Hi m name is Bub. I was diagnosed back in august of 2020. Been on tysabri for a year and a few months. Tysabri was good to me but had to switch to ocrevus according to my neurologist due to JCV antibodies detection . I just received my first ocrevus infusion earlier today. Only side effects were runny nose and itchy throat followed by a little coughing, body was itching but it all calmed down after a few hours. Just wanted to share to get others feed back on ocrevus. My mom is on ocrevus as well and she says it’s not helping her. I know all ms cases are not the same. So I was ok with starting it to see if it’s a good medication for me. I’m praying it is. Also praying that my mom finds the best medication to help her out as well. Hope all ms warriors are in good spirits and striving to be better everyday !