I’m on the viatris program and get my medicine for free. With that being said I do not qualify for Medicaid or even the free clinic in my town, I have no doctor nor can I afford to go to the neurologist. I’m married and I work part time my husband works full time. I always have to include both incom...

Hi guys!! So I did my first 6 months follow up mri, two new lesions came up… but I’ve been on Tysabri for 6 months…but from October (when my first mri was) to January ( when I started tysabri) I’m guessing I just feel a little defeated… looking for either words of wisdom or some insight on your exp...

Him and I have been together going on 6 yrs its our 2nd time 1st was a month he got deployed and didn't want me to get that knock on my door 2012 then he finds me again Jan 2021 we haven't been separated since then we both just got divorced from our mistakes and want to be each other's last we r b...

Anyone else on tysabri and gets sick all the time?? I’m on my third infusion and the second time I’m sick 🫠

So I am starting a relapse after being diagnosed in Feb. I have only had one infusion in May and the bloodwork i had from my follow up at tge end of June has shown more nerve injury regardless of the infusion. They have put me on high oral dose steroids and pushing to get me in for MRIs but im scare...

Anyone deal with mood changes. I seem to have several days or longer that I feel great and full of energy and positivity then I seem to get depressed a little and then usually really irritable and emotional. Its like the sky is falling g ove night. I dont want to take meds like antidepressants bit ...

Not posted in a while but I’ve really started to struggle lately and I feel like my family just don’t or can’t understand. I’ve started with the cramping basically all over my body but the worst in my legs and arms, my family have said they have noticed significant change in my memory and my emotion...