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ME/CFS and Beating the Clock
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Sodium salicylate inhibits mast cell degranulation

Discussion in 'Mast Cell Disorders/Mastocytosis' started by Violeta, May 4, 2014.

  1. xchocoholic

    xchocoholic Senior Member

    Hi @Sherlock

    Thanks for the pdf link. I'm still reviewing it but I was surprised at how long the list is. Makes me wonder what all has been looked at in me/cfs.

    On the enzymes, I'm still mostly clueless but I've spoken with Enzymedica reps a few times and they've been helpful. There used to be a forum called enzymes for autism. If it's still there you may find some answers there too.

    I can't digest food without enzymes. Labs show I'm low on elastase. I take a variety of Enzymedica based on what I'm eating and creon.

    Tc ... x
  2. Gondwanaland

    Gondwanaland Senior Member

    South America
    After further researching on salicylates, I found a comment at Chris Kresser's article "3 reasons why coconut milk may not be your friend" (where BTW he totally misses the point) where a reader shares very interesting info:

    Note to self: remember to check supplements based on MCT or olive oil (like vit D)...
  3. MeSci

    MeSci ME/CFS since 1995; activity level 6

    Cornwall, UK
    Sorry no one's answered. I don't know enough to say for sure, but would guess that a distilled product might be tolerable. Don't quote me on that!

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