u/Julynn2021

▲ 3 r/MCAS

How To Find Doctor?!

I'm losing my mind. I have mcas symptoms all year, but like twice a year , EVERYTHING makes me react. That's happening right now. I'm only eating all natural popsicles, caprisuns, a very specific fried tofu, and (sometimes) box gluten free vegan Mac and cheese. I'm so hungry and miserable. And I don't have the money to just not eat the food that I bought. I've seen people, but they say th3y can only treat it, not diagnose it. Amd they can't refer me to someone to diagnose it. So I don't know what to do. I meet to find someone that takes my insurance. I don't know where to look. I found a place, they said online they diagnose it. We called beforehand, and they confirmed that they diagnose it, we got all the way there, they say they don't diagnose it 🙃. At my wits end.

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u/Julynn2021 — 8 days ago