First MRI after my first Ocrevus infusion / after almost a year being diagnosed.
Do we get these via post? Or do we have an appointment with the Neurologist? I've tried asking my MS nurse but no-one has got back to me as of yet.
I only ask because I don't want the results unless I absolutely need to have them. Like I know I've got this crap ass disease but i don't want to know anything else unless I'm being bumped up to primary progressive or whatever.
Normally comes by letter about a month after scan. You could get a someone else to read it and only tell you about it if it meets your criteria. Personally I would want to know though.
Well I see you are in the UK but in the States depending on which State your in it’s usually “no news is good news”, at the next appt they’ll tell you what they saw or if there’s no changes