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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...

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...

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 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.

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 have just received my new driving licence from the D.V.L.A. After my diagnosis, three years ago, I was issued with a three-year driving licence. Today, out of the blue, I received a one-year licence. There was no explanation for the downgrade. Has this happened to anyone else?

Morning all, my name is Matt (aka R-F-J) I have recently found this site and hope that it will benefit me going forwards. I was diagnosed last year with PPMS and waiting for vaccines before I start DMTs of Ocrevus later in the year all being well. This has turned my life upside down, as am a keen ...

I am the husband of the person who was diagnosed with multiple scerolsis. My butiful wife is Sarah and she is only 41 we recently moved across the country and shortly after that I started noticing that her hair and balance were giving her trouble. It was so bad that police officers have stopped her ...