Hello. I am 44 now. Wasn't officially diagnosed until 4.5 years ago. They believe it started in my early 20's. Back then they just kept saying it was mono then it was "chronic fatigue" then "ebstein barr". I was sick all the time with anything within 50 miles

. I continued to work full time, get married and live like anyone else. The big "break through" was when I woke up with my new constant companions of tingling, pins and needles, fatigue and major spasticity. Had mri's ...confirmed ms diagnosis and then fibromyalgia, the only true change is I don't work full time outside the home. I have a full time job here at home taking care of things here and I can rest when I need to. There are days when driving is not an option but there is always things to do here.
I love pilates. I use a pilates machine not the kind you just do on a mat. I have a treadmill and walk alot on days I can or as much as I can. I do not use the injectable medication. I take a multiple vitamin and vit. d supplement and get as much sun as possible in this state!
I live a very full life. Many, many people with MS and other autoimmune diseases do. The thing with these types of conditions is that they are all so "individual" and affect everyone differently. There are common symptoms but to what degree seems to be the biggest difference.
Hope this answers some questions.
Lisa
p.s. no such thing as stupid question! ask away!