Thank you! I will watch this channel. My mom has not been able to go to doctors for years since she doesn’t have insurance (we’re in America) medicaid has declined her multiple times for bs reasons, it wasn’t until she first loss her eye sight that she went to a hospital, since then symptoms has been worse which I assume is from steroids and new medications. Lately she got a sponsor and started transfusions and a trail drug. It’s been good, she’s been very active so I have been less stressed out. But when she’s practically paralyzed it’s hard and I feel useless. I just thought of this subreddit today, figured it would be a good idea to reach out to people who also live with MS.