New Atmosphere, New Vision: Gibson and Whittemore Kick Off Invest in ME Conference 2016
Mark Berry reports on Dr. Gibson's introduction and Dr. Whittemore's keynote speech, at the 11th Invest in ME International ME Conference in London.
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MAF 878 Available - Anyone already using it?

Discussion in 'GcMAF' started by shannah, Jun 3, 2012.

  1. deuce


    Hey Suzanne or others

    Any news to report on the MAF878?

    I've been taking it for about 1month now and notice no real benefits yet. Did notice at 75mls it was too strong and I felt tired, exhausted and a bit fluish. Reduced it to about 25mls and its easier to take. Wish I could report benefits so far but not yet.

    Keen to hear any other news
  2. suzanne

    suzanne Senior Member


    I can offer you a bit of a story around why I have stalled on GcMAF- for what it is worth.

    I have my MAF 878 from Dr Enlander sitting in my fridge. I was hoping on giviing it a 'go' as I thought it may cause a less inflammatory response.
    The reason I haven't trialled it yet is because I am still SO inflamed!
    I have tried in vain over the last 6 months to get the inflammation down, but have had no luck on any of the supplements- in fact they all make me feel worse.

    I am currently taking some bile acids that my dr suggesed due to some bad bugs in my gut- and guess what - more inflammation!

    Also, my big and surprising news is that I have had a recent ( last week) diagnosis of lyme - borrelia, and I live in Australia, like you. Who would believe? But there is no mistaking it as it is a positive result from a PCR test.

    In fact the lyme and possible co infections (I have some more test results that are still pending) may help to explain my impossible reactions to tiny doses of GcMAF.

    So for now, I am waiting to see if I need to treat the lyme and co infections - get the pathogen load down a bit and then try the GcMAF again.

    Like everyone else, this is turning into a long, painful and hideous process. I hope that a treatment pathway emerges soon, that I can stick with. The treatment options are going to be had to decide on, but I am researching that now.

    I think until you have been on the MAF for 3 months it will be difficult to see the results. Perhaps just hang in there, if you can.
  3. lnester7

    lnester7 Seven

    Any update using MAF 878?? I just ordered mine and was wondering how you are all doing on it. Also if you did bad have you been diagnosed with Lyme since using it?
  4. knackers323

    knackers323 Senior Member

    Anything to report anyone?

    Is the 878 as time consuming to make as the 314?

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