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9th Invest in ME International ME Conference, 2014 - Part 2: Pathogens and the Gut
Mark Berry continues his series of articles on the 9th Invest in ME International ME Conference in London, with the emphasis shifting from autoimmunity to pathogens and the gut ...
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Please Help: Antivirals or Ampligen?

Discussion in 'Antivirals, Antibiotics and Immune Modulators' started by Riley, Jan 4, 2011.

  1. alice1

    alice1 Senior Member

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    Toronto
    Klimas suggested it.
     
  2. Crappy

    Crappy Senior Member

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    TX
    I have experienced this

    The closest thing I could find to explain my symptoms is an old article from Dr. Cheney, here:
    http://www.ei-resource.org/articles...cheney:-balance-the-immune-system-(th1th2)-/

    As he stated in this part, "it is also chewing up human messenger RNA, inhibiting all the enzymes in the body, disrupting protein synthesis, and generally making patients miserable. As RNase L grinds away, it eventually shifts into "after-burner" desperation mode - the more powerful and deadly low molecular weight form", this statement coincides with what I have experienced similar to your description.

    If my layman interpretation is correct, you are suffering significant pathogen reactivation, a loss of enzyme activity, and loss of protein synthesis. What helps me is Human Growth Hormone replacement. Using the Hormone directly is detrimental, you need professional help for a way to supplement, that causes your body to make more. I use http://www.transd.com/ , immediately you could try predigested protein and supplement enzymes to supply elemental building blocks.
    http://www.nextag.com/predigested-protein/stores-html
    http://www.bizrate.com/vitamins-nutrition/enzymes/

    I theorize what Cheney describes causes the nervous system lining to become more porous and the pathogens and immune cells penetrate it at an increasing rate.

    I don't know about you, but I cannot travel like that. I would find someone close by to get quick help with what I outlined and then make plans to find a good ME Dr.
     
  3. Crappy

    Crappy Senior Member

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    TX
    Dr. Sharp

    I notice many quick to follow Cindy Willis positive post regarding Dr. Sharp in Texas. I suspect she is a plant by an advocate of Dr. Sharp.

    NOT REALLY!

    I believe Cindy Willis was an easy case, as disclosed by herself, and has experienced the miracle recovery we all deserve.

    I have known Dr. Sharp for two years and have been sadly disappointed. Much like many of the comments about Gordon Inc. here:
    http://forums.aboutmecfs.org/showth...r-with-WPI)-Mikovts-lecture-and-XMRV-Findings

    For those of you new to this struggle (less than five years), I urge caution when seeking treatment. If you are lucky enough to be ill less than five years I think treatments are coming around to help you regain your life. But caution in choosing a Dr. is advised, most are BIG on SALES, and SHORT on RESULTS! I have been as gullible as anyone. Just acknowledging CFS/ME is a good start.

    I have been sick 10 yrs., I have paid Dr. Sharp a few thousand with no results yet, and like Gordon Inc. patients, I am not alone . To make matters worse Dr. Sharp promised a revised Dr. Cheney protocol the first November and he has yet to deliver on it.
     

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