First entry to bring things up to date

I was having problems swallowing, with my speech and nasal drainage. Visited my General Practioner and he decided we would start by sending me to ear,nose and throat dr. Went 2/5/16.  ENT checked drainage did nasal X-ray, prescribed nasal sprays. Said I rhinitis and to try neurology next.  Over weekend thought I had allergic reaction to nasal spray, but in hindsight it was a mg flare. Slurred speecH and tingling cheeks. Took me off of nasal sprays and symptoms went away. Went back to General Practioner 2/18/16. He suggested I may have myasthenia gravis but said he would send me to a neurologist to verify. Went to neurologist 2/29/16. Neurologist also thought I may have mg. She ordered a blood test and MRI which I had 3/3/16. They called and said blood test positive for mg and they wanted CAT scan of chest to check thymus gland. Had CAT 3/8/16. Went back to neurologist 3/11/16. Found out I had a tumor on my thymus gland. She said once it was removed I would be cured (yeah right).  She said may just be a small incision at my collar bone to remove. Sent me to cardiac surgeon to discuss surgery. Went to cardio surgeon 3/16/16. Discovered I would need the equivalent of open heart surgery to remove tumor and no, would not 'cure' mg, but may lessen symptoms. Surgery was scheduled for the following Thurs, 3/24/16--the Thurs before Easter. The kids were out of school, the whole break I would be in the hospital. Sad moment for me. I had surgery, found that tumor had also wrapped around my left frenic nerve of my chest, so that was removed as well.  Left hospital 3/29/16.  
 
Was as hoping to finish this, but too pooped at moment. I know I need to journal. Will catch up tomorrow.