My name is Eddie. I was diagnosed in 2008 with MG due to multiple positive blood tests for the ACHR. It took almost 2 years to get a diagnoses. I was having weird facial tingling, slurred speech at times, and what I thought, was my tounge feeling heavy/numb. I also had problems with my throat. It took my current Neuro, the only one to test me for EVERYTHING including MS, to realize I had MG. I have been blessed for almost 5 years and I have never taken meds. I have good days and other days are ok. I mainly have issues with the bulbar muscles, I only have mild eye lid weakness, and fatigue. For the most part I have been putting along. What changed was in April was my vision became wavy. When I look at patterns or even when I read the lines and letters very slowly wave about. It's not normal and not consistent with MG. I've tried covering one eye and both eyes do this. My doctor immediately had me come in and ordered tons of blood work for EVERYTHING, MRA, MRI with and without contrast of the brain, eyes, and C Spine. According to him, everything looked good. I even had Evoked Potentials and the eyes and ears came back fine. The SSEP said the right foot was slower than the left but he isn't concerned with it. I saw three eye doctors, an Optician, Neuro Opthamologist, and a Retina Specialist. The only thing that was found was eye lid weakness (no optic neuritis). I had a lumbar puncture and waiting on the results. I'm pretty scared guys and just want someone to talk to.