Sylvie,
I posted this a while ago on a separate thread and in the old mast cell thread you started, but here it is again in case you didn't see it:
https://chriskresser.com/quercetin-heal-leaky-gut/
One way that I'm seeing whether I have MCAS is by using quercetin to see if there are any changes, which is one method of checking, though in medical settings they use antihistamines. But this is also relevant, since testing for MCAS is wholly inadequate with plenty of false negatives.
Either way, good luck with everything.
Quote:
Originally Posted by SylvieM
Dear Boiler,
Gosh, your guy must be planning to move to a prestigious teaching hospital in NYC!
I'm glad you wrote me! The new neuro I just saw at Mt. Sinai (the silent one) also spent nearly a decade at the Cleveland Clinic....
I'm hoping the testing for Mast Cell Activation Syndrome (MCAS) will be fruitful....but I'll see who they assign me to in the other fields before I fully commit. There is a Dr. Shields there who I hear is good for dysautonomia... is this the doc you saw?
Good to get your feedback...Thank you.
S
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