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Hi, After having Lemtrada in 2016/2017 & being relapse free since, I've had two back to back relapses and will be switching treatments. The neuro is keen on Tysabri, but has also talked about Ocrelizumab, Kesimpta and Cladribine. I feel overwhelmed 😕 Does anyone have personal experience of these dr...

Hello. I was diagnosed in 2019 with RRMS and really only had the initial balance and optic issues and then 2 months later a numb face. Can people who have had no relapses for 4 years have one out of the blue? I thought with RRMS you might have a relapse every year. I am worried that my luck might...

Does anyone else find that they rarely have totally symptom free days, which are worsened by (extra!!) tiredness or stress? And during relapses, 'old' symptoms tend to flare up, too?

Hi, I was diagnosed with MS summer 2019. At that point I had had some minor symptoms such as numbness in my hands and feet and some blurred vision. Optic neuritis led to my diagnosis. Since then my day to day experience has got progressively worse. I have struggled to walk any distance at times and ...

Any advice? Generally I have relapses - one every three years, and I am not on DMT. This year, my left leg slowly fades away. Stairs, walking for a longer period now becomes a challenge.

Hey friends! So I am just wondering what peoples experience and/or knowledge of cold sores is with regards to MS relapses? I can feel my first cold sore brewing since my diagnosis and I’m feeling super fatigued. Not sure if the cold sore is a symptom of me being a bit run down, or if the cold sore i...

I've got a soft diagnosis of "very likely RRMS". They've done the lumbar puncture and two MRIs and Ive got an appointment to go through all the results on Monday with neurology. It's all happened since February (though I now recognise first relapse was December) so still getting to grips with it al...

I'm relatively new to MS, diagnosed in 2020 initially with "very mild benign RRMS" when actually by 2022 new MRI shows 2 legions on the spine and 2 on the brain (the spine were there originally in 2020 and missed). I've been wary of "everything becomes MS" from the diagnosis and I tend to avoid "bo...

As part of #WorldMSDay 2019 Shift.ms released #Relapses24x24 - 24 stories of relapses as told by MSer's. We've stitched these stories together so you can see the various stages MSer's go through with relapses. What we learnt from these stories is that if you're experiencing symptoms that are not nor...

Hi! Not sure if anyone else has experienced this but before my first relapse I had the most horrific headache, photophobia - unable to move for 24 hours and then relapsed approx 2 weeks later. I’ve just been discharged from hospital as I had another one this week and they kept me in overnight, CT s...