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Has anyone else gone night blind? I suffered from optic neurosis (fainted and came round blind in one eye)it led to my ms diagnosis 2 days later. After my sight mostly came back I have found I can nolonger see in the dark and hence can no longer drive after sunset which is rubbish in winter when I c...

Hi everyone! I hope you're all doing OK. I was just wondering if anyone has any experience with eye twitching? My left eye has been twitching for about a month now and I experienced some pain in the eye last week, but haven't had the pain since however, the twitching persists. The twitching is ha...

I had a relapse in april which is 5 months ago with optic neuritis as my symptom. I was fine after steroids my symptoms subsided and now 5 months later i have the same symptoms again for more than 2 days. Can relapses happen this frequent?

Hi I have RRMS, I got optic neuritis in January 2023 & an MRI showed lesions on my brain & spine I also have problems with my left leg (drop foot/Numbness) I was put on Tecfidera in January 2024 but I haven’t noticed any real changes yet, sorry I’m new to this & was just wondering if anyone else is ...

hi everyone just discovered this app and thought i’d introduce myself. i’m tanya 38, from the north east. was diagnosed in june this year after a couple of years back and forth to my GP with numerous symptoms but hey ho! thank you optic neuritis for showing yourself and getting health professionals ...

I read that in most cases of OP , the eyesight is restored some if not completely after time has passed with or without steroids, however i have had optic neuritis in my right eye with no improvement for 19 years. Anybody else? I can see everything through a very dim view like when you come in a ro...

*LONG WINDED POST IM AFRAID * It's been 7 years since i was diagnosed with Fibromyalgia. I spent the first few months after that diagnosis on such strong painkillers, I was almost constantly nauseous and I struggled to get out of bed most days. I became depressed, because i felt like i couldnt do a...

Hello, I'm pretty sure I have ms, going to Moorfields tomorrow for probably optic neuritis and various other symptoms too. Ten days ago I thought I was fine - I'm 44 so that's adding anxiety. I know noone can solve this for me but if anyone has some words of courage, I'd really appreciate it. Thank ...

Hi everyone! This is more of an introductory post I guess. My names Hannah and I am newly diagnosed. I was first diagnosed with Fibromyalgia in 2017. They started to suspect MS in 2020 after I developed Optic Neuritis. I have not started treatment yet, but I am due to give my decision to my MS nurs...

Hi all, I’m in need of a bit of a rant and to hear any tips/advice you might have. I’ve only been diagnosed for 6 months and recently as I have told more of the people close to me about my experiences and symptoms I’m getting A LOT of people saying ‘oh yeah, I get that too’ and I’m finding it extr...