Home Forums General Discussion Very exciting! New Immune regulator GcMaf

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  • #306077
    nspiker
    Participant

    I recently learned of a new product, GcMaf, available in Europe, which has the potential to be extremely beneficial in regulating the immune system. It’s exciting, especially for those of us with illness from a “turned on” immune system that is attacking itself. Better Healthy Guy blogs about this product:

    http://www.betterhealthguy.com/joomla/blog/247-gcmaf
    http://www.gcmaf.eu/info/

    From gcmaf.eu, “In its role of immune system regulator, research shows GcMAF can reverse other diseases that attack the immune system like Autism, CFS, XMRV, Lyme disease, Aids, HIV, Fibromyalgia, osteoporosis, Hodgkin’s, Lupus, MS, Parkinson

    #359722
    Lisabuf
    Participant

    Is this a prescription drug?
    Please keep us posted on what you find out. I believe that the answer to controlling or stopping my disease is out there somewhere…I just have to find it. So I’m always glad to hear of new possibilities.

    #359723
    Trudi
    Participant

    Very, very interesting. Keep us posted 🙂

    Lyme/RA; AP 4/2008 off and on to 3/2010; past use of quinolones may be the cause of my current problems, (including wheelchair use); all supplements (which can aggravate the condition) were discontinued on 10/14/2012. Am now treating for the homozygous MTHFR 1298 mutation. Off of all pain meds since Spring '14 (was on them for years--doctor is amazed--me too). Back on pain med 1/2017. Reinfected? Frozen shoulder?

    #359724
    nspiker
    Participant

    I just learned GcMaf idoes NOT require a prescription. As you will see in the link below, the cost is about $450 a month, but it may only be needed for three months. It has been used in Europe and Japan for years for Cancer and HIV. Also, Vitamin D levels must be high enough to begin treatment.

    Here’s a link from lymenet:

    http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/111722

    #359725
    Krys
    Participant

    FASCINATING!!!! Thank you, Nancy.

    #359726
    hopefulmama
    Participant

    There is an amazing woman/member of our board (who recovered from SD a few years ago) who has actually just conquered lymphoma using GcMaf in conjunction with other therapies and AP. I’m sure she would have a lot to say about the experience. I consider her to be a treasured friend and a true inspiration. She allowed me to share her story in my blog last April – she is the bravest, most incredible person. Like everyone on this board!

    http://yearofmeaning.blogspot.com/2011/04/april-19-2011-day-131-warrior-racing.html

    #359727
    cavalier
    Participant

    Hi I am new to this forum – I have SD Diffuse along with 2ndary Sjogrens & Raynauds. In reading the gal’s blog who had SD now in remission – I cant help but wonder since SD patients have a increased risk of cancer if the virus just mutated perhaps – the good news is reading GcMaf is if it works it seems to beat risk for cancer and possibly autoimmune diseases for good – but how many success stories are our there for SD – hard to say. It does look interesting. I wonder if the IAT in Bermuda would ever use this on a SD patient? Good news is while expensive it is a short term treatment. Thanks for the info. Best Jill

    #359728
    cavalier
    Participant

    Just FYI – there is 2 doc’s that are using this treatment one in Asheville NC who uses it to treat C.F. & one in Florida –

    NC is http://www.cheneyclinic.com
    Fl is Dr Bradstreet in Melbourne Fl.
    I have not called either office however to confirm this nor do i know if they are open to using this for other conditions. They both just came up in a search for the SE.
    I just found it interesting to see that some practiconers in the states are using this med.

    Jill

    #359729
    nspiker
    Participant

    Cavalier,

    Dr. K. in Seattle is also using GcMaf. It will be interesting to see if the upcoming ILADS conference will address this product. Thanks for the info on Dr. Cheney – he’s been a pioneer in the CFS community for years.

    nancy

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