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So, I haven't driven a car in years, was never a confident driver and since optic neuritis never even tried getting behind the wheel.My vision recovered mostly in one eye but not completely in the other. I am not sure how to go back to driving. Do I have to tell DVLA or take another test?

Has anyone lost all vision in their eye(s), as in complete darkness, even after doing rounds of steroids and plasma phersis?

Hi, i had optic neuritis in my left eye in october, i didnt loose my sight but i had blurry vision and pain when moving my eye. I was treated with steroids at the time which made the pain completely go. Since then my eye is much better but i do get like little black what i can only describe as float...

Dies anyone have any wisdom or information to share on Optic Neuritis? It was my 3rd relapse &the one that got me my diagnosis. Each time I’ve had a check up my neurologist seems to move the goalposts with how long it may last. I started with it in April 2021, it isn’t as bad but my vision still is...

Hi, just a little bit of background I was diagnosed with ms in 2020 following an episode of optic neuritis and a severe relapse about 2 months after. I fully recovered from my second relapse, however the optic neuritis never fully recovered. I went complexly blind in my left eye and I am now left w...

How do I deal with his temper in the mood swings with Thomas and his iMessage, and so bad that he falls a lot more than normal

Hi all, I have had a blurred eye (periferal vision) since end of July. It goes away and then comes back worse. I cam see out of it but blurry and such an effort to focus. Do I contact my GP? Told MS Nurse in August but they just took notes. So frustrating not hurting. I feel like the muscles need re...

Hi all, My partner was diagnosed with MS a few months ago after a bout of quite severe optic neuritis. Some vision has luckily recovered, but they can still see very poorly with the affected eye. It has been more than 6 months now and I am wondering if anyone has experienced any recovery in ON afte...

Hey, I was just diagnosed with optic neuritis and also seem to have signs of previous inflammation in my brain — I don’t have an official MS diagnosis at this point but they think it’s one of the autoimmune diseases or something in the “MS family” of diseases— not sure what that means. I received a ...

Hello there, Decided to reach out because I am at a crossroads. Diagnosed with relapsing remitting MS in 1998 and started Avonex that same year. Been on Avonex Ever since. Over the last 10 years my MS has remained stable with some noticeable weakness in my legs since the pandemic, I contribute that ...