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something specific?

Hello All, Im seeking some guidance on how one might feel when moving to ocrevus from tysabri, is it better similar or you feel no difference at all? Does it improce symptoms is it good in the long run? Will one feel better? Thanks

Hi I've not been on the site recently, had some personal issues. I went to see my neurologist, after being off treatment for nearly two years, I've had a scan and it's bought up another legion, so he's offered me 3 separate treatments, HELP! Has anyone tried any or had good/ bad experiences of them...

Hello Every one I want to know how it is wen startiing ocrevus does the fatigue go sky high and spasms in crease and energy loss, pains in arms legs and feet issue walking? Woukd really like to know before I start calling my ms team as they do take time to get back. Thanks

Hi guys I’ve had first neurologist appointment which had confirmed it for me i have RRMS and I’m going onto octevus I’m a bit nervous about it and speaking with a MS nurse 🤔

I had my first treatment of ocrevus on thurday 15th aug and I have had ever since a bad headache and felt sick has anybody else felt like this after your treatment ?

Hi, I’m Mia. I’m 22 and live in Cambridgeshire in the UK. A couple of weeks ago I was diagnosed with RRMS. It’s been tough as a lot has happened in a very short space of time and it’s all still very new to me. I’m looking for other people my age for advice and their experiences living with MS as I d...

I wonder so people change their MS treatment after a length of time? I’m on Gilenya 11 years

Hi, I’m Mia. I’m 22 and live in Cambridgeshire in the UK. A couple of weeks ago I was diagnosed with RRMS. It’s been tough as a lot has happened in a very short space of time and it’s all still very new to me. I’m looking for other people my age for advice and their experiences living with MS as I d...

Hi all! Just wanted to know if anyone here lives in Australia/New Zealand and if they could tell me a bit about getting treatment over there? I live in England and my treatments covered by the NHS so am worried about how I’d get treatment over there when I go travelling or if I’d have to make differ...

Hi all, I'm new to this site but have been diagnosed with MS for a couple of years. It has been suggested that stem cell treatment could be a good thing for me to have but may mean being off work for up to 6 months. As a contractor I won't get paid if not working so was wondering if there was any f...