I always feel depressed afterwards :'(

Been on Tysabri for 10 years and my consultant has just suggested I change to Ocrevus. I’ve been relapse free on Tysabri, so I’m wary of changing. However, the lesser PML risk is something to consider. Has anyone changed to Ocrevus? How did it go? Do you get any side effects?

Dimethyl Fumarate DMF It has been up to 10 years to take it.

I literally just got diagnosed. Im overwhelmed, scared, and still waiting for some results. My body hurts and the spinal tap didnt help that pain any. Im feeling lost....

Looking for as much info as I can find. Was diagnosed in 2015 when I had "wet feet" that eventually creeptd to to my feet legs up to my theighs - numb tingling.. Didn't hinder anything, just a nuisance at that time. Over the years since then small patches on my body would have pins and needles in - ...

I got a bad cold and took an at home test for Covid after a few days because it was getting worse even though I started an antibiotic. The test came back positive. I were I get Covid more than anyone I know and I am careful. Anyway, my doctor wouldn’t prescribe an antiviral and it’s been like 7 days...

How are you ladies dealing with this? I reached out to my neurologist and she’s been out of the office but I’m feeling terrible and it just dawned on me that I’m in perimenopause and I’m feeling like I’m in a relapse. Also, I’m wondering if it progressed your MS.

Does anyone also get random blood pressure readings? Like it can be fine, Then all of a sudden your heart start racing? Just took mine and it was off the roof. Does anyone else ever have that experience?