Hello to all my fellow #LongCovid and #mecfs advocacy orgs and advocates here. Brief intro. I'm a black long covid advocate from the first wave and mom of a genius long Covid kid. Still recovering. POTS, MCAS, EDS, and who knows what else. I'm always fighting the good fight in disability and equity often with just my keyboard. I'm knee-deep in policy, legislation, research and writing. Feel free to follow me. #longcovid19 #longcovidKid #longhauler

@CynthiaAdinig Hi! Welcome!

I also got #LongCovid. Been difficult.

@Aaidanbird Fortunately and unfortunately it seems as if we have a lot more than long covid in common. Nice to virtually meet you.

@CynthiaAdinig Glad to meet you too!

Any projects you're currently working on?

I've been working on a petition to get all medical clinics and hospitals in my city to reinstate mask mandates. It's baffling and harmful to make it optional as if airborne diseases aren't real... I view masks similar to handwashing. Both reduce viral and bacteria load in air and on hands significantly, and are needed for safer and cleaner spaces for patients and medical employees. Hoping to launch it December 1st.

@Aaidanbird I'm in the process of launching a company that will systematically meet with hospital networks with the purpose of streamlining care for illnesses commonly developed from long covid illnesses. Such as dysautonomia, MCAS, and MCS. Alongside tackling equity with medical staff and researchers. I'm also working on a variety of diagnostic tests.

@CynthiaAdinig

Hello, I also have EDS. Weak wave from my corner of the internet

@morgandawn my wrists feel this comment so much. Lids that screw on are my daily arch nemesis😅

@CynthiaAdinig My first wrist #subluxation was trying to open a Dijon mustard jar. Since then, mustard jars have been on my #nemesis list. The list expands every year. These foes are wily and can circumvent many assistive devices and power tools. Be on the lookout!!

#EDS #hypermobility

@morgandawn my son's daily arch nemesis is a Gatorade lid. It feels good to be able to actually open it for him and show him the things I learned, after spending my childhood using pliers and scissors on various lids while being judged by my family who all have EDS but somehow didnt struggle with lids.