I am going into my second Rituxan infusion this week after being diagnosed with MS last May. I can't help but get extremely anxious in the weeks before and the weeks following infusion due to the reminder of the very rare risk of PML. I think I get so anxious because it is so unknown, my neurologist and nursing team never discussed these risks with me and so I've been left to discover what I do know from google. And we all know that google isn't always kind. I just wondered if anyone get anxious about this as well, or if anyone has any information they can share that isn't so scary. Thanks <3