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Just want to vent really as It’s all so new and I have no one to relate to! My story starts with Lhermitte’s sign out of the blue from the 1st September 2024, it was initially so intense and every time I looked down. I also noticed deteriorating vision at the same time which lead to a stronger gla...

In the past week, I've had the MS add spasms and neuropathy to a sciatica I'd been wrangling in the past month. I used to be not sporty by any measure, but active. Keen in walking, 12k+ a day. Now I walk with a stick. It is difficult to come to terms with, but I am blessed with a great clinical tea...

I thought I knew #ChronicPain ( and I don't mean being unable to score some sticky Icky) Then, during a month long attack of #sciatica (not my first) I developed a fucked ankle (not a medical term) - presumably #MS #spasticity in the peroneal muscle (shin/calf - not per_I_neal!). Can't walk (got t...

Hiya Shifies, I've been having sciatica for the past month or so - nothing new, had had it before and after Dx. But then my ankle started going weird on the same leg. Foot will naturally fall pointing out, and tilting out. It doesn't feel like a "weakness", more like an excess of strength - rang...

Hi all, Hope you’re all ok. Question.. my MS nurse has asked me to have the puemonococal vaccine before I have my infusion, however has mentioned it’s only advisory and not something mandatory to prevent me having the infusion. Just wondered if some of you have had this, and is it better to do...

You can watch YouTube till you're blue in the face. Some stretches are completely useless. Should I show shift ms how to stretch these muscles

Hi everyone - this is a bit of a sensitive one, but hoping to get people's views on what to do, or if anyone has experienced something similar. My last MRI was in November 2022 and the results were reported as stable compared to previous years since having treatment (Cladribine) in 2018 and 2019. I...

Hi, I've been reading all the posts on here for a little while before I plucked up the courage to post. I've had really bad headaches for many years but I was constantly being told it was just stress/anxiety even though I felt there was more to it several doctors said the same I even took myself to ...

Hello. I’m new here but not new to MS. I’m one of those who also has a bunch of other diagnoses, of the sort which often along with MS. Most of them predated it. Bipolar disorder, narcolepsy, fibromyalgia, psoriatic arthritis. My mobility is not noticeably affected, although I know what’ll happ...

I somehow injured my back over a week ago and not only it is sending my sciatica through the roof, it is also sending my other ms symptoms crazy as well. Pretty much feeling fed up at the moment