What's it like going from AC chemo to weekly Taxol treatments?

Many people find that transitioning from AC to Taxol brings different side effects and experiences, with some finding Taxol more manageable overall. Each person's response can vary, so connecting with others who've been through this same treatment sequence can provide valuable insights and support during this phase of your journey.

I had this regimen. Doxycycline/cyclophosphamide treatments were way worse than the 12 paclitaxel. All manageable.

I did 16 weeks of taxol. ice your feet in your hands every time or you will get neuropathy. Drink a lot of hydrated water at least 150 ounces a day. I made it through it. You can make it through it.

Everyone is different, but I found the AC harder. My HR and LFTs went up, my WBCs went down to 0. If I stood too long, I got dizzy. I did 12 weeks of Paclitaxel, it was better, I even went back to work during the Paclitaxel.

@Timothy-can you elaborate, please? did you use ice after or during the treatment?

I did 12 weeks of Taxol and then 4 treatments of AC over 8 weeks. The AC was way worse. I was exercising getting the Taxol and totally exhausted and knocked out by the AC. I did ice hands and feet during Taxol and would recommend for AC as well. Despite AC being worse it was manageable.

I did AC and I’m doing Abraxane instead of Taxol because I have Raynauds Syndrome. Had to fight insurance. I still somewhat ice the hands and feet as much as I can stand. The AC was rough but doable. I fasted before and that helped a ton. The one time I didn’t I regretted. I did walk a lot which helped a ton. The Abraxane is a breeze! It’s the same thing as Taxol with the preservative. Highly recommend.

Oh and be sure to suck/eat ice while getting the A push. It will help you avoid the mouth sores. Don’t bother cold capping on AC in my opinion. Just shave your head after the 2nd one because that hair is going bye bye!