Tuesday, April 27, 2010

Back in the Saddle Again

I had my first treatment in a long time today, and I'm glad to be back. The doctor is going to give me a shot for the white blood cells on Thursday when I get my pump disconnected, so we're hoping that won't be a problem anymore. You never know.

It's been a while - I'm feeling very tired, and that metallic taste in my mouth, and the sensitivity to cold... but I'm still happy we got it done. Time to kill some cancer cells!

Friday, April 23, 2010

New Doc, New Treatment, 19th Nervous Breakdown

I had a nervous breakdown yesterday. I was going to say I almost "lost it" but I actually did lose it. It was when UnitedHealthcare did not approve a CT scan my new doctor requested. I don't know why they did not approve it - I've already had two of them done at the same place. I'm getting convinced that they will deny any claim, no matter what. I'm fighting them on several fronts - they still claim a common drug used for colorectal cancer I received is "experimental". They want me to pony up $7500 for each of six treatments. I'm not sure how much that is but I know I don't have that much in my savings account.

The CT scan was finally approved after about 4 hours on the phone and I'm going in this morning. It's important that it gets done today so the doctor can review it this afternoon and we can start treatment next week. I haven't had treatment in several weeks and my markers are going up, so I'm ready to get back on track.

The good news is that I really like my new doctor and she is ready to get aggressive with the new treatment. So we're going to get after the cancer - now I need to work on my mental health!

Sunday, April 4, 2010

Easter Weekend


It's been a nice Easter weekend. John and Elsie are in town and we had a huge Easter feast today. Yesterday I actually went swimming - if only for a very short time. I've been avoiding the pool because one of the side effects from the chemo is a hyper-sensitivity to cold. For a few days after treatment, I can't drink anything cold and if I touch something cold I get a tingling and numb feeling in my fingers. It's very uncomfortable and a dip in Barton Springs is out of the question. Fortunately, it doesn't last forever and after last treatment it didn't seem so bad.

I have another treatment this week (provided my white blood cell count is high enough). I also have an appointment with the surgeon and he's going to check out the tumor once again. I'm not really looking forward to the week, but I really enjoyed this weekend.