Some of you have asked what exactly my treatments are, so here is the breakdown:
Week 1 - I get 4 different drugs through my port. First they give me an anti-nausea medication called Zofran and a steroid called Dexamethasone. Then a drug called Taxotere, next is Cytoxan and one called Herceptin and last is Perjeta. In all in takes about 4 hours.
Then the next day I go back and get a shot called Neulasta.
Week 2 - This treatment is just one drug through my port again, this one is called Herceptin. This round only takes about an hour.
Week 3 - Same as week 2.
Then is starts all over again.
There is also all the medications to help with the side effects...
But they have side effects too.
I also go in the Thursday before week 1 and have my blood draw. They check the numbers and make sure I am well enough to have the big round of chemo. I also meet with my oncologist.
I remember doing a lot of research on all of these drugs and honestly the side effects scared me so much that I didn't want to learn any more. I hope they do what they are supposed to and don't cause too many long term side effects.
After 3 rounds, I will have another MRI and Muga Scan, which they will compare to the ones I had before I started chemo.
After 6 rounds, I will have surgery, most likely a mastectomy, possibly a double mastectomy.
Then I will have a year of Herceptin, every 3 weeks.
THEN I WILL BE DONE WITH THIS, NEVER TO HAVE TO DEAL WITH IT AGAIN!!!!!!!
Sending extra prayers and love your way, Kim! I think about you all of the time! You are wonderful and I know you can fight this! Hang in there! Love you tons!
ReplyDelete