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Life swallows you up and you forget you're seriously ill until you have another relapse. I have to laugh otherwise I'll cry. Luckily, it's nowhere near as severe as my last just incredibly uncomfortable and is making work and study difficult. I'm also going to be starting my DMDs soon, I'm going to ...

Hey guys! So, I’ve had right hand pain for 3 weeks. My job requires me to type so I’m pretty much typing every daily . At first I thought it was carpal but there is no pain in my wrist. I think it’s MS related. The pain is on and off and really present when using my hand. I wear copper gloves when ...

Today Nuro doctor been in touch and asked which treatment I would like to start Ocrevus or Kesimpta. Didn’t think I would be getting a choice, how do I know which is best for me, hardly got used to the fact I have ms. Any guidance would be much appreciated, I am 52 work 6 days a week, don’t cope wel...

Since the UK heat wave started, my brain has been rotting. These last few weeks I do the bare minimum and just can’t seem to function properly throughout the rest of the day. Never in the mood to do anything. Left tasks undone and just been feeling so guilty because I’ve not been doing anything arou...

I finished work for the summer on Friday and the night before I started getting shocks in my face. I came off meds for this in May and made a big fuss about cancelling my repeat prescription. The shocks are getting more frequent and it's unbearable! Do you think this is a sign that my MS is progres...

Hi, i just been diagnosed this month after a LP for the final results! I had tingling toes last November, when the whole adiagnosis process stated! I asked before, but didn’t get any answers! I am currently dealing with my legs being numb and tingling all the way up to my hips! I am not sure if the ...

Past two weeks or so my feet feel like they are burning. It gets so much worse when I’m back home after working for 10 hours. This is a new symptom for me and I’ve recently switched to Briumvi from Ocrevus. I was on ocrevus since 2019 and I was very stable, some flaring of old symptoms but never a...

just need to get this off my chest because it’s hit me like a train today. I had to stop working a few years ago. I volunteer when I can but I’ve realised I don’t actually have any friends anymore. The people I volunteer with are lovely, but they’re mostly a lot older than me, so we’re just not rea...

I have a really supportive husband. We've been together almost 20yrs and still in love, but MS is becoming a third wheel in our relationship, and I'm struggling to find support for either of us... I'd really appreciate advice from anyone else navigating this. We want to keep our relationship strong ...