I think MCAS causes the majority of my symptoms
Hey all. I’ve been ill since 2023 after EBV and multiple Covid infections. I was wondering how many others suffer with severe MCAS and how they’re coping? I think it drives most of my symptoms and it has got progressively worse for me the last year. I’m on antihistamines and started a mast cell stabiliser, which slightly helps, but not massively. Whenever I eat something slightly high in histamine, I still have awful reactions. Apart from that, I don’t really know what I’m supposed to do. I just wish there was more research into it as I feel like the mast cells might be playing a key role.