18 July

I know at least 3 people exhibiting symptoms of MCAS. All of them have had Covid. MCAS is quite common after Covid infection. It can be torture to live with. It has no cure. Many GPs won't recognise it nor link it to Covid, a medical specialist friend who treats people with Long Covid told me the connection. Sharing in case you or anybody you know has symptoms similar to this, and you've had Covid. The chronic after-effects of Covid infection will be mostly ignored by society and medicine, to admit they exist is to admit living with Covid was a catastrophic mistake. You'll be on your own. https://www.webmd.com/allergies/what-is-mast-cell-activation-syndrome