MS symptoms started being noticeable in my late teens. I started getting resp. infections, all body weakness and severe muscle contractions and jerks on my left side. I was not diagnosed until I was 50 years old. It was caught by my doctor trying to prove that I did not have MS or Parkinsons. He thought the symptoms were not going away due to an antidepressant enhancer drug I was taking. Well, it didn't work out that way. My family did not take the news well and no longer communicate with me. My spouse believes it sometimes and sometimes not. I am looking for some sort of support group and gathering any information from this group that may help me deal with PPMS. Everything from not sleeping to dealing with physical changes and mood changes. Also, I am interested in hearing about diet that have helped some of you feel better.