I had never heard of it when I first got told of my probable-diagnosis, but once I was told it was probably MS and I mentioned it to other people, almost everybody replied that someone else they knew also had it.
As an MSer, I feel like I’m kinda late to the party with regards to understanding how important the ADA is. I was diagnosed in 1991 but didn’t really experience physical disability until later in my life.
I've had this disease a long time and am thankful that it is not life-threatening to me right now. But sadly I have had to give up some things.
Nothing found here should be considered medical advice. Please consult your doctor before making any changes.