When I was diagnosed with MS I was terrified, I knew nothing about it. I was in the hospital with a lot of symptoms (unable to walk, vision issues, half of the body was numb) but no diagnosis for a few weeks. The doctors at the hospital weren’t too helpful with providing information. Although I was suffering a lot of mental anguish with this diagnosis — nothing they could say would have reassured me at the time. Later, I was transferred to a rehab center.
At the rehab center they gave me some outdated information — I didn’t know at this time. This information was way too much for me to handle and caused my bipolar brain to become unstable. The item that struck me the most was the mention of a wheelchair for 80 percent of those diagnosed after ten years. I was 37 at the time and I had a lot of fear about being in a wheelchair by the time I was 50.