2nd Herceptin Treatment
Yesterday I went in for my 2nd Herceptin treatment. I was very apprehensive as this was the drug that caused me to go into spasms (the nurses called it “chills”) when I had my first Taxol treatment two weeks ago. I managed to not vomit the entire time, but boy was it close. My half hour treatment lasted 4 hours as it took forever to mix the drugs then the nurse decided to put me on a slower drip to make sure I did not spasm and then I had to periodically stop and take 15 minute breaks to stop my gagging. I was wiped out when I got home and fell asleep for two hours before dinner. Of course, not sleeping through the night for weeks does not help any either. I have been experiencing muscle and bone pain plus tons of hot flashes that wake me up in the middle night. These are side effects of the chemo. My oncologist has put me on a new medication, which should help with these symptoms in addition to the extremity numbness, and tingling that I should begin experiencing after my third Taxol dosage. My spirits are up knowing that the end is getting closer. Radiation sounds like a party compared to what I have been going through. Plus, once chemo ends my hair will begin to grow again.
Thank you for all your love, cards, gifts and support as we hobble down this path.
Thank you for all your love, cards, gifts and support as we hobble down this path.

4 Comments:
At 2:33 PM, September 07, 2006,
Anonymous said…
Hey Cheryl,
I am so glad to read that you are making it through the treatments. You may have heard through the SATech grapevine that I am pregnant. Every morning about 3:00 am I have to get up and get a snack. As I eat my eggo, you and your family always come to my mind and I pray for you during this time! Just wanted you to know that even the baby inside my belly is thinking about you!
Hope each day brings you more hope and strength.
Love,
Diana (at SA Tech)
ps - I have also been saving the breast cancer awareness lids from the gallons of yogart I've been eating in your honor. :)
At 6:45 AM, September 08, 2006,
Anonymous said…
Hi, Cheryl: Will we see you on Sunday morning? I miss you and glad the worst to close to being behind you. Cute headscarf, though.
xoxo
Barbara
At 6:38 PM, September 08, 2006,
Anonymous said…
You said: "Thank you for all your love, cards, gifts and support as we hobble down this path." It may feel like hobbling to you, and I'm sure it does, but your spirit and outlook come across much more like a victory march. So glad to hear you are nearing the end of chemo! Hug your kids for me. No need to kiss Mark for me, though.
Chuck
At 8:19 PM, September 08, 2006,
Anonymous said…
Dear Cheryl:
Just to let you know you are still in our thoughts and prayers.Just continue with your good attitude and keep your spirits up-this helps so much for you recovery.May God keep you strong and positive while on this difficult path you must take.I know it is hard to believe-but- this too will end.
Fondly
The Mannino's in Florida
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