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Hello all, I’ve had numb feet since a relapse last year. Any tips for helping with this? It’s affecting my balance alongside hyperreflexia (wobbly when going from sitting to standing) Any help much appreciated and sending all the positive vibes to all you MS warriors

Hi everyone, I’m so glad to have a place to come I’m only diagnosed a few weeks very nervous, my symptoms r ms hug which is nothing like a hug I have had , numbness in my hands torso and right leg. I also have ulcerative colitis so they have to find a medication to do both , the one they have picke...

It's funny how quickly my mind goes to "well it was fun while it lasted. Time to end things." In general I'm a very positive person and people compliment me a lot for being so positive, you always hear wiser (usually old )people say "it could be worse", and between that and MS, I've gotten through...

After diagnosis last January and my neurologist not perpepared to identify my sub type although he says it more than likely PPMS. I've decided to take the bull by horns and go for HSCT in Mexico in November. EDSS currently 3.5. I know Dr Burt and NHS health experts do not recommend HSCT for PPMS a...

So I am currently on Tysabri but I have to change due to coming up to my 2 years on it and being JCV positive. My two options are Ocrevus and Kesimpta. I know they both work in a very similar way but does anyone have any advice around side effects for both etc? My nurse told me Ocrevus has an incr...

I m normally a very positive person but today I just can't stop feeling sorry for myself I m just having one of those days where ms is a forefront of everything getting frustrated over not being able to do a simple task feeling like my future has been robbed I just needed to get it out but do ther p...

One benefit of covid, other than people having to stay away from me (joke, I am actually really sociable!) was that I massively got into fitness, although you wouldn’t tell now! This was pre diagnosis, but I lost 2 stone (again, put most of it back on!) and I actually really enjoyed working out. I’m...

Hello! Has anybody tried the Wahls protocol diet? Any success stories, or otherwise?! I have done a lot of research and reading and it all sounds very positive, I tried it for a month and I must admit I felt amazing. Although I don’t really have severe symptoms to notice a massive change, but the fe...

My neuro wants to start me on Tec as I’ve not done well with other DMT’s and he wants me on something. I’m also JC virus positive, bringing the risk of PML into the picture. Anyone out there made the decision to go ahead on a DMT after testing JC positive? Knowing the risk of PML in the equation? No...

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...