[quote RainbowZebraWarrior]**@ofwarren* and @LilyRed*
So Mast Cell Activation syndrome is basically mast cells which react angrily to environmental factors. Could be chemicals, heat intolerance etc. So symptoms can vary such as asthma type reactions, skin sensitivity or allergic reactions to foods. At the extreme level, it can cause anaphylaxis.
It is interesting as I've read a lot about allergies/ asthma being closely linked with ASD. I also have Ehlers-Danlos syndrome, and 40% of patients also have ASD. I find it fascinating, although obviously hugely bloody frustrating at times too.
Treatment for MCAS is antihistamines and other meds, EpiPens if necessary. The biggest factor is to avoid the triggers so is a very limited diet with as little exposure as possible to chemicals and other irritants.[/quote]
Being nosy, do you have any symptoms of dysautonomia too?
I have EDS, and MCAS, no diagnosis of ASD but I've been told I'm "odd, quirky, different" so many times I've lost count. My son is the same. I had no idea so many people with EDS also have ASD.
Dysautonomia for me effects digestion, sleep, I'm always cold even in very hot weather, low blood pressure, brain fog, migraine, feeling dizzy, POTS.
I've never pursued an ASD diagnosis, but I'm almost tempted to.