Head Shave! and Chemo Cycle 2

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.




So….the appointment on Friday the 24th turned out to be with the doctor’s nurse only. I was given prescriptions for Decadron (dexamethasone), Zofran (mylan ondansetron) and Metoclopramide.

Some of the pills have to be taken beginning on the day prior to the chemotherapy.

On Monday, I was awake early, and at the cancer centre in plenty of time. All of the people in the waiting room seemed so OLD.

A nurse escorted me and my husband to one of the large rooms, where beds are available. Since I was going to be there for 2 and a half hours, and it was the first time, I had to be in a bed. Not undressed, though, and the port was easily available and it did not hurt at all when she inserted the needle!

The nurse went very carefully over all the possible side effects and what to watch out for. Then the first chemo drug was started by IV. After an hour and a half, it was done. The port was flushed, and the second chemo drug was started. There are volunteers who come around every so often, with coffee, juice, cookies and crackers. It is possible to get up to use the bathroom as the IV is portable.

I was very glad to have this first session over with,and no ill effects – no allergic reactions.

I have been very tired yesterday and today (day 3 and 4 since the chemo on Monday). The worst effects are days 3, 4 and 5 according to the doctor.

I next have to go for blood work on June 14, and see the doctor again. Then June 17th is Chemotherapy 2 of four.

The anti-nausea pills are working well. I’ve only needed them once or twice the last two days. Of course, I expect to be much more ill but here is how I look at it – If I am sick it means the drugs are working. To me, I think of chemotherapy as a ‘reboot’ of my body., much like when you ‘reboot’ a computer. All the cells are going to be killed off and restart. That may not be very accurate!  But it helps me to face what is coming.

Until next time.