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Nine months ago, my life changed when I was diagnosed with MS in 2023. The journey since has been nothing short of transformative—physically, mentally, and emotionally. I’ve faced challenges I never imagined: enduring relentless relapses, the disconnection of not being able to feel my hands, feet, o...

I've been diagnosed with RRMS in 2020 and started Tysabri in 2021, everything went and is great, no relapses since but I just cannot stop thinking about Tysabri's side effects and what bad things does to my body. I wasn't sure I wanted to go with it in the first place and I'm stressed and frustrated...

Hi all! I am due to be starting Ocrevus in the next few weeks and wondered if anyone had any tips, or any feedback on how the treatment is, or any side effects they had? I have been through many treatments during my MS journey (Rebif, Tysabri and Lemtrada) but have recently had more activity on my...

This has now taken over 12 months with lots of false promises from my neurologists secretary , I have attended an nhs driving assessment (on a manual car ) which I passed with ease ,is this usual practice ?, has anyone else gone through this and what can be done?..all I require is a straight and tr...

I had my annual check up with my consultant 2 hours ago at RUH Bath. Here is a brain dump of our discussion, while it's fresh in my mind, in case it helps anyone else with RRMS/SPMS who takes a T Cell based DMD: - Lymp count was 1.3 and right where they want it. - The very slow annual increase in...

Hello everyone, I was diagnosed with relapse remitting MS in 2010. Like everyone it’s been unpredictable, painful and downright frustrating having the disease. My question is though since I hit my early 50’s my relapses have stopped and still yay DMT Tecfidera. Has anybody else had the same experien...

Hope youre all well. Saw my Neurologist last week. I've had a lot of relapses in the last couple of years. He thinks a change of DMD. Ocrevus and also Kesimpta has been mentioned. I'm getting info about it in the post. I know one is an infusion and the other to inject it myself. Does anyone know a...

Hey there, I just joined shift.ms today and I hope it's okay to ask that question here and that maybe some of you can help me with this question. Btw sorry if I make too many mistakes in English; it's not my mother tongue. My question is: I have been diagnosed with RRMS in 2015/6 and only had some...

Hi, I'm new to the app. I was diagnosed with RRMS in August 2019 but my journey began in April 2017. I have been very fortunate and have had no relapses since beginning my DMD in October 2019 with my MRIs remaining "stable" since then. I have spent the last 4 days with a severe stomach bug, not...

Hi. Hope your great where ever you are in your journey with MS. I have a question for all those on Tysabri infusions or have used it. I have been on the infusions for last couple yrs and I have been having relapses that have been ignored. Now a mri has shown new changes and they have offered me HSCT...