So last Wednesday, Day 16 since the first chemotherapy treatment I went to the salon that specializes in products and services for cancer patients.
I had a free head shave, which was a real relief for the scalp. The day before, when I shampooed my hair, it hurt down at the roots, so I am truly glad to have it gone right now.
The stylist then trimmed my new blond wig, and showed me how to put it on, as well as giving instructions on the care of the wig. I chose a synthetic wig and find it is just a real looking as a real hair wig. It was rather expensive, yes, but our health plan will cover some of the costs. And I can wear it when my own hair grows back.
On Friday I had a blood test so that the doctor would know if my platelets were back up, so I could have chemotherapy again on Monday. They were. She gave me a new prescription for the numbness I had felt in both arms right after the first treatment, and said it should also help with the back pain. These are unusual symptoms, she said, but they can occur.
This Monday, June 17th I had the second chemotherapy IV, this time with Herceptin added. It took 5 hours total. The Herceptin was injected slowly, over 90 minutes, since it was the first time, and then there was a hour wait for any side effects or complications to occur. That was followed by the other two drugs, Docataxel and Cyclophosphamide.
I feel fine today. Must drink 3 liters of water per day, to help flush out the drugs. And of course, I am again taking the Decadron (dexamethasone), Zofran (mylan ondansetron) and Metoclopramide.
I am ready for days 3 to 5 when symptoms are the worst. I have learned that days 10 to 14 are when the platelets are lowest and that is when one must be careful of developing a fever (an emergency) and of exposure to germs etc.
That’s it for this time! Thanks for reading and thank you for the kind wishes from so many of you.