Hi all.
As some of you may have seen elsewhere, I suspect my POIS is caused by some kind of mast cell activation disorder, and I'm being diagnosed by an endocrinologist at the moment.
My tryptase level was normal and there was no unusual mast cell activity in my skin biopsy. To my horror I found out today that my doctor thought I meant Mastocytosis when I mentioned MCAS to him before, and it turns out he hasn't even heard of MCAS. MCAS has similar symptoms to Mastocytosis but has no reliable biomarkers.
Thankfully he's willing to entertain the idea of untimely mast cell activation without biomarkers. To test this hypothesis he prescribed Lomudal oral, which AFAIK is similar or identical to Cromolyn Sodium oral, which has been discussed on the forum here and there.
So what sucks is that apparently I can't get it reimbursed as it's not an officially recognised medication here in Norway. And it's quite expensive: 2100 NOK for 100 x 10 ml. I got the impression that I may be able to get future purchases reimbursed if we can prove that it's working for me.
To those who have tried Cromolyn Sodium: How well did it work for you? And did you have to take it regularly, or did you take it only when symptomatic? (My doc suggested the latter.)
Thanks for reading!