Can I talk to the ladies who are doing the TAC chemotherapy
I will be starting this July 22nd. (Taxotere, Adriymycin, Cytoxan ) Yes I am terrified. Can those of you that have gone through this treatment or are going through it tell me how it went for you?
Thanks,
Nancy
Comments
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Nancy, I am starting the same on the 17th. Looks like we'll be in it together. I am ready to get started, but more than a little scared about what to expect. Good luck to you. I'll try to keep in touch! I joined a thread for starting chemo July 2014. There are several women active on that thread.
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i did TAC, 6 rounds. I was dehydrated a lot so had fluids the day of chemo and daily for 4 days. It's definitely cumulative so by round 4 my body really felt it. Chemo infusion took about 6- 8 hours. Listen to your body, rest when you can, be active when you can and eat what you can. Be kind to yourself. I always said i can do 6 and had a count down board. xo
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i did TAC, 6 rounds. I was dehydrated a lot so had fluids the day of chemo and daily for 4 days. It's definitely cumulative so by round 4 my body really felt it. Chemo infusion took about 6- 8 hours. Listen to your body, rest when you can, be active when you can and eat what you can. Be kind to yourself. I always said i can do 6 and had a count down board. xo
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I did TAC last year. 6 cycles every three weeks. I finished the last week of June 2013. In fact, I went Thursday got my hair colored and cut. I feel like I am a new woman.
I am still going through reconstruction.
Not sure what questions you would like to ask but I will be happy to help anyway I can. I did all 3 drugs at once, I only met about 3 ladies doing TAC x 6.
I know you are anxious, I was too but I did go into treatment #1 prepared.
I took a full cup of shaved ice to eat during treatment to try to ease mouth soreness. After a couple of days mouth got very sore anyways. I used lemon drops to suck on which helped but not enough, talked to MO and he suggested a mouth wash. 1 part children's bendrylll, 1 part children's Advil, 1 part Maalox and a few drops of prescription lydocaine for numbing. Hopefully you will not have this side effect, it really limited what I could eat. My tongue got very raw. But healed by the start of week 3 each treatment.
I did not use frozen peas for fingers and toes. I don't know if it would have helped but I did get minor neuropathy in my fingers and toes and still have tingling and minor numbness in toes and fingers to this day. The MO says it can still take a while to go away. I did lose both big toenails a couple of weeks after last treatment. They have both grown back in completely. Several nails lifted but I did not lose them. Keep a clear coat on your nails for strength but clear so you can see what is happening underneath.
I did have the Neulasta shot on day after treatment. First one I took a Claritin day of then for 5 days after. I had pretty severe bone pain in my thighs. The rest of the treatments I took the Claritin for 2 days before and 7 days after and had very mild pain.
As far as general health and stamina I did really well. Days 3 through 5 were my hardest but perked up beginning day 7. The more I walked the better I felt. After treatment 3 on day 8 I walked a 5k walk with my team. On day 5 following my last treatment I went out of town and attended my grandsons rehearsal dinner and wedding the following day and did remarkably well.
This my be more than you want to hear, but I wanted to know these items before I started so I could be prepared.
Not everyone will have all the SE's but some will. I don't want to scare anyone, I would do this again in a heartbeat.
Three weeks after my first treatment my tumor had shrunk by at least 40%. At time of surgery only a couple of mm were left but not active; an almost complete pathological response.
That is the most important part. Cancer free.
Good luck and feel free to ask me anything.
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Hi,
I just did my second round of TACx6 on Thursday and noticed that no one else is doing all 3 at once on my board (August 2014) wanted to know how you were doing now that you are probably done with 3.
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I actually got switched after my first treatment of TAC. I didn't handle it well and my WBC dropped to .7 even with neulasta. I am now doing AC+T (taxol) which has been easier for me. One more AC then weekly taxol. Everyone is different though ( I guess I am a wimp). I had a friend who did TAC 10 years ago and she tolerated it well.
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I did AC four times, every two weeks. Super exhausted. Diarrhea. But it ends. Have had two of 12 weekly taxol treatments. So easy compared to the others.
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I did AC four times, every two weeks. Super exhausted. Diarrhea. But it ends. Have had two of 12 weekly taxol treatments. So easy compared to the others.
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