help for mercury

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- I sent this out several weeks ago I think. Its a site to help you find alternative MDs in your area. Its how I found one. You have to have a prescription for Oral chelation if its what you need - but they can also help you determine if thats what you need.

http://www.acam.org/

Mercury poisoning is all too common but the country as a whole is in denial about it. May not be the whole root to Fibromyalgia and/or its removal may not cause immediate healing - but there are other factors and problems it causes that may need addressed too if it is the culprit. I'm attacking it all. Doing the oral chelation (once I remove all metal which I can't finish till August) - working on parasite cleansing - liver cleansing - kidney cleansing (cleansing period), exercise, etc. etc. The info is out there for the taking on how to do these things. I am on a program through Awareness for colon, parasite and immune system building and now that its warming up here intend to start cleansing when I have the time to take it easy. Dr. Baker doesn't believe in doing all this now till the mercury is gone( as far as parasite cleansing cause parasites actually live off the mercury), and I am following her advice and am not doing the full parasite cleanse yet - but am enough to keep candida in check at least. I feel the difference. Diet of course is important. Sugar is a bad thing for me. Doing the Eat Right 4 Your Type diet. I lived in VA and know there isn't necessarily a lot of support for all this type of stuff where you are. Living in AK has its drawbacks - but its surprisingly progressive. We have a wonderful Iridologist up here - Naturopaths, etc. and I found Alternative MDs in the southern part of the state. Good luck in your search. I know you are miserable at times. I am going to see an Orthopedic up here next week about my neck cause i am pretty sure there is more going on than just spasming. Anyway - let us know how it goes. You seem like a very sweet person. jeanie

antibiotics for FMS/CFS>>> Hi everyone; I am new to this list; my name is ph; I'm 23/m with fibro > for about 10 years; in LA county. I will do a longer intro soon; but for now > let me say I've had major success for pain; about 80% better; with > medications (klonopin and methadone) and malic acid/magnesium malate. Other > things I focus on are diet, supplements, exercise, and spiritual stuff. I'm > better than my severe pain/zombie state 3 years ago; My fatigue and brainfog > continue to make life a struggle however; working 20 hrs per week as a > cashier i feel I'm really pushing myself. Although I havent been tested I > believe its very likely I have mycoplasmas, and would be helped a lot with > the fatigue and brainfog if I took the antibiotics route. Its very tempting; > but some of the books I've read talk of people who's health was ruined from > excessive abx. Also; Im a member of CFSFMExperimental@onelist and when i > asked the 400 members if anyone had SUSTAINED improvement after stopping abx > no one answered that they had. Once they stopped the abx they went back to > the way they were. And a few people responded that abx had ruined their > health. > I'd like to pose the same question here. well, what I'd like to know is > anyone's experience with using abx for FMS or CFS, the more detailed the > response the better. > thank you all very much. BTW here's my website:> http://www.geocities.com/hotsprings/villa/6171> ~~ph>> ------------------------------------------------------------------------> eGroups eLerts> It's Easy. It's Fun. Best of All, it's Free!> http://click./1/3079/7/ /452863/ /955953421/> ------------------------------------------------------------------------>>