Hey everyone, I know I've occasionally talked about my disorder, but now I desperately need help. My insurance will no longer cover my epi pens, a life saving medicine. I have been on the decline with hEDS, POTS and MCAS diegnosis. Mcas is my biggest scare as it is life threatening. Back in May of 2023, I had a CT, where I was anaphylactic to iodine contrast. Since then I have had 11 anaphylactic reactions to anything from heat to a food. Anaphylactic shock can kill you in minutes. This month alone I have had four episodes, three of which back to back and landing me in the ED twice. Without my epipen I live in fear of what I am near could kill me waiting for EMS to arrive and give me life saving medicine. I do not have specific triggers I can avoid with this disorder. I desperately need help being able to fund my epi pens. Anything can help.



