To be honest, everyone around me is really understanding, especially my family and friends. Work is also understanding about it all but I’m lucky in respects that I really only get fatigue and a few aches and pains that didn’t really happen till recently. Think I can put that down to what’s happening in the world though. Worst thing I’ve had said to me was from my ex, just said that I’m now classed as disabled so I can get disability pay 🤦🏻♀️😂.
I don’t see my MS as a curse or hindrance but that’s me, I’ve done more in my life in a short space of time since my diagnosis than I probably would have before 😊.