I’m responding to the “first wheelchair” question. Having adult onset (MD type 2) I didn’t know what to expect. It’s such a rare disease and the symptoms in two different people even getting the disease from the same source, (like my siblings), are extremely varied. I first realized I needed something to get longer distances than I could any longer walk without risking falling. So I bought one of those cheap electric two wheeled scooters. After a while I got to where I couldn’t balance and was always dragging my feet. So I next got a Segway with a seat (not the i-pod). It was fun and fast, but not very safe because it moves to stay under your center of gravity. So whenever I would sneeze or have a hand spasm it would jump to stay under me and got me off the sidewalk and into trouble a lot. Finally after that I fell into a power chair and never looked back! It took me so long to admit that that was what I needed, but it makes going places pleasurable and safe and easy! Why does it take so long for us to admit that?