u/Still-Battle-5167

▲ 3 r/MCAS

Need suggestions

Have an oral thrush and intertigo due to my gp giving me prednisolone for calming my mcas . Well he didn't realize that it makes things very much worse for people like me with SAD deficiency and now I'm stuck with how do I treat them like there's this fear of severe mcas flares God forbid but at the same time their making my mcas worse i literally react to almost all antifungals I just don't know what to do wanna cry at my helplessness and misery ❤‍🩹😭

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u/Still-Battle-5167 — 2 days ago

Suffering from mcas heds, pots.

Hi everyone I'm 18 F suffer from a few chronic illnesses which have started to make me quite lonely as people around me don't understand me if anyone going through the same conditions as me and is female (18-22) please DM if your interested.

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u/Still-Battle-5167 — 2 days ago

Suffering from mcas heds, pots.

Hey everyone I suffer from heds, pots , SAD Deficiency , Adhd and the worst MCAS. Since I got mcas last year after a bad stomach infection im quite depressed because the worst part is I live in some what a third world country so not much support for me even from doctors.Family doesn't really care about me. I don't sleep at night or eat properly during the day all day im just yearning over the my past self and how much I miss eating anything without worrying about mcas flares. I miss being able to do skincare use makeup without having reactions . I can't get out of this grief doing therapy but in stuck in an abusive environment too so it's apparently not working though. Just needed some people wholl listen to me and my grief and just ingeneral some kind hearted friends.

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u/Still-Battle-5167 — 2 days ago