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Hi! I’m Jenny-May,I’m 21 and I’ve recently been diagnosed with relapsing remitting MS. I’ve been advised to join because I’m quite ‘lonely’ as my therapist says 🤦🏼

After nearly 3 years of searching for answers to my wife's rapid cognitive decline, multiple tests and MRIs and second opinions it is clear she has a the syndrome of Dementia. Our local neurologist as well as the team at UCLA agree that the cause is MS. Images show significant brain atrophy. I ...

Does anyone else get the terrible MS related toe pain ? Omg it is awful 😔

I was diagnosed with RRMS last week. The neuro gave me some options in regards to treatment; I'm to take a week to educate myself and hopefully come to a decision. Tomorrow will be one week. I'm leaning towards Tecfidera, but I'm absolutely terrified. I'm terrified about all of this, but in regards ...

I'm going to be on ocrevus in a few weeks, what are the best options for treatment so far?

Hi all, hope you are keeping well and safe in these unusual times. I am newly diagnosed in March, first symptoms 18 months ago and 1 minor relapse 6 months ago. Other than that I am lucky not to have any symptoms of note. I discussed with my MS nurse DMT drugs early March and my neurologist recom...

From MS Society With shielding set to be paused in all four nations of the UK in August, we want the UK Government to support people with MS who can’t safely go back to work. We’re campaigning with Age UK, the Trade Union Congress (TUC) and 9 other charities. Together, we’re calling for the furlou...

I have MS disanosed when I was 24 Ms doc said I had since I was 9 n I'm 45 now with my 10 yr old son

Hi everyone, even though I’ve had MS for over ten years I’m pretty new to the forum scene. I haven’t really spoke or sort advise on anything like this? I’m thinking of purchasing an electric wheelchair as my mobility over the last couple of years as become worse. Can anyone make any recommendations,...

Hi guys. First post, so here goes - I've gone from R/R to PPMS. It's a bit frightening but it's nice to talk to people who understand. I've been put on the W/L for Rituximab infusions although from what I'm reading the results aren't great for PPMS - anyone here have any experience? I'm determin...