Im in the process of getting an official diagnosis, RNS next week, but since my occular symptoms have improved a lot since starting pyridostigmine my neurologist said I probably do have MG. Since we talked about MG even being a possibility 2 months ago I feel like im noticing a lot more signs that line up with it or at least noticing them more frequently. Things like easy arm fatigue, fatigue with chewing or swallowing, decreased walking speed from over all fatigue, etc. I know i felt them… read more
Before I was even diagnosed with MG I did notice fatigue and being tired especially at work and after dinner I’d fall asleep in the chair watching rv for maybe 15 min. But who knows maybe I had other subtle signs and just never noticed them??? I do know about 2 months after my femur surgery thats when every symptom started and I thought I was having a stroke. It’s been almost a year and I’ve come along way I still have leg weakness, bowel issues at times but all in all the meds have helped with all my other MG symptoms and I had every one except breathing issues.
Is it possible that getting a myasthenia gravis diagnosis has made symptoms feel more noticeable or intense? This is actually a really common experience — and it makes complete sense.
Before a diagnosis, many people push through symptoms without fully registering them. Once there's a name for what's happening, the brain Show Full Answer