Would there be any campers and bike riders?

As anyone on this group got MS after the covid vaccine,

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

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 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. ❤️‍🩹

It seems that these conversations are between young people who have children, jobs, and many other priorities than a retired 60-something has while managing MS. CAN WE OLDER FOLK CONNECT?

Hi, I got told by Neurologist yesterday I have MS. I’m feeling a bit lost and confused and worried about how different my life will look now I have this condition. I’d be grateful to know if there are any things people wish they knew when they were first diagnosed that may help? I’ve just finish...

And I miss not peeing myself. I don’t even want to go anywhere, I can’t remember the last time I left my house to do something that wasn’t a doctor’s appointment. I feel like I’m stuck in an endless cycle of grief.