My son was diagnosed 2 years ago, he has seen Neurologist twice and not been told how far advanced his MS is. It worries him greatly, and me as mum is terrified as I can already see how it’s affecting him The Neurologist said it’s slow processing and he will have an MRI again, at later date. Can anyone advice whether he just waits or can he ask to see him again. This waiting game is hard not knowing what’s going on
has your son had any treatment?
slow processing? or do you mean slow progressing?
slow progress is a good thing but even so, your son should be on a DMT.
does your hospital have email contacts for the consultants?
that could be a way to inform the consultant that your son is concerned.