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I was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...

Have you heard about the new restaurant called ‘Karma?’ There’s no menu—you get what you deserve

New to forum. I am 49 and I won't be able to live on my own very soon. What resources are out there to find housing (group or other) for an under 50 year old? Been looking online, but places are all 55+. I prefer a warm climate, but other than that can live anywhere.

Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...