I have Leimyosarcoma. Diagnosed in 2020. Post hysterectomy, necrosis fascitis complications, chemo, and radiation. I am told my cancer is "inoperable". I am lucky as I am doing well the 4 yrs since dx. Wondering if anyone else told "inoperable" and what follow up care they are having. I feel very abandoned and can't get answers as to what to expect.