August 8th, 2016: Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis
Jody Smith joins with other ME voices in honor of Understanding and Remembrance Day for Severe Myalgic Encephalomyelitis.
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GCMAF factory closed down in the UK

Discussion in 'GcMAF' started by ukxmrv, Feb 4, 2015.

  1. Olena

    Olena

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    Ukraine
    I on GcMaf for almost 3 years and KDM said to continue.
     
  2. Hello,

    I have been away from this forum for a while. I am an autism mom whose son did extremely well on GcMAF and Goleic. My son was a patient of Dr. Bradstreet's from Sept 2012 until Dr. B's death.

    I am posting to ask for advice for an autism mom friend of mine who needs GcMAF. She was diagnosed with breast cancer in December (2016). She has mets to her lungs and possibly liver. She lives in the upper Midwest USA.

    Do any of you have suggestions for the best route for her to take in obtaining GcMAF? Is the GcMAF from Canada GcMAF or Goleic?

    My son, who is 10 years old with multiple auto-immune disorders and moderate level autism, has started Rerum injections. He is improving with Rerum. The results are not as dramatic as they were with GcMAF.

    Thanks in advance for any direction you can give me for my friend.

    (Edited to say that I read the rules about all posts needing to be about ME. I feel that several of the disorders are related. My BIL has had ME for 20+ years. I have thought that I may have it, but I believe that my severe fatigue problems are related to grief. I grew .75 inches during my 40s b/c I spent so much time in bed. I am not sure of why I have a difficult time staying well. I am sick much of the time.)

    Madison
     
    Last edited: Feb 16, 2017

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