I'm usually pretty open about my health. You guys know I've been sick for a while now (about 2 1/2 years). My doctors and I assumed it was my autoimmune disease because the symptoms were indicative of that. So, we've been treating it that way. I wasn't getting any better though. So, last December, I insisted that my GI doc do an endoscopy to check on some issues. Well, on March 13th, she informed me that one of the samples she had taken for biopsy turned out to be neuroendocrine cancer (the bad news). Turns out neuroendocrine cancer, which is rare, also has a lot of the same symptoms of my autoimmune disease.
I saw an oncologist and he ordered a PET scan, which I found out yesterday showed the cancer had not spread (the good news). Also good news is that they caught it early, it's a slow growing cancer, and it's just in the right spot to totally avoid chemo and/or radiation. I really didn't want to talk about it until I knew exactly what I was dealing with. It has been a crazy rollercoaster ride. I'm mostly upbeat and positive, but there are times when it's incredibly hard, especially when the severe fatigue and GI symptoms hit.
I'll be having surgery soon to remove the tumor and recovery might take a few months. You're in good hands with Hoss looking after the place though.