Comparing Ampyra vs Ocrevus

For Multiple Sclerosis: I've has MS for 5 years now. I was diagnosed with RRMS but think I'm much worse. I know I had something going on as far back as 2010 ( 9 years ago) but unable to get a diagnosis till 2014. Because of this, I have many lesions. I started taking Amprya 2 years ago. I felt if it helps me a little bit it would be worth it. Well it helped me a little bit. Enough that 2 years later I had to go without for 2 weeks. Insurance reasons. When I came off of it I noticed the difference. So now I have to start taking the generic now because of my Insurance. (Dalfampridine) is the name. So it is the same actual drug dalfampridine but made by a different company which makes is at a cheaper price. My generic brand is made in India.

For Multiple Sclerosis: Not a cure and I may have been expecting (hoping for) more, but it's working for me. I still use a cane to walk to the office (.33 mile), but I now get around the office without the cane, including going to the restroom, going for lunch, etc.

For Multiple Sclerosis: I was diagnosed with PPMS in 2017. In 2018 I began being treated with Ocrevus infusions. Subsequent MRIs revealed no additional lesions. This past fall I was diagnosed with breast cancer and had the tumor surgically removed. I am 71 years old. There is no record of cancer by anyone in my family. My oncologist stated he never heard of a male developing breast cancer at my age. My neurological team says there was evidence of breast cancer in women during the Ocrevus trial period. My dilemma is do I risk additional cancers or do I stop the Ocrevus treatments and allow the PPMS to proceed uninhibited.

For Multiple Sclerosis: I've had MS for 29 years. No relapses for a while, no worsening MRIs for a long time. So it would seem I'm in secondary progressive stage. I was on Tecfedera since the week it was approved by the FDA, about 10 years ago. But I've been declining slowly with the usual MS stuff - fatigue, cognitive, walking is slow, right side is weak, and falling. So I decided I wanted to get more aggressive with my treatment than my neurologist was willing to, so I switched to another neurologist knowing he would put me on Ocrevus. I had 2 first time infusions about 5 weeks ago. Well now I'm scared. Since then I had complete numbness on right side for about 24 hours but it did go away. Bladder has never been as bad as it is now. I feel like I have numbness traveling from foot to foot, hands, back, stomach. I'm pretty nervous. Thinking I might have made a mistake,