Talk:Cynthia Adinig

Important health information is missing
I, Cynthia Adinig the subject matter or whatever wikipedia calls me , am currently living with severe disabilities from long covid as the article should reflect but doesn't yet. Alongside Long covid, I've been diagnosed with POTS, MECFS, MCAS, MCS. These becoming disabling all stemming from mild covid. I also developed severe cognitive impairment, including short term memory loss and executive function deficits that is often associated with MECFS and Long Covid in 2020. I'm slowly recovering from these symptoms. (Please also keep this part in mind with all interactions on this page.) https://www.ameridisability.com/long-haul-voices-series-patients-talk-about-living-with-long-covid/

From (MCAS) Mast Cell Activation syndrome, I developed allergic reactions to eating all food and even drinking water. I need high doses of antihistamine to eat or drink each day. or https://www.washingtonpost.com/video/topics/coronavirus/why-this-black-woman-with-long-covid-feels-the-medical-community-has-failed-her/2021/02/02/68ce212c-f1ba-4983-8d07-d2fd5e8e4429_video.html

From Multiple Chemical Sensitivity (MCS), I developed allergic reactions to air outside, or any smells really ( multiple chemical sensitivity,) a little over a year into long covid, which makes any work I do as an activist and advocate, in person, harmful to my health. I need air filters around the clock via a mask or air purifiers to breath function each day. https://www.usatoday.com/in-depth/news/health/2022/09/14/long-covid-treatment-research-challenges/10255796002/

A good place to source my litany of symptoms is from my written or video Testimony before the Select Subcommittee on the Coronavirus Crisis https://www.congress.gov/117/meeting/house/115020/witnesses/HHRG-117-VC00-Wstate-AdinigC-20220719.pdf Thanks CynthiaAdinig (talk) 22:45, 25 March 2023 (UTC)