I am having a hard time finding information about mast cell disease, aside from a few sources that all say the same basic things and veterinary med sources!
Isn’t it sad when the animals get more attention than we do? 🙂 I like tmsforacure.org — and they have a conference coming up! mastocytosis.ca/ has a Patient Experience Letter that is worth downloading and sharing with your doctors, too. It mentions the direct link to EDS and dysautonomia!
Thanks so much! I’m hoping to get some help with this since I’m itchy again despite my claritin and singulair. You’re awesome.