Can I please ask, those of you in the uk that have been diagnosed a while but not on treatment, what is the reason for this? NHS or a personal choice ?
Hello! I was diagnosed with RRMS in Jan this year and despite the fact that myself and my neuro consultant have chosen Mavenclad to try first, I'm still waiting to actually be put onto it. How long have others taken to be put into treatment? I understand I'm not the only person in the world so I'm n...
Hi all, I have a question. Is there anybody on a treatment that is working well for them and they can see and feel a good improvement in their situation.
Personally I'm not on any medication at the moment only a daily vitimum d supliment tab.
KESIMPTA OR OCREVUS ANY GOOD??
Good days and bad days ar...
My neurologist has given me a list of treatments, that she believes I will be eligible for, to look into to help me make a decision.
People currently on treatment....did you make the choice on your own or go off what your neurologist most recommended?
I've been doing some research and am finding ...
Has anyone else had to wait over 3 months for the neurologist to give the ok on some treatment? I’m still waiting after 3 months and I think I’m having a relapse. I’m fed up with waiting and very angry
It’s my first dose of Ocrevus tomorrow. I have the iPad charged, snacks and food sorted. Luckily I love meeting and talking to new people so I’ll make friends ☺️