← Return to dysautonomia and /or MCAS

Discussion
monikka avatar

dysautonomia and /or MCAS

Post-COVID Recovery & COVID-19 | Last Active: Sep 20 11:50am | Replies (6)

Comment receiving replies
Profile picture for vostie @vostie

I have tried to find an allergist who can officially diagnosis MCAS for me but they are few and far between. I developed multiple food allergies following covid along with sporadic shortness of breath, tremendous itchy rashes on my legs, hot red cheeks after eating or drinking specific foods, fatigue, fluctuating pulse/blood pressure, nasal congestion, palpitations, and diarrhea. All of the food allergies are new post covid and my reactions initially were pretty severe. After 1 year on LDN, I have less reactions but when I do, they are significant. I do take Montelukast and a daily antihistamine but have yet to try cromolyn sodium. I do not take a histamine-2 blocker as I do not want to turn off most of the acid production in my stomach.

Jump to this post


Replies to "I have tried to find an allergist who can officially diagnosis MCAS for me but they..."

@vostie
Thank you