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Any connection between Neuropathy and MCAS?

Neuropathy | Last Active: Dec 21 12:25am | Replies (9)

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Profile picture for lewin @lewin

Yes, I feel there is but finding a doctor who understands the connection is a problem. There are mast cell facebook pages for many states and general ones. I would suggest going there.

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Replies to "Yes, I feel there is but finding a doctor who understands the connection is a problem...."

I see an allergist/immunologist and he is wonderful. I’ve been to Philly a few times to see a hematologist and an allergist. Then I saw Dr Maryanna Castells in Brigham and Women’s hospital in Boston who diagnosed me with the mcas. Funny thing is my present Dr was just 45 minutes away from where I live.