Greetings , hugs and salutations .
Hello beautiful people , I'm Frank Florimonte fro. Sanford , NC (originally from Bklyn NY) , but came down to chickenland after pandemic wiped out my family in NY. It's ok , they were against vaccines and rude with my MS . I've had MS for 25 years now - lost vision , couldn't walk, slurred speech , hugs , a triple attack after skin cancer surgery , i thought i was going to die attack after colon cancer surgery too .
So I'm new here , been on other MS sites before . Can anyone on SSI explain to me the steps and level of difficulty ir is ??
I was diagnosed in 1996, after I went blind in my right eye, sent me to a teaching hospital in Portland Oregon, started me on blood steroids after a few weeks my vision came back. Started on my first medication, interferon. Shots once a week I hated it. I had to give them to myself. intermuscular,
@Jaymie63 yeah I did interferon injections too for a decade . I stopped it becasue melanoma. Went on the pill , then went to first monthly infusion till JC virus, then ritoxam , then on the bi similar of ritoxam (can't remember name ) and last two insurance wouldn't cover it , so finally now on Briumvi . I think Ritoxam has been the best one . I don't feel yuk , but everything is bit harder