I just had my ninth round of chemo . . . ¾ done! After consulting both oncologists, I decided to drop the chemo drug that is causing most of my neuropathy and give my body a rest. The oncologists were concerned about permanent nerve damage in my hands, feet, and mouth.
I consulted some kindly people on a colon cancer forum, and their input and the oncologists’ opinions helped me make this decision. It was tough, actually. It’s hard to know all the implications, and even the doctors don’t know it all. There’s so much uncharted territory yet.
I have very happy to have received an “all clear” from the PET/CT scan radiologist. I’m aware that the scanner only sees activity that is 3mm or larger. It doesn’t see the tiny stuff. So I really don’t know what remains inside me.
Still, I am celebrating the scan results. They could have been so much different. I take the good when it comes and bask in it as long as I can!
During the weekend, I was down with a chemo-related migraine that I couldn’t seem to control with pain meds. I am predictably getting a migraine during the second week of chemo, usually on the weekend. So I ride it out.
I had a long day yesterday (but the headache was gone!) — getting chemo for 4 hours and seeing both oncologists (one is far away) takes a while. I left the house at 8am and didn’t return until 5pm – a normal workday for most people but exhausting for me.
Fortunately, my very kind son drove me to and from the distant appointment, and I was so grateful in my weary state not to have to gear myself up and concentrate on commuter traffic.
Today I feel so good and peaceful and rested, even though I’m still wearing the chemo unit which is dispensing a drug into my body 24/7.
All the same, this is a rare day, when I feel so serene during chemo. I will get outside and walk the dog and admire the autumn leaves, which is always refreshing.


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