For the last two weeks I have been more tired than ever before. I have no enthusiasm, I can’t focus my thoughts, my body has been giving me some crazy sensations and I just want to curl up in a ball and fall asleep but kindly my insomnia has said no. Not asking anyone for a magic cure, I know we’re ...

Any tips for taking a bath in bed?

People ask me how I stay so calm. Truth is, I don't. I've just become incredibly selective with where I spend my f**ks. You can even check the field where I grow them. It's barren. The soil's given up. Even the scarecrow packed his bags and left. I don't give a single, solitary f**k. Not one. If ...

Today I can’t take anymore. Nothing anyone can say or do can help but if you have MS you will understand. To the outside world I appear as if everything is okay because who wants a moaner and I don’t think I have it in me even to do that. I was bought up to be polite and make an effort but I can’t. ...

What is your experience with strength training and exercise? I noticed when I lift heavy my gate is good for that day and the next and I have a little bit more balance, but I also am having a hard time defining that red line where if I go any further, I’ll push myself over the edge and pay for it w...

I have SPMS but for the last few years I've also had worsening arthritis and my hips have been terrible, so I bought an electric wheelchair - a Drive Autofold power chair. It has been great, comfortable and easy to drive and use, but in the last year I've had both hips replaced and now I don't need ...

I got a couple things that bother me cognitively. for example, I cannot just make a damn decision about anything, which bothers me. Also, sounds crazy but i feel like MS has kinda made me dyslexic, sort of. Anyway, just asking. Thx.

I am a beacon of light in the darkness. I am the solution to my problems. There is nothing i cannot conquer. I find the answers inside when i stop looking outward. Love and appreciation for all in existence. Thank you for existing.

I have RRMS. Been denied for social security 5 times and I'm losing hope. Is it really that hard to prove I'm disabled? I have attorneys, but I'm struggling even with them. 😭

I live in the north west england UK and I was diagnosed with RRMS in 2022. Since then I have been denied DMTs despite requesting every time I see my Nuerologist. Since diagnosis I have decorated ALOT I have had quite a few attacks (each has gave me a lovely new symptom). But when ever I see my neuro...