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I just had a call with an optician, got my driving license taken off me by DVLA 5 years ago and the optician today said the damage to my eyes had been done from optic nuritis 9 years ago and it’s just got worse.. it’s causing me every day walking problems etc and it’s really getting me down how do I...

If you could go back to a year before your multiple sclerosis diagnosis, which year would it be? I choose 1998: the year I passed my driving test 🚗 before losing sight in right eye due to optic neuritis 👁 and England were also supposed to win the World Cup. Go! 🏴󠁧󠁢󠁥󠁮󠁧󠁿🇧🇷🇩🇪🇦🇷🇮🇹🇦🇷...

Hi all, I was diagnosed in Jan of this year after a severe bout of optic neuritis. During the diagnostic process i developed a spinal leak and headache from the lumbar puncture and have had residual pain and nerve issues in my lower back after the epidural blood patch to seal it. My eyesight improv...

I’d love to hear people’s stories with optic neuritis. Like when did it start? Do you experience it with Uthoffs? How long? One of the major first symptoms I had was double vision. I got it after getting COVID. The double vision went away but I still experience brightness, especially when hot. If ...

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 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'm almost 28 and am still waiting for an official diagnosis. Just had 3 more MRIs today and got the results back on my phone immediately. Follow up appointment isn't until next month but from what I gathered from the results, it's just a confirmation of what they already suspected. This all started...

Hello, I’m not sure how many lesions I have, I had optic neuritis 3 times and then an attack in my feet before I was diagnosed with MS, since I’ve been on treatment I’ve no more attacks, noticeable ones anyway, I was originally on Copaxone, then Techfadera (Which killed my white blood count) and hav...