So I had my first real flare up with MS actually at the end of 2023 and I didn't get officially diagnosed until the end of 2024 (it was a pain to set up all those MRI appointments, which was why it took so long) Anywho, sometime after I got the diagnosis, I had to return to my day job at a fast foo...

Does anyone find them selves quickly annoyed w people?😮😣

Stressed annoyed. I exercise 4 to 5 times a week I eat healthy i try and walk about afew times a week not easy when relying on chair. I do not drink alcohol more then once a month. I drink more water then a fish but I cannot get below 86kg bmi 21. I know meds affects body but I do core exercises tha...

Where do I start. I work 3 days a week. 7am to 3pm. I stand all day packing veg in a packhouse. I'm the only one with a 'health condition'. We have stools to sit on because I asked for one as my legs are in constant pain. If it's not my legs, it's my hips. The pain is that bad that sometimes i could...

Is anyone else having trouble with the app it's constantly logging me out getting very annoyed

I was diagnosed with MS after a MRI scan in Gloucestershire Hospital via letter and was basically left hanging. In the interim I moved to Birmingham and re-registered GP and they quickly had me in with a neurologist, MS nurse and took my case to board to discuss and consider treatment options. All i...

Does anyone else feel so so much anger? If I’m not annoyed I’m crying it’s like my emotions are on high alert and just switch within seconds, I snap at everyone close to me for stupid things then feel so awful afterwards.. they understand why I’m emotional but is this normal?

I just want to say a massive thank you to this forum. I don’t know why I stopped myself from participating in it from the beginning of my MS journey. It probably would have helped me a lot during some very dark times. I’ve just sat laid on this bed, quiet for the past 4 hours. Everyone has continu...

I was diagnosed in 2000 with MS. Gradually gone from walking and active, to now not being able to walk needing Carers and having a catheter. Today I am really fed up as I am bypassing a lot and we are meant to be going out tonight. I just felt so low and not sure I will enjoy it. I am annoyed the MS...

Everyone close to me has recently had a cold/flu symptoms. I'm on ocrevus and you can probably guess....I've come down with it. Today is the worst I've felt and all I've done is sleep the day away. I'm then told to get over myself, it's flu.....we've all had it and that they are watching me waste aw...