Thank you, Sue! That is wonderfully encouraging. I see my neuro on March 1, and I have new, much more typical mg symptoms to describe to him now. I have some confidence in him, because he ordered the MG tests on the basis of the symptoms I had a month ago, which were a lot vaguer. Maybe he will be willing to consider the possibility that this is MG even if the tests aren't conclusive. Maybe he'll try me on Mestinon. If not, you and the others here have given me hope that if he won't consider it, another neurologist might.