I was diagnosed with Myasthenia Gravis 4 weeks ago. On Mestinon and Prednisone. Still having some double vision. I cut down Prednisone dose myself because of side effects. I do experience fatigue, occasional shortness of breath,and sores on lips and inside cheeks as if I bit inside of cheek but I didn’t. My husband passed in November and the only family I have is my adult son who I am very grateful for. We are both mourning the death and now dealing with this. I’m a cancer survivor and feel this is so unfair, I’m in denial at times, angry and having a difficult time trying to adjust living with MG. I don’t have anybody that I can talk to that understands.Don’t know what prognosis is for me but as I research, it could be a bumpy ride. Any advice?