Hi everyone, hope everyone is doing ok. Just wanted to ask if anyone has experienced almost blindness to your disability. I was diagnosed with rrms 2 years ago. For me, ms came after a stressful period at 42 years old. To me it came out of the blue, generally I have been ok since then, my balance is off and my walking is limited now, but I’ve still been able to hold onto a full time job as a teacher. However, recently I have been falling, eg 3 times in the past month and I get quite exhausted when cooking/ cleaning etc but my husband and kids really don’t see it and really don’t understand, i am trying my best because though this disability has come upon me, I don’t regard myself as disabled , but just want them to sort of see how difficult very regular things have become for me now. Does anyone have any golden nuggets? I have said it to them but they don’t really make any adjustments lol and things carry on as normal..