MCS...for Michele

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I thought this was a bit inspiring....from another group. (Dr. testimonials) Michele, have you ever done a liver flush? If I remember right, I believe that a clogged or sluggish liver may play a very large part in MCS. Once you do a series of liver flushes and get that sluggishness fixed, you may find your MCS significantly lessened. I've done them and had good results, as has Rogene, and Kathy that I know of for sure. Patty >"Is MCS (Multiple Chemical Sensitivity) Incurable?"> >By W. Gilbert, Ph.D.> ><claire@b...>> >Copyright 2000> >> >Open Letter to Kauppi> >> >Editor and Publisher> >Heavy Metal Bulletin> >Lilla Aspuddsv. 10,> >S-12649 Hagersten, Sweden> ><heavymetal.bulletin@s...>> >> >Dear

,> >> > I just received Heavy Metal Bulletin (10/00) and can hardly> >wait to read it, from the scanning "In this issue" on Page 1. I am> >also exceedingly eager to see the next issue featuring the role of> >oral infections in systematic disease because I am going to be> >writing about the very same subject myself, perhaps from a> >different standpoint.> > I planned immediately to acknowledge to you receiving your> >latest edition, but after looking at the back page -- at "JoAnne> >never had MCS" -- a letter from of the Chemical> >Injury Information Network -- I am doubly motivated to write.> > denounces Chinese Medicine as "quackery" and without ever> >seeing the patient who was cured of MCS from a quack, concludes the> >patient never had MCS.>

> It sounds so much like oncologists who say patients "never had> >cancer" after a cure is obtained by a quack -- such as by the use> >of herbs and nutrition. "The patient never had cancer" is> >proclaimed by the "expert" despite the his or her earlier diagnosis> >of cancer and the supporting tests.> > sent Blazing Tattles and an angry letter, too, once for> >an article which discussed the role of ideas, thoughts, or beliefs,> >in the creation and cure of illness.> > I would tell , by way of this letter, that one of the> >standard maxims of my discipline (sociology) in which I hold a> >Ph.D. is "As a thing is believed real, it becomes real in its> >consequences." Few people with MCS who believe they are incurable> >are ever going to get well. In fact, accepting such

a believe can> >be a death sentence for some, as their bodies shut down.> > I have been diagnosed with MCS by members of the American> >Academy of Environmental Medicine in every geographical area in> >which I've lived. I am a "universal reactor," also, meaning that> >almost anything for which I've been tested, I react to.> > I was first diagnosed with MCS in New York City in 1980, then> >in Boca Raton, Florida, in 1989, and later in Saratoga, California,> >in 1992. I've been diagnosed with MCS also by a forensic> >pathologist, chiropractors, and nutritionists. I have been> >"certified" by Social Security and New York State as being disabled> >from MCS.> > My first doctor told me there was nothing I could do to> >recover. He said I had to accept my brain injury (from>

>formaldehyde fumes) and the ultra, exquisite sensitivity I> >developed to levels of chemicals that a normal person wouldn't even> >detect.> > I was bedridden a good part of the time and semi-home bound.> >My IQ was severely reduced. I accepted I was incurable.> > However, I did what I could including, when I had a double> >migraine and could not get out of bed, affirming: "Every day in> >every way I am getting better and better and better." I read in> >Food, Mind, and Mood, in a footnote, that some doctor said every> >patient he had that affirmed that -- three times a day -- got well.> > At one point a couple of years after I was diagnosed as> >"irreversible," I decided to act as if MCS was not irreversible.> >I didn't believe I could ever be well, but I figured I had nothing>

>to lose to believe I could get well. Yet, I did not expect it to> >happen.> > Through the years, through medical professionals as well as> >quacks, I have gradually learned how to live with MCS and improve> >my health. I've done such a large number of different things to> >foster the creation of my own health that it would take a book> >length manuscript to describe them. I still devote a lot of> >attention to making myself healthy.> > I cannot work in the labor force at a nine to five job> >because I would quickly loose my health due to the same reasons> >I became ill working in the first place, but -- as long as I take> >excellent care of myself and avoid continuous exposure to common> >chemicals -- the startling thing is that I am becoming healthy> >beyond my wildest expectations in terms

of how I feel.> > I feel better and better. Many days I feel fantastic and> >function very well for an "incurably ill" MCS. I am free from pain> >almost all the time now, including migrains which I no longer have.> > Those who loudly proclaim to know that MCS (lupus,> >fibromyalgia, hypoglyemcia, candida, acquired porphyria, chronic> >fatigue syndrome, candida, Gulf War Illness, etc.) is incurable do> >not help anyone at all, in my opinion. Also, saying MCS is> >incurable flies in the face of many who are recovering.> > All diseases -- except perhaps those you have at birth -- are> >reversible. The body wants very much to be healthy, and if you> >remove your toxic dental materials, infections, and parasites --> >which provide a steady supply of chemicals within your body --

plus> >do a couple of other "clean ups" as described by Hulda R. ,> >Ph.D., N.D., in her books* you can be healthy once more.> > Those of us with MCS who learn how to get well are among the> >lucky ones on this earth, for we know all the pitfalls. As we> >watch so-called "healthy" people run their bodies aground,> >guaranteeing later, disasterous health problems, we rejoice in> >gratitude for having been given an opporunity to learn many, many> >lessons from our sensitivity.> >> >*If one is going to follow , please consult her latest book,> >The Cure for All Advanced Cancers," for her latest dental findings.> >> >> >--> > W. Gilbert, Ph.D.

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