But since being off pyridostigmine (test requirement) I have started to decline...plus the stimulation of my eye area has left me with eye weakness and a facial drooping feeling...as if heading into a flare.
When I had my single fiber test I had the same issues being off the medicine. Don’t know results yet but the test was really tough for me and stopped being able to take air in and the dr didn’t seem concerned. Also troubled that my regular MG dr didn’t seem to think it was a big deal either - just go to the er if concerned. Getting back in the meds has started to help.
Thank you so very much! This has been a 3 year process and since starting pyridostigmine in January 26, I have improved so much. I am fearful of losing something that has literally given me my independence back...it has been the difference between night and day...I will contact my neurologist tomorrow and let him know of my status. He did give me the okay to restart my medication before this test, come off of it for the test, then start it back up. After your response, I am heading to bed as I believe I can sleep now. Thanks so very much!
That sounds like a really frustrating and exhausting day — traveling for testing, stopping your medication, and then feeling worse afterward is a lot to deal with all at once.
Normal EMG and single fiber EMG results don't automatically rule out myasthenia gravis. These tests aren't perfect, and false negatives can happen Show Full Answer