording this correctly). I remember reading somewhere that in Africa for instance GERD is pretty rare… It would be interesting to take a look at countries where GERD is relatively rare, and see if the native diet has anything to do with it… Mark

Response:

> Does anyone have any info on what countries have what incidence rates > for GERD (not sure if I am wording this correctly). I remember reading > somewhere that in Africa for instance GERD is pretty rare… > It would be interesting to take a look at countries where GERD is > relatively rare, and see if the native diet has anything to do with > it…

Obesity is a very substantial contributing factor to GERD. Since obesity is so rampantly epidemic here in the US, it’s not surprising that GERD is too. Likewise, there is some correlation between lower incidence of GERD and lower incidence of obesity in countries where the amount and type of food is less obesity-inducing. Diet does not cause GERD. GERD is caused by a dysfunctional lower esophageal sphincter. That dysfunction causing reflux symptoms is exacerbated by the increased intraabdominal pressure associated with obesity. So, to the extent that diet contributes to obesity, GERD is indeed diet -associated, and the classic American diet definitely makes it more common in the US. HMc

Response:

increasingly worse gastric reflux

Aciphex is a medication used to treat gestational acid reflux disease (GERD) and ulcers. Buy aciphex medication and feel better today!

Question:

> Alot of doctors suggest that peptic ulcers are caused by H pylori. Alot of > pharmaceutical companies dont really care. Antacids are big business.

Peptic ulcers have nothing to do with acid reflux, which is the cause of most "heartburn". Helicobacter pylori is indeed the cause of about 70% of peptic ulcers, but H pylori has nothing to do with acid reflux either. Antacids are indeed big business. But how do you think H. pylori-mediated peptic ulcers are treated? With anti-secretory medication (Prevacid, Prilosec, Zantac, Tagamet etc etc) and antibiotics (which the pharmaceutical companies also make, right?). Just treating with antibiotics alone doesn’t work. In fact, TAP Pharmaceuticals (makers of Prevacid) also markets a standard treatment for H pylori-mediated peptic ulcers called PrevPac, which is a single package that contains Prevacid and an antibiotic. Look at http://tinyurl.com/lq0l HMc

Response:

– Hide quoted text — Show quoted text -> Alot of doctors suggest that peptic ulcers are caused by H pylori. Alot of > pharmaceutical companies dont really care. Antacids are big business. > Peptic ulcers have nothing to do with acid reflux, which is the cause of > most "heartburn". > Helicobacter pylori is indeed the cause of about 70% of peptic ulcers, but H > pylori has nothing to do with acid reflux either. > Antacids are indeed big business. But how do you think H. pylori-mediated > peptic ulcers are treated? With anti-secretory medication (Prevacid, > Prilosec, Zantac, Tagamet etc etc) and antibiotics (which the pharmaceutical > companies also make, right?). Just treating with antibiotics alone doesn’t > work.

I have worked with some top notch doctors that beg to differ outside of their practice. A simple over the counter antacid can work just fine while treating it with anti biotics. Yes pharaceutical companies sell the antibiotics, but do you think they push the antibiotic for the treatment? How many doctors do you know suggest using the antibiotic to treat the ulcer? ALMOST NONE in the USA. WHY? Because there arent the big kickbacks they can get by continually prescribing antacids. I amnot suggesting the doctor is willfully trying to hurt the person but they see through green colored glasses sometimes… > In fact, TAP Pharmaceuticals (makers of Prevacid) also markets a standard > treatment for H pylori-mediated peptic ulcers called PrevPac, which is a > single package that contains Prevacid and an antibiotic. Look at > http://tinyurl.com/lq0l

I will check that out. If that is what they are doing then bravo! – Hide quoted text — Show quoted text -> HMc

Response:

> Hmm…haven’t tried raisins lately.  Have to see if I can handle those; I > don’t guess they should be bad.  Haven’t tried the tums smooth dissolve yet. > I’ve used a lot of maalox max, though, and it seems to work well.

Try some tums smooth disolve if you get the chance. One of > the nice things about the liquid is that you can keep it in the fridge, and > the cold is nice.

Is the Malox mint flavored?  I also have a "GI cocktail," which is a prescription mix > of mylanta, benadryl, a numbing agent, and something else I can’t remember > right off.

Yeah a purple lady like they give in the doctors office for peptic ulcers. I am about to try something called active Manuka honey for my peptic ulcers which has an abundance of anti bacterial and anti oxidents in it. It is all natural but better than origonal honey. They use it in Australia for peptic ulcers and even doctors suggest it commonly. So I figure its not worth hurting to take a chance. Alot of doctors suggest that peptic ulcers are caused by H pylori. Alot of pharmaceutical companies dont really care. Antacids are big business. It litterally numbs your GI tract from the back of your tongue > down.  I’ve hardly had to use it since I’ve been on the AcipHex, though. > Maybe I’ll get some of those tums to have something I can keep in my

pocket. As I said they gave me a purple lady at the hospital… Great for an all out attack. I have been trying to limit my antacid intake to only when i really need it. I have been trying an all pure diet. It seems to be helping. Less meats and stuff help. – Hide quoted text — Show quoted text -> > I’ve basically given up on fruit and fruit juice, except for bananas > when > > I’m having particularly bad stomach problems.  Those don’t really help, > but > > they’re about the only thing that doesn’t taste too bad coming back up. > :- > Well let me tell you something. Rasins are high in anti oxidents so I eat > them. I have no problem with them. I eat dole fruit cups for breakfast. It > all depends on your stomach though. > BTW have you tried tums smooth disolve? Seems to work with me. > > > > Tomatoes are ‘acidy’ do you find any problems with apples or citrus > > > fruits? > > > > Derek. > > > I dont find any problems with fresh citrus fruits like oranges or > anything > > > like that, but grapefruit yes, and an obvious yes to lemon or lime…. > > > Orange Juice is an obvious dont drink… > > > Choclate is very acidic… Mint should not be eaten either because it > > > relaxes the sphincter muscle which shouldnt be relaxed…. > > > > > Hey, just like to say that AcipHex has been a miracle drug for my > > GERD. > > > > One > > > > > pill every morning, and I’ve gone from sleeping a few hours in a > > > recliner > > > > > because of the pain when I’d lie down to having only minor > discomfort > > > once > > > > a > > > > > week or so.  Might be worth asking your doctor about.  Also, and > this > > is > > > a > > > > > little odd, avoiding tomato products seems to help.  Something > about > > > > tomatos > > > > > can really irritate GERD. > > > > > Hope you and your son feel better. > > > > > Mike > > > > > > > It can feel like it is your heart but you have classic > symptoms > of > > > > > gerd… > > > > > > > gerd can feel like a heart problem when it isnt… this > ofcourse > > can > > > > > give > > > > > > > you panic attack feelings… and anxiety… or the gerd can be > > > caused > > > > by > > > > > > > anxiety… > > > > > > > any questions > > > > > > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > > > > > > Anyway, thanks for replying…. > > > > > > Yeah..it is gerd by the looks of it. Although my doctor now > thinks > I > > > may > > > > > > have an ulcer as well. > > > > > > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty > food > > > has > > > > > > made a difference. The pain in my stomach is worse and I have > been > > > given > > > > > an > > > > > > a strong ant  acid and an anaesthetic suspension to take > together > > to > > > > ease > > > > > > the discomfort. What are your symptoms, does it get any better? > It > > > seems > > > > > > stress does indeed  makes it worse…. > > > > > > I was meant to go for an endoscopy but my son has been in > hospital > ( > > > > > > recently diagnosed with juvenile diabetes) so life has been > > incredibly > > > > > > hectic…..

Response:

Hmm…haven’t tried raisins lately.  Have to see if I can handle those; I don’t guess they should be bad.  Haven’t tried the tums smooth dissolve yet. I’ve used a lot of maalox max, though, and it seems to work well.  One of the nice things about the liquid is that you can keep it in the fridge, and the cold is nice.  I also have a "GI cocktail," which is a prescription mix of mylanta, benadryl, a numbing agent, and something else I can’t remember right off.  It litterally numbs your GI tract from the back of your tongue down.  I’ve hardly had to use it since I’ve been on the AcipHex, though. Maybe I’ll get some of those tums to have something I can keep in my pocket.

– Hide quoted text — Show quoted text -> I’ve basically given up on fruit and fruit juice, except for bananas when > I’m having particularly bad stomach problems.  Those don’t really help, > but > they’re about the only thing that doesn’t taste too bad coming back up. > :- > Well let me tell you something. Rasins are high in anti oxidents so I eat > them. I have no problem with them. I eat dole fruit cups for breakfast. It > all depends on your stomach though. > BTW have you tried tums smooth disolve? Seems to work with me. > > > Tomatoes are ‘acidy’ do you find any problems with apples or citrus > > fruits? > > > Derek. > > I dont find any problems with fresh citrus fruits like oranges or > anything > > like that, but grapefruit yes, and an obvious yes to lemon or lime…. > > Orange Juice is an obvious dont drink… > > Choclate is very acidic… Mint should not be eaten either because it > > relaxes the sphincter muscle which shouldnt be relaxed…. > > > > Hey, just like to say that AcipHex has been a miracle drug for my > GERD. > > > One > > > > pill every morning, and I’ve gone from sleeping a few hours in a > > recliner > > > > because of the pain when I’d lie down to having only minor > discomfort > > once > > > a > > > > week or so.  Might be worth asking your doctor about.  Also, and > this > is > > a > > > > little odd, avoiding tomato products seems to help.  Something about > > > tomatos > > > > can really irritate GERD. > > > > Hope you and your son feel better. > > > > Mike > > > > > > It can feel like it is your heart but you have classic symptoms > of > > > > gerd… > > > > > > gerd can feel like a heart problem when it isnt… this ofcourse > can > > > > give > > > > > > you panic attack feelings… and anxiety… or the gerd can be > > caused > > > by > > > > > > anxiety… > > > > > > any questions > > > > > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > > > > > Anyway, thanks for replying…. > > > > > Yeah..it is gerd by the looks of it. Although my doctor now thinks > I > > may > > > > > have an ulcer as well. > > > > > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty > food > > has > > > > > made a difference. The pain in my stomach is worse and I have been > > given > > > > an > > > > > a strong ant  acid and an anaesthetic suspension to take together > to > > > ease > > > > > the discomfort. What are your symptoms, does it get any better? It > > seems > > > > > stress does indeed  makes it worse…. > > > > > I was meant to go for an endoscopy but my son has been in hospital > ( > > > > > recently diagnosed with juvenile diabetes) so life has been > incredibly > > > > > hectic…..

Response:

> I’ve basically given up on fruit and fruit juice, except for bananas when > I’m having particularly bad stomach problems.  Those don’t really help, but > they’re about the only thing that doesn’t taste too bad coming back up.

:- Well let me tell you something. Rasins are high in anti oxidents so I eat them. I have no problem with them. I eat dole fruit cups for breakfast. It all depends on your stomach though. BTW have you tried tums smooth disolve? Seems to work with me. – Hide quoted text — Show quoted text -> > Tomatoes are ‘acidy’ do you find any problems with apples or citrus > fruits? > > Derek. > I dont find any problems with fresh citrus fruits like oranges or anything > like that, but grapefruit yes, and an obvious yes to lemon or lime…. > Orange Juice is an obvious dont drink… > Choclate is very acidic… Mint should not be eaten either because it > relaxes the sphincter muscle which shouldnt be relaxed…. > > > Hey, just like to say that AcipHex has been a miracle drug for my > GERD. > > One > > > pill every morning, and I’ve gone from sleeping a few hours in a > recliner > > > because of the pain when I’d lie down to having only minor discomfort > once > > a > > > week or so.  Might be worth asking your doctor about.  Also, and this > is > a > > > little odd, avoiding tomato products seems to help.  Something about > > tomatos > > > can really irritate GERD. > > > Hope you and your son feel better. > > > Mike > > > > > It can feel like it is your heart but you have classic symptoms of > > > gerd… > > > > > gerd can feel like a heart problem when it isnt… this ofcourse > can > > > give > > > > > you panic attack feelings… and anxiety… or the gerd can be > caused > > by > > > > > anxiety… > > > > > any questions > > > > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > > > > Anyway, thanks for replying…. > > > > Yeah..it is gerd by the looks of it. Although my doctor now thinks I > may > > > > have an ulcer as well. > > > > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food > has > > > > made a difference. The pain in my stomach is worse and I have been > given > > > an > > > > a strong ant  acid and an anaesthetic suspension to take together > to > > ease > > > > the discomfort. What are your symptoms, does it get any better? It > seems > > > > stress does indeed  makes it worse…. > > > > I was meant to go for an endoscopy but my son has been in hospital ( > > > > recently diagnosed with juvenile diabetes) so life has been > incredibly > > > > hectic…..

Response:

I’ve basically given up on fruit and fruit juice, except for bananas when I’m having particularly bad stomach problems.  Those don’t really help, but they’re about the only thing that doesn’t taste too bad coming back up.  :-

– Hide quoted text — Show quoted text -> Tomatoes are ‘acidy’ do you find any problems with apples or citrus > fruits? > Derek. > I dont find any problems with fresh citrus fruits like oranges or anything > like that, but grapefruit yes, and an obvious yes to lemon or lime…. > Orange Juice is an obvious dont drink… > Choclate is very acidic… Mint should not be eaten either because it > relaxes the sphincter muscle which shouldnt be relaxed…. > > Hey, just like to say that AcipHex has been a miracle drug for my GERD. > One > > pill every morning, and I’ve gone from sleeping a few hours in a > recliner > > because of the pain when I’d lie down to having only minor discomfort > once > a > > week or so.  Might be worth asking your doctor about.  Also, and this is > a > > little odd, avoiding tomato products seems to help.  Something about > tomatos > > can really irritate GERD. > > Hope you and your son feel better. > > Mike > > > > It can feel like it is your heart but you have classic symptoms of > > gerd… > > > > gerd can feel like a heart problem when it isnt… this ofcourse can > > give > > > > you panic attack feelings… and anxiety… or the gerd can be > caused > by > > > > anxiety… > > > > any questions > > > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > > > Anyway, thanks for replying…. > > > Yeah..it is gerd by the looks of it. Although my doctor now thinks I > may > > > have an ulcer as well. > > > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food > has > > > made a difference. The pain in my stomach is worse and I have been > given > > an > > > a strong ant  acid and an anaesthetic suspension to take together to > ease > > > the discomfort. What are your symptoms, does it get any better? It > seems > > > stress does indeed  makes it worse…. > > > I was meant to go for an endoscopy but my son has been in hospital ( > > > recently diagnosed with juvenile diabetes) so life has been incredibly > > > hectic…..

Response:

> Tomatoes are ‘acidy’ do you find any problems with apples or citrus fruits? > Derek.

I dont find any problems with fresh citrus fruits like oranges or anything like that, but grapefruit yes, and an obvious yes to lemon or lime…. Orange Juice is an obvious dont drink… Choclate is very acidic… Mint should not be eaten either because it relaxes the sphincter muscle which shouldnt be relaxed…. – Hide quoted text — Show quoted text -> Hey, just like to say that AcipHex has been a miracle drug for my GERD. > One > pill every morning, and I’ve gone from sleeping a few hours in a recliner > because of the pain when I’d lie down to having only minor discomfort once > a > week or so.  Might be worth asking your doctor about.  Also, and this is a > little odd, avoiding tomato products seems to help.  Something about > tomatos > can really irritate GERD. > Hope you and your son feel better. > Mike > > > It can feel like it is your heart but you have classic symptoms of > gerd… > > > gerd can feel like a heart problem when it isnt… this ofcourse can > give > > > you panic attack feelings… and anxiety… or the gerd can be caused > by > > > anxiety… > > > any questions > > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > > Anyway, thanks for replying…. > > Yeah..it is gerd by the looks of it. Although my doctor now thinks I may > > have an ulcer as well. > > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food has > > made a difference. The pain in my stomach is worse and I have been given > an > > a strong ant  acid and an anaesthetic suspension to take together  to > ease > > the discomfort. What are your symptoms, does it get any better? It seems > > stress does indeed  makes it worse…. > > I was meant to go for an endoscopy but my son has been in hospital ( > > recently diagnosed with juvenile diabetes) so life has been incredibly > > hectic…..

Response:

Hey, just like to say that AcipHex has been a miracle drug for my GERD.  One pill every morning, and I’ve gone from sleeping a few hours in a recliner because of the pain when I’d lie down to having only minor discomfort once a week or so.  Might be worth asking your doctor about.  Also, and this is a little odd, avoiding tomato products seems to help.  Something about tomatos can really irritate GERD. Hope you and your son feel better. Mike

– Hide quoted text — Show quoted text -> It can feel like it is your heart but you have classic symptoms of gerd… > gerd can feel like a heart problem when it isnt… this ofcourse can give > you panic attack feelings… and anxiety… or the gerd can be caused by > anxiety… > any questions > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > Anyway, thanks for replying…. > Yeah..it is gerd by the looks of it. Although my doctor now thinks I may > have an ulcer as well. > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food has > made a difference. The pain in my stomach is worse and I have been given an > a strong ant  acid and an anaesthetic suspension to take together  to ease > the discomfort. What are your symptoms, does it get any better? It seems > stress does indeed  makes it worse…. > I was meant to go for an endoscopy but my son has been in hospital ( > recently diagnosed with juvenile diabetes) so life has been incredibly > hectic…..

Response:

Tomatoes are ‘acidy’ do you find any problems with apples or citrus fruits? Derek.

– Hide quoted text — Show quoted text -> Hey, just like to say that AcipHex has been a miracle drug for my GERD. One > pill every morning, and I’ve gone from sleeping a few hours in a recliner > because of the pain when I’d lie down to having only minor discomfort once a > week or so.  Might be worth asking your doctor about.  Also, and this is a > little odd, avoiding tomato products seems to help.  Something about tomatos > can really irritate GERD. > Hope you and your son feel better. > Mike > > It can feel like it is your heart but you have classic symptoms of > gerd… > > gerd can feel like a heart problem when it isnt… this ofcourse can > give > > you panic attack feelings… and anxiety… or the gerd can be caused by > > anxiety… > > any questions > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > Anyway, thanks for replying…. > Yeah..it is gerd by the looks of it. Although my doctor now thinks I may > have an ulcer as well. > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food has > made a difference. The pain in my stomach is worse and I have been given > an > a strong ant  acid and an anaesthetic suspension to take together  to ease > the discomfort. What are your symptoms, does it get any better? It seems > stress does indeed  makes it worse…. > I was meant to go for an endoscopy but my son has been in hospital ( > recently diagnosed with juvenile diabetes) so life has been incredibly > hectic…..

Response:

> It can feel like it is your heart but you have classic symptoms of gerd… > gerd can feel like a heart problem when it isnt… this ofcourse can give > you panic attack feelings… and anxiety… or the gerd can be caused by > anxiety… > any questions

Hey Douglas !! I see you on alt. religion Mormon..how are you??? Anyway, thanks for replying…. Yeah..it is gerd by the looks of it. Although my doctor now thinks I may have an ulcer as well. Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food has made a difference. The pain in my stomach is worse and I have been given an a strong ant  acid and an anaesthetic suspension to take together  to ease the discomfort. What are your symptoms, does it get any better? It seems stress does indeed  makes it worse…. I was meant to go for an endoscopy but my son has been in hospital ( recently diagnosed with juvenile diabetes) so life has been incredibly hectic…..

Response:

– Hide quoted text — Show quoted text -> It can feel like it is your heart but you have classic symptoms of gerd… > gerd can feel like a heart problem when it isnt… this ofcourse can give > you panic attack feelings… and anxiety… or the gerd can be caused by > anxiety… > any questions > Hey Douglas !! I see you on alt. religion Mormon..how are you??? > Anyway, thanks for replying…. > Yeah..it is gerd by the looks of it. Although my doctor now thinks I may > have an ulcer as well. > Wiping out  coffee from my diet  ( I weep!) and spicy and fatty food has > made a difference. The pain in my stomach is worse and I have been given an > a strong ant  acid and an anaesthetic suspension to take together  to ease > the discomfort. What are your symptoms, does it get any better? It seems > stress does indeed  makes it worse…. > I was meant to go for an endoscopy but my son has been in hospital ( > recently diagnosed with juvenile diabetes) so life has been incredibly > hectic…..

Well yes I am a "Mormon". I dont really go to the newsgroup anymore because so many bashers. Well yeah I figured you probablly had gerd, and peptic ulcers are usual with it. I am about to read a book soon called the PH miracle (you can get it on amazon for like 4 bucks). One lady who had the same symtpoms suggested it and said she is cured from her problems. I know her very well.. As far as the coffee and so forth is concerned the "Mormon" religion is really strict on dieting. For instance limiting the meats you eat, not drinking hot drinks, and staying away from any herb you dont need are just a few suggestions. I can only assume the reason this country has more problems with GERD than any other is because of the amount of chemicals and perservatives we take in. Caffine is horrible for the stomach, and especially sodas. I have gone back to a more pure diet involving fruits, grains, and very little meat. I have noticed some major changes but it will take time for my body to adapt…. I drink water and pure apple juice such as (langers). I figure not only will this cure my body from alot of illnesses but will give me longer life and less stress as it has shown so far. Will I miss foods? Sure but I can indulge everyonce in a blue moon. However I have learned to enjoy moderation more than I enjoyed the food. It is a hard habit to break but it can be done certainly.

Response:

– Hide quoted text — Show quoted text -> Hi all. > I have been having shocking reflux and stomach pain for over two years on > and off. > I went for an endoscopy eighteen months ago and was told I had very inflamed > stomach lining. No follow up. > All was fine for a while but a about five moths ago I felt like there was a > particle of food stuck in my throat ( after eating some spicy Thai food) I > went to a throat specialist who had a look and said my throat was irritated > due to reflux. Since then I have been getting increasingly worse reflux with > knife like pain under my breast bone. The pain radiated into my arm and > shoulder so my doctor ordered blood works and an ECG and of course did basic > obs.( pulse, BP and respiratory ) all normal. Yet I still get  a tad panicky > and think the pain is related to my heart even though the ECG was normal. > The pain on my left side ( under the ribs) is quite crippling at times and > when ever I bend over my reflux  gets much  worse.as does the pain in my > sternum and under the breast bone.My doctor palpated my stomach and said it > is extremely tender and has refereed me to a gastro specialist with the idea > to also do another endoscopy. Any one else here been through this?  Can you > tell me what to expect , is stress making it worse,any chance it is a cardio > vascular  thing?Can anxiety exacerbate   the  symptoms? > Much obliged for any replies……. > Helen

It can feel like it is your heart but you have classic symptoms of gerd… gerd can feel like a heart problem when it isnt… this ofcourse can give you panic attack feelings… and anxiety… or the gerd can be caused by anxiety… any questions

Response:

Hi all. I have been having shocking reflux and stomach pain for over two years on and off. I went for an endoscopy eighteen months ago and was told I had very inflamed stomach lining. No follow up. All was fine for a while but a about five moths ago I felt like there was a particle of food stuck in my throat ( after eating some spicy Thai food) I went to a throat specialist who had a look and said my throat was irritated due to reflux. Since then I have been getting increasingly worse reflux with knife like pain under my breast bone. The pain radiated into my arm and shoulder so my doctor ordered blood works and an ECG and of course did basic obs.( pulse, BP and respiratory ) all normal. Yet I still get  a tad panicky and think the pain is related to my heart even though the ECG was normal. The pain on my left side ( under the ribs) is quite crippling at times and when ever I bend over my reflux  gets much  worse.as does the pain in my sternum and under the breast bone.My doctor palpated my stomach and said it is extremely tender and has refereed me to a gastro specialist with the idea to also do another endoscopy. Any one else here been through this?  Can you tell me what to expect , is stress making it worse,any chance it is a cardio vascular  thing?Can anxiety exacerbate   the  symptoms? Much obliged for any replies……. Helen

Response:

Surgery for GERD

Esomeprazole is a medication used to treat gestational acid reflux disease (GERD). Buy esomeprazole drug and feel better today!

Question:

> I just recently switch doctors (about 6 months ago) over the last 5 years I > have been switch from one drug to the other, now nothing is working and I am > continually having heartburn.  My current doctor placed me back on Aciphex > and sugested that I give it a try for 3-4 weeks and if I do not get relief > then I should start to consider surgery.  I am currenlty not only > experiancing the heartburn but get acid and food backup whenever I bend > over, anytime…….  I am only 38 years old, slightly overwight (+20 lbs),

In my case, I found that the "lose some weight, even a few pounds" advice from my MD was also advice that helped a *lot*.  Losing 5lbs greatly reduced my GERD problems (and I was not, and am not, even close to being overweight: 5′10" and 160 lbs). — Richard W Kaszeta http://www.kaszeta.org/rich

Response:

Not had it done myself but know of someone that has had the fundoplication procedure done and is very happy with the results e.g. eats what she wants when she wants. I think everyone has a different way of dealing with GERD, for me it was to loose some weight, watch my diet, try to get a handle on what I can eat and what I can’t and  get some type of regular exercise. I still have events but they  are minor and can be controlled with a little Mylanta. (well most times). I am on 1x 40mg of Somac (pantoprazole) / day. If you don’t have a motility problem and at 38 y/o it sound like you are a good candidate for for surgery. Have you had a Acid PH and Motilty study done? Casey

Response:

I have not had the PH test nor the Motility tests done, I understand what the PH test does but I am not quite sure what the motility test does?  Now that I think about it, awhile ago I went in and had several tests taken where I drank some stuff and they took pictures as I swallowed, then I drank some fizzy stuff and they took more pictures to see the reflux.  They also took pictures of my upper GI.  I have never had any problems swallowing or have never had any feeling of unswallowed food, quite the opposite, if I even bend over slightly after eating I will reflux my meal back into my throat and mouth.  I would like to be able to exercise without that fear! Thanks Rob

– Hide quoted text — Show quoted text -> Not had it done myself but know of someone that has had the fundoplication > procedure done and is very happy with the results e.g. eats what she wants > when she wants. > I think everyone has a different way of dealing with GERD, for me it was to > loose some weight, watch my diet, try to get a handle on what I can eat and > what I can’t and  get some type of regular exercise. > I still have events but they  are minor and can be controlled with a little > Mylanta. (well most times). > I am on 1x 40mg of Somac (pantoprazole) / day. > If you don’t have a motility problem and at 38 y/o it sound like you are a > good candidate for for surgery. > Have you had a Acid PH and Motilty study done? > Casey

Response:

Hi Rob Sound like you had a Barium Swallow and X-rays done. PH and Motility study requires a small tube down the throat into the oesophagus area (via the nose). The first is the Motility and you are required to swallow water and the motility is recorded on a machine. The second tube, PH (fitted straight after the first is removed) is left there for 24 hours and has a monitor attached to you belt (or on a harness). You are able to do all you normal activities in this time (within reason of course). The monitor has an "event" button on it so that if you have some reflux and or regurgitating you the press this button and the event is "flagged" as need to be looked at. This monitor record the whole 24 hours (not just the events) and is removed after that. I had no trouble with this procedure at all and only felt a little discomfort. The motility study is required if you oft for the surgery (determines the amount of tightness they set the sphincter).  Hope this is some help. Cheers Casey P.S. Motility is the natural rhythm of the oesophagus to move food down to the stomach. <snip>

– Hide quoted text — Show quoted text -> I have not had the PH test nor the Motility tests done, I understand what

Response:

When was the last time you have had a total checkup and especially a check internally.  I have not had the surgery, but have heard that if it is needed it is needed.  Dumb statement but true.

– Hide quoted text — Show quoted text -> Just wondering if anyone has undergone the surgery to correct GERD.  I have > been on medication for numerous years and they have all stopped working. If > anyone has undergone the surgery could you post your experiances?? > Thanks > Rob

Response:

I just recently switch doctors (about 6 months ago) over the last 5 years I have been switch from one drug to the other, now nothing is working and I am continually having heartburn.  My current doctor placed me back on Aciphex and sugested that I give it a try for 3-4 weeks and if I do not get relief then I should start to consider surgery.  I am currenlty not only experiancing the heartburn but get acid and food backup whenever I bend over, anytime…….  I am only 38 years old, slightly overwight (+20 lbs), have migranes and glaucoma. I have been on: Priolosec, Previced, Aciphex, Nexium……. Thanks Rob

– Hide quoted text — Show quoted text -> When was the last time you have had a total checkup and especially a check > internally.  I have not had the surgery, but have heard that if it is needed > it is needed.  Dumb statement but true. > Just wondering if anyone has undergone the surgery to correct GERD.  I > have > been on medication for numerous years and they have all stopped working. > If > anyone has undergone the surgery could you post your experiances?? > Thanks > Rob

Response:

Just wondering if anyone has undergone the surgery to correct GERD.  I have been on medication for numerous years and they have all stopped working.  If anyone has undergone the surgery could you post your experiances?? Thanks Rob

Response:

> Just wondering if anyone has undergone the surgery to correct GERD.  I have > been on medication for numerous years and they have all stopped working.  If > anyone has undergone the surgery could you post your experiances??

Sure, I had a Nissen Fundoplication done in ‘01.  Here’s the short version: 1. Prior to the surgery, I was almsot completely unresponsive to medication (including Zantac, Prevacid, and Prilosec), and was recommended for a Nissen. 2. Had the nissen, which went fairly well except for a rather nasty bout of crepitus (trapped air under the skin) after surgery. 3. For about 3 weeks after the surgery, I couldn’t swallow anything solid, but then regained the ability to swallow.  Alas, at that time my GERD symptoms reappeared. 4. However, post-Nissen I have been a *lot* more responsive to medication, and am currently taking Nexium 2x a day, and an occasional Zantac prior to going to bed, and have regained a more or less normal life. — Richard W Kaszeta http://www.kaszeta.org/rich

Response:

Fish Oil Capsule's

Question:

This post not CC’d by email >This post not CC’d by email >>http://www.usnews.com/usnews/issue/021202/usnews/2week.lede.htm >>Check labels to make sure you’re getting 1,000 mg of DHA and EPA fatty >>acids. To avoid a fishy aftertaste, keep the gel tabs in the freezer, >>and take them at bedtime. >G’day G’day, Quenten >I forgot to ask you my original question for making the posting.  What >do you think about freezing get capsules, like fish oil and Vitamin E? >Not for odor, but, for freshness.

G’day G’day,  That is one question I can answer simply.   I don’t know. Fish oil capsules come with an expiry date. I simply look at that and buy the ones with the longest time to go.  In hot climates it probably makes sense to keep them in the fridge. People do a lot of worrying about oxidation.  Where temperatures are low and the fish oil high grade such oxidation as does occur might even be beneficial.  Part of the reason I say I don’t know is because things aren’t always simple and obvious. BTW.  One caveat I should have added to my previous post is to consult with your doctor/GP when taking high doses of fish oil.  So many people are on so many meds these days that few people are well represented in all respects by the sort of averages dealt with in studies. Best wishes, — Quentin Grady       ^  ^  / New Zealand,       >#,#< [                     / /     "… and the blind dog was leading." http://homepages.paradise.net.nz/quentin

Response:

This post not CC’d by email >http://www.usnews.com/usnews/issue/021202/usnews/2week.lede.htm >Check labels to make sure you’re getting 1,000 mg of DHA and EPA fatty >acids. To avoid a fishy aftertaste, keep the gel tabs in the freezer, >and take them at bedtime.

G’day G’day,  Most fish oil tablets contain 1000 mg of refined fish oil containing 180 mg of EPA and 120 mg of DHA.  Some tablets provide more either by having 1200 mg of refined fish oil or by increasing the concentration of EPA and DHA by further distillation. As with many news articles the science gets a bit garbled.  To get 1000 mg of DHA and EPA one would have to have sufficient fish oil to get 1000 mg of DHA since it is the one in the lesser amount.  Well … to get over 1000 mg would take nine of the standard size capsules. The after taste is avoided by buying a brand that has an enteric coat. They label describes them as reflux free. Though it is probably irrelevant to anyone else I am currently taking five a day. My lipid profiles are normal and I have little incentive to do more or less.  The containers suggests three. >Hey Quentin, does a tsp of cod liver oil have the same cholesterol >busting abilities as fish oil capsules?

Barry Sears puts 4 capsules of pharmaceutical grade fish oil as equivalent to 1 TABLESPOON of cod liver oil. Interestingly he makes the following suggestion if one’s TG:HDL ratio is less than 2 using US mg/100ml units (0.9 on mmol/L units), then ones diet should contain 2.5 grams of long-chain omega-3 per day.   Notice that he is lumping EPA and DHA together.       1 gram fish oil -> 0.3 gram of long chain omega-3       ? gram fish oil -> 2.5 gram of long chain omega-3 To solve the direct proportionality, two numbers must be multiplied and the third one divided.  Use the one on the diagonal for division. (1 x 2.5) / 0.3 = 8.3 capsules.   OK so to meet Barry Sears recommendation one is back to nine capsules per day if one doesn’t have other source of long chain omega-3s in one’s diet.   But wait … brace yourself. If your triglyceride:HDL is greater than 2 (US) or 0.9 (others) then one is meant to take double that dose for a month.  That is eighteen capsules per day. Well what could be wrong with that?   <grin> Firstly one needs to increase the dosage of active oils slowly. Secondly we are talking 18 grams of fat = 162 Calories.   Basically adding calories isn’t usually the most successful strategy. Put simply one has to take out fat calories from somewhere else. That 162 grams is 9% of one’s calorie intake on a 1800 Calorie per day diet. Remembering that the ADA suggested maximum calories from fat is 30%, about one third of one’s fat intake from other sources has to go. Thirdly readers here are mostly diabetics, many of them T2s.  T2s are notorious for having high TG:HDL ratios so much so that is makes an excellent marker for insulin resistance, the hallmark of the condition. If one simply adds fats bumping up calorie intake then blood glucose levels are likely also to rise. If one REPLACES other fats with long chain omega-3s then this problem usually doesn’t arise. Still YMMV and it does with fish oil supplementation.  Some people find their blood glucose control improves and some that it worsens. The average seems to stay unchanged but hey, who is average around here. If you embark on taking fish oil supplementation then do what you always do TEST, TEST, TEST. Hope this helps. With the AHA recommending fish oil, I’ll have to run a little harder to stay ahead of the game. <grin> — Quentin Grady       ^  ^  / New Zealand,       >#,#< [                     / /     "… and the blind dog was leading." http://homepages.paradise.net.nz/quentin

Response:

Personal preference

Question:

From Guy Williams I was put on metaformin and it was a disaster.  It has since been proven that it was not needed.  It was a combination ignorance of it’s action and a speil be a drug salesmen. It is indicated in many cases, but this should NOT be WAG decision. Like ALL drugs it has pluses and minuses.  Any drug  should be used with good reasons.   Most drugs harm someone. Anyone that had a job where productivity is their job requirement should not be expected to publicize the negatives of their product.

Response:

– Hide quoted text — Show quoted text -> From Guy Williams > I was put on metaformin and it was a disaster.  It has > since been proven that it was not needed.  It was > a combination ignorance of it’s action and a speil > be a drug salesmen. > It is indicated in many cases, but this should NOT be > WAG decision. > Like ALL drugs it has pluses and minuses.  Any > drug  should be used with good reasons.   Most > drugs harm someone. > Anyone that had a job where productivity is their > job requirement should not be expected to publicize > the negatives of their product.

I also had a very nasty experience with metformin. It is still being urged on me by well meaning doctors. The account of my experience is viewed with suspicion. My only defence is a stubborn refusal to ever use this medication again. Annette

Response:

>It is still being urged on me by well meaning doctors. The account >of my experience is viewed with suspicion. >My only defence is a stubborn refusal to ever use this medication >again.

Annette, I feel the same way about Actos.  Even though my blood sugar was EXCELLENT with Actos, I’m convinced  the side effects themselves would have killed me eventually.   First visit with a new PCP last year, she said, "I’m thinking about Actos for you."  I told her not to bother, I wouldn’t be taking that again anytime soon, after experiencing a rapid weight gain of 30lbs, constant pressure in my head, feeling unable to breathe, and pitted edema so bad I sprang a leak that wouldn’t dry up till I abruptly quit taking the Actos and went on Lasix. My experience with Avandia wasn’t much better, although the side effects were limited to edema, a 20lb weight gain and frequent headaches. Glucophage is my only reasonable option at this point.  I cannot exceed 850mg regular Glucophage per day, or I become ill.  I cannot take Glucophage XR at all, as it seems to cause me MORE gastric upset, (heartburn, nausea) than the regular. My husband is on XR, and has had pretty good results with it.  I don’t know why it doesn’t work for me.  I just consider myself lucky that I can now buy generic metformin at a cheaper copay……lol.. Bev Remove the "SpamFree" for email, please.  

Response:

In my opinion for the many that glucophage has an adverse affect, I feel that the scale towards the postiive aspects of this drug outweigh the negatives.  It is a case of YMMV  and for my mileage Glucophage is doing great.  I hope as I condinue to lose weight that I can reduce the amount of meds.  i have already reduced six mgs of amaryl. Loretta In tribute to the United States of America and the State of Israel, two bastions of strength in a world filled with strife and terrorism.

Response:

Eric's question – "What would you do without…."

Question:

Sorry, to restart a thread like this; I can’t find the continuity of the conversation last night.  I remembered something important regarding Eric’s question to me: "I wonder where you would be without your lithium Squiggles?" I remembered that some years back, when I was working, that I decided to quit the lithium. Within 2 months, I lost an awful lot of weight; so much so that people were wondering to me what kind of diet I was on.  But by the end of about 3 months, I remember I started getting very depressed and crying, and decided that it was not a good idea, and I went back on the lithium and felt OK. Was this depression a result of lithium withdrawal or the underlying depression coming through – this must be a perennial question right? Also, speaking of diets, I am on a practically NO carbohydrate diet – just protein – fish, chicken, beef, fruit, vegetables and cheese – all at small amounts through the day.  Does anyone know if NO carbs can lead to ketosis, because with my lithium that might be dangerous. Thanks all I hope to get to most of your posts today – will try. Squiggles

Response:

– Hide quoted text — Show quoted text -> Sorry, to restart a thread like this; > I can’t find the continuity of the conversation > last night.  I remembered something important > regarding Eric’s question to me: "I wonder where > you would be without your lithium Squiggles?" > I remembered that some years back, when I was > working, that I decided to quit the lithium. > Within 2 months, I lost an awful lot of weight; > so much so that people were wondering to me what > kind of diet I was on.  But by the end of about > 3 months, I remember I started getting very > depressed and crying, and decided that it was > not a good idea, and I went back on the lithium > and felt OK. > Was this depression a result of lithium withdrawal > or the underlying depression coming through – this > must be a perennial question right? > Also, speaking of diets, I am on a practically NO carbohydrate > diet – just protein – fish, chicken, beef, fruit, vegetables > and cheese – all at small amounts through the day.  Does > anyone know if NO carbs can lead to ketosis, because with > my lithium that might be dangerous. > Thanks all > I hope to get to most of your posts today – will try. > Squiggles

Hey Squiggles. The best correlate to your personal diet is the Zone series of books. They’d be at the library or Chapters, if you wanted to look through them. You could develop insulin resistance on this diet, but it’s probably less likely than on more typical carbohydrate diets. The best way to maintain insulin sensitivity is to make sure you get a good portion of omega-3 fatty acids. This only works, though, before the pancreas poops out. Regards, Larry

Response:

- Hide quoted text — Show quoted text -> Sorry, to restart a thread like this; > I can’t find the continuity of the conversation > last night.  I remembered something important > regarding Eric’s question to me: "I wonder where > you would be without your lithium Squiggles?" > I remembered that some years back, when I was > working, that I decided to quit the lithium. > Within 2 months, I lost an awful lot of weight; > so much so that people were wondering to me what > kind of diet I was on.  But by the end of about > 3 months, I remember I started getting very > depressed and crying, and decided that it was > not a good idea, and I went back on the lithium > and felt OK. > Was this depression a result of lithium withdrawal > or the underlying depression coming through – this > must be a perennial question right? > Also, speaking of diets, I am on a practically NO carbohydrate > diet – just protein – fish, chicken, beef, fruit, vegetables > and cheese – all at small amounts through the day.  Does > anyone know if NO carbs can lead to ketosis, because with > my lithium that might be dangerous. > Thanks all > I hope to get to most of your posts today – will try. > Squiggles > Hey Squiggles. The best correlate to your personal diet is the Zone series > of books. They’d be at the library or Chapters, if you wanted to look > through them. You could develop insulin resistance on this diet, but it’s > probably less likely than on more typical carbohydrate diets. The best way > to maintain insulin sensitivity is to make sure you get a good portion of > omega-3 fatty acids. This only works, though, before the pancreas poops out. > Regards, > Larry

Uhm, the ZONE diets – OK – I will look when I got Chapters, because I still want to get that book by David Healy – it is scholarly and likely not to be there though – maybe I will try Indigo down the street.  Yes, I know low carb diet has to do with insulin, but I am not diabetic – just overweight – I just thought that since the kidneys have to work overtime with lithium excretion that perhaps this is not the best diet for me.  But I think that it is precisly the ketosis that makes you lose, I don’t know.  I am willing to just follow something that will bring me back to size 10. Squiggles

Response:

– Hide quoted text — Show quoted text -> Hey Squiggles. The best correlate to your personal diet is the Zone series > of books. They’d be at the library or Chapters, if you wanted to look > through them. You could develop insulin resistance on this diet, but it’s > probably less likely than on more typical carbohydrate diets. The best way > to maintain insulin sensitivity is to make sure you get a good portion of > omega-3 fatty acids. This only works, though, before the pancreas poops out. > Regards, > Larry > Uhm, the ZONE diets – OK – I will look when I got Chapters, because > I still want to get that book by David Healy – it is scholarly > and likely not to be there though – maybe I will try Indigo down > the street.  Yes, I know low carb diet has to do with insulin, > but I am not diabetic – just overweight – I just thought that since > the kidneys have to work overtime with lithium excretion that perhaps > this is not the best diet for me.  But I think that it is precisly > the ketosis that makes you lose, I don’t know.  I am willing to > just follow something that will bring me back to size 10. > Squiggles

Ketosis occurs when the body is unable to burn glucose and other sugars for fuel, and instead turns to burning fats. On the surface, that seems desirable, but it’s generally not. In type 2 diabetes (adult onset), insulin resistance, and what is known as Syndrome X, glucose uptake is reduced or even absent because the insulin-dependent uptake of sugars across the cell membrane does not function properly. Cells then burn fats (and proteins to some extent) as energy sources. Poly-unsaturated fats do not burn "cleanly", as the unsaturated bonds oxidize to ketones. It’s not clear if it’s the high serum glucose content, or the increase in ketones in the blood, or both together, which lead to the neuropathies seen in diabetes and its related syndromes. Artificial ketogenic situations come in two flavours: the ketogenic diet, and fasting. A true ketogenic diet is low in both carbohydrate and protein calories, and derives most of its energy inputs from fats. This extreme situation has been found to help control treatment-unresponsive epilepsy. It’s not for most people. Fasting induces ketogenesis in healthy people after the body has depleted its stores of quickly available sugars. The liver retains a reserve in the form of glucagon (sp?) for emergency energy, and there are other resources within cells via anaerobic processes, but by and large, ketosis is a starvation process. It’s believed that episodic ketogenesis actually trains the body to store a higher proportion of fat than it otherwise would, which is counter-productive to your cause. I think the Zone series will give you good insight into what you’re trying to accomplish. I, too, rely on a high-protein, low-carb diet. I just do better that way. Regards, Larry

Response:

- Hide quoted text — Show quoted text -> > Hey Squiggles. The best correlate to your personal diet is the Zone > series > > of books. They’d be at the library or Chapters, if you wanted to look > > through them. You could develop insulin resistance on this diet, but > it’s > > probably less likely than on more typical carbohydrate diets. The best > way > > to maintain insulin sensitivity is to make sure you get a good portion > of > > omega-3 fatty acids. This only works, though, before the pancreas poops > out. > > Regards, > > Larry > Uhm, the ZONE diets – OK – I will look when I got Chapters, because > I still want to get that book by David Healy – it is scholarly > and likely not to be there though – maybe I will try Indigo down > the street.  Yes, I know low carb diet has to do with insulin, > but I am not diabetic – just overweight – I just thought that since > the kidneys have to work overtime with lithium excretion that perhaps > this is not the best diet for me.  But I think that it is precisly > the ketosis that makes you lose, I don’t know.  I am willing to > just follow something that will bring me back to size 10. > Squiggles > Ketosis occurs when the body is unable to burn glucose and other sugars for > fuel, and instead turns to burning fats. On the surface, that seems > desirable, but it’s generally not. > In type 2 diabetes (adult onset), insulin resistance, and what is known as > Syndrome X, glucose uptake is reduced or even absent because the > insulin-dependent uptake of sugars across the cell membrane does not > function properly. Cells then burn fats (and proteins to some extent) as > energy sources. Poly-unsaturated fats do not burn "cleanly", as the > unsaturated bonds oxidize to ketones. It’s not clear if it’s the high serum > glucose content, or the increase in ketones in the blood, or both together, > which lead to the neuropathies seen in diabetes and its related syndromes. > Artificial ketogenic situations come in two flavours: the ketogenic diet, > and fasting. > A true ketogenic diet is low in both carbohydrate and protein calories, and > derives most of its energy inputs from fats. This extreme situation has been > found to help control treatment-unresponsive epilepsy. It’s not for most > people. > Fasting induces ketogenesis in healthy people after the body has depleted > its stores of quickly available sugars. The liver retains a reserve in the > form of glucagon (sp?) for emergency energy, and there are other resources > within cells via anaerobic processes, but by and large, ketosis is a > starvation process. It’s believed that episodic ketogenesis actually trains > the body to store a higher proportion of fat than it otherwise would, which > is counter-productive to your cause. > I think the Zone series will give you good insight into what you’re trying > to accomplish. I, too, rely on a high-protein, low-carb diet. I just do > better that way. > Regards, > Larry

Thanks Larry, You  must be a Nutriotionist – doctor?  Yes, what you say is consistent with what I read on the net, as well as the fact that my doctor checked me for diabetes – which I do not have, but I am overweight and I have peripheral neuropathy- I have no idea where it came from.  I have a number of suspects: one of which is that it happened close to ingestion of Canola oil in a salad.  I am waiting for those EMG, etc. tests – but I think I will try to follow the high protein – low carb diet in moderation. I bet you find you have more energy with that. take care Squiggles

Response:

- Hide quoted text — Show quoted text ->Was this depression a result of lithium withdrawal >or the underlying depression coming through – this >must be a perennial question right? > Squiggles, use some common sense. You have been off the lithium for three > months when you crashed right? That is more than enough time to have gone thru > any "lithium withdrawal." I never heard of anybody having "lithium withdrawal" > anyway. Lithium’s not addictive at all like Klonopin. It never has had a > reputation for having severe withdrawal like say, Paxil or Effexor (due to > short half life). > Even if you did have lithium withdrawal, it would have been long gone before > three months was up. To put it bluntly, Id say any crashing you had was cause > you were off lithium and this allowed whatever mental condition to return in > spades. The lithium was protecting you. > If you doubt lithium was protecting you or that you have a serious medical > condition, and would like to go by your Freud which you hold so dear, Id > suggest totally going off all drugs for at least six months, probably a year > and aggressively pursue talk therapy. Read Freud and other psychology oriented > self help books. Go off your drugs Squiggles and begin working you ass off on > those underlying "issues" which are the root cause of your psychiatric > condition. > Then after youve done this for a year report back to us how you feel drug free > and off meds and after having undergone aggressive talk therapy and "issue" > resolvement. I want to hear how it went for you. > Eric

You may be right.  I don’t know frankly.  I just looked at the American Family Physician site, and it says a control group and a lithium group of women were tested for discontinuation syndromes, and after 40 weeks, both were the same. I have not had the time to search for more – got to go out. At any rate, just because I am critical does not mean I am not frightened and btw I am still on 0.50 mg Klonopin as I suffered something like a seizure going down and had to raise it again. One thing you don’t know is the kind of torture they put me through at McGill – I will not go into details because it involves harrassment which I was subjected to while having to cover the entire Ph.D. programme in 2 years, with 4 TAships; not only was I exhausted, but I was under threat the whole time. I believe what I experienced at the time of breakdown was severe disassociation of personality.  The faculty and the administration turned a blind eye to the harrassment for a number of self-interested reasons. You don’t any of that and you never will, but I think it contributed and possibly was the cause of my breakdown (the Valium I was taking may have also had a lot to do with it). I will never ever ever go back to school.  The wound I received from that, will never be erased in my memory. Anyway, I hope the Seroquel helped you and one thing Eric, I would like you ever so much more if you were not anti-Semitic- if you wish I will send you some URLs – those people – innocent – they suffered the pains of the damned.  I hope you will change. Life is to be enjoyed. Squiggles http://www.aafp.org/afp/20000801/tips/16.html

Response:

– Hide quoted text — Show quoted text -> > > Hey Squiggles. The best correlate to your personal diet is the Zone > series > > > of books. They’d be at the library or Chapters, if you wanted to look > > > through them. You could develop insulin resistance on this diet, but > it’s > > > probably less likely than on more typical carbohydrate diets. The best > way > > > to maintain insulin sensitivity is to make sure you get a good portion > of > > > omega-3 fatty acids. This only works, though, before the pancreas poops > out. > > > Regards, > > > Larry > > Uhm, the ZONE diets – OK – I will look when I got Chapters, because > > I still want to get that book by David Healy – it is scholarly > > and likely not to be there though – maybe I will try Indigo down > > the street.  Yes, I know low carb diet has to do with insulin, > > but I am not diabetic – just overweight – I just thought that since > > the kidneys have to work overtime with lithium excretion that perhaps > > this is not the best diet for me.  But I think that it is precisly > > the ketosis that makes you lose, I don’t know.  I am willing to > > just follow something that will bring me back to size 10. > > Squiggles > Ketosis occurs when the body is unable to burn glucose and other sugars for > fuel, and instead turns to burning fats. On the surface, that seems > desirable, but it’s generally not. > In type 2 diabetes (adult onset), insulin resistance, and what is known as > Syndrome X, glucose uptake is reduced or even absent because the > insulin-dependent uptake of sugars across the cell membrane does not > function properly. Cells then burn fats (and proteins to some extent) as > energy sources. Poly-unsaturated fats do not burn "cleanly", as the > unsaturated bonds oxidize to ketones. It’s not clear if it’s the high serum > glucose content, or the increase in ketones in the blood, or both together, > which lead to the neuropathies seen in diabetes and its related syndromes. > Artificial ketogenic situations come in two flavours: the ketogenic diet, > and fasting. > A true ketogenic diet is low in both carbohydrate and protein calories, and > derives most of its energy inputs from fats. This extreme situation has been > found to help control treatment-unresponsive epilepsy. It’s not for most > people. > Fasting induces ketogenesis in healthy people after the body has depleted > its stores of quickly available sugars. The liver retains a reserve in the > form of glucagon (sp?) for emergency energy, and there are other resources > within cells via anaerobic processes, but by and large, ketosis is a > starvation process. It’s believed that episodic ketogenesis actually trains > the body to store a higher proportion of fat than it otherwise would, which > is counter-productive to your cause. > I think the Zone series will give you good insight into what you’re trying > to accomplish. I, too, rely on a high-protein, low-carb diet. I just do > better that way. > Regards, > Larry > Thanks Larry, > You  must be a Nutriotionist – doctor?

Part schooling, part avocation. You can’t have a healthy mind in a sick body, is my way of looking at the problems we face. > Yes, what you say > is consistent with what I read on the net, as well as > the fact that my doctor checked me for diabetes – which I do > not have, but I am overweight and I have peripheral neuropathy- > I have no idea where it came from.

How’s your digestion? No graphic descriptions required, but are you stable, or troubled? There are many reasons for peripheral neuropathy, but some stem from malnutrition. Despite "common knowledge" you can have functional deficits in nutrients despite having a balanced diet. Did your doctor check B12 status? > I have a number of suspects: > one of which is that it happened close to ingestion of > Canola oil in a salad.

Erucic acid levels in canola are closely monitored. I doubt there’s a link, but you could be allergic to the traces of proteins that remain in refined vegetable oils. Erucic acid is a substance produced at about 2% in rapeseed. This fatty acid was eliminated through intensive selection and some genetic manipulation. The result, a Canadian first, a safe-for-humans vegetable oil from rapeseed, Canada oil, or canola. > I am waiting for those EMG, etc. tests –

Now, they are a thrill a minute. Nerve conduction studies are quite bizarre to experience. > but I think I will try to follow the high protein – low carb > diet in moderation. > I bet you find you have more energy with that.

Indeed. The whole point is to maintain energy. I get all slowed down on high carbs. > take care > Squiggles

You too. Happy Thanksgiving. Larry

Response:

- Hide quoted text — Show quoted text – > You may be right.  I don’t know frankly.  I just looked at the > American Family Physician site, and it says a control group and > a lithium group of women were tested for discontinuation syndromes, > and after 40 weeks, both were the same. > I have not had the time to search for more – got to go out. At > any rate, just because I am critical does not mean I am not > frightened and btw I am still on 0.50 mg Klonopin as I suffered > something like a seizure going down and had to raise it again. > One thing you don’t know is the kind of torture they put me > through at McGill – I will not go into details because it > involves harrassment which I was subjected to while having > to cover the entire Ph.D. programme in 2 years, with 4 TAships; > not only was I exhausted, but I was under threat the whole time. > I believe what I experienced at the time of breakdown was > severe disassociation of personality.  The faculty and the > administration turned a blind eye to the harrassment for > a number of self-interested reasons. > You don’t any of that and you never will, but I think it > contributed and possibly was the cause of my breakdown (the > Valium I was taking may have also had a lot to do with it). > I will never ever ever go back to school.  The wound I received > from that, will never be erased in my memory.

what a horrible story. there is so much pressure in the ‘real world’. im not sure i understand it…. well dont give up on school. i didnt have the greatest time there > Anyway, I hope the Seroquel helped you and one thing Eric, > I would like you ever so much more if you were not anti-Semitic- > if you wish I will send you some URLs – those people – innocent – > they suffered the pains of the damned.  I hope you will change. > Life is to be enjoyed.

i really do not think he is truly anti-semitic. think of the area in which he lives now… that does make a difference….. sometimes americans dont think about what they are saying…… i think eric -would- like to enjoy life a lot and is pissed cause hes not enjoying anything much at all right now and hates that…… thats what i think. i hope the seroquel helps too.. hmm… yes definitely.. whatever it takes is what i think these days. but, do not stay on a med if you dont like it too. that is a bad problem i think too… <<<<<take care>>>>>…. anna > Squiggles > http://www.aafp.org/afp/20000801/tips/16.html

– blackbird singin in the dead of night take these broken eyes and learn to see all your life you were only waiting for this moment to be free ~

Response:

– Hide quoted text — Show quoted text -> >Was this depression a result of lithium withdrawal > >or the underlying depression coming through – this > >must be a perennial question right? > Squiggles, use some common sense. You have been off the lithium for three > months when you crashed right? That is more than enough time to have gone thru > any "lithium withdrawal." I never heard of anybody having "lithium withdrawal" > anyway. Lithium’s not addictive at all like Klonopin. It never has had a > reputation for having severe withdrawal like say, Paxil or Effexor (due to > short half life). > Even if you did have lithium withdrawal, it would have been long gone before > three months was up. To put it bluntly, Id say any crashing you had was cause > you were off lithium and this allowed whatever mental condition to return in > spades. The lithium was protecting you. > If you doubt lithium was protecting you or that you have a serious medical > condition, and would like to go by your Freud which you hold so dear, Id > suggest totally going off all drugs for at least six months, probably a year > and aggressively pursue talk therapy. Read Freud and other psychology oriented > self help books. Go off your drugs Squiggles and begin working you ass off on > those underlying "issues" which are the root cause of your psychiatric > condition. > Then after youve done this for a year report back to us how you feel drug free > and off meds and after having undergone aggressive talk therapy and "issue" > resolvement. I want to hear how it went for you. > Eric > You may be right.  I don’t know frankly.  I just looked at the > American Family Physician site, and it says a control group and > a lithium group of women were tested for discontinuation syndromes, > and after 40 weeks, both were the same. > I have not had the time to search for more – got to go out. At > any rate, just because I am critical does not mean I am not > frightened and btw I am still on 0.50 mg Klonopin as I suffered > something like a seizure going down and had to raise it again. > One thing you don’t know is the kind of torture they put me > through at McGill – I will not go into details because it > involves harrassment which I was subjected to while having > to cover the entire Ph.D. programme in 2 years, with 4 TAships; > not only was I exhausted, but I was under threat the whole time. > I believe what I experienced at the time of breakdown was > severe disassociation of personality.  The faculty and the > administration turned a blind eye to the harrassment for > a number of self-interested reasons. > You don’t any of that and you never will, but I think it > contributed and possibly was the cause of my breakdown (the > Valium I was taking may have also had a lot to do with it). > I will never ever ever go back to school.  The wound I received > from that, will never be erased in my memory.

I am sorry anyone put you through that….and stole your ability to feel safe in the academic envirnment  which you seem so suitable for. I relate…as something similiar occuring to me 11 years ago..is pivotal to my problems.  A situation occurred stole my ability to feel safe at work..so I will not go back  to doing what I otherwise loved..professional career…etc.  Who are these people..who can steal away a all one worked for from the age of 16… Lot more to it of course…I been stressed for three years prior..having my son…born with congenital birth defects needing operations that failed and made his problems worse..having to litigate for two years with his father…to ensure insurance was maintained…etc…so I took the trauma of being held against my will  real bad…and have yet to find a way home from it….did the poker thing instead   own boss and all for a decade…now I really should find a way home…but dont know how to…  I stopped saying I will NEVER go back…though thats an improvement…. I am  sorry it happened to you… – Hide quoted text — Show quoted text -> Anyway, I hope the Seroquel helped you and one thing Eric, > I would like you ever so much more if you were not anti-Semitic- > if you wish I will send you some URLs – those people – innocent – > they suffered the pains of the damned.  I hope you will change. > Life is to be enjoyed. > Squiggles > http://www.aafp.org/afp/20000801/tips/16.html

Response:

- Hide quoted text — Show quoted text -> Thanks Larry, > You  must be a Nutriotionist – doctor? > Part schooling, part avocation. You can’t have a healthy mind in a sick > body, is my way of looking at the problems we face. > Yes, what you say > is consistent with what I read on the net, as well as > the fact that my doctor checked me for diabetes – which I do > not have, but I am overweight and I have peripheral neuropathy- > I have no idea where it came from. > How’s your digestion? No graphic descriptions required, but are you stable, > or troubled? There are many reasons for peripheral neuropathy, but some stem > from malnutrition. Despite "common knowledge" you can have functional > deficits in nutrients despite having a balanced diet. Did your doctor check > B12 status? > I have a number of suspects: > one of which is that it happened close to ingestion of > Canola oil in a salad. > Erucic acid levels in canola are closely monitored. I doubt there’s a link, > but you could be allergic to the traces of proteins that remain in refined > vegetable oils. Erucic acid is a substance produced at about 2% in rapeseed. > This fatty acid was eliminated through intensive selection and some genetic > manipulation. The result, a Canadian first, a safe-for-humans vegetable oil > from rapeseed, Canada oil, or canola. > I am waiting for those EMG, etc. tests – > Now, they are a thrill a minute. Nerve conduction studies are quite bizarre > to experience. > but I think I will try to follow the high protein – low carb > diet in moderation. > I bet you find you have more energy with that. > Indeed. The whole point is to maintain energy. I get all slowed down on high > carbs. > take care > Squiggles > You too. Happy Thanksgiving. > Larry

Hi Larry, Thank you for your good wishes and explanation. About digestion – well it has not been the same for a year or so; that is because of my benzo withdrawal – among many other side effects of that withdrawal – indigestion, heartburn, daily diarrhea, which has now gotten better on account of raising the dose, and of course a physical anxiety which seems to have changed all my gastro-perspiration everything having to do with fluids in my body.  No doubt there may be a connection.   There are many possible causes of course – the weird thing about my carpal tunnel  was that it was so acute.  I was sitting at my chair, and all of sudden I got a histaminic-like reaction, that felt as if my hands were stung by a million bees – and what followed what was pretty severe carpal tunnel requiring braces – I was quite terrified. Maybe w/d, maybe a nerve in the back, maybe canola allergy, who knows. Tx – good to have a nutriotinist on board – you guys know so much. Squiggles

Response:

> I am sorry anyone put you through that….and stole your ability to feel > safe in the academic envirnment  which you seem so suitable for.

Hi Linda, Thanks – I don’t like to repeat the experiences in my memory – I am afraid it left a mark. But I appreciate your sympathetic reply very much. > I relate…as something similiar occuring to me 11 years ago..is pivotal to > my problems.  A situation occurred stole my ability to feel safe at work..so > I will not go back  to doing what I otherwise loved..professional > career…etc.

I wonder what that is – I don’t think you ever told. >  Who are these people..who can steal away a all one worked for from the age > of 16… > Lot more to it of course…I been stressed for three years prior..having my > son…born with congenital birth defects needing operations that failed and > made his problems worse..having to litigate for two years with his > father…to ensure insurance was maintained…etc…so I took the trauma of > being held against my will  real bad…and have yet to find a way home from > it….did the poker thing instead   own boss and all for a decade…now I > really should find a way home…but dont know how to…  I stopped saying I > will NEVER go back…though thats an improvement…. > I am  sorry it happened to you…

Oh gee, I am sorry Linda.  I have been so selfish to think that not getting a Ph.D is such a big deal.  These things you describe would touch you personally, I am sure.  I am glad you are able to talk about it here. Squiggles

Response:

> Whats the problem with the harassment at school got to do with you TODAY > Squiggles? It suffices to say that the harassment you received in school was > the environmental stress which caused you to have your nervous breakdown and > get put on lithium. However it was a LONG time ago. Its over with. The change > in your brain occured a LONG time ago. Its over with.

Hi Eric, The point is, that the "change" in my brain may have been transient under the stress – are you saying stress can make a person bipolar? Is there no possibility I would have gotten over it?  I am asking seriously, because I do not know the answer to that question. > The fact of the matter is that you have the here and now to deal with. You are > no longer the same as before you had your nervous breakdown. The breakdown > obviously caused some major changes in your body and health…changes which are > most likely chronic.

Well, I don’t know – do you?  You seem so sure. > I dont go around obsessing about moping about the original environmental > stresses which occured to me four years ago and led to me developing major > depression.

No need to chastise me.  I am not obsessing – it’s just an injustice that changed my life, and necessitated further possibly unnecessary drugs when really the cause was stress and the drugs themselves.  In a way I hope you are right, because I am not about to make major med changes after many years.   I must say though, that memory tends to romanticize things; and it is true that I never get depressed with lithium though I did before I ever took it.  I am very curious to find out if it has that effects on normals – I think I saw a study on Virtual Hospital, but I don’t think it was conclusive. Anyway, about the Jews – I think I should send you some URLs, though they will probably make me sick to look at – you must know what happened – I can’t believe that you are ignorant and if you are not, that you are so heartless. Squiggles

Response:

- Hide quoted text — Show quoted text – > It used to be … > A psych or neurological dx was highly dependent upon ones responsiveness to > meds.. > you presented with symptoms.. they take a stab or a WAG at your dx… >  then they experiment with meds…beginining with those for the initial > DX…and  if you respond positively to the med…thats the dx.. > .if you dont….well they try others meds in that category.. > .if still no response..and they have to change the type of RX you used to > get a dx change.. >  nowadays…they are using all the meds to treat all the dx’s and see > nothing wrong with a dx of depression or PTSD while  giving you mood > stabilizers..and AP’s etc.. > and now they are treating depression and PTSD with AP’s and mood stablizers > cause they found those disorders respond to those meds…too….  someone > who responded to one of those meds way back when…  has to question whether > if they presented today..they get that  DX  or PTSD and depression instead.. > … > not sure the rx is wrong though….Squiggles..you do so well on the LI.. > . > . > >Hi Eric, > >The point is, that the "change" in my brain may have been transient > >under the stress – are you saying stress can make a person bipolar? > >Is there no possibility I would have gotten over it?  I am asking > >seriously, because I do not know the answer to that question. > Squiggles…please dont smart ass me. Its well known that mental illness > oftentimes is activated by severe stress. My point is that once it > develops, > lessening the stress or eliminating it doesnt tend to make the mental > illness > go away. Unfortunately it doesnt work that way I wish it did. > With milder mood disorders (dysthymia) this might be the case many times, > removing or decreasing the stress gets rid of dysthymia…this may or may > not > work. > You dont even have clinical depression I dont even know why Im bothering > to > explain this to you. This is what has happened to this NG in the past year > we’ve gotten so many bipolar folks on this NG as regulars who DO NOT HAVE > clinical depression but instead have manic depression. Its obvious reading > your > stuff you never experienced major depression. > >> The fact of the matter is that you have the here and now to deal with. > You > >are > >> no longer the same as before you had your nervous breakdown. The > breakdown > >> obviously caused some major changes in your body and health…changes > which > >are > >> most likely chronic. > >Well, I don’t know – do you?  You seem so sure. > Yes Squiggles. Bipolar manic depression is well known to be a > chronic…oftentimes lifetime disease. Again…dont smartass me. Go ask > your > doctor this question. You know what the answer will be. > >> I dont go around obsessing about moping about the original > environmental > >> stresses which occured to me four years ago and led to me developing > major > >> depression. > >No need to chastise me.  I am not obsessing – it’s just an > >injustice that changed my life, and necessitated further > >possibly unnecessary drugs when really the cause was stress > >and the drugs themselves.  In a way I hope you are right, because > >I am not about to make major med changes after many years. > Well why do you bring it up? > >I must say though, that memory tends to romanticize things; > >and it is true that I never get depressed with lithium though > >I did before I ever took it.  I am very curious to find out if > >it has that effects on normals – I think I saw a study on Virtual > >Hospital, but I don’t think it was conclusive. > >Anyway, about the Jews – I think I should send you some URLs, > >though they will probably make me sick to look at – you must > >know what happened – I can’t believe that you are ignorant > >and if you are not, that you are so heartless. > Dont send me any fucking URLs. > Eric > Steroids caused my depression…prednisone should be used conservatively. > http://groups.yahoo.com/group/FactsAndFallaciesOfDepression > MIBS (Minimally Invasive Brain Stimulation) > http://www.musc.edu/psychiatry/fnrd/tms.htm

Linda, One thing that is very encouraging about lithium – it seems to work wonders on so many conditions: Unipolar Bipolar Post Traumatic Anorexia Parkinson’s Alzheimer’s Aggression Insomnia Hyperthyroidism Leukemia It’s dynamite.  And I suspect that I am better than normals with respect to depression, heck why stop there :-) Squiggles

Response:

> The best thing about it is its natural.. > I want to use it anytime I feel myself getting triggered and feel like I am > manifesting PTSD… course they want me to use the benzo……but I know the > Lithium works better …cause I took that til I could see my doctor…and it > just STPPED the  escalating PTSD symptoms right in their track.. > sigh….I guess there is a problems prescribing  ’ LI as needed"   they dont > have prescriging  benzo’s as needed.. > ..

Linda, It does feel "natural" too – this is the amazing thing about lithium – it feel like water – it does not feel like a drug at all and your head and consciousness is entirely clear.  I know that is not the case with the synthetic drugs because I have tried them, and I know that until you get used to them at least you are always aware that they are drugs.  Of course lithium can be deadly if overdosed and toxic if too high and then I imagine you feel very sick — I have not felt that yet I don’t think – the problem with polypharmacy is — right now I am still feeling the w/d from Klonopin and sometimes you cannot tell one apart from the other.  I feel for people who have AIDS or cancer and have to take so many drugs.  The last time I was at the pharmacy I saw a poor senior citizen with his vial compartment of oh, must have been 9 drugs in each pocket.  Poor man. Yes, lithium on low doses I am certain would be good for many ailments, and who knows maybe it will be soon used that way. Squiggles – Hide quoted text — Show quoted text -> Squiggles

Response:

You have a big ego Eric – but that’s OK – cause I think I have an even bigger one  – LOL Yes, it is indeed sublime that we can see eye to eye on something, as microscopically miniscule as it may be. Yup, lithium has been known to calm people throughout history. I have a theory about Greek civilization – that is became great because the water contained lithium – they used to go to the springs for inspiration and a cool head. > she gets normal again. Ive wondered if maybe its that small amount of lithium > in those vitamins thats keeping her on "even keel?" You think so? > This sounds like the sort of thing Linda would be interested in.

As for your mother, I rather doubt that the small amount would make that much of a difference but who knows – they used to use it in 7UP the soft drink, at around the same time they used cocaine in Coca Cola. Squiggles

Response:

Pain Clinic

Question:

When I see this subject line, I am reading it like Jimmy Dean (the sausage man) has a pain clinic named after him…the "Jimmy Dean Pain Clinic"…sorry..just trying to put some humor in here :) Nikki "… lost in the darkness of my own circumstance, criticizing echoes leaving me awake in the night… the barrier and blockades that keep me safe and in control while I pretend that I am okay… "

Response:

>When I see this subject line, I am reading it like Jimmy Dean (the sausage >man) >has a pain clinic named after him…the "Jimmy Dean Pain >Clinic"…sorry..just >trying to put some humor in here :) >Nikki

Nikki, you’re showing your age!  I know Jimmy Dean as a country singer & I think had his own TV show for a while, THEN he got into the sausage business. Debbie Life is a test. It is only a test. If this were real life, we would have been given better instructions.

Response:

I guess you missed the comment:  "which is why I’m asking, not accusing." What makes me wonder now is that she hasn’t answered. — The Mouse No cute quote; deal with it. AIM ID:  JSHMTE ICQ# 9049058

: Hello, : :      Why must you look for the evil in posters(especially new posters) : right from the get go.  Why must you play net police?  Why cant you : start from the aspect that maybe Julie wants to help others like you : want to help others and work from there?  Suspicion is even written in : someones reply and then her website is investigated all the while she : didn’t even give a web address.  Maybe, just maybe, she can help someone : on this group but she could be runoff before even given the chance, and : what is her crime and at this point why is there any need to be : suspicious or to investigate?  Yo Cagney and Lacey take a day off and : let Julie post in a guilt free environment. : : respect everybody…fear nobody

: > : > : What website?  There is not one included in any post she has made that : > : I can find. : > : > I just followed the site in her address (aboutcts.com, I believe) and found : > all kinds of goodies for sale.  It made me leary, which is why I’m asking, : > not accusing.  I do find it odd that someone who claims to do what she says : > she does can’t spell massiter muscle correctly, which is what first got my : > attention. : > : > Mouse : > : > : : > : Don’t take this wrong — I have the same sneaking suspicion you have : > : (there have been far too many of them not to have).  But I haven’t yet : > : seen anything to confirm the suspicion or even really give me cause to : > : question.  She is not including a link to a website.  She is sounding : > : like many of the others who come here and start by saying  "I know the : > : cure for you" and it evolves to  "pay me and I will tell you", she : > : just has not done the "pay me" part yet.  I am suspecting that she : > : will get to that, in fact I am watching for it.   I was going to let : > : her hang herself though. : > : : > : > Julie:  Are you selling the packages advertised on your website?  Or : > : are you : > : > going to give out the information and assistance here free of : > : charge? : > : > : > : > — : > : > The Mouse : > : > : > : > No cute quote; deal with it. : > : > AIM ID:  JSHMTE : > : > ICQ# 9049058 : > : > : Jimmy – please look for the response I just wrote to "I need : > : advice on : > : > back : > : > : and leg pain" from Clarington Jackson.  I have been helping people : > : who : > : > have : > : > : chronic joint pain for 14 years.  The treatments are extremely : > : successful : > : > : and involve deep muscle therapy.  I am not looking for new clients : > : (I have : > : > : plenty of them) but I do want to help people find therapists that : > : are : > : > right : > : > : for them.  I can also talk you through some self-treatment : > : techniques. I : > : > do : > : > : that all the time with my own patients, and it’s also successful. : > : > : : > : > : Please feel free to contact me.  Our medical office has been : > : successful : > : > with : > : > : hundreds of people.  Many, many times the problem is muscular – : > : except in : > : > : the USA there is no specialty for muscles, and as a result you : > : won’t : > : > easily : > : > : find the therapist who can help you. I will help you direct your : > : search : > : > for : > : > : the person who is best qualified to help you. : > : > : : > : > : : > : > : : > : > : : > : > : > : > : > : : > :

Response:

Hello,      Why must you look for the evil in posters(especially new posters) right from the get go.  Why must you play net police?  Why cant you start from the aspect that maybe Julie wants to help others like you want to help others and work from there?  Suspicion is even written in someones reply and then her website is investigated all the while she didn’t even give a web address.  Maybe, just maybe, she can help someone on this group but she could be runoff before even given the chance, and what is her crime and at this point why is there any need to be suspicious or to investigate?  Yo Cagney and Lacey take a day off and let Julie post in a guilt free environment.   respect everybody…fear nobody – Hide quoted text — Show quoted text – > : What website?  There is not one included in any post she has made that > : I can find. > I just followed the site in her address (aboutcts.com, I believe) and found > all kinds of goodies for sale.  It made me leary, which is why I’m asking, > not accusing.  I do find it odd that someone who claims to do what she says > she does can’t spell massiter muscle correctly, which is what first got my > attention. > Mouse > : > : Don’t take this wrong — I have the same sneaking suspicion you have > : (there have been far too many of them not to have).  But I haven’t yet > : seen anything to confirm the suspicion or even really give me cause to > : question.  She is not including a link to a website.  She is sounding > : like many of the others who come here and start by saying  "I know the > : cure for you" and it evolves to  "pay me and I will tell you", she > : just has not done the "pay me" part yet.  I am suspecting that she > : will get to that, in fact I am watching for it.   I was going to let > : her hang herself though. > : > : > Julie:  Are you selling the packages advertised on your website?  Or > : are you > : > going to give out the information and assistance here free of > : charge? > : > > : > — > : > The Mouse > : > > : > No cute quote; deal with it. > : > AIM ID:  JSHMTE > : > ICQ# 9049058 > : > : Jimmy – please look for the response I just wrote to "I need > : advice on > : > back > : > : and leg pain" from Clarington Jackson.  I have been helping people > : who > : > have > : > : chronic joint pain for 14 years.  The treatments are extremely > : successful > : > : and involve deep muscle therapy.  I am not looking for new clients > : (I have > : > : plenty of them) but I do want to help people find therapists that > : are > : > right > : > : for them.  I can also talk you through some self-treatment > : techniques. I > : > do > : > : that all the time with my own patients, and it’s also successful. > : > : > : > : Please feel free to contact me.  Our medical office has been > : successful > : > with > : > : hundreds of people.  Many, many times the problem is muscular – > : except in > : > : the USA there is no specialty for muscles, and as a result you > : won’t > : > easily > : > : find the therapist who can help you. I will help you direct your > : search > : > for > : > : the person who is best qualified to help you. > : > : > : > : > : > : > : > : > : > > : > > : > :

Response:

Hi Ruada ,     Just turn the add’y into a http url and you will find the web site. The *aboutcts* title refers to carpal tunnel syndrome and the site sells info on how to heal yourself of muscle related problems . Wishing you the best with your food problems . Peace , Richard

– Hide quoted text — Show quoted text -> What website?  There is not one included in any post she has made that > I can find. > Don’t take this wrong — I have the same sneaking suspicion you have > (there have been far too many of them not to have).  But I haven’t yet > seen anything to confirm the suspicion or even really give me cause to > question.  She is not including a link to a website.  She is sounding > like many of the others who come here and start by saying  "I know the > cure for you" and it evolves to  "pay me and I will tell you", she > just has not done the "pay me" part yet.  I am suspecting that she > will get to that, in fact I am watching for it.   I was going to let > her hang herself though. > Julie:  Are you selling the packages advertised on your website?  Or > are you > going to give out the information and assistance here free of > charge? > — > The Mouse > No cute quote; deal with it. > AIM ID:  JSHMTE > ICQ# 9049058 > : Jimmy – please look for the response I just wrote to "I need > advice on > back > : and leg pain" from Clarington Jackson.  I have been helping people > who > have > : chronic joint pain for 14 years.  The treatments are extremely > successful > : and involve deep muscle therapy.  I am not looking for new clients > (I have > : plenty of them) but I do want to help people find therapists that > are > right > : for them.  I can also talk you through some self-treatment > techniques. I > do > : that all the time with my own patients, and it’s also successful. > : > : Please feel free to contact me.  Our medical office has been > successful > with > : hundreds of people.  Many, many times the problem is muscular – > except in > : the USA there is no specialty for muscles, and as a result you > won’t > easily > : find the therapist who can help you. I will help you direct your > search > for > : the person who is best qualified to help you. > : > : > : > :

Response:

: What website?  There is not one included in any post she has made that : I can find. I just followed the site in her address (aboutcts.com, I believe) and found all kinds of goodies for sale.  It made me leary, which is why I’m asking, not accusing.  I do find it odd that someone who claims to do what she says she does can’t spell massiter muscle correctly, which is what first got my attention. Mouse : : Don’t take this wrong — I have the same sneaking suspicion you have : (there have been far too many of them not to have).  But I haven’t yet : seen anything to confirm the suspicion or even really give me cause to : question.  She is not including a link to a website.  She is sounding : like many of the others who come here and start by saying  "I know the : cure for you" and it evolves to  "pay me and I will tell you", she : just has not done the "pay me" part yet.  I am suspecting that she : will get to that, in fact I am watching for it.   I was going to let : her hang herself though. : : > Julie:  Are you selling the packages advertised on your website?  Or : are you : > going to give out the information and assistance here free of : charge? : > : > — : > The Mouse : > : > No cute quote; deal with it. : > AIM ID:  JSHMTE : > ICQ# 9049058 : > : Jimmy – please look for the response I just wrote to "I need : advice on : > back : > : and leg pain" from Clarington Jackson.  I have been helping people : who : > have : > : chronic joint pain for 14 years.  The treatments are extremely : successful : > : and involve deep muscle therapy.  I am not looking for new clients : (I have : > : plenty of them) but I do want to help people find therapists that : are : > right : > : for them.  I can also talk you through some self-treatment : techniques. I : > do : > : that all the time with my own patients, and it’s also successful. : > : : > : Please feel free to contact me.  Our medical office has been : successful : > with : > : hundreds of people.  Many, many times the problem is muscular – : except in : > : the USA there is no specialty for muscles, and as a result you : won’t : > easily : > : find the therapist who can help you. I will help you direct your : search : > for : > : the person who is best qualified to help you. : > : : > : : > : : > : : > : > : :

Response:

What website?  There is not one included in any post she has made that I can find. Don’t take this wrong — I have the same sneaking suspicion you have (there have been far too many of them not to have).  But I haven’t yet seen anything to confirm the suspicion or even really give me cause to question.  She is not including a link to a website.  She is sounding like many of the others who come here and start by saying  "I know the cure for you" and it evolves to  "pay me and I will tell you", she just has not done the "pay me" part yet.  I am suspecting that she will get to that, in fact I am watching for it.   I was going to let her hang herself though.

– Hide quoted text — Show quoted text -> Julie:  Are you selling the packages advertised on your website?  Or are you > going to give out the information and assistance here free of charge? > — > The Mouse > No cute quote; deal with it. > AIM ID:  JSHMTE > ICQ# 9049058 > : Jimmy – please look for the response I just wrote to "I need advice on > back > : and leg pain" from Clarington Jackson.  I have been helping people who > have > : chronic joint pain for 14 years.  The treatments are extremely successful > : and involve deep muscle therapy.  I am not looking for new clients (I have > : plenty of them) but I do want to help people find therapists that are > right > : for them.  I can also talk you through some self-treatment techniques. I > do > : that all the time with my own patients, and it’s also successful. > : > : Please feel free to contact me.  Our medical office has been successful > with > : hundreds of people.  Many, many times the problem is muscular – except in > : the USA there is no specialty for muscles, and as a result you won’t > easily > : find the therapist who can help you. I will help you direct your search > for > : the person who is best qualified to help you. > : > : > : > :

Response:

Julie:  Are you selling the packages advertised on your website?  Or are you going to give out the information and assistance here free of charge? — The Mouse No cute quote; deal with it. AIM ID:  JSHMTE ICQ# 9049058

: Jimmy – please look for the response I just wrote to "I need advice on back : and leg pain" from Clarington Jackson.  I have been helping people who have : chronic joint pain for 14 years.  The treatments are extremely successful : and involve deep muscle therapy.  I am not looking for new clients (I have : plenty of them) but I do want to help people find therapists that are right : for them.  I can also talk you through some self-treatment techniques. I do : that all the time with my own patients, and it’s also successful. : : Please feel free to contact me.  Our medical office has been successful with : hundreds of people.  Many, many times the problem is muscular – except in : the USA there is no specialty for muscles, and as a result you won’t easily : find the therapist who can help you. I will help you direct your search for : the person who is best qualified to help you. : : : :

Response:

Jimmy – please look for the response I just wrote to "I need advice on back and leg pain" from Clarington Jackson.  I have been helping people who have chronic joint pain for 14 years.  The treatments are extremely successful and involve deep muscle therapy.  I am not looking for new clients (I have plenty of them) but I do want to help people find therapists that are right for them.  I can also talk you through some self-treatment techniques. I do that all the time with my own patients, and it’s also successful. Please feel free to contact me.  Our medical office has been successful with hundreds of people.  Many, many times the problem is muscular – except in the USA there is no specialty for muscles, and as a result you won’t easily find the therapist who can help you. I will help you direct your search for the person who is best qualified to help you.

Response:

> > "nerve blocks"? > I put it in quotes because many doctors proclaim them to be miracle cures > ..My experience indicates they aren’t  – but as they say, YMMV!    I went > to one of those pain clinics, er tourture clinics, a few years ago for a > problem I had.   They tried several different treatments, none of which > worked, and it ended up causing me more pain and trouble in the long run.

According to their statistics, nerve blocks are effective in about 50% of cases.  I don’t know how they define effective.  Mine worked for 36 hours, which they told me was not effective. Then they lost interest in me (I guess I’m not a good patient — I didn’t respond to their treatment). Nonetheless, with appropriate information available to the patient, I think nerve blocks are an important part of the arsenal against pain. Jon Miller

Response:

SAG, Why won’t your Dr. prescribe (not subscribe….unless he is giving 12 months of GQ ;o)…) the Oxycontin, since you have been on it?  Is this the same MD that was writing your meds before? I do not know if you are in the States, but you did mention trying to get to your regular "RN."  RN’s, at least in the States, are not able to write prescriptions.  Some states will allow PA-c (Physician’s Assistants) to write an Rx. I do think you need to sit down with whomever it was that sent you to the Dr. that ordered the MRI and Nerve Studies and decide who is going to write your Prescription’s.  It is not right to leave you hanging until someone refill’s your meds.  They evidently found a reason for your pain.  If they do not want to Rx an Opiate, there are meds out there to help with nerve pain, such as Topamax and Neurontin.  But to give you a shot in the neck, and a few muscle relaxers, is cruel.  If you’ve been on OxyContin for awhile, they need to either wean you off, if they do not want you on it, or give you something else.  To just stop it, could put you in withdrawal, and anyone that has been through that, knows it isn’t a bed of roses! I do hope you get some help. Robin >Path: >lobby!newstf02.news.aol.com!portc01.blue.aol.com!news.stealth.net!newscon

02.news.prodigy.com!prodigy.com!cyclone.swbell.net!nnrp3.sbc.net.POSTED!no t-for-mail – Hide quoted text — Show quoted text – >Newsgroups: alt.support.chronic-pain >Lines: 10 >X-Priority: 3 >X-MSMail-Priority: Normal >X-Newsreader: Microsoft Outlook Express 5.50.4133.2400 >X-MimeOLE: Produced By Microsoft MimeOLE V5.50.4133.2400 >NNTP-Posting-Host: 216.63.21.97 >Organization: SBC Internet Services >I went a got an MRI and a nerve test done and while both showed some damage >all they did was give me a steroid shot in my neck and a script for 15 >zanaflex which all I call tell made me nod off all day long. I asked for >refill of the Oxycontin my regular pain meds but the Doc subscribed said >they didn’t subscribe narcotics at the pain clinic. The shot didn’t do >anything and now I’m stuck with trying to get my regular RN to keep managing >my pain which he is reluctant to do. Any thoughts. >SAG

I am *not* a Medical Doctor (MD) or *any* other type of Medical Professional. PLEASE consult your own Dr. for medical advice.  The information posted is information I have learned from researching or learning from my own disease.

Response:

My rheumatologist ran out of ideas when I couldn’t tolerate the 20 mg Oxycontin and sent me to a pain management clinic.  I took my most recent MRI and scans and he said all they did was injections and blocks and since I have rheumatoid arthritis in every joint, it wouldn’t do me any good. He sent me back to my RD who changed me to 10 mg Oxycontin.  onight was my first dose. Wish me luck.

– Hide quoted text — Show quoted text -> What kind of pain clinic is this that does not prescribe pain medicines > (narcotics)?   If they don’t prescribe narcotics, they are no different than > the other opiataphobe doctors that love prescribing NSAIDs that now only > ruin peoples digestive systems, but provide little to no pain relief! What > a crock of shit!

Response:

For Matt — There are quite a few "so called" pain clinics that are being run with usually a single doctor who has some experience in doing nerve blocks and trigger point injections and this is about all they offer. No meds or suggesting that one go elsewhere for better care given the disorder. The doc’s will do epidurals, subarachnoid, facet nerve block injections. Since there are only certain types of pain likely to respond and of these, the results are very short term, they have the patient return for repeated injections, some saying that it takes more than one or two." From my personal experience, every nerve block I underwent lasted no longer than the anesthetic in the injection would allow. The same pain always returned. But there are thousands of these types of "clinics" and for the most part, it seems the bottom line comes before all else. Its always wise to seek out info before seeking and seeing a new doc. Ask that they mail a brochure that lists the services offered (if they have one). If you have a good relationship with your pharmacist, ask (s)he for suggestions. If the doc is board certified, such as the American Academy of Family Physicians (who recently published a policy statement supporting the use opioid analgesics for chronic/terminal pain), you may have a better chance of gaining relief . Also, the receptionist may be able to either bite your head off or respond honestly when asked to describe the treatment options the clinic offers, if the treatment includes "weaning the patient off of pain medicine," and it can’t hurt to ask what non-drug treatments they offer. It can an art form in progress when seeking out a new pain doc. The following includes many of the board certification web sites as well as a number of physician/pain clinic links Check out the National Chronic Pain Outreach Assn; they offer a free physician referral service, doing so since 1978 http://painlinks.org/paindoc.html Good Luck Dave L

– Hide quoted text — Show quoted text -> They don’t prescribe narcotics at a pain clinic?  I guess irony never made > it into their vocabulary. > Did you check this so-called pain clinic out at Skip Baker’s site about fake > pain clinics? > — > The Mouse > No cute quote; deal with it. > AIM ID:  JSHMTE > ICQ# 9049058 > : I went a got an MRI and a nerve test done and while both showed some > damage > : all they did was give me a steroid shot in my neck and a script for 15 > : zanaflex which all I call tell made me nod off all day long. I asked for > : refill of the Oxycontin my regular pain meds but the Doc subscribed said > : they didn’t subscribe narcotics at the pain clinic. The shot didn’t do > : anything and now I’m stuck with trying to get my regular RN to keep > managing > : my pain which he is reluctant to do. Any thoughts. > : SAG > : > :

Response:

> As far as their other treatments, I suspect it’s probably the normal "nerve > blocks"

Why in quotes?  Do you disbelieve in nerve blocks, or are there nerve blocks and "nerve blocks"? Jon Miller

Response:

> > As far as their other treatments, I suspect it’s probably the normal "nerve > blocks" > Why in quotes?  Do you disbelieve in nerve blocks, or are there nerve blocks and > "nerve blocks"?

I put it in quotes because many doctors proclaim them to be miracle cures ..My experience indicates they aren’t  – but as they say, YMMV!    I went to one of those pain clinics, er tourture clinics, a few years ago for a problem I had.   They tried several different treatments, none of which worked, and it ended up causing me more pain and trouble in the long run. Skippy

Response:

> I went a got an MRI and a nerve test done and while both showed some damage > all they did was give me a steroid shot in my neck and a script for 15 > zanaflex which all I call tell made me nod off all day long. I asked for > refill of the Oxycontin my regular pain meds but the Doc subscribed said > they didn’t subscribe narcotics at the pain clinic. The shot didn’t do > anything and now I’m stuck with trying to get my regular RN to keep managing > my pain which he is reluctant to do. Any thoughts. > SAG

What kind of pain clinic is this that does not prescribe pain medicines (narcotics)?   If they don’t prescribe narcotics, they are no different than the other opiataphobe doctors that love prescribing NSAIDs that now only ruin peoples digestive systems, but provide little to no pain relief!  What a crock of shit! As far as their other treatments, I suspect it’s probably the normal "nerve blocks", cortizone injections, and the physical therapy bit that many people on here report as torture when done alone..  Don’t get me wrong as they can be valuable treatments, but when a clinic uses just these to relieve EVERYONES pain, they often end up putting the patient in more pain from what I have heard. So, instead of a pain clinic, how bout just calling it a Torture Clinic? Skippy

Response:

They don’t prescribe narcotics at a pain clinic?  I guess irony never made it into their vocabulary. Did you check this so-called pain clinic out at Skip Baker’s site about fake pain clinics? — The Mouse No cute quote; deal with it. AIM ID:  JSHMTE ICQ# 9049058

: I went a got an MRI and a nerve test done and while both showed some damage : all they did was give me a steroid shot in my neck and a script for 15 : zanaflex which all I call tell made me nod off all day long. I asked for : refill of the Oxycontin my regular pain meds but the Doc subscribed said : they didn’t subscribe narcotics at the pain clinic. The shot didn’t do : anything and now I’m stuck with trying to get my regular RN to keep managing : my pain which he is reluctant to do. Any thoughts. : SAG : :

Response:

I went a got an MRI and a nerve test done and while both showed some damage all they did was give me a steroid shot in my neck and a script for 15 zanaflex which all I call tell made me nod off all day long. I asked for refill of the Oxycontin my regular pain meds but the Doc subscribed said they didn’t subscribe narcotics at the pain clinic. The shot didn’t do anything and now I’m stuck with trying to get my regular RN to keep managing my pain which he is reluctant to do. Any thoughts. SAG

Response:

Tramadol’s brand name is Ultram..you can access information on it at: http://www.rxlist.com

Response:

I wrote up a few evaluations of my personal experiences with this drug.  You could do a power search on Deja News using my email and Ultram to find them. I’ve decided to stop using it.  It takes ALOT to keep my breakthru pain under control (appx 15 tabs per day).  I get the most headaches from the pharmacists when I get my prescriptions (Ultram is a a pseudo-scheduled drug here in the states…..the pharmacists look for anyone who take large doses of it). Hope you experience is better in Aus–the drug WILL work at higher dosages with a narcotic. – Jon – Hide quoted text — Show quoted text – >:University teaching hospitals’ pain clinics can also offer the latest treatments >:and in some cases treatments/medications that have not been released to >:the public. >Just returned from my my first visit to the pain clinic. They’ve put me on >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It >hasn’t been fully released in Australia yet – does anyone have feedback on >its success, side effects etc?

Response:

Tramadol is Ultram. :) > – Hide quoted text — Show quoted text – > :University teaching hospitals’ pain clinics can also offer the latest treatments > :and in some cases treatments/medications that have not been released to > :the public. > Just returned from my my first visit to the pain clinic. They’ve put me on > Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It > hasn’t been fully released in Australia yet – does anyone have feedback on > its success, side effects etc?

Response:

> Just returned from my my first visit to the pain clinic. They’ve put me on > Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It > hasn’t been fully released in Australia yet – does anyone have feedback on > its success, side effects etc?

I have had bad experiences with "new" drugs.Make sure you are aware of all reported side effects BEFORE you start taking it Don’t know this one,but be careful with experimental pain meds.I was taking Ketalar when they were first trialing it.It seemed OK for my pain,then I broke my toe caught it on a stool,didn’t take much notice(these things happen). A week later I went face first into the tiled floor,after I missed the step(the afore mentioned toe was no help)Broke my nose had 7 or so stitches in my forehead. Next visit to the pain clinic"Oh my God what happened to you"  Then he tells me Ketelar disassociates mind and body and this was the most probable cause for my for my fall and the broken toe.I stopped taking it and only then did people start telling me how distant and disconected I had been. aussie annieb

Response:

Dear Scarlet, I’ve been casually using Ultram against lower back pain since 10 years. I think that there are not many people who have been taking this med for such a long time.Two years ago I started going to a pain-clinic, where the doctors recommended me to take 200 – 300 mg daily  (up to 400 mg).  I can say that this medication helped me to cut the highest pain-level. For me (and fore some other people of this ng) Tramal has an antidepressant effect too. When I first took Ultram/Tramal, I only needed the half dose to get a recognizable pain relief. Since it has no severe side-effects for me, I don’t had a problem with upping the dose. My doc told me that the possibility of  withdrawal effects can be ruled out. In spite of this I am concerned about addiction because if I foget to take my morning pill I feel pretty bad – like catching a cold, very tired and simultaneously cold and hot. This could be withdrawl symtoms. I hope this information helps you, Sigrid – Hide quoted text — Show quoted text ->Just returned from my my first visit to the pain clinic. They’ve put me on >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It >hasn’t been fully released in Australia yet – does anyone have feedback on >its success, side effects etc?

Response:

Just go to the place on your keyboard (go to) write in www. pain clinic.com  it will tell you of clinics in your home town or close by.It did for me.                  Good luck,Donnie

God Be With You, Donnie & Judy

Response:

Scarlet, I have been taking Ultram (Tramadol) for several months now. I take them with my hydrocodone (5 vicodins a day)  to "boost" it. I’ve tried taking it alone and I didn’t get any pain relief.  I’ve tried taking it with 2 extra strength tylenol ( yes, that’s right, OTC tylenol ) and got some relief. I feel it is a pretty worthwhile antidepressant though, which is to say I must get something out of it, any change in the way I view my pain is appreciated. Perhaps I am looking for it to act like a narcotic and when it doesn’t (no itching, no need for the deep breath, no warm fuzzy feeling, etc), I feel it’s not any good.  If I could ever get over this herniated disc problem in my neck and get back to my regular arthritis, I would like to try it for just those symptoms. My friend with fibromyalgia thinks they work great and I’ve heard others say they liked the pain relief it gives them. Shauna – Hide quoted text — Show quoted text – > :University teaching hospitals’ pain clinics can also offer the latest treatments > :and in some cases treatments/medications that have not been released to > :the public. > Just returned from my my first visit to the pain clinic. They’ve put me on > Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It > hasn’t been fully released in Australia yet – does anyone have feedback on > its success, side effects etc?

Response:

I’ve been taking Ultam for about four years and I swear by it. It seem to help the pain that the narcotics don’t touch. It wears off after four hours, so it’s not hard to tell whether it’s working or not. I also take the equivalent of 16 Vicodins a day, so Ultam isn’t my primary pain drug, but I wouldn’t give it up. I think it has done a job on my stomach, though. I never had heartburn before. Now it’s like lava. Don’t know for sure if there’s a connection, but a lot of H2O seems to help. Purple – Hide quoted text — Show quoted text – >:University teaching hospitals’ pain clinics can also offer the latest treatments >:and in some cases treatments/medications that have not been released to >:the public. >Just returned from my my first visit to the pain clinic. They’ve put me on >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It >hasn’t been fully released in Australia yet – does anyone have feedback on >its success, side effects etc?

Response:

I’ve been suffering from back pain for some time now (a few months) and I too find that Tramadol helps and gives some kind of antidepressant effect.  I’m not on many pain killers now but I find if I take  50mg pill before I go to bed I can rise easily in the morning and feel ready to go to work. If I don’t I find it really hard to get out of bed and feel tired all day.  Could be related to the pain causing a shut down of the sympathetic nervous system and when the pain is gone the system comes back and performs more "normally". Just a hypothesis. – Hide quoted text — Show quoted text -> Dear Scarlet, > I’ve been casually using Ultram against lower back pain since 10 years. I > think that there are not many people who have been taking this med for such > a long time.Two years ago I started > going to a pain-clinic, where the doctors recommended me to take 200 – 300 > mg daily  (up to 400 mg).  I can say that this medication helped me to cut > the highest pain-level. > For me (and fore some other people of this ng) Tramal has an antidepressant > effect too. > When I first took Ultram/Tramal, I only needed the half dose to get a > recognizable pain relief. Since it has no severe side-effects for me, I > don’t had a problem with upping the dose. > My doc told me that the possibility of  withdrawal effects can be ruled out. > In spite of this I am concerned about addiction because if I foget to take > my morning pill I feel pretty bad – like catching a cold, very tired and > simultaneously cold and hot. This could be withdrawl symtoms. > I hope this information helps you, > Sigrid >Just returned from my my first visit to the pain clinic. They’ve put me on >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It >hasn’t been fully released in Australia yet – does anyone have feedback on >its success, side effects etc?

Response:

Hey….me too. In fact, I find that this effect lasts about 2-4 hours longer than the pain relief.  I can’t be sure, but I think it’s at least partially related to the stimulant properties of Ultram.  The antidepressant effects might contribute too.  At first, I put it off as simply a result of getting a GOOD night’s sleep finally.  But I don’t know that I believe that anymore. It seems to be realted to the drug, and is dose dependant (up to a point). Anyone else got ideas on why Ultram does this? Spiggy – Hide quoted text — Show quoted text – > I’ve been suffering from back pain for some time now (a few months) and I too > find that Tramadol helps and gives some kind of antidepressant effect.     I’m > not on many pain killers now but I find if I take  50mg pill before I go to > bed I can rise easily in the morning and feel ready to go to work. If I don’t > I find it really hard to get out of bed and feel tired all day.  Could be > related to the pain causing a shut down of the sympathetic nervous system and > when the pain is gone the system comes back and performs more "normally". > Just a hypothesis. > Dear Scarlet, > I’ve been casually using Ultram against lower back pain since 10 years. I > think that there are not many people who have been taking this med for such > a long time.Two years ago I started > going to a pain-clinic, where the doctors recommended me to take 200 – 300 > mg daily  (up to 400 mg).  I can say that this medication helped me to cut > the highest pain-level. > For me (and fore some other people of this ng) Tramal has an antidepressant > effect too. > When I first took Ultram/Tramal, I only needed the half dose to get a > recognizable pain relief. Since it has no severe side-effects for me, I > don’t had a problem with upping the dose. > My doc told me that the possibility of  withdrawal effects can be ruled out. > In spite of this I am concerned about addiction because if I foget to take > my morning pill I feel pretty bad – like catching a cold, very tired and > simultaneously cold and hot. This could be withdrawl symtoms. > I hope this information helps you, > Sigrid > >Just returned from my my first visit to the pain clinic. They’ve put me on > >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It > >hasn’t been fully released in Australia yet – does anyone have feedback on > >its success, side effects etc?

Response:

When I was taking 300-400mg a day I was getting reasonable sleep simply because the pain was relieved.  Now that I only occasionally take tramadol, I find that if I take it before going to bed I don’t sleep as well, I’m restless and a bit itchy but I can get out of bed easy in the morning.  It seems as if I don’t get as deep a sleep as I would normally do. Sunday night I took 50mg when I went to bed and I managed to do a full days work starting at 8.30 in the morning.  I didn’t take any since then and although I’m not in pain, I got to work at 10.30 na dI’m struggling to lift my hands to the keyboard.  I’ve got to get this sorted. Steve – Hide quoted text — Show quoted text – > Hey….me too. In fact, I find that this effect lasts about 2-4 hours longer > than the pain relief.  I can’t be sure, but I think it’s at least partially > related to the stimulant properties of Ultram.     The antidepressant effects > might contribute too.  At first, I put it off as simply a result of getting a > GOOD night’s sleep finally.  But I don’t know that I believe that anymore. > It seems to be realted to the drug, and is dose dependant (up to a point). > Anyone else got ideas on why Ultram does this? > Spiggy > I’ve been suffering from back pain for some time now (a few months) and I too > find that Tramadol helps and gives some kind of antidepressant effect. I’m > not on many pain killers now but I find if I take  50mg pill before I go to > bed I can rise easily in the morning and feel ready to go to work. If I don’t > I find it really hard to get out of bed and feel tired all day.  Could be > related to the pain causing a shut down of the sympathetic nervous system and > when the pain is gone the system comes back and performs more "normally". > Just a hypothesis. > > Dear Scarlet, > > I’ve been casually using Ultram against lower back pain since 10 years. I > > think that there are not many people who have been taking this med for such > > a long time.Two years ago I started > > going to a pain-clinic, where the doctors recommended me to take 200 – 300 > > mg daily  (up to 400 mg).  I can say that this medication helped me to cut > > the highest pain-level. > > For me (and fore some other people of this ng) Tramal has an antidepressant > > effect too. > > When I first took Ultram/Tramal, I only needed the half dose to get a > > recognizable pain relief. Since it has no severe side-effects for me, I > > don’t had a problem with upping the dose. > > My doc told me that the possibility of  withdrawal effects can be ruled out. > > In spite of this I am concerned about addiction because if I foget to take > > my morning pill I feel pretty bad – like catching a cold, very tired and > > simultaneously cold and hot. This could be withdrawl symtoms. > > I hope this information helps you, > > Sigrid > > >Just returned from my my first visit to the pain clinic. They’ve put me on > > >Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It > > >hasn’t been fully released in Australia yet – does anyone have feedback on > > >its success, side effects etc?

Response:

:When I was taking 300-400mg a day I was getting reasonable sleep simply :because the pain was relieved. That’s all I want. A good night sleep. Is that too much too ask??? Apparently so. Today my G.P refused to give me another prescription for Panadeine forte. Her theory is that the reason I’m not sleeping at night is because I’m not getting up early in the day, so my sleep pattern is out of whack. She completely ignored the fact that the reason I don’t get up ’til noon is ‘cos I didn’t get to sleep ’til 4 am. Why? Because of the *pain*. She just could not grasp the concept. I had to bite my tongue to stop myself from bursting into tears. I have experienced negative attitudes regarding codeine etc. but from *my own doctor*???? Pah!! She also is concerned that I have been on Panadeine forte for 6 months now, & is concerned about the long term side effects. What about my present sanity??? :        Now that I only occasionally take tramadol, I :find that if I take it before going to bed I don’t sleep as well, I’m :restless and a bit itchy but I can get out of bed easy in the morning. It :seems as if I don’t get as deep a sleep as I would normally do. Sorry ’bout that rant, but I’m extremely frustrated…back on topic… I was taking 150mg Ultram a day for a week & it didn’t do much. When I told my doctor (not the aforementioned. This was at the pain clinic.) this, he said "it’s not the drug for you then". This was disappointing, as from what I’ve read it seemed to be the perfect drug for me. I’m also taking anti-depressants (depression caused by my pain), & maybe I could’ve stopped them if Ultram has anti-depressant side effects. Scarlet

Response:

Sandra, If you are in the US, you might be able to find a pain doctor through this website. I hope it helps. http://www.abpm.org/ Lily Women do come with instructions….ask them! Artificial Intelligence is no match for natural stupidity. *delete the colour of my hair from my address to send e-mail to me*

Response:

> Can anyone tell me what resources there are to find a chronic pain clinic? > Sandy D.

Your local phone book.  A recommendation from your doctor.  Your insurance company. Chris Owens

Response:

:University teaching hospitals’ pain clinics can also offer the latest treatments :and in some cases treatments/medications that have not been released to :the public. Just returned from my my first visit to the pain clinic. They’ve put me on Tramal (Tramadol hydrochloride) as a substitute for Panedeine forte. It hasn’t been fully released in Australia yet – does anyone have feedback on its success, side effects etc?

Response:

Can anyone tell me what resources there are to find a chronic pain clinic? Sandy D.

Response:

Hi Sandra!!      There are a lot of resources here.  If you don’t find what you need please get back to us!!  ;-) http://www.c2corp.com/painresource1.html Hugz,  Jane

|Can anyone tell me what resources there are to find a chronic pain clinic? |Sandy D. | |

Response:

Pain clinics, like other specialized clinics, offer a wider range of treatment options then a doctor’s office that doesn’t specialize in pain treatment.  Depending on the disorder that causes your pain, pain clinics offer everything from botox injections, epidural blocks, electric stimulation, medication pumps to narcotic therapy. University teaching hospitals’ pain clinics can also offer the latest treatments and in some cases treatments/medications that have not been released to the public.  Its always best to see a specialist when dealing with a chronic disorder. Good luck.

Response:

Well, I went to the pain clinic today. I met with the doctor and told him what I wanted and he agreed to give it to me if I agreed to take his class. It’s a three week class… 8-4/M-F. I agreed to start classes today since there weren’t any openings for the next three weeks. I got in because some people canceled out due to weather this week. The only thing the doctor and I didn’t agree on is the use of breakthru meds. He feels that the base drug should be titrated so that breakthru meds aren’t needed. I guess he doesn’t figure people do different levels of physical activity and need that extra boost. His reasoning was… of course… fear of addiction with the IR meds. He did tell me I could continue using my hydrocodone PRN while we’re adjusting the base med. Oh, and he wrote me a script for oxycontin before we finished the meeting. I’m waiting to take my first one tonight to get on the correct 12 hour dosing schedule. For those interested in what happened during my day at the pain clinic… it started with the nurse taking blood pressure, temp, pulse, and asking pain level (they’re JCAHO). :) I guess they do that routine every morning. Then I talked to the doctor. After that, I started the actual class. Since I wasn’t there in the morning for class, I missed the physician lecture, stretch and flex, and group bio feedback. I did sit in on the nutrition class and the stress management class. The stress management one was interesting… we talked about sexual side effects of different drugs people take who have chronic pain… AD’s, opiates, etc.. I also talked to some lady who will do the bio feedback stuff when it comes around again. I was sent to physical therapy where we discussed doing water therapy and what to do about my ankle. I missed my appointment with the nurse to do a full intake, so that will be fit in tomorrow. Tomorrow I will be starting at the ungodly hour of 8 in the morning with a private water therapy session. I expressed concern at getting into a swimming pool since I don’t know how to swim and that I might panic. Therefore, I will start with a private session instead of the group one as most people do. They seem to try to tailor the program to your individual needs. There are some things you do as a group and other things you do individually based on personal needs. I’ll be spending more time with physical therapy because I have that ankle pain and the edema that they would like to get under control. They did offer a psychologist… but it’s completely at my discretion and I would need to request a consultation… it’s not required. They’re also going to teach me some basic simple exercises that help with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation period each day too. I guess you just sit in a recliner and relax. lol. But the best part is that they give you a free meal ticket for lunch. :) Each Friday they have a group meeting where you can bring family or friends for a "Concerned Persons Group." It was explained that they attempt to educate your family and friends what it’s like to have chronic pain and how to deal with it. Overall, it seems like a harmless class that could actually help in the long run. And they stress that it’s a holistic approach that is done in conjunction with proper pain meds, not in place of. My goals is to get my pain under control with the pain meds and the strengthening exercises so that I can start working a 40 hour week soon. Anything beyond that is a plus for me. I imagine all pain clinics are different, but I thought I’d share what the one I went to was like. Oh… and when I told them that I didn’t bring any of my pain meds because I didn’t know I’d be staying all day… they offered to get some sent up from the pharmacy. Will

Response:

Will ,    Thanks for the fill in on what the pain clinic is doing . So much of the stuff I ridiculed two years ago ( stress mgmt. , relaxation , ) I surely wish I had a better handle on now . See if you can find out if they are using this approach with RSD , specifically full body. As a pain patient who has lived with severe anxiety  , I think it is time for me to explore other avenues to compliment the medication approach . I will be interested to see what you think of their approach down the road a bit . Thanks !! Peace Richard > Well, I went to the pain clinic today. I met with the doctor and told > him what I wanted and he agreed to give it to me if I agreed to take his > class. It’s a three week class… 8-4/M-F. I agreed to start classes > today since there weren’t any openings for the next three weeks. I got > in because some people canceled out due to weather this week. The only > thing the doctor and I didn’t agree on is the use of breakthru meds. He > feels that the base drug should be titrated so that breakthru meds > aren’t needed. I guess he doesn’t figure people do different levels of > physical activity and need that extra boost. His reasoning was… of > course… fear of addiction with the IR meds. He did tell me I could > continue using my hydrocodone PRN while we’re adjusting the base med. > Oh, and he wrote me a script for oxycontin before we finished the > meeting. I’m waiting to take my first one tonight to get on the correct > 12 hour dosing schedule.

       < snip for space >

Response:

I like the holistic approach with medication. I could never afford three weeks off work, though.  I am self-employed and that would ruin me. Kay

Response:

Richard… it’s basically the same routine for everyone who comes to the clinic. They have a basic time schedule you follow that has the things I listed on it… water therapy, biofeedback, relaxation, nutrition, stress management, etc.. Then you also have an hour or two per day where they have you do individual things you request or need. For me it was physical therapy. Others might choose the psychologist, more pool time, or whatever. We did have a couple of people there for fibromyalgia who were also being given opioids. I think I remember people talking about that being one of the chronic pain diseases that they have a problem getting doctors to believe. So it appears that everyone is treated equally and they go primarily by what you state is your pain level. The doctor didn’t even glance at the x-rays I brought with me… and sent them home with me too… so he isn’t going to be looking at them later either. I felt he was just totally taking my word on everything I told him… including my pain level. I think agreeing to take the class for three weeks where he can monitor me did make a big difference though. He’ll have the opportunity to see firsthand that I’m not abusing them or anything. I was impressed that when he wrote the script he told me that these probably aren’t going to be strong enough, but that we have to start somewhere and see what works and he didn’t want me driving high in the morning to come back to the clinic. Since I’m going to be monitored every day for three weeks and can up the dosage just by asking, I have no problem starting low and moving up as needed. I’ll probably keep you all posted each day what goes on unless everyone isn’t interested. I just took my first oxycontin about 45 minutes ago… :) Will – Hide quoted text — Show quoted text – > Will , >    Thanks for the fill in on what the pain clinic is doing . So much of the > stuff I ridiculed two years ago ( stress mgmt. , relaxation , ) I surely wish > I had a better handle on now . See if you can find out if they are using this > approach with RSD , specifically full body. As a pain patient who has lived > with severe anxiety  , I think it is time for me to explore other avenues to > compliment the medication approach . I will be interested to see what you > think of their approach down the road a bit . Thanks !! > Peace > Richard

Response:

- Hide quoted text — Show quoted text ->Well, I went to the pain clinic today. I met with the doctor and told >him what I wanted and he agreed to give it to me if I agreed to take his >class. It’s a three week class… 8-4/M-F. I agreed to start classes >today since there weren’t any openings for the next three weeks. I got >in because some people canceled out due to weather this week. The only >thing the doctor and I didn’t agree on is the use of breakthru meds. He >feels that the base drug should be titrated so that breakthru meds >aren’t needed. I guess he doesn’t figure people do different levels of >physical activity and need that extra boost. His reasoning was… of >course… fear of addiction with the IR meds. He did tell me I could >continue using my hydrocodone PRN while we’re adjusting the base med. >Oh, and he wrote me a script for oxycontin before we finished the >meeting. I’m waiting to take my first one tonight to get on the correct >12 hour dosing schedule. >For those interested in what happened during my day at the pain >clinic… it started with the nurse taking blood pressure, temp, pulse, >and asking pain level (they’re JCAHO). :) I guess they do that routine >every morning. Then I talked to the doctor. After that, I started the >actual class. Since I wasn’t there in the morning for class, I missed >the physician lecture, stretch and flex, and group bio feedback. I did >sit in on the nutrition class and the stress management class. The >stress management one was interesting… we talked about sexual side >effects of different drugs people take who have chronic pain… AD’s, >opiates, etc.. I also talked to some lady who will do the bio feedback >stuff when it comes around again. I was sent to physical therapy where >we discussed doing water therapy and what to do about my ankle. I missed >my appointment with the nurse to do a full intake, so that will be fit >in tomorrow. >Tomorrow I will be starting at the ungodly hour of 8 in the morning with >a private water therapy session. I expressed concern at getting into a >swimming pool since I don’t know how to swim and that I might panic. >Therefore, I will start with a private session instead of the group one >as most people do. They seem to try to tailor the program to your >individual needs. There are some things you do as a group and other >things you do individually based on personal needs. I’ll be spending >more time with physical therapy because I have that ankle pain and the >edema that they would like to get under control. They did offer a >psychologist… but it’s completely at my discretion and I would need to >request a consultation… it’s not required. >They’re also going to teach me some basic simple exercises that help >with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation >period each day too. I guess you just sit in a recliner and relax. lol. >But the best part is that they give you a free meal ticket for lunch. :) >Each Friday they have a group meeting where you can bring family or >friends for a "Concerned Persons Group." It was explained that they >attempt to educate your family and friends what it’s like to have >chronic pain and how to deal with it. >Overall, it seems like a harmless class that could actually help in the >long run. And they stress that it’s a holistic approach that is done in >conjunction with proper pain meds, not in place of. My goals is to get >my pain under control with the pain meds and the strengthening exercises >so that I can start working a 40 hour week soon. Anything beyond that is >a plus for me. I imagine all pain clinics are different, but I thought >I’d share what the one I went to was like. Oh… and when I told them >that I didn’t bring any of my pain meds because I didn’t know I’d be >staying all day… they offered to get some sent up from the pharmacy. >Will > Well, sheeeit…..three weeks? Is this good news?<g> > Crafty

Good that I’m now on oxycontin… bad that I just postponed interviewing and looking at jobs for another three weeks. Cash donations will be accepted. :) Will

Response:

Hi Kay Yeah, they kind of are asking a lot to give up three weeks for most people. I’m lucky (?) that I’m on SSDI right now and can do it. However, I just put out about a dozen resumes in the last week or two and it does postpone starting work anywhere for awhile. We do get out early on Friday afternoon though, so I can go to an interview if one should come up. I went to this pain clinic last year and they sent a recommendation to my primary care doctor to start me on hydrocodone. They didn’t make me take the class for those. I think with the big gun opioids they want to monitor you is part of the reason for the class. At least that’s the feeling I get besides the basic education/holistic part of it all. Will – Hide quoted text — Show quoted text – > I like the holistic approach with medication. I could never afford three weeks > off work, though.  I am self-employed and that would ruin me. > Kay

Response:

sounds like extortion…you can have meds if you sign up for a course….sorry…but that sounds like extortion to me…but I hope it is helpful and look forward to hearing about your experiences.  Good Luck..

– Hide quoted text — Show quoted text -> Well, I went to the pain clinic today. I met with the doctor and told > him what I wanted and he agreed to give it to me if I agreed to take his > class. It’s a three week class… 8-4/M-F. I agreed to start classes > today since there weren’t any openings for the next three weeks. I got > in because some people canceled out due to weather this week. The only > thing the doctor and I didn’t agree on is the use of breakthru meds. He > feels that the base drug should be titrated so that breakthru meds > aren’t needed. I guess he doesn’t figure people do different levels of > physical activity and need that extra boost. His reasoning was… of > course… fear of addiction with the IR meds. He did tell me I could > continue using my hydrocodone PRN while we’re adjusting the base med. > Oh, and he wrote me a script for oxycontin before we finished the > meeting. I’m waiting to take my first one tonight to get on the correct > 12 hour dosing schedule. > For those interested in what happened during my day at the pain > clinic… it started with the nurse taking blood pressure, temp, pulse, > and asking pain level (they’re JCAHO). :) I guess they do that routine > every morning. Then I talked to the doctor. After that, I started the > actual class. Since I wasn’t there in the morning for class, I missed > the physician lecture, stretch and flex, and group bio feedback. I did > sit in on the nutrition class and the stress management class. The > stress management one was interesting… we talked about sexual side > effects of different drugs people take who have chronic pain… AD’s, > opiates, etc.. I also talked to some lady who will do the bio feedback > stuff when it comes around again. I was sent to physical therapy where > we discussed doing water therapy and what to do about my ankle. I missed > my appointment with the nurse to do a full intake, so that will be fit > in tomorrow. > Tomorrow I will be starting at the ungodly hour of 8 in the morning with > a private water therapy session. I expressed concern at getting into a > swimming pool since I don’t know how to swim and that I might panic. > Therefore, I will start with a private session instead of the group one > as most people do. They seem to try to tailor the program to your > individual needs. There are some things you do as a group and other > things you do individually based on personal needs. I’ll be spending > more time with physical therapy because I have that ankle pain and the > edema that they would like to get under control. They did offer a > psychologist… but it’s completely at my discretion and I would need to > request a consultation… it’s not required. > They’re also going to teach me some basic simple exercises that help > with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation > period each day too. I guess you just sit in a recliner and relax. lol. > But the best part is that they give you a free meal ticket for lunch. :) > Each Friday they have a group meeting where you can bring family or > friends for a "Concerned Persons Group." It was explained that they > attempt to educate your family and friends what it’s like to have > chronic pain and how to deal with it. > Overall, it seems like a harmless class that could actually help in the > long run. And they stress that it’s a holistic approach that is done in > conjunction with proper pain meds, not in place of. My goals is to get > my pain under control with the pain meds and the strengthening exercises > so that I can start working a 40 hour week soon. Anything beyond that is > a plus for me. I imagine all pain clinics are different, but I thought > I’d share what the one I went to was like. Oh… and when I told them > that I didn’t bring any of my pain meds because I didn’t know I’d be > staying all day… they offered to get some sent up from the pharmacy. > Will

Response:

I am sorry to say I have been looking for work for over 12 months after completing a Network Engineering Technology (4.0 GPA/Honor Role/Deans List) course with certifications in Novell and Microsoft (CNE & MCSE) and there is a catch 22 to actually getting hired….OSHA precludes allowing you to work while on the medications and you are uninsurable for Workman’s Comp and other liability issues…even though we all know that our alertness is not effected by the medications, we are pinned with a sign that says stay away from this person because they are high risk…employers can get information on any person who is on SSDI/Medicare including a full pharmacology report when prescribed class 2 narcotics..your life is an open book and even without your permission they can find this information and refuse to hire or follow up after an initial interview and getting your SSI number on an application. I have been fighting this in Congress with my local representatives and there is pending legislation (forget about it being signed by Bush) to limit the access to this information by employers..until then we are going to be refused an opportunity to return to the working world while on class 2’s A very sad state of affairs but reality and truth.  In addition, I don’t know anyone who has gone through the long wait of determination of benefits and the additional 24 month waiting period for Medicare coverage that has not been financially harmed resulting in negative items on a credit report…also a source of information for employers and many will not hire if you have credit problems…another sad but truthful fact… SUCKS!..and I am angry and frustrated…I am able and willing to work if someone would look past my physical problems that do not effect the ability to get the job done and do it well.. I wish you luck in your job search but be prepared for what I have just detailed of my own personal experiences.. Alan

– Hide quoted text — Show quoted text -> >Well, I went to the pain clinic today. I met with the doctor and told > >him what I wanted and he agreed to give it to me if I agreed to take his > >class. It’s a three week class… 8-4/M-F. I agreed to start classes > >today since there weren’t any openings for the next three weeks. I got > >in because some people canceled out due to weather this week. The only > >thing the doctor and I didn’t agree on is the use of breakthru meds. He > >feels that the base drug should be titrated so that breakthru meds > >aren’t needed. I guess he doesn’t figure people do different levels of > >physical activity and need that extra boost. His reasoning was… of > >course… fear of addiction with the IR meds. He did tell me I could > >continue using my hydrocodone PRN while we’re adjusting the base med. > >Oh, and he wrote me a script for oxycontin before we finished the > >meeting. I’m waiting to take my first one tonight to get on the correct > >12 hour dosing schedule. > >For those interested in what happened during my day at the pain > >clinic… it started with the nurse taking blood pressure, temp, pulse, > >and asking pain level (they’re JCAHO). :) I guess they do that routine > >every morning. Then I talked to the doctor. After that, I started the > >actual class. Since I wasn’t there in the morning for class, I missed > >the physician lecture, stretch and flex, and group bio feedback. I did > >sit in on the nutrition class and the stress management class. The > >stress management one was interesting… we talked about sexual side > >effects of different drugs people take who have chronic pain… AD’s, > >opiates, etc.. I also talked to some lady who will do the bio feedback > >stuff when it comes around again. I was sent to physical therapy where > >we discussed doing water therapy and what to do about my ankle. I missed > >my appointment with the nurse to do a full intake, so that will be fit > >in tomorrow. > >Tomorrow I will be starting at the ungodly hour of 8 in the morning with > >a private water therapy session. I expressed concern at getting into a > >swimming pool since I don’t know how to swim and that I might panic. > >Therefore, I will start with a private session instead of the group one > >as most people do. They seem to try to tailor the program to your > >individual needs. There are some things you do as a group and other > >things you do individually based on personal needs. I’ll be spending > >more time with physical therapy because I have that ankle pain and the > >edema that they would like to get under control. They did offer a > >psychologist… but it’s completely at my discretion and I would need to > >request a consultation… it’s not required. > >They’re also going to teach me some basic simple exercises that help > >with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation > >period each day too. I guess you just sit in a recliner and relax. lol. > >But the best part is that they give you a free meal ticket for lunch. :) > >Each Friday they have a group meeting where you can bring family or > >friends for a "Concerned Persons Group." It was explained that they > >attempt to educate your family and friends what it’s like to have > >chronic pain and how to deal with it. > >Overall, it seems like a harmless class that could actually help in the > >long run. And they stress that it’s a holistic approach that is done in > >conjunction with proper pain meds, not in place of. My goals is to get > >my pain under control with the pain meds and the strengthening exercises > >so that I can start working a 40 hour week soon. Anything beyond that is > >a plus for me. I imagine all pain clinics are different, but I thought > >I’d share what the one I went to was like. Oh… and when I told them > >that I didn’t bring any of my pain meds because I didn’t know I’d be > >staying all day… they offered to get some sent up from the pharmacy. > >Will > Well, sheeeit…..three weeks? Is this good news?<g> > Crafty > Good that I’m now on oxycontin… bad that I just postponed interviewing and > looking at jobs for another three weeks. Cash donations will be accepted. :) > Will

Response:

Please keep us up to date on your experiences…I would like to see if extortion really works…sorry…if your program works…I should not be so quick to the fire on this one..I am very interested in how your days go and how you are treated.. Alan

– Hide quoted text — Show quoted text -> Richard… it’s basically the same routine for everyone who comes to the clinic. > They have a basic time schedule you follow that has the things I listed on it… > water therapy, biofeedback, relaxation, nutrition, stress management, etc.. Then > you also have an hour or two per day where they have you do individual things > you request or need. For me it was physical therapy. Others might choose the > psychologist, more pool time, or whatever. We did have a couple of people there > for fibromyalgia who were also being given opioids. I think I remember people > talking about that being one of the chronic pain diseases that they have a > problem getting doctors to believe. So it appears that everyone is treated > equally and they go primarily by what you state is your pain level. The doctor > didn’t even glance at the x-rays I brought with me… and sent them home with me > too… so he isn’t going to be looking at them later either. I felt he was just > totally taking my word on everything I told him… including my pain level. I > think agreeing to take the class for three weeks where he can monitor me did > make a big difference though. He’ll have the opportunity to see firsthand that > I’m not abusing them or anything. I was impressed that when he wrote the script > he told me that these probably aren’t going to be strong enough, but that we > have to start somewhere and see what works and he didn’t want me driving high in > the morning to come back to the clinic. Since I’m going to be monitored every > day for three weeks and can up the dosage just by asking, I have no problem > starting low and moving up as needed. I’ll probably keep you all posted each day > what goes on unless everyone isn’t interested. I just took my first oxycontin > about 45 minutes ago… :) > Will > Will , >    Thanks for the fill in on what the pain clinic is doing . So much of the > stuff I ridiculed two years ago ( stress mgmt. , relaxation , ) I surely wish > I had a better handle on now . See if you can find out if they are using this > approach with RSD , specifically full body. As a pain patient who has lived > with severe anxiety  , I think it is time for me to explore other avenues to > compliment the medication approach . I will be interested to see what you > think of their approach down the road a bit . Thanks !! > Peace > Richard

Response:

Will, Good luck with the classes.  Keep us posted. The Dr. at the hospital where I go, who runs the pain clinic and the pain service for inpatients also does not believe in breakthrough meds and that your base med should be titrated up…..who knows…. Feel better.  I hope the oxycontin works well for you. Robin I am *not* a Medical Doctor (MD) or *any* other type of Medical Professional. PLEASE consult your own Dr. for medical advice.  The information posted is information I have learned from researching or learning from my own disease.

Response:

Will, sounds like a winning situation. When you saw this pain doctor last year you weren’t ready to try alternatives to medication. I don’t see this decision to participate in the pain clinic as giving into extortion but more as you being ready to look at your life in a more holistic way. Plus you are planning to return to full-time employment so it makes sense to have as many useful ideas as possible for handling pain issues. And last, you are having these severe edema and ankle problems and this gives you nearly three weeks of daily contact with physical therapists and other medical professionals. Good luck and do let us know how it goes. Jennie…. – Hide quoted text — Show quoted text -> Well, I went to the pain clinic today. I met with the doctor and told > him what I wanted and he agreed to give it to me if I agreed to take his > class. It’s a three week class… 8-4/M-F. I agreed to start classes > today since there weren’t any openings for the next three weeks. I got > in because some people canceled out due to weather this week. The only > thing the doctor and I didn’t agree on is the use of breakthru meds. He > feels that the base drug should be titrated so that breakthru meds > aren’t needed. I guess he doesn’t figure people do different levels of > physical activity and need that extra boost. His reasoning was… of > course… fear of addiction with the IR meds. He did tell me I could > continue using my hydrocodone PRN while we’re adjusting the base med. > Oh, and he wrote me a script for oxycontin before we finished the > meeting. I’m waiting to take my first one tonight to get on the correct > 12 hour dosing schedule. > For those interested in what happened during my day at the pain > clinic… it started with the nurse taking blood pressure, temp, pulse, > and asking pain level (they’re JCAHO). :) I guess they do that routine > every morning. Then I talked to the doctor. After that, I started the > actual class. Since I wasn’t there in the morning for class, I missed > the physician lecture, stretch and flex, and group bio feedback. I did > sit in on the nutrition class and the stress management class. The > stress management one was interesting… we talked about sexual side > effects of different drugs people take who have chronic pain… AD’s, > opiates, etc.. I also talked to some lady who will do the bio feedback > stuff when it comes around again. I was sent to physical therapy where > we discussed doing water therapy and what to do about my ankle. I missed > my appointment with the nurse to do a full intake, so that will be fit > in tomorrow. > Tomorrow I will be starting at the ungodly hour of 8 in the morning with > a private water therapy session. I expressed concern at getting into a > swimming pool since I don’t know how to swim and that I might panic. > Therefore, I will start with a private session instead of the group one > as most people do. They seem to try to tailor the program to your > individual needs. There are some things you do as a group and other > things you do individually based on personal needs. I’ll be spending > more time with physical therapy because I have that ankle pain and the > edema that they would like to get under control. They did offer a > psychologist… but it’s completely at my discretion and I would need to > request a consultation… it’s not required. > They’re also going to teach me some basic simple exercises that help > with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation > period each day too. I guess you just sit in a recliner and relax. lol. > But the best part is that they give you a free meal ticket for lunch. :) > Each Friday they have a group meeting where you can bring family or > friends for a "Concerned Persons Group." It was explained that they > attempt to educate your family and friends what it’s like to have > chronic pain and how to deal with it. > Overall, it seems like a harmless class that could actually help in the > long run. And they stress that it’s a holistic approach that is done in > conjunction with proper pain meds, not in place of. My goals is to get > my pain under control with the pain meds and the strengthening exercises > so that I can start working a 40 hour week soon. Anything beyond that is > a plus for me. I imagine all pain clinics are different, but I thought > I’d share what the one I went to was like. Oh… and when I told them > that I didn’t bring any of my pain meds because I didn’t know I’d be > staying all day… they offered to get some sent up from the pharmacy.

Response:

>> For those interested in what happened during my day at the pain

clinic… it started with the nurse taking blood pressure, temp, pulse, and asking pain level << The anti-narcotic and narcotics are evil messages will begin soon. !^NavFont02F00C00007RGHHGC1D9E3 !N3

Response:

Interesting . . . some of it (biofeedback, nursing management, relaxation) sounds a lot like what I did last year in the psych program as an outpatient at a local hospital.  Sounds like it could be really useful, Will. mary – Hide quoted text — Show quoted text – >Well, I went to the pain clinic today. I met with the doctor and told >him what I wanted and he agreed to give it to me if I agreed to take his >class. It’s a three week class… 8-4/M-F. I agreed to start classes >today since there weren’t any openings for the next three weeks. I got >in because some people canceled out due to weather this week. The only >thing the doctor and I didn’t agree on is the use of breakthru meds. He >feels that the base drug should be titrated so that breakthru meds >aren’t needed. I guess he doesn’t figure people do different levels of >physical activity and need that extra boost. His reasoning was… of >course… fear of addiction with the IR meds. He did tell me I could >continue using my hydrocodone PRN while we’re adjusting the base med. >Oh, and he wrote me a script for oxycontin before we finished the >meeting. I’m waiting to take my first one tonight to get on the correct >12 hour dosing schedule. >For those interested in what happened during my day at the pain >clinic… it started with the nurse taking blood pressure, temp, pulse, >and asking pain level (they’re JCAHO). :) I guess they do that routine >every morning. Then I talked to the doctor. After that, I started the >actual class. Since I wasn’t there in the morning for class, I missed >the physician lecture, stretch and flex, and group bio feedback. I did >sit in on the nutrition class and the stress management class. The >stress management one was interesting… we talked about sexual side >effects of different drugs people take who have chronic pain… AD’s, >opiates, etc.. I also talked to some lady who will do the bio feedback >stuff when it comes around again. I was sent to physical therapy where >we discussed doing water therapy and what to do about my ankle. I missed >my appointment with the nurse to do a full intake, so that will be fit >in tomorrow. >Tomorrow I will be starting at the ungodly hour of 8 in the morning with >a private water therapy session. I expressed concern at getting into a >swimming pool since I don’t know how to swim and that I might panic. >Therefore, I will start with a private session instead of the group one >as most people do. They seem to try to tailor the program to your >individual needs. There are some things you do as a group and other >things you do individually based on personal needs. I’ll be spending >more time with physical therapy because I have that ankle pain and the >edema that they would like to get under control. They did offer a >psychologist… but it’s completely at my discretion and I would need to >request a consultation… it’s not required. >They’re also going to teach me some basic simple exercises that help >with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation >period each day too. I guess you just sit in a recliner and relax. lol. >But the best part is that they give you a free meal ticket for lunch. :) >Each Friday they have a group meeting where you can bring family or >friends for a "Concerned Persons Group." It was explained that they >attempt to educate your family and friends what it’s like to have >chronic pain and how to deal with it. >Overall, it seems like a harmless class that could actually help in the >long run. And they stress that it’s a holistic approach that is done in >conjunction with proper pain meds, not in place of. My goals is to get >my pain under control with the pain meds and the strengthening exercises >so that I can start working a 40 hour week soon. Anything beyond that is >a plus for me. I imagine all pain clinics are different, but I thought >I’d share what the one I went to was like. Oh… and when I told them >that I didn’t bring any of my pain meds because I didn’t know I’d be >staying all day… they offered to get some sent up from the pharmacy. >Will

Response:

>sounds like extortion…you can have > meds if you sign up for a > course….sorry…but that sounds like > extortion to me…but I hope it is helpful > and look forward to hearing about your > experiences. Good Luck..

  ===  ===  === Alan,    Prior to going on opioids for chronic (read lifetime) use, I had to go to a pain clinic, also.  At the time, I felt like you.    Looking back, it was one of the best moves I ever made.  I actually turned down the opportunity 2 years earlier, thinking, "I’m not gonna let some shrink poke around in my head AND pay for his Ferrari!".  Now I see the reasoning behind it.    For one thing, they have a chance to interact with you over an extended period of time.  They see your good days and the days where you’d rather be dead.  They see you when you hurt so bad a bowel movement is nearly impossible.    Second … trust is built.  The begin to take you at your word, and don’t get suspicious when you suggest things, or ask for your meds to be upped.  In other words, they LISTEN.    I’m still going to my pain clinic.  I see my psych guy every couple months, or whenever my pain starts to get the better of me.  There’s new coping skills being developed every day, as well as new PT modalities. The pain clinic helps me to make informed decisions about where I want to go, as far as my pain’s concerned.    They know I’m telling the truth and are truthful to me in return. I’m allowed to try different meds, but always go back to methadone, as it has *no* side-effects on me — not even constipation!    A GOOD pain clinic could be the first step in reclaiming your life. Pain doesn’t *have* to win. — Harley "Can’t hang with the big dogs?  Stay on the porch!"

Response:

>Well, I went to the pain clinic today. I met with the doctor and told >him what I wanted and he agreed to give it to me if I agreed to take his >class. It’s a three week class… 8-4/M-F. I agreed to start classes >today since there weren’t any openings for the next three week

I think,  but I could be wrong, that some doctors use this idea to get someone to take a class, then after the three weeks they come out and say something similiar to "see you truly don’t need pain medications as if you were in that much pain you would not have been able to go through a complete three week course".  Then you go back and say that you pushed yourself, or were just barely able to do it, etc.  But it’ll end with him saying something along the lines of "you can do whatever you can if you set your mind to it..including not taking pain medications and beating the pain".  All of this may or may not be good for you, depending on the situation.   Just a heads up there for you. George

Response:

I could have probably talked my way out of the classes. I did last year when I saw him and got a reference letter for hydrocodone to take to my PCP. I was actually kind of open to taking the class before I went there. I get to see a PT, a nutritionist, nurses, and all these other people every day for three weeks and they’re helping me to work on my pain with other things than just meds. I’ve noticed that my physical strength and stamina has gone downhill over the past few months since getting out of school. I’ve become much more sedentary because of the pain. So they will be helping to teach me non weight bearing exercises and monitoring me so I don’t have a heart attack and all that other neat stuff that you can’t get doing it yourself at home. Will – Hide quoted text — Show quoted text – > sounds like extortion…you can have meds if you sign up for a > course….sorry…but that sounds like extortion to me…but I hope it is > helpful and look forward to hearing about your experiences.  Good Luck.. > Well, I went to the pain clinic today. I met with the doctor and told > him what I wanted and he agreed to give it to me if I agreed to take his > class. It’s a three week class… 8-4/M-F. I agreed to start classes > today since there weren’t any openings for the next three weeks. I got > in because some people canceled out due to weather this week. The only > thing the doctor and I didn’t agree on is the use of breakthru meds. He > feels that the base drug should be titrated so that breakthru meds > aren’t needed. I guess he doesn’t figure people do different levels of > physical activity and need that extra boost. His reasoning was… of > course… fear of addiction with the IR meds. He did tell me I could > continue using my hydrocodone PRN while we’re adjusting the base med. > Oh, and he wrote me a script for oxycontin before we finished the > meeting. I’m waiting to take my first one tonight to get on the correct > 12 hour dosing schedule. > For those interested in what happened during my day at the pain > clinic… it started with the nurse taking blood pressure, temp, pulse, > and asking pain level (they’re JCAHO). :) I guess they do that routine > every morning. Then I talked to the doctor. After that, I started the > actual class. Since I wasn’t there in the morning for class, I missed > the physician lecture, stretch and flex, and group bio feedback. I did > sit in on the nutrition class and the stress management class. The > stress management one was interesting… we talked about sexual side > effects of different drugs people take who have chronic pain… AD’s, > opiates, etc.. I also talked to some lady who will do the bio feedback > stuff when it comes around again. I was sent to physical therapy where > we discussed doing water therapy and what to do about my ankle. I missed > my appointment with the nurse to do a full intake, so that will be fit > in tomorrow. > Tomorrow I will be starting at the ungodly hour of 8 in the morning with > a private water therapy session. I expressed concern at getting into a > swimming pool since I don’t know how to swim and that I might panic. > Therefore, I will start with a private session instead of the group one > as most people do. They seem to try to tailor the program to your > individual needs. There are some things you do as a group and other > things you do individually based on personal needs. I’ll be spending > more time with physical therapy because I have that ankle pain and the > edema that they would like to get under control. They did offer a > psychologist… but it’s completely at my discretion and I would need to > request a consultation… it’s not required. > They’re also going to teach me some basic simple exercises that help > with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation > period each day too. I guess you just sit in a recliner and relax. lol. > But the best part is that they give you a free meal ticket for lunch. :) > Each Friday they have a group meeting where you can bring family or > friends for a "Concerned Persons Group." It was explained that they > attempt to educate your family and friends what it’s like to have > chronic pain and how to deal with it. > Overall, it seems like a harmless class that could actually help in the > long run. And they stress that it’s a holistic approach that is done in > conjunction with proper pain meds, not in place of. My goals is to get > my pain under control with the pain meds and the strengthening exercises > so that I can start working a 40 hour week soon. Anything beyond that is > a plus for me. I imagine all pain clinics are different, but I thought > I’d share what the one I went to was like. Oh… and when I told them > that I didn’t bring any of my pain meds because I didn’t know I’d be > staying all day… they offered to get some sent up from the pharmacy. > Will

Response:

Thanks for the well wishes and the info, Alan. I hadn’t heard about the employers accessing SSA records before. Is there somewhere on the net I can go to read about it more? Will – Hide quoted text — Show quoted text – > I am sorry to say I have been looking for work for over 12 months after > completing a Network Engineering Technology (4.0 GPA/Honor Role/Deans List) > course with certifications in Novell and Microsoft (CNE & MCSE) and there is > a catch 22 to actually getting hired….OSHA precludes allowing you to work > while on the medications and you are uninsurable for Workman’s Comp and > other liability issues…even though we all know that our alertness is not > effected by the medications, we are pinned with a sign that says stay away > from this person because they are high risk…employers can get information > on any person who is on SSDI/Medicare including a full pharmacology report > when prescribed class 2 narcotics..your life is an open book and even > without your permission they can find this information and refuse to hire or > follow up after an initial interview and getting your SSI number on an > application. > I have been fighting this in Congress with my local representatives and > there is pending legislation (forget about it being signed by Bush) to limit > the access to this information by employers..until then we are going to be > refused an opportunity to return to the working world while on class 2’s > A very sad state of affairs but reality and truth.  In addition, I don’t > know anyone who has gone through the long wait of determination of benefits > and the additional 24 month waiting period for Medicare coverage that has > not been financially harmed resulting in negative items on a credit > report…also a source of information for employers and many will not hire > if you have credit problems…another sad but truthful fact… > SUCKS!..and I am angry and frustrated…I am able and willing to work if > someone would look past my physical problems that do not effect the ability > to get the job done and do it well.. > I wish you luck in your job search but be prepared for what I have just > detailed of my own personal experiences.. > Alan > > >Well, I went to the pain clinic today. I met with the doctor and told > > >him what I wanted and he agreed to give it to me if I agreed to take > his > > >class. It’s a three week class… 8-4/M-F. I agreed to start classes > > >today since there weren’t any openings for the next three weeks. I got > > >in because some people canceled out due to weather this week. The only > > >thing the doctor and I didn’t agree on is the use of breakthru meds. He > > >feels that the base drug should be titrated so that breakthru meds > > >aren’t needed. I guess he doesn’t figure people do different levels of > > >physical activity and need that extra boost. His reasoning was… of > > >course… fear of addiction with the IR meds. He did tell me I could > > >continue using my hydrocodone PRN while we’re adjusting the base med. > > >Oh, and he wrote me a script for oxycontin before we finished the > > >meeting. I’m waiting to take my first one tonight to get on the correct > > >12 hour dosing schedule. > > >For those interested in what happened during my day at the pain > > >clinic… it started with the nurse taking blood pressure, temp, pulse, > > >and asking pain level (they’re JCAHO). :) I guess they do that routine > > >every morning. Then I talked to the doctor. After that, I started the > > >actual class. Since I wasn’t there in the morning for class, I missed > > >the physician lecture, stretch and flex, and group bio feedback. I did > > >sit in on the nutrition class and the stress management class. The > > >stress management one was interesting… we talked about sexual side > > >effects of different drugs people take who have chronic pain… AD’s, > > >opiates, etc.. I also talked to some lady who will do the bio feedback > > >stuff when it comes around again. I was sent to physical therapy where > > >we discussed doing water therapy and what to do about my ankle. I > missed > > >my appointment with the nurse to do a full intake, so that will be fit > > >in tomorrow. > > >Tomorrow I will be starting at the ungodly hour of 8 in the morning > with > > >a private water therapy session. I expressed concern at getting into a > > >swimming pool since I don’t know how to swim and that I might panic. > > >Therefore, I will start with a private session instead of the group one > > >as most people do. They seem to try to tailor the program to your > > >individual needs. There are some things you do as a group and other > > >things you do individually based on personal needs. I’ll be spending > > >more time with physical therapy because I have that ankle pain and the > > >edema that they would like to get under control. They did offer a > > >psychologist… but it’s completely at my discretion and I would need > to > > >request a consultation… it’s not required. > > >They’re also going to teach me some basic simple exercises that help > > >with arthritis type of pain. We’ll see. :) Oh, and we have a relaxation > > >period each day too. I guess you just sit in a recliner and relax. lol. > > >But the best part is that they give you a free meal ticket for lunch. > :) > > >Each Friday they have a group meeting where you can bring family or > > >friends for a "Concerned Persons Group." It was explained that they > > >attempt to educate your family and friends what it’s like to have > > >chronic pain and how to deal with it. > > >Overall, it seems like a harmless class that could actually help in the > > >long run. And they stress that it’s a holistic approach that is done in > > >conjunction with proper pain meds, not in place of. My goals is to get > > >my pain under control with the pain meds and the strengthening > exercises > > >so that I can start working a 40 hour week soon. Anything beyond that > is > > >a plus for me. I imagine all pain clinics are different, but I thought > > >I’d share what the one I went to was like. Oh… and when I told them > > >that I didn’t bring any of my pain meds because I didn’t know I’d be > > >staying all day… they offered to get some sent up from the pharmacy. > > >Will > > Well, sheeeit…..three weeks? Is this good news?<g> > > Crafty > Good that I’m now on oxycontin… bad that I just postponed interviewing > and > looking at jobs for another three weeks. Cash donations will be accepted. > :) > Will

Response:

I’ll keep you all posted. And it’s not as bad as it sounds. I’m impressed with them so far. Will – Hide quoted text — Show quoted text – > Please keep us up to date on your experiences…I would like to see if > extortion really works…sorry…if your program works…I should not be so > quick to the fire on this one..I am very interested in how your days go and > how you are treated.. > Alan > Richard… it’s basically the same routine for everyone who comes to the > clinic. > They have a basic time schedule you follow that has the things I listed on > it… > water therapy, biofeedback, relaxation, nutrition, stress management, > etc.. Then > you also have an hour or two per day where they have you do individual > things > you request or need. For me it was physical therapy. Others might choose > the > psychologist, more pool time, or whatever. We did have a couple of people > there > for fibromyalgia who were also being given opioids. I think I remember > people > talking about that being one of the chronic pain diseases that they have a > problem getting doctors to believe. So it appears that everyone is treated > equally and they go primarily by what you state is your pain level. The > doctor > didn’t even glance at the x-rays I brought with me… and sent them home > with me > too… so he isn’t going to be looking at them later either. I felt he was > just > totally taking my word on everything I told him… including my pain > level. I > think agreeing to take the class for three weeks where he can monitor me > did > make a big difference though. He’ll have the opportunity to see firsthand > that > I’m not abusing them or anything. I was impressed that when he wrote the > script > he told me that these probably aren’t going to be strong enough, but that > we > have to start somewhere and see what works and he didn’t want me driving > high in > the morning to come back to the clinic. Since I’m going to be monitored > every > day for three weeks and can up the dosage just by asking, I have no > problem > starting low and moving up as needed. I’ll probably keep you all posted > each day > what goes on unless everyone isn’t interested. I just took my first > oxycontin > about 45 minutes ago… :) > Will > > Will , > >    Thanks for the fill in on what the pain clinic is doing . So much of > the > > stuff I ridiculed two years ago ( stress mgmt. , relaxation , ) I surely > wish > > I had a better handle on now . See if you can find out if they are using > this > > approach with RSD , specifically full body. As a pain patient who has > lived > > with severe anxiety  , I think it is time for me to explore other > avenues to > > compliment the medication approach . I will be interested to see what > you > > think of their approach down the road a bit . Thanks !! > > Peace > > Richard

Response:

Thanks Robin :) The 10 mg he started me on did nothing… no pain relief, no high, nothing. Might as well have been candy. The doctor was really busy today because being behind due to weather issues this week… so I didn’t get in to see him. However, I talked to the nurse and she said that there would be no problem increasing my dosage… but I need to see the doctor to do it. She promised she would get me in tomorrow. An interesting comment she made to me too… she said in an offhand kind of way that I’m no where near what my dose will be when I leave in three weeks. That sounded promising to me. :) Will – Hide quoted text — Show quoted text – > Will, > Good luck with the classes.  Keep us posted. > The Dr. at the hospital where I go, who runs the pain clinic and the pain > service for inpatients also does not believe in breakthrough meds and that your > base med should be titrated up…..who knows…. > Feel better.  I hope the oxycontin works well for you. > Robin > I am *not* a Medical Doctor (MD) or *any* other type of Medical Professional. > PLEASE consult your own Dr. for medical advice.  The information posted is > information I have learned from researching or learning from my own disease.

Response:

I don’t see it as extortion either, Jennie. I could have talked my way out of the classes if I really wanted to. As much as I gripe about stuff, I think deep down I knew the classes would be good for me and I kinda wanted to take them. There’s also the personal and professional interest in learning what they do at a pain clinic. I wish I could talk them into offering some basic voc rehab counseling to exiting clients and hire me to do it. :) I talked to a physical rehab guy today. We’re going to figure out some non weight bearing exercises for me to do. My stamina is way down since finishing school and I need to get it back up if I ever want to last a forty hour work week. I’m going to be fitted for a custom stocking thing to help control the edema. It’s some kind of compression stocking. However, they don’t have them to fit me, so I’m going to get a custom one made just for me. I am in really bad pain after being there doing things all day today… but a lot of it is muscle pain from once again using those muscles I forgot I had. I also used my free lunch pass today and hit the salad bar in the hospital cafeteria. The free lunch pass doesn’t work at the McDonalds located in the hospital. lol. Anyway, I ate so much salad that I was tired after lunch. I’m not used to eating lunch. Oh, and I found out what relaxation time is… we sit in recliners in a dimly lit room and listen to those mood tapes where the guy with deep voice almost hypnotizes you. And I went to the pool today too. They had a bar thing set up where I could stay between the two bars and never let go. It wasn’t as bad as I thought it would be. It’s amazing how heavy you are when you walk out of the pool though. You go from weighing nothing to weighing like ten tons it feels like. First time in a pool for me… so I didn’t know about that phenomena. Stress management was on depression and sexual side effects again. Strawberries and whipped cream where recommended by the psychologist teaching the class to increase interest in sexual relations. Nutrition class was boring again… we learned the five basic food groups… that pyramid thing. Let’s see… oh, the only other class was the exercise one. We sat in chairs and lifted these one pound weights. Nothing big… no running a mile or anything like that. :) The most exercise I got was walking from the pain center all the way to the other end of the hospital to get to the cafeteria at lunch… and then all the way back too. lol. So that was my day today. I’m going to meet with the doctor tomorrow to get my oxycontin dosage increased. What I’m taking now doesn’t do anything at all for pain. I’m not sure they’re even as good as a vicodin as far as pain control. So, I’m hoping he’ll at least double my dosage. First thing tomorrow is physical therapy for my ankle. Will – Hide quoted text — Show quoted text – > Will, sounds like a winning situation. When you saw this pain doctor last > year you weren’t ready to try alternatives to medication. I don’t see this > decision to participate in the pain clinic as giving into extortion but > more as you being ready to look at your life in a more holistic way. Plus > you are planning to return to full-time employment so it makes sense to > have as many useful ideas as possible for handling pain issues. And last, > you are having these severe edema and ankle problems and this gives you > nearly three weeks of daily contact with physical therapists and other > medical professionals. Good luck and do let us know how it goes. > Jennie….

Response:

> >> For those interested in what happened during my day at the pain > clinic… it started with the nurse taking blood pressure, temp, pulse, > and asking pain level << > The anti-narcotic and narcotics are evil messages will begin soon.

Nope… getting a script for oxycontin was next. :) Will

Response:

My pain has gotten worse because of inactivity as much as anything in the last few months. If any of this helps me get some stamina and strength back, then I’m all for it. I haven’t gotten to do the biofeedback yet because I started the program later then the others during the week… but I’m looking forward to learning more about what it is about. The part I like with this program is that they consider the opiates to be an important part of the overall program. Their goal is to get you titrated by the end of the three weeks of classes. Hey, a little exercise and some education about pain management can’t hurt anyone. :) – Hide quoted text — Show quoted text – > Interesting . . . some of it (biofeedback, nursing management, relaxation) > sounds a lot like what I did last year in the psych program as an outpatient > at a local hospital.  Sounds like it could be really useful, Will. > mary

Response:

> Hehe, good luck Will….that class sounds like torture to me<g>. > Crafty

Thanks Crafty. For me… besides the personal reasons for taking the classes, I also have a professional interest in learning more about these things. I want to help people with disabilities to get jobs. So the more I can learn about different disabilities and how the impact the person, the better counselor I can become. I get to talk in person with my fellow pain patients there each day about their disabilities and how it has affected their life. I also get to talk to the doctors and professionals and get their perspective on things. Heck, if I could make a career out of it, I’d go back to school forever. :) Will

Response:

- Hide quoted text — Show quoted text ->sounds like extortion…you can have > meds if you sign up for a > course….sorry…but that sounds like > extortion to me…but I hope it is helpful > and look forward to hearing about your > experiences. Good Luck.. >   ===  ===  === > Alan, >    Prior to going on opioids for chronic (read lifetime) use, I had to go > to a pain clinic, also.  At the time, I felt like you. >    Looking back, it was one of the best moves I ever made.  I actually > turned down the opportunity 2 years earlier, thinking, "I’m not gonna let > some shrink poke around in my head AND pay for his Ferrari!".  Now I see > the reasoning behind it. >    For one thing, they have a chance to interact with you over an extended > period of time.  They see your good days and the days where you’d rather > be dead.  They see you when you hurt so bad a bowel movement is nearly > impossible. >    Second … trust is built.  The begin to take you at your word, and > don’t get suspicious when you suggest things, or ask for your meds to be > upped.  In other words, they LISTEN. >    I’m still going to my pain clinic.  I see my psych guy every couple > months, or whenever my pain starts to get the better of me.  There’s new > coping skills being developed every day, as well as new PT modalities. The > pain clinic helps me to make informed decisions about where I want to go, > as far as my pain’s concerned. >    They know I’m telling the truth and are truthful to me in return. I’m > allowed to try different meds, but always go back to methadone, as it has > *no* side-effects on me — not even constipation! >    A GOOD pain clinic could be the first step in reclaiming your life. > Pain doesn’t *have* to win. > — > Harley > "Can’t hang with the big dogs?  Stay on the porch!"

Right on, Harley! We’ve all heard of the scam pain clinics that just do the other stuff and not the pain meds. But I feel that one that just does the pain meds and doesn’t do any of the other things could be just as bad. While I may not utilize all of the things I learn at this pain clinic, at least I was given the opportunity to try them and find out first hand if they would work for me. I am also being educated on what to expect with these pain meds. How many questions do we see here every day that should have been answered by the doctor before ever scripting the meds? This pain center is making sure people know all the good and all the bad and how to overcome some of the bad stuff instead of just handing them a script and sending ‘em out to learn it on their own. Will

Response:

- Hide quoted text — Show quoted text ->Well, I went to the pain clinic today. I met with the doctor and told >him what I wanted and he agreed to give it to me if I agreed to take his >class. It’s a three week class… 8-4/M-F. I agreed to start classes >today since there weren’t any openings for the next three week > I think,  but I could be wrong, that some doctors use this idea to get someone to > take a class, then after the three weeks they come out and say something similiar > to "see you truly don’t need pain medications as if you were in that much pain > you would not have been able to go through a complete three week course".  Then > you go back and say that you pushed yourself, or were just barely able to do it, > etc.  But it’ll end with him saying something along the lines of "you can do > whatever you can if you set your mind to it..including not taking pain > medications and beating the pain".  All of this may or may not be good for you, > depending on the situation. > Just a heads up there for you. > George

Thanks for the heads up… but I don’t feel that this pain center is the way you describe. They started me on my oxycontin the first day there and will titrate it to the proper amount while I’m there. Therefore, they can say I made it the three weeks, but only because I was on the oxycontin that they scripted me from the very beginning. They don’t make you take the classes with the promise of drugs later… they give the drugs and then you start classes. Will

Response:

Greetings. Has anyone here been referred to a pain clinic? If so, what can I expect? Has anyone found benefit?? Many thanks. dee

Response:

 Be very very careful because there are quite a few of these pain facilities that are nothing but a scam.  They tend to detox you off of any pain medication youmay be taking and then try to teach you to handle the pain by changing your thought process. Some are good tho. Ted – Hide quoted text — Show quoted text – > Greetings. > Has anyone here been referred to a pain clinic? If so, what can I > expect? > Has anyone found benefit?? Many thanks. dee

Response:

Hi Dee, There are different "philosophies" among clinics just as there are among MD’s or RN’s or any other profession. Some believe in getting you off all meds (the detox philosophy) and there are those that promote "all natural" methods and there are those that use a multitude of approaches and techniques. Unfortunately there is no set of guidelines accepted and/or approved by all. My personal philosophy is to seek a "group" of clinicians dedicated to the relief of pain. The multi-disciplinary approach makes the most sense to me. Since pain involves a multitude of systems (body, mind, spirit), then the approach should include treatment for the affected. I know there are many who would disagree with this approach and that’s there right. But to isolate treatment to one aspect is to ignore the depth of suffering in the areas ignored. Unrelieved pain is one of the leading causes of suicide, destruction of a marriage and family, loss of time from work, destruction of "self", and obliteration of "spirit". Clinicians included in this multi-disciplinary approach include anesthesiologists/anesthetists, internal medicine, orthopedic/neurosurgery/neurologist, psychiatry/psychology, physical/occupational therapy, spiritual guidance (priest, rabbi, minister, etc.), nurse practitioner, nurse clinicians, and others. Family inclusion and education is important also since unrelieved pain can be as destructive to other members of the family as it is to the person experiencing the pain. Education about medications and therapies is important for all involved. Dr. David Leak (www.painnet.com) has provided us with important questions to ask of any clinic or single practitioner to assist in the decision to choose the practitioner that will meet our needs. Questions YOU Should Ask of People That Are Treating Your Pain and Some of the Answers YOU Should Get When Sent to a Pain Specialist or Center Q. Is this practice dedicated solely to the diagnosis and treatment of pain? A. Answer should be:      Yes, we practice full-time in the practice of pain medicine / management. Q. Are all the staff fully dedicated to the diagnosis and treatment of pain? A. Answer should be:      Yes, except for part-time filing personnel or "generic" ancillary staff ( people who      collect lab specimens, other medical technicians ). Q. How many full time staff are on the team? A. Answer should be:      Minimally a secretary / receptionist, a nurse, a behavioral specialist, and a physician. 3a.) What are their specialties? Q. Do you have part time staff? A. Answer should be:      Yes, or no, but the physician and primary nursing staff should not be part time. 4a.) What are their specialties?      Physical therapy, occupational therapy, phlebotomy, dietary, social work, radiology      technician, and administrative personnel. Q. Did you train specifically in the diagnosis and treatment of pain? A. Answer should be:      Yes!!      * Note economic pressures have caused many physicians to practice in the area of      pain medicine / management without adequate training! Q. How long was your training in pain? A. Answer should be for a physician :      Fellowships ( Fellowship, a period of intense medical specialty training after completion      of residency training ) prior to 1993, six (6 ) months were wide spread, however, from      1993 forward fellowships of one year were more common. Q. Where did you do your training specifically in pain? A. Answer should be:      At a university or with a proctor for an extended period of time (6-36 months).      Week-end orientation courses or short visits with experts do not count as training.      Orientation courses can only attest to physical presence at a course, not to      demonstrated mastery knowledge or skills. Q. What do you use to monitor outcomes? A. Answer should be:      Master Piece Medical, or an equivalent. If a test is ordered: 9a.) What is the purpose of the test? 9b.) What difference will this test make in my treatment? If a consult ( the opinion or evaluation of another specialist ) is requested: 10a.) What type of specialist is being consulted, and why? 10b.) Will the consult make any difference in my treatment? If a procedure is recommended: 11a.) What is the purpose of the procedure ?      i. Diagnostic ( to tell what the problem is )      ii. Therapeutic ( for treatment )      iii. Pre-emptive ( to prevent pain from becoming worse due to a planned surgery )      11b.) Where did you learn this procedure?      11c.) How many of these procedures have you done?      11d.) What is likely to happen if the procedure is not done? One additional question: What is your philosophy of using opioids for pain if more conservative therapies are ineffectual in relieving my pain? Answer: If it’s necessary, I’ll prescribe them for as long as necessary. If I can be of any other assistance, let me know. Feel free to visit my web site for additional links and information. — Jack Stem Midwest Anesthesia Consultants Conscious Sedation, Pain Management, PICC Lines, Chart Review http://www.bergsmyriad.com/macindex.htm "One person CAN make a difference. Be that person" – Hide quoted text — Show quoted text – > Greetings. > Has anyone here been referred to a pain clinic? If so, what can I > expect? > Has anyone found benefit?? Many thanks. dee

Response:

The one I go to likes to use nerve block shots, but not working well for me. They have been trying to find some kind of morphine I can take that won’t make me sick . I get mad at them a lot but that is the nature of the pain and it is nice to have them call once a week to see how I am doing. I am in TN, could not even get good pain meds til I went to Pain Clinic. Am also going to chiropractor in spite of Harrington rods from L3 to T4 and physical therapy and keep thinking about the life I am going to have once we get the pain under control. Every good day I do all I can to make worthwhile….read somewhere that hard times breed character. Karen Shelton "Giving up is not an option" – Hide quoted text — Show quoted text – > Be very very careful because there are quite a few of these pain facilities >that are nothing but a scam.  They tend to detox you off of any pain >medication youmay be taking and then try to teach you to handle the pain by >changing your thought process. >Some are good tho. >Ted > Greetings. > Has anyone here been referred to a pain clinic? If so, what can I > expect? > Has anyone found benefit?? Many thanks. dee

Response:

prevacid, how long before it works

Question:

Prilosec reaches peak effectiveness after taking it for a few days. It is a real powerful Proton Pump Inhibitor that stops most of the acid the stomach produces. Sometimes any minor side effects go away once your body adjusts to the drug. Some people find that they can take the drug for a couple of months and then stop without reoccurrence of the symptoms. Others have to be on the drug continually. Glad you were able to get some free samples. Don’t be afraid to ask for more the next time you visit your doctor. Heartburn and Gastro Esophageal Reflux web page: http://www.heartburn-help.com

Response:

> Prilosec reaches peak effectiveness after taking it for a few days. It is a > real powerful Proton Pump Inhibitor that stops most of the acid the stomach > produces. Sometimes any minor side effects go away once your body adjusts to > the drug. Some people find that they can take the drug for a couple of months > and then stop without reoccurrence of the symptoms. Others have to be on the > drug continually. Glad you were able to get some free samples. Don’t be afraid > to ask for more the next time you visit your doctor. > Heartburn and Gastro Esophageal Reflux web page:

http://www.heartburn-help.com As far as I’m concerned, an in my particular case, it’s a miracle drug.  I had a chat with my Doc. as I was leaving his office and we discussed first (antacids), second (Zantac, et. al.) and third (Prilosec and Prevacid) generation acid reducers and how each worked, and how much acid they reduced and patents and when things go over the counter, and generics and such.  Very interesting to hear his knowledge on the subject.  He said that Prilosec (and, I assume Prevacid too..).. won’t go OTC for 15-20 years. Like the H2 blockers, Zantac, Pepcid, Axid, and so on, did a few years ago, and now there are even cheap generics available for those "..dine"s.   So it’s gonna stay expensive and Rx for a long time as long as only one company can make and sell it. Harv

Response:

>He said that Prilosec (and, I assume Prevacid too..).. won’t go OTC for 15-20

years.>> The Prilosec people just made a pitch to the FDA to take Prilosec over the counter.  Members of the Food and Drug Administration (FDA) committee said they believed Prilosec could be safe and effective as a nonprescription product. But a majority of panelists said they needed more information on long-term use before recommending that Prilosec be made readily available on drugstore shelves. They were concerned about the labeling and how the consumer might use the drug. The Prilosec people put a positive spin on everything saying it is quite common for the FDA to want more information and they were quite encouraged. A generic version of Prilosec will be available in some countries outside the USA maybe as early as next year. I am glad that Prilosec is working well for you Harv. I have been taking it for over 3 years now and it has been a miracle drug for me as well. Heartburn and Gastro Esophageal Reflux web page: http://www.heartburn-help.com

Response:

> Sounds like you are producing some extra stomach acid when you are under stress > and your lower esophageal sphincter is a little on the weak side. Chocolate is > a known trigger food. I have similar symptoms.

Ding! and also Ding!.. you got that right.  I was an idiot to eat all those leftover chocolate bars after Halloween.. plus stress piled upon stress as I explained.  But when you feel fine, it’s hard to remember what it’s like when the burn starts.. so you do dumb things thinking it’ll be okay.  Well, another hard lesson learned.. > When I get a little out of > control I back off to a bland diet for a while and try to reduce the

amount of I’m curious what your "bland diet" consists of.. could you detail what you switch to during your episodes? > stress I am under. (Not easy sometimes to do that) Some people respond better > to the compounds that make up one of the Proton Pump Inhibitors than the other. > If you find one does not work well then switch to another. Try to get some > samples of Prilosec for times like you are experiencing now. It is much better > to get things under control as soon as possible. The recovery time is much > shorter.

I went through a bout of this a year ago, and the year before that.  I put off calling the Doc but just made an appointment for tomorrow.  He’s seen me for this condition twice before.. it seems to be a yearly thing with me and I haven’t had the burn for a year, but with the combination of the stress and the chocolate, blammo, back it came.  Exactly the same symptoms. Prilosec did it for me the last time, so I’m going to ask him for it again, as I had success with it. Thanks, Harv

Response:

Try asking your doctor for some samples of Prilosec. Sometimes they will give you a handful. Bland diet. I stick with things that I know do not bother me. Pears in the can and the juice. Toast, Chicken, potatoes, lots of water but a little at a time if too much makes you reflux. Then once I am feeling better I start introducing the next level. Red meat etc. I found onions, nutmeg and tomatoes are a big trigger for me so I stay away from these even when I am feeling good. When the urge for pizza get real bad my wife makes some with just a little tomato sauce. I add some cheese and hamburger with a little Tummy Tamer to neutralize the acid and I can get away with it. Heartburn and Gastro Esophageal Reflux web page: http://www.heartburn-help.com

Response:

> Try asking your doctor for some samples of Prilosec. Sometimes they will give > you a handful.

I saw my Doc. two days ago.  He put me back on Prilosec, 40mg. caps this time instead of 20mg. that I had last year.  He handed me two sample boxes with seven caps each ($3.00 each cap, if filled from an Rx typically). I’ve taken three so far.  The burn is 3/4ths gone already.  It’s either a miracle drug (for me) or it’s utter coincidence.  Choose one.  Side effects?  None that I’ve noticed, except for some gas. He also gave me an Rx good for 2 months’ worth in case I need to stay on it after the 14 free caps are gone. Harv

Response:

Background – I am having a bout of hiatal hernia/ulcer right now and am about ready to call the doc again.. I had it last year (and have had it in previous years) and am 100% convinced it is brought on by stress  and trigger foods – a close friend recently passed away causing much stress and angst and emotion, then Halloween came and I bought 100 mini chocolate bars to give to kids who never came so over the course of a few days I ate them all myself.. I think the chocolate is an irritant that might have pushed my condition over the edge.. since then, financial woes, plus the election.. add it all up and I have a real good burn going under that bottom little lump of my breastbone, exactly as I had a year ago.  I can feel it when I press it hard with a couple fingers, just as the last time. Funny thing is, I can sleep fine.. it’s only after I get up and the day’s travails start to hit me that the burn comes back.  I’m trying to change my diet, trying different things, but it also kills my appetite when I’m in this condition.  Glugging down antacids and taking Axid which seems not to help at all. So.. to get back to your question, and realizing everyone is different.. Last year my Doc put me on Prevacid.. first with three or four sample packages, and then with one or two full Rx refills.. it didn’t do squat. Did not help one iota. Nothing.  So I asked him to switch me to Prilosec. With a few days I felt the burn going away, I took it for about two months (which at $3.00 per cap, 2 caps a day, cost me over $500.00 for the two drugs.. out of pocket!..).. but for me, and speaking only for myself, Prilosec worked, and Prevacid didn’t do diddley.  Either that or it was simply time that healed it, although I tend to believe the Prilosec is what did it. Harv — Founder of AmigaZone. Supporting Amiga owners since 1985! Go here for info or to join: http://www.amigazone.com

– Hide quoted text — Show quoted text -> supposed to start taking prevacid.  how long before it starts to work? > thnks, > M.

Response:

Sounds like you are producing some extra stomach acid when you are under stress and your lower esophageal sphincter is a little on the weak side. Chocolate is a known trigger food. I have similar symptoms. When I get a little out of control I back off to a bland diet for a while and try to reduce the amount of stress I am under. (Not easy sometimes to do that) Some people respond better to the compounds that make up one of the Proton Pump Inhibitors than the other. If you find one does not work well then switch to another. Try to get some samples of Prilosec for times like you are experiencing now. It is much better to get things under control as soon as possible. The recovery time is much shorter. Heartburn and Gastro Esophageal Reflux web page: http://www.heartburn-help.com

Response:

supposed to start taking prevacid.  how long before it starts to work? thnks, M.

Response:

>supposed to start taking prevacid.  how long before it starts to work? >thnks, >M.

   When I started taking it, it worked immediately – that same day! I felt wonderful. However, if I forget to take it – it stops working right on cue. It’s been a godsend for me. I hope it does the trick for you too. Debi

Response:

Pain causing panic?

Question:

    Hi, I have posted here earlier regarding a chronic headache clinic. My new question has to do with panic attacks, which I believe are a function of extreme pain. My head hurts so bad, and my symptoms are so disturbing, that I often times feel like I’m going to have a stroke/convulsion and die.     Generally what happens is that my neck and face start hurting all over, and my vision gets messed up, then I go into a migraine. At this point I’m very afraid, afraid that there is something really wrong with me, and I’m going to die. This problem has intensified in the last few months.      Anybody else here have pain so intense or symptoms so disturbing they have serious panic?

Response:

A5d,       You should see a couple hundred hands in the air. Just as pain will raise your BP, some of the pain is so intense, it’s hard to believe there is not something mortally wrong. Valium helps me, but I do get afraid . I have had panic attacks so long. I can usually wait them out. That doesn’t make them better. Also , yours sound a heck of a lot more intense in the beginning. I bet the " I’m gonna die "  panic attack is pretty well distributed throughout ASC-P. Peace, Richard

– Hide quoted text — Show quoted text ->     Hi, I have posted here earlier regarding a chronic headache clinic. My new > question has to do with panic attacks, which I believe are a function of > extreme pain. My head hurts so bad, and my symptoms are so disturbing, that I > often times feel like I’m going to have a stroke/convulsion and die. >     Generally what happens is that my neck and face start hurting all over, and > my vision gets messed up, then I go into a migraine. At this point I’m very > afraid, afraid that there is something really wrong with me, and I’m going to > die. This problem has intensified in the last few months. >      Anybody else here have pain so intense or symptoms so disturbing they have > serious panic?

Response:

I’m sorry you’re going through this.  Have you had an MRI and ruled out anything else? If so, then I can tell you first hand that panic does set in for me when nothing is working well to treat the pain, or I have nothing for it. Then, it’s a vicious circle as the meds don’t work while you’re in an advanced state of anxiety.  I’ve worked with relaxation etc.- but find a valium or ativan along with the pain meds makes them much more effective . But please get checked out, if you haven’t. ,Best of luck, and let us know how it goes, codeeee – Hide quoted text — Show quoted text ->     Hi, I have posted here earlier regarding a chronic headache clinic. My new > question has to do with panic attacks, which I believe are a function of > extreme pain. My head hurts so bad, and my symptoms are so disturbing, that I > often times feel like I’m going to have a stroke/convulsion and die. >     Generally what happens is that my neck and face start hurting all over, and > my vision gets messed up, then I go into a migraine. At this point I’m very > afraid, afraid that there is something really wrong with me, and I’m going to > die. This problem has intensified in the last few months. >      Anybody else here have pain so intense or symptoms so disturbing they have > serious panic?

Before you buy.

Response:

Do you mean the panic that comes out of no-where and have no clue as to what’s causing the feeling that you’re going to jump out of your skin,hyperventilate, maybe die?  Opposed to a feeling of panic from a known source like pain? I don;t know why you can’t have both . some attacks are triggered by previously normal events like driving,leaving the house fear of heights etc. I’m probably way off base about this, so if you can clear it up and maybe offer some solutions, it would be great Jack,  All I know, Is when you have a genuine one – there’s no mistaking it. Thank you, codeee , – Hide quoted text — Show quoted text -> You may feel panic, but you really haven’t described a "panic attack". > In no way am I trying to minimize what you’re going through. > Jack >     Hi, I have posted here earlier regarding a chronic headache clinic. My new > question has to do with panic attacks, which I believe are a function of > extreme pain. My head hurts so bad, and my symptoms are so disturbing, that I > often times feel like I’m going to have a stroke/convulsion and die. >     Generally what happens is that my neck and face start hurting all over, and > my vision gets messed up, then I go into a migraine. At this point I’m very > afraid, afraid that there is something really wrong with me, and I’m going to > die. This problem has intensified in the last few months. >      Anybody else here have pain so intense or symptoms so

disturbing they have > serious panic?

Before you buy.

Response:

I have had panic attacks in the absense of pain before. Was at the ER or ICU five times within one week in June. They did the EEGs and chest x-rays and so forth, and reassured me there was nothing wrong with my heart – thought maybe I was stressed out because my father had died a week before. The ER doctor wrote down ‘panic disorder’ on the charts, and my psychiatrist, neurologist and regular doctor agreed.       Anyway, I know what it’s like to have panic attacks. The hyperventilation,losing your breath, chest pain, misinterpretation of what your body’s doing, fear of going crazy, sweating, and so forth.     What I’m saying is that my head pain becomes so severe that it induces a panic attack. Anything that elevates anxiety will probably be prone – in my case – to cause panic. Severe head pain elevates my anxiety, and hence I become panic prone.      I have anti-anxiety medication I can take when I get these panic attacks. I have a long history of panic/anxiety. However, it wasn’t the case until recently that headaches induced panic attacks. This is a recent development; probably because the intensity of the pain has increased. I think I’m going to request an MRI because the headaches have worsened. Thanks <<<<<<<<Do you mean the panic that comes out of no-where and have no clue as to what’s causing the feeling that you’re going to jump out of your skin,hyperventilate, maybe die?  Opposed to a feeling of panic from a known source like pain? I don;t know why you can’t have both . some attacks are triggered by previously normal events like driving,leaving the house fear of heights etc. I’m probably way off base about this, so if you can clear it up and maybe offer some solutions, it would be great Jack,  All I know, Is when you have a genuine one – there’s no mistaking it. Thank you, codeee

Response:

You may feel panic, but you really haven’t described a "panic attack". In no way am I trying to minimize what you’re going through. Jack – Hide quoted text — Show quoted text – >     Hi, I have posted here earlier regarding a chronic headache clinic. My new > question has to do with panic attacks, which I believe are a function of > extreme pain. My head hurts so bad, and my symptoms are so disturbing, that I > often times feel like I’m going to have a stroke/convulsion and die. >     Generally what happens is that my neck and face start hurting all over, and > my vision gets messed up, then I go into a migraine. At this point I’m very > afraid, afraid that there is something really wrong with me, and I’m going to > die. This problem has intensified in the last few months. >      Anybody else here have pain so intense or symptoms so disturbing they have > serious panic?

Response:

"USUALLY", a "panic attack" wakes up a person from sleep, and consists of hyperventilation, rapid pulse, sweating, and a feeling of impending doom, WITHOUT being able to attribute the panic feeling to a specific cause. The person feels like they can’t "get enough air", when, in fact they are getting too much, which is why re-breathing air into a paper bag can help. These are "usually" self-limiting within a short time. I can’t overemphasize the "fear" aspect, and panic attacks account for a reasonable number of calls to 911 in the middle of the night. They do not end with a headache. There are variations on this theme (such as daytime attacks), but this is what they "usually" consists of. Yes, you can "panic" for a number of specific reasons, without a "panic attack", and you can have both at different times. If a panic attack was triggered by "driving", as in your example, you wouldn’t be able to drive. Panic, yes; panic attack, no. If they end up as a migraine (which I know something about), then the feelings you have may be a migraine prodrome, as may be the "vision" problems. However, the "feeling that you’re going to die" is NOT part of a migraine prodrome or a migraine. Wanting to die, perhaps; feeling that you will die, no. There’s just not a box to check for everything. Jack – Hide quoted text — Show quoted text – > Do you mean the panic that comes out of no-where and have no clue as > to what’s causing the feeling that you’re going to jump out of your > skin,hyperventilate, maybe die?  Opposed to a feeling of panic from a > known source like pain? I don;t know why you can’t have both . some > attacks are triggered by previously normal events like driving,leaving > the house fear of heights etc. I’m probably way off base about this, so > if you can clear it up and maybe offer some solutions, it would be great > Jack,  All I know, Is when you have a genuine one – there’s no mistaking > it. > Thank you, > codeee > , > You may feel panic, but you really haven’t described a "panic attack". > In no way am I trying to minimize what you’re going through. > Jack > >     Hi, I have posted here earlier regarding a chronic headache > clinic. My new > > question has to do with panic attacks, which I believe are a > function of > > extreme pain. My head hurts so bad, and my symptoms are so > disturbing, that I > > often times feel like I’m going to have a stroke/convulsion and die. > >     Generally what happens is that my neck and face start hurting > all over, and > > my vision gets messed up, then I go into a migraine. At this point > I’m very > > afraid, afraid that there is something really wrong with me, and I’m > going to > > die. This problem has intensified in the last few months. > >      Anybody else here have pain so intense or symptoms so > disturbing they have > > serious panic? > Before you buy.

Response:

I am sure that someone has tried you on Celexa or another SSRI, right? Those are tailor-made for panic disorder. — Bill Work

– Hide quoted text — Show quoted text -> I have had panic attacks in the absense of pain before. Was at the ER or ICU > five times within one week in June. They did the EEGs and chest x-rays and so > forth, and reassured me there was nothing wrong with my heart – thought maybe I > was stressed out because my father had died a week before. The ER doctor wrote > down ‘panic disorder’ on the charts, and my psychiatrist, neurologist and > regular doctor agreed. >     Anyway, I know what it’s like to have panic attacks. The > hyperventilation,losing your breath, chest pain, misinterpretation of what your > body’s doing, fear of going crazy, sweating, and so forth. >     What I’m saying is that my head pain becomes so severe that it induces a > panic attack. Anything that elevates anxiety will probably be prone – in my > case – to cause panic. Severe head pain elevates my anxiety, and hence I become > panic prone. >      I have anti-anxiety medication I can take when I get these panic attacks. > I have a long history of panic/anxiety. However, it wasn’t the case until > recently that headaches induced panic attacks. This is a recent development; > probably because the intensity of the pain has increased. I think I’m going to > request an MRI because the headaches have worsened. > Thanks > <<<<<<<<Do you mean the panic that comes out of no-where and have no clue as > to what’s causing the feeling that you’re going to jump out of your > skin,hyperventilate, maybe die?  Opposed to a feeling of panic from a > known source like pain? I don;t know why you can’t have both . some > attacks are triggered by previously normal events like driving,leaving > the house fear of heights etc. I’m probably way off base about this, so > if you can clear it up and maybe offer some solutions, it would be great > Jack,  All I know, Is when you have a genuine one – there’s no mistaking > it. > Thank you, > codeee

Response:

Hi Dr. Work, I cannot take SSRI antidepressant medication because for me it induces panic attacks, racing thoughts, sleeplessness, migraine and other unpleasant symptoms.      Last time I tried an SSRI I ended up in the psychiatric facility. I have a medication sensitivity problem and become ‘manicky’ when taking drugs Paxil, Prozac, Celexa, Luvox,  Zoloft and the other ones. More than one psychiatrist said it would be malpractice to give me these again, as they believed I had bipolar disorder.       That’s why I was curious about trying the Nardil; maybe this drug won’t cause the above problems?

Response:

Nardil is used as a drug of last resort.  Since you have tried others, perhaps this is the last one for you…good luck finding someone to put you on it…out of my league. — Bill Work

– Hide quoted text — Show quoted text -> Hi Dr. Work, I cannot take SSRI antidepressant medication because for me it > induces panic attacks, racing thoughts, sleeplessness, migraine and other > unpleasant symptoms. >      Last time I tried an SSRI I ended up in the psychiatric facility. I have a > medication sensitivity problem and become ‘manicky’ when taking drugs Paxil, > Prozac, Celexa, Luvox,  Zoloft and the other ones. More than one psychiatrist > said it would be malpractice to give me these again, as they believed I had > bipolar disorder. >       That’s why I was curious about trying the Nardil; maybe this drug won’t > cause the above problems?

Response:

Have you not tried lithium carbonate for bi-polar? – Hide quoted text — Show quoted text -> Nardil is used as a drug of last resort.  Since you have tried others, > perhaps this is the last one for you…good luck finding someone to put you > on it…out of my league. > — > Bill Work > Hi Dr. Work, I cannot take SSRI antidepressant medication because for me > it > induces panic attacks, racing thoughts, sleeplessness, migraine and other > unpleasant symptoms. >      Last time I tried an SSRI I ended up in the psychiatric facility. I > have a > medication sensitivity problem and become ‘manicky’ when taking drugs > Paxil, > Prozac, Celexa, Luvox,  Zoloft and the other ones. More than one > psychiatrist > said it would be malpractice to give me these again, as they believed I > had > bipolar disorder. >       That’s why I was curious about trying the Nardil; maybe this drug > won’t > cause the above problems?

Response:

  Have you not tried lithium carbonate for bi-polar? Yes, I took Lithobid for about 5 months at doses ranging from 600 to 2100mgs. The side-effects of the medication were intolerable, even with the addition of prilosec and inderal. Kept on getting flu-like symptoms, hand tremor, nausea, etc.     I don’t think the diagnosis of bipolar was necessarily valid anyway. I think most of my mental symptoms are a product of having chronic headaches, tmj, and neck pain. Psychiatry: 90 percent speculation and the 10 percent guess work.

Response:

   I have had several panic attacks due to heartburn (I think).  My head felt cold but sweat profusely, could not catch my breath and pain in my chest that felt like my heart wanted out.  Their was pain in my arms, jaw and hands and could not swallow.  I didn’t know if I wanted to stand, sit down or run.  Many images raced threw my mind then complete confusion.  I literally thought I was having a heart attach and this was it.  I eventually calmed down and drank a glass of milk and ate a few Tums.  The "attack" left as abruptly as it came.  The cause was narrowed down to the consumption of four large coffees on an empty stomach.  Scariest thing that ever happened to me in my life.   I have also noticed that since my injuries that I have an exaggerated fear of heights.  I don’t like elevators that go farther than 3 floors and will climb stairs rather than go for the ride.  Climbing stairs is tuff work but my fear prevents me from riding elevators.  I also live close to the US/Canadian Border that has about a two year old bridge.  If I can’t drive over the bridge without stopping, I will not go.  This Friday my wife and I are invited to go out for dinner on the American side, I am very concerned about the trip over this bridge and am seriously considering canceling out due to this. I feel very embarrassed about this fear and cannot get threw to my wife how disturbing this is to me.  It is very difficult communicating this fear to people, especially my wife.  She wants to jump out of a perfectly good airplane!    The odd thing is that before my injuries I used to work 60% of the time over 100 feet in the air.  This does not make sense intellectually but the fear still exists. Rob Hartley

– Hide quoted text — Show quoted text -> Do you mean the panic that comes out of no-where and have no clue as > to what’s causing the feeling that you’re going to jump out of your > skin,hyperventilate, maybe die?  Opposed to a feeling of panic from a > known source like pain? I don;t know why you can’t have both . some > attacks are triggered by previously normal events like driving,leaving > the house fear of heights etc. I’m probably way off base about this, so > if you can clear it up and maybe offer some solutions, it would be great > Jack,  All I know, Is when you have a genuine one – there’s no mistaking > it. > Thank you, > codeee > , > You may feel panic, but you really haven’t described a "panic attack". > In no way am I trying to minimize what you’re going through. > Jack > Before you buy.

Response:

Hi Jack :) Hmmmm. I agree with your statement. Maybe we confuse ‘panicdisorder’ with ‘panic attacks’.  My aunt has had them badly, and she refers to them as ’scream  dreams’.  I have had one panicattack, ( I have an anxiety/panic disorder ) because it was around 3 am.( EXTREME clausterphobia and inability to breathe/move ) All the other times, I get anxiety attacks, which are ‘milder’ ( but bladdy debilitating ). All the symptoms the above poster posted. So what makes the difference between panic disorder and anxiety disorders? My doctor sais I have ‘both’ which she misleadingly refers to both as ‘the same thing’. Though, the panic type, seems more severe. I am happy to report, that with therapy ( and no drugs!!!! ) that my aunt was able to ‘cure’ or at least put her ’scream dreams’ into remission. So there are happy endings. I prefer not to use meds, because they dont decrease my anxiety, so I am using Cognitive Behaviour Therapy to help me. That is *my*  preferred method, as I simply do not want to take Benzos. It’s helping – I can now recognise how temporary they ( anxiety attacks )are, and breathe myself through them. In fact, every time I go to refill my meds, I get one. I call going to the doc, an exercise in breathing control – and an excellent ’staged’ anxiety attack, which ‘experts’ recommend you ‘deal with’ and face and conquer. It worked the last time! Thanks and have a great day, Shauna

– Hide quoted text — Show quoted text -> "USUALLY", a "panic attack" wakes up a person from sleep, and consists > of hyperventilation, rapid pulse, sweating, and a feeling of impending > doom, WITHOUT being able to attribute the panic feeling to a specific > cause. The person feels like they can’t "get enough air", when, in fact > they are getting too much, which is why re-breathing air into a paper > bag can help. > These are "usually" self-limiting within a short time. I can’t > overemphasize the "fear" aspect, and panic attacks account for a > reasonable number of calls to 911 in the middle of the night. They do > not end with a headache. > There are variations on this theme (such as daytime attacks), but this > is what they "usually" consists of. > Yes, you can "panic" for a number of specific reasons, without a "panic > attack", and you can have both at different times. > If a panic attack was triggered by "driving", as in your example, you > wouldn’t be able to drive. Panic, yes; panic attack, no. > If they end up as a migraine (which I know something about), then the > feelings you have may be a migraine prodrome, as may be the "vision" > problems. However, the "feeling that you’re going to die" is NOT part of > a migraine prodrome or a migraine. Wanting to die, perhaps; feeling that > you will die, no. > There’s just not a box to check for everything. > Jack

Response:

My friend was on Nardil for many years for Anxiety. Worked like a charm. She discontinued after 15 years. I know it is not agood drug – my neuro would rather die than put anyone on them – but for some people – on a last resort basis, it needn’t be too bad. It worked for my friend.  We live in Canada ) Shauna

– Hide quoted text — Show quoted text -> Hi Dr. Work, I cannot take SSRI antidepressant medication because for me it > induces panic attacks, racing thoughts, sleeplessness, migraine and other > unpleasant symptoms. >      Last time I tried an SSRI I ended up in the psychiatric facility. I have a > medication sensitivity problem and become ‘manicky’ when taking drugs Paxil, > Prozac, Celexa, Luvox,  Zoloft and the other ones. More than one psychiatrist > said it would be malpractice to give me these again, as they believed I had > bipolar disorder. >       That’s why I was curious about trying the Nardil; maybe this drug won’t > cause the above problems?

Response:

Lithium has such a narrow therapeutic range…glad I don’t play with it. — Bill Work

– Hide quoted text — Show quoted text -> 2100 mg. is, IMO, a very toxic dose. 900 comes close for many. Nausea is > usually the first sign of toxicity. >   Have you not tried lithium carbonate for bi-polar? > Yes, I took Lithobid for about 5 months at doses ranging from 600 to 2100mgs. > The side-effects of the medication were intolerable, even with the addition of > prilosec and inderal. Kept on getting flu-like symptoms, hand tremor, nausea, > etc. >     I don’t think the diagnosis of bipolar was necessarily valid anyway. I > think most of my mental symptoms are a product of having chronic headaches, > tmj, and neck pain. > Psychiatry: 90 percent speculation and the 10 percent guess work.

Response:

You need to have your heart checked out. I had quadruple by-pass a year and a half ago.My biggest symptoms were anxiety and panic attacks.If you haven’t done so allready,don’t wait,check it out. Good Luck Lem

Response:

2100 mg. is, IMO, a very toxic dose. 900 comes close for many. Nausea is usually the first sign of toxicity. – Hide quoted text — Show quoted text – >   Have you not tried lithium carbonate for bi-polar? > Yes, I took Lithobid for about 5 months at doses ranging from 600 to 2100mgs. > The side-effects of the medication were intolerable, even with the addition of > prilosec and inderal. Kept on getting flu-like symptoms, hand tremor, nausea, > etc. >     I don’t think the diagnosis of bipolar was necessarily valid anyway. I > think most of my mental symptoms are a product of having chronic headaches, > tmj, and neck pain. > Psychiatry: 90 percent speculation and the 10 percent guess work.

Response:

This post is too confusing to offer an intelligent response. It also belongs in the appropriate ng. – Hide quoted text — Show quoted text – > Hi Jack :) > Hmmmm. > I agree with your statement. Maybe we confuse ‘panicdisorder’ with ‘panic > attacks’. >  My aunt has had them badly, and she refers to them as ’scream  dreams’.  I > have had one panicattack, ( I have an anxiety/panic disorder ) because it > was around 3 am.( EXTREME clausterphobia and inability to breathe/move ) All > the other times, I get anxiety attacks, which are ‘milder’ ( but bladdy > debilitating ). All the symptoms the above poster posted. > So what makes the difference between panic disorder and anxiety disorders? > My doctor sais I have ‘both’ which she misleadingly refers to both as ‘the > same thing’. Though, the panic type, seems more severe. > I am happy to report, that with therapy ( and no drugs!!!! ) that my aunt > was able to ‘cure’ or at least put > her ’scream dreams’ into remission. So there are happy endings. I prefer not > to use meds, because they > dont decrease my anxiety, so I am using Cognitive Behaviour Therapy to help > me. That is *my*  preferred method, > as I simply do not want to take Benzos. It’s helping – I can now recognise > how temporary they ( anxiety attacks )are, and breathe myself through them. > In fact, every time I go to refill my meds, I get one. I call going to the > doc, an exercise in breathing control – and an excellent > ’staged’ anxiety attack, which ‘experts’ recommend you ‘deal with’ and face > and conquer. It worked the last time! > Thanks and have a great day, > Shauna > "USUALLY", a "panic attack" wakes up a person from sleep, and consists > of hyperventilation, rapid pulse, sweating, and a feeling of impending > doom, WITHOUT being able to attribute the panic feeling to a specific > cause. The person feels like they can’t "get enough air", when, in fact > they are getting too much, which is why re-breathing air into a paper > bag can help. > These are "usually" self-limiting within a short time. I can’t > overemphasize the "fear" aspect, and panic attacks account for a > reasonable number of calls to 911 in the middle of the night. They do > not end with a headache. > There are variations on this theme (such as daytime attacks), but this > is what they "usually" consists of. > Yes, you can "panic" for a number of specific reasons, without a "panic > attack", and you can have both at different times. > If a panic attack was triggered by "driving", as in your example, you > wouldn’t be able to drive. Panic, yes; panic attack, no. > If they end up as a migraine (which I know something about), then the > feelings you have may be a migraine prodrome, as may be the "vision" > problems. However, the "feeling that you’re going to die" is NOT part of > a migraine prodrome or a migraine. Wanting to die, perhaps; feeling that > you will die, no. > There’s just not a box to check for everything. > Jack

Response:

 so I am using Cognitive Behaviour Therapy to help > me.

That is a great way to deal with anxiety, not panic attacks.

Response:

Yes, but the doses have come WAY down (from the standard 900 mg), and the signs of reversable toxicity are easily recognized by the patient. It has made many outpatients out of inpatients. It is also found in "almost therapeutic" levels in some drinking water, and is a very safe drug, IMHO. Worst problems are the interactions with everything from HCTZ to ibuprofen, but they’re not serious interactions—-just affect clearance time, and raise levels. Again, patients recognize the light nausea, sometimes tinnitus, and just skip a dose. A lot safer than buying 3 Cadillacs one weekend as has happened. And, a lot cheaper. A former internist of mine thought (only half jokingly) that it should be added to LA’s water supply—–to sorta mellow out the city. That was in the 60’s——remember those?   – Hide quoted text — Show quoted text -> Lithium has such a narrow therapeutic range…glad I don’t play with it. > — > Bill Work > 2100 mg. is, IMO, a very toxic dose. 900 comes close for many. Nausea is > usually the first sign of toxicity. > >   Have you not tried lithium carbonate for bi-polar? > > Yes, I took Lithobid for about 5 months at doses ranging from 600 to > 2100mgs. > > The side-effects of the medication were intolerable, even with the > addition of > > prilosec and inderal. Kept on getting flu-like symptoms, hand tremor, > nausea, > > etc. > >     I don’t think the diagnosis of bipolar was necessarily valid anyway. > I > > think most of my mental symptoms are a product of having chronic > headaches, > > tmj, and neck pain. > > Psychiatry: 90 percent speculation and the 10 percent guess work.

Response:

Only neuro in town (where we used to live) put my husband on lithium, of all things, for cluster and tension H.A’s.(not frequent) After a week of dragging him around and waking him in a sitting position, we figured we’d given it a shot. It seemed like a drastic measure for that kind of H.A. New doc…all he needs now is some t-4 once in a great while, geeez. codeee – Hide quoted text — Show quoted text -> Lithium has such a narrow therapeutic range…glad I don’t play with it. > — > Bill Work > 2100 mg. is, IMO, a very toxic dose. 900 comes close for many. Nausea is > usually the first sign of toxicity. > >   Have you not tried lithium carbonate for bi-polar? > > Yes, I took Lithobid for about 5 months at doses ranging from 600 to > 2100mgs. > > The side-effects of the medication were intolerable, even with the > addition of > > prilosec and inderal. Kept on getting flu-like symptoms, hand tremor, > nausea, > > etc. > >     I don’t think the diagnosis of bipolar was necessarily valid anyway. > I > > think most of my mental symptoms are a product of having chronic > headaches, > > tmj, and neck pain. > > Psychiatry: 90 percent speculation and the 10 percent guess work.

Before you buy.

Response: