Last week MSAA and MS Pathfinder sent out an email of a new informational tool to help answer your covid questions!
mymsaa.org/covid-19-and-ms-...
Have you checked it out yet? What do you think of it? Does it help answer your questions? Put at least some of your fears to rest?
Fill me in!
🤗💕
J🌠
I thought to begin with it was an app that they were trying to introduce but it is geared at you guys in the States and insurance, so I hope you all find it useful 👍
I didn’t check it out because I don’t have any questions.
Thanks for sharing! Good to see people with ms not more at risk and the on immunosuppressants doing better than though
I looked at it & it had what I already knew about COVID-19.
Nice simple straightforward. I was disappointed however in hearing that interferons which kept me from getting so much as a sniffle for the many years I was on them, did not seem to have much affect with COVID-19. Was thinking of going back on the non-stop flue-like symptom generating DMT I did for years that way. Didn't help my M.S. according to my neurologists, plural, who after years had me stop them, BUT, it did keep me from getting anything, even when my home was full of people suffering with the flue. I thought I could boast how see, on this med I can't get sick, then I realized, yeah, I'm essentially sick all the time on this med. Fever and shakes from the fever, achy days,... I may not be sick, but it felt like it. For years.
I would change too! Being sick all the time? Not my idea of helping!😒🤗💕🌠
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