I’m a woman who was diagnosed with MG in August 2020 at the age of 70. My symptoms then included double vision, droopy eyelids, impaired speech, difficulty swallowing, weak neck muscles and tiredness. I was put on Mestinon and Prednisone and I had minimally invasive Thymectomy surgery in November 2020 at University of MI Hospital. I was informed by my surgeon, who was excellent, that I did have a Thymoma but it was not malignant. I had no complications from this surgery. However, in December 2020, I had a very bad MG flareup and I was admitted to the Emergency Department of the same hospital. I was an inpatient at this hospital for 12 days and I was discharged with a NG feeding tube which I had to have for about 7 weeks until I was again able to swallow food. My neurologist is also on staff at this Hospital and he has been excellent thru out this MG experience. I later had home IVIG infusions, starting bi-weekly and then later every 6 weeks (with Privigen), for a total of about 18 months. I also had transitioned to Cellcept as my only MG medication. As of January of this year (2023), I’ve now been off the Cellcept and I’ve not had any MG symptoms and I feel like I’ve never had this problem. I’m hoping and praying that I’m either cured or in remission. This was my Thymectomy experience and I hope all of you contemplating this surgery have the same result that I’m now so fortunate to be having.