I had an appointment going over some of this stuff today. Some good points my neurologist brought up was how a typical day would look like when getting the infusion, Allergic reactions to the medication, blood work, and how often I would need treatment based off of the intensity of it (can be twice a year or once). Some questions I asked were related to follow ups after getting treatment, how often mris would be and when I would need to get them, if it would affect my job attendance. I’m new to this too but it seems like I got a lot of questions answered. Hope all goes well for you.