Good morning everybody I just thought I’ll come on and introduce myself. I’m Dave David MS trucker on Tiktok. I’m also an MS champion for MS Society. I’m here to help an answer questions if anybody’s looking for somebody to reach out to I was diagnosed in 2019 with rrms

Is MS a long term condition like Parkinson's? I had thought that it was until I saw a few comments recently on here where people said that their Neurologist had said that their MS had gone. Is it to much to hope that it clears up after say 10/15 years? Or is it that MS treats everyone differently?

Does anyone have those days where they really just cant function, eyes hurt to open, brain cant cope with any info, limbs hurt to lift. Do they find it affects there mood, I get into really dark places mentally when like this. One of those days today, still trying to work and have mum duties later ...

Living with MS is not easy. Some days, I smile even when I’m hurting inside. Going through a relapse is exhausting, frightening, and emotionally draining. There are days when I feel strong and days when I silently wish things were different. But I’m taking it one day at a time, holding on to hope, ...

How do you cope?

I have been referred to gynaecology for severe pelvic, back and leg pain. The pain comes in suddenly and throughout the month - not correlated with my period but pain is similar to period pain except far more intense. I shake with the pain, my legs feel like they're buzzing when I go into a pain fla...

Living with relapsing MS is a battle no one truly sees. Some days are harder than others, but I’m still here, taking it one day at a time. Tired, scared, but still hanging on. ❤️‍🩹

I’m I the only one but when I go out with my family on days out I feel like a burden as I’m so tired and always in pain