In MS fatigue is very common. Fatigue is different from normal tiredness or exhaustion and can cause sudden losses of energy which may interrupt your daily life. It affects everyone differently but often feels like being weighed down or trying to wade through quicksand.
I’m so unbelievably anxious that I may lose my job…since August last year I’ve been off sick multiple times, MS investigations, infusions, MRI’s, Lumbar puncture, adverse effects of kesimpta, surgery, insanely bad fatigue, bed bound with vertigo, my work has been so lovely the whole time and I came ...
I was initially diagnosed with Clinical Isolated Syndrome following a bout of left optic neuritis in April 2023 - from here until September 2024 my fatigue levels started to drop and started to get really bad pins and needles in both of my lower legs - my neurologist ordered another MRI and in Janua...
Hi, I’m 52, born without my right leg due to mild spina bifida… I’ve always had problems with my hip/pelvis as it was deformed at birth and X-ray shows massive difference in the two hips.. had to stop wearing false leg in 2010. I’ve suffered with different types of spasms as well as hip pain for yea...
Hi there- I’ve been on Kesimpta since the end of September- I still feel rough some days, optic neuritis, headaches, dizziness, balance issues body aches and endless fatigue- everyone keeps telling me it will take time for me and my body/MS to adjust to treatment but when have these things started t...
I feel hopeless, doctors still don't listen, ms team are useless, so many follow-ups just never happen. I'm progressively getting worse and I can't afford to pay for help, I cannot rest, there's always a new problem adding on to the already massive list, I can't get a grip on anything and trying to ...
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Hey everyone!
My name is Zara and I am an MSc Occupational therapy student from City St Georges, University of London. I am currently conducting a research study which investigates the impact of ms fatigue on occupational participation acro...