Guest guest Posted January 22, 2008 Report Share Posted January 22, 2008 *Every* time I see one of those commericals for the treatment of FMG with Lyrica (that drug seems to get another indicaiton about every six months - I think this is probably on purpose), I think about Dr. Lowes research on FMG treatment.. I find it a bit amusing they say " the only *FDA approved* treatment for FMG. " I think, " umm.. what about *unapproved* treatments.. Like T3! " And of course, Lyrica doesn't (as far as I know) do anything about the cause(s) of FMG. As much as we know about the causes, that is. Jim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2008 Report Share Posted January 22, 2008 Lol! I saw that one too! Cherie Experience: that most brutal of teachers. But you learn, my God do you learn.--C.S. > *Every* time I see one of those commericals for the treatment of > FMG with Lyrica (that drug seems to get another indicaiton about > every six months - I think this is probably on purpose), I think > about Dr. Lowes research on FMG treatment.. I find it a bit amusing > they say " the only *FDA approved* treatment for FMG. " I think, > " umm.. what about *unapproved* treatments.. Like T3! " > > And of course, Lyrica doesn't (as far as I know) do anything about > the cause(s) of FMG. As much as we know about the causes, that is. > > Jim > >> No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.5.516 / Virus Database: 269.19.8/1235 - Release Date: 1/21/2008 9:39 AM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2008 Report Share Posted January 22, 2008 Does Dr. Lowe have a proven method that works for Fibro???? I have Fibro, but don't even bother to do much of anything for it, but do believe it is connected to the endocrine system being out of whack...from lack of sleep on down. I didn't notice it getting any better, even when I was on armour And cytomel - the cytomel made my T3 go up to 1024, so had to eliminate that. What have people on here found helps with it?? SeaLady *Every* time I see one of those commericals for the treatment of FMG with Lyrica (that drug seems to get another indicaiton about every six months - I think this is probably on purpose), I think about Dr. Lowes research on FMG treatment.. I find it a bit amusing they say " the only *FDA approved* treatment for FMG. " I think, " umm.. what about *unapproved* treatments.. Like T3! " And of course, Lyrica doesn't (as far as I know) do anything about the cause(s) of FMG. As much as we know about the causes, that is. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2008 Report Share Posted January 23, 2008 Sol, any idea why avoiding mint is a part of that protocol? I drink so much of the tea, I'm almost afraid to ask. Thank's, Pat Re: AARGGH! Yet another damn Lyrica commercial for FMG.. Hi Jim, You should be on the FM lists I'm on (maybe you are on some?). People are taking Lyrica right and left, and many have had awful side effects, and as you say it doesn't fix the cause at all. The side effects people have written about are freaking scary. Driving someplace and then not knowing how they got there " sleep walking " int he daytime. Falling alseep at the wheel............. I refer to or comment on thyroid or adrenal causes of FM from time to time, but no one has ever commented nor has anyone EVER asked for more info. It falls on deaf ears/eyes. But they sure suck up the ideas of Dr. St. Amand, in which basically people go on a very restrictive way of life (no topical salicylates) which means no herbals no toothpaste or anything with mint, and on and on and on, plus his guaifenesin treatment puts them into more pain, which they say is good and a sign it is working. I actually tried his protocol for 8 months, but it didn't work for me at all. I also couldn't stand the replacement products for sal-full ones--the replacements may not have salicylates but they are full of toxic chemicals and preservatives. The only benefit I got from the protocol was a return to a low carb diet, which did benefit me hugely. Given that people will fall all over themselves to ask about the guaifenesin, and are willing to be in MORE pain on that protocol, as well as the willingness to take every horrible drug they can get their hands on, it strikes me so weird they won't even LOOK at the idea FM could be thyroid/adrenal. It amazes me. sol Jim Witte wrote: > *Every* time I see one of those commericals for the treatment of > FMG with Lyrica (that drug seems to get another indicaiton about > every six months - I think this is probably on purpose), I think > about Dr. Lowes research on FMG treatment.. I find it a bit amusing > they say " the only *FDA approved* treatment for FMG. " I think, > " umm.. what about *unapproved* treatments.. Like T3! " > > And of course, Lyrica doesn't (as far as I know) do anything about > the cause(s) of FMG. As much as we know about the causes, that is. > > ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG Free Edition. Version: 7.5.516 / Virus Database: 269.19.9/1237 - Release Date: 1/22/2008 11:04 AM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2008 Report Share Posted January 23, 2008 Because mint contains salicylates, one of the highest sources. So no mint mouthwash, no mint toothpaste (which is virtually ALL of the regular toothpastes), no mint tea, no shampoo, lotion or anything with any mint at all. The idea is that topical salicylates block the action of guaifenesin. Also no regular tea, again because of salicylates. Some people say they can't brush against plants, can't garden without gloves, can't walk barefoot in grass, etc. I might be still taking guai if it had helped me but it didn't. A good pain med and a low carb diet DID help! And I hope I'm now addressing the root causes of my " fibromyalgia " , myofascial pain syndrome, and chronic fatigue. Funny how all the symptoms of those are also symptoms of low cortisol and hypothyroid. Guai is supposed to remove excess phosphate from muscles, tendons, and joints, which excess phosphate is supposed to the cause of fibromyalgia. Excess phosphate is thought to interfere with the ATP production in the cells. The " phosphate hypothesis " seemed possible when I was nearly unable to walk and was desperate, but honestly it seems like a really loopy idea to me now. And over the last couple years, I have come to believe what guaiers see as " cycling " is just normal flare and remissionof symptoms, which I had experienced for 20 + years. Still a lot of people swear it has helped them. You can read the protocol and lists of sall-full and sal-free products here-- http://www.psha-inc.com/guai-support/ And a discussion with references on guaifenesin http://web.mit.edu/london/www/guai.html The guai advocates pooh-pooh the London article, but I followed a couple of the references, and they say what he says they say. The Mark London critics do not have references which convince me. sol pat wrote: > Sol, any idea why avoiding mint is a part of that protocol? I drink so much of the tea, I'm almost afraid to ask. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2008 Report Share Posted January 23, 2008 Because mint contains salicylates, one of the highest sources. So no mint mouthwash, no mint toothpaste (which is virtually ALL of the regular toothpastes), no mint tea, no shampoo, lotion or anything with any mint at all. The idea is that topical salicylates block the action of guaifenesin. Also no regular tea, again because of salicylates. Some people say they can't brush against plants, can't garden without gloves, can't walk barefoot in grass, etc. I might be still taking guai if it had helped me but it didn't. A good pain med and a low carb diet DID help! And I hope I'm now addressing the root causes of my " fibromyalgia " , myofascial pain syndrome, and chronic fatigue. Funny how all the symptoms of those are also symptoms of low cortisol and hypothyroid. Guai is supposed to remove excess phosphate from muscles, tendons, and joints, which excess phosphate is supposed to the cause of fibromyalgia. Excess phosphate is thought to interfere with the ATP production in the cells. The " phosphate hypothesis " seemed possible when I was nearly unable to walk and was desperate, but honestly it seems like a really loopy idea to me now. And over the last couple years, I have come to believe what guaiers see as " cycling " is just normal flare and remissionof symptoms, which I had experienced for 20 + years. Still a lot of people swear it has helped them. You can read the protocol and lists of sall-full and sal-free products here-- http://www.psha-inc.com/guai-support/ And a discussion with references on guaifenesin http://web.mit.edu/london/www/guai.html The guai advocates pooh-pooh the London article, but I followed a couple of the references, and they say what he says they say. The Mark London critics do not have references which convince me. sol pat wrote: > Sol, any idea why avoiding mint is a part of that protocol? I drink so much of the tea, I'm almost afraid to ask. > > Quote Link to comment Share on other sites More sharing options...
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