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Hi this is the first time I’ve posted on anything but I’ve just got that angry and upset I need to do something. I was diagnosed with rrms in 2018 having symptoms for 3 years. I applied for pip after my last relapse, late last year that got me diagnosed with ataxia that has robed me of my balance I ...

Hi all, I've was diagnosed almost 10 years ago now and was just wondering how do you know once you've gone to SPMS/PPMS? Sorry if this sounds a silly question.

Howdy all, I'm new to this site after my MS nurse pointed me in this direction. A little about me: I'm a 34 year old Male. Married with a young son, 7 months old. I Live in Southampton. I enjoy paddle boarding, going out on my mountain bike. I did enjoy the gym but haven't really been since Aug 2...

I’ve recently just been diagnosed and have been given the option of which medication I could try out the most promising one is Tecfidera but has some unpleasant side effects and I was just wondering if you are on this medication, how long did the symptoms last or do you still have them?

Hello Lovely People.... I have RRMS, late diagnosis at 55, after 20 years of misdiagnosis. I’m on Tecfidera. I am experiencing more and disabling issues. I have to use walking sticks and by the end of the day, a mobility scooter. I have extreme pain in both feet, some evening spasms and string elect...

Hi I was sent email about having MS buddy today which I would love to happen as recently been diagnosed and waiting to see neurologist. I’m have 404 error. Can someone help x Thanks K x

I've had symptoms for the past 8 years but was only officially diagnosed in February. I thought I was handling it ok - wasn't looking to change anything I'd been doing just maybe not push myself as hard - then Covid-19 hit. Again was ok at the start but now my fatigue is hitting me earlier and earli...

Hi I’m teide I’m 24 and I have RRMS. I was diagnosed in October 2018.. I spent 1 1/2 years on tecfidera but my ms just kept progressing. I started ocrevus last Tuesday and had my first 1/2 dose.. Tuesday I felt ok! I was surprised how well I felt on Wednesday but since then it’s been horrific! Sle...

<p>I have been reading the posts about working as a nurse with MS, and have a quandary – I am a therapist, with RRMS, due to start Ocrevus post-lockdown.</p> <p>The MS does not interfere with my ability to work. A colleague (the only one who knows about the MS) is anxious as to whether my employers ...</p>

<p>My 14 month old granddaughter lives with us (along with her parents) plus my other sons. 2 are mental health key workers, my daughter in law is a nursery nurse key worker (currently furloughed) and my youngest at uni is earning money working part time as a key worker in Farmfoods frozen food shop...</p>