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Hi guys. Just want to know if there is anyone else out there that has had optic neuritis due to having MS. Iv just been diagnosed with MS.

Hi guys. Just want to know if there is anyone else out there that has had optic neuritis due to having MS. Iv just been diagnosed with MS.

Hi all, I'm a 52 year old male just diagnosed with Primary Progressive MS. It's mostly affecting my left leg so far, with foot drop, altered gait and weakness. I can no longer stand up from a squat on that leg, which is scary for a guy who's been healthy, strong and physically active his whole life....

I would like to reassure anyone who gets newly diagnosed with MS that it really is not the end.” In a brave fashion, sheridanallison reveals how her recent MS diagnosis affected her mental health and caused her to grow scared of things she usually loved. Welcoming in 2022, she looks ahead to her car...

I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

Hi I have Ms for the last 8years , diagnosed at 21, I haven’t luckily had many pains up till now, basically haven’t been able to sleep due to spasm in feet , now given beclomec but don’t find it works , have any followers or volunteers heard of anything that does, nuisance as much as pain uncomforta...

I am new to this site and wondered how many people with PPMS used it? Really interested to hear other people's experience of PPMS. I was diagnosed three year ago after investigations into what was then a mild gait/drop foot problem. Over the past 18 months I have experienced significantly greater...

Hi everyone. I'm 33 years old and not so long ago I been diagnosed with RRMS. It took me a while to accept it and figured out what's happening with me. Still very new to it, trying to get as much information as possible. Thanks to everyone for sharing their stories, it's really helps.

I usually kee things bottled up but here goes im struggling to let the fact I’ve been diagnosed with ms sink in I feel like guilty for putting my gf and family through it and my temper sometimes gets the better of me and I say stuff I don’t mean I’m on tysabri round 5 coming up soon and diluxatine f...

Hi All, I was diagnosed November 2019 with RRMS. I was put on Rebif which the only complaint i have is the red marks it leaves but would have happily gone on with it. Yesterday i met with a new neurologist after my previous one had left. I had an MRI in advance and there was one small new very sma...