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I need some advice in regards to 2 types of medication that’s been prescribed to me to start taking opposite from the previous medication I was taking which was Copaxone. I have been advised to make a decision to take Ocrevus or Kesimpta. I need some advice who can advise me whoever has been taking ...

When it comes to the 15th of every month. I get nervous to do my injection. I feel so down and nervous I keep thinking why me all the time But when I have done it I feel better about it

Hi everyone I have not been on here for a short while lol, I just got my lumber puncture results which came back clear they said oligoclonal bands were present in both the cerebrospinal fluid and serum and that with MS the typical finding for oligoclonal bands are to be present in the CSF fluid onl...

hello.... I was wondering if anyone is on Tysabri or mavenclad? and how you find it I am on tecfidera and had a relapse in august I was given steroids and had an MRI... I have seen my MS nurse today and they want to escalate my treatments I really don't know which one to go with so any advice would ...

Is it strange that I was diagnosed in February but my doctor hasn’t started me on ANY medication?

I was diagnosed with ms 4 years ago and had only 1 MRI done during that time is that normal?? I also have one new lesson during thous 4 years is that a common thing

Hi just looking for some advice I'm diagnosed a year now and I'm finding it very hard to come to terms with. At first I was ok with it as i was told for 10 years it was all in my head so when i was diagnosed i was so relieved. But now I'm really struggling with it. Is this a normal feeling.

Hi all Not diagnosed yet but after spending 10 weeks with symptoms and looking over various forums this seems the most sane and non cynical one. Just wondered if during a relapse symptoms can come and go and change? Started with lhermittes that got strong around mid jan, since then had hand tingling...

I am turning 27 years old and my ocrevus treatment is about to start from next month. What would you guys suggest to me?

I was diagnosed 5 years ago roughly with RRMS. I do deal with it best I can but does anyone know any groups or just folk who can listen or talk I know this is basically this group but I'm talking about out of this ???