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dysautonomia and /or MCAS
Livivng with Long Covid for two years. It took me a while to realize I was not myself anymore. My doctor told me that the symptoms might go away after a year . My other provider finally said I might be dealing with post covid dysautonomia. Based on my own research on line I might be dealing either with dysautonomia and/or MCAS . Has anybody in this group has been diagnosed with these Dxs?
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Check out the Cleveland Clinic MCAS Guide. They have done a lot of Research to figure out the Treatment for Multiple Symptoms ,that Affect People Differently. It is " Work in Progress " for all Involved trying to figure out COVID ...Now I'm not a Licensed Medical Doctor, I just do my own Research for my own Knowledge and Health Bennifits...
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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.