Looking for
something specific?

From Barbados, doesn’t have MS but apparently knows someone who does and Ocrevus is mentioned. I’m assuming it’s fake to declined offer

Hello to everyone, I have just joined you. I was initially diagnosed in 2009 with ADEM & thought it was benign MS. I have had ongoing symptoms over recent years which led to a recent MRI showing multiple lesions. The Consultant has diagnosed MS and referred me to Queens Square in London. I ...

I am victim of domestic abuse due to having ms it sucks

MS is stressing. We MSers know that first hand. Unfortunately seems that my boyfriend of 6 years is only now realizing that. We have been fighting a lot and he has said very hurtful things to me. Its true that he apologizes when his temper has cooled off but truth is that for the past few months we ...

I was diagnosed with MS Nov 97 so nearly 23 years. I have been on various treatments . I am now on Ocrevus 6 monthly infusion. But because of COVID-19 my treatment has been delayed my last dose was the 26th September 2019 I was supposed to have my next dose In March . I just wanted to know if anyo...

I have a conflict of interest to declare: I am on the UK MS Register committee. - The MS Register here struggles to get more sign-ups. Everything you share is to further the cause of MS research. Your data is secured properly and never ever shared, outside of the anonymised research data. - The Fre...

I'm wondering if any men have experienced fertility issues? I'm on Ocrevus and wondering if the drug (or MS in general) can affect my sperm count/motility. Was it harder to conceive or were you even able to get your girlfriends/wives pregnant at all?

Hey, I have been in lockdown with my family since 17th March and as of recent (the past week or so), I have really struggled with my mental health. I suffer from depression which is believed to be due to MS, so I take 50mg Sertraline a day. As I have been extremely down the past few days my partne...

I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

New here and not sure how to find friends. Is this like FB for MS?