Hi my name is Peter and in the early part of this year I was diagnosed with Myasthenia Gravis I was then made aware that with this condition I may have a thymoma. Yes they were right. Between then and know I have had an operation to remove my thymus but things did not go quite as planned. My thymoma was quite advanced and now I am at the point of waiting for my first of 25 doses of radio therapy. I am quite happy to talk to anyone about my experiences so far and If anyone wants to let me know more about radio therapy ie side effects long term etc I would be quite happy to hear.