Meech • I saw my opthamologist last year for double vision ... no diagnosis, only a suggestion that it might be MG. He suggested that I see a neuro-opthamologist which I did - twice - and who ran a series of tests but could not come up with an MG diagnosis, altho she suspected it. She referred me to a neuromuscular doctor whom I saw and who ran some tests and diagnosed the Myasthenia syndrome. One of the tests done was a MuSK antibody test which took eight weeks for the report to reach my doctor. I’m in Arizona and the blood work was sent to a lab in Massachusetts.

To me, the whole project felt a bit like running in circles but eventually answers were found. I agree with pingpongman that you are getting great advice, and with AnnieB3, that ‘waiting is the hardest part’. Have faith, Meech, you’ll get there.