Dose dense paclitaxel
Hi everyone I’m about to have my last of 4 dose dense AC (fortnightly) treatments soon, and it’s got me thinking about the next step which is dose dense Paclitaxel. Ive seen on the forum a lot of people have had weekly paclitaxel after AC but hoping to hear from anyone who has had dose dense (fortnightly) paclitaxel after AC, and how you found it in comparison to the AC. Thanks 😊 Claire.
Doxorubicin for 3 rounds and 12 weekly Paclitaxol
Hi All, I was diagnosed with ER + BC in Dec 2020, Grade 3 stage 2b, as it reached two lymph nodes. I had a pet scan after surgery biopsy results from lumpectomy, and there was no distant metastasis anywhere. I have just completed my third round of doxorubicin and Cyclophosphamide with one more too go. Hair has started well and truly coming out. I have 12 weeks of paclitaxol after this. I have heard that hair does come back during paclitaxol. If anyone can please let me know of your experience I would be very great full xx
Has anyone had Vertigo on Paclitaxel
I've been experiencing vertigo, towards the end of my Paclitaxel, and are still experiencing 7 weeks later. It's not severe, but usually occurs in bed turning my head side to side. My Oncologist doesn't think it relates to my Chemo. Maybe it's just a coincidence. Has anyone else experienced this?
First cycle of Paclitaxel dose dense
@Locksley So starting my premedication last night with 5 Dexamethasone & 1 Famotidine and then the same dose this morning plus 1 Loratadine 60min before treatment starts, totally dosed up ready, I had an appointment with my oncologist first to talk about possible side effects and how I'm going so far. Then had my Paclitaxel without any allergic reactions at all such a relief it did take a lot longer than getting AC 3.5 hours compared to 2 hours but that's ok as its one of my few outings. So I'm hoping it's a sign of how my next 3 cycles will go. Hope everyone's going good in their treatments. xo
Paclitaxel
Hi all, my next lot of treatments are Paclitaxel when I am well enough to start, and would like to know from anybody that has gone through this one or going through, helpful hints on side effects, recommendations on how to handle myself through these treatments as I am rather concerned , as my body was only able to handle 3 rounds of ac. thanks for any information that you can give Hugs xx
Paclitaxel & Hot spotty hands, spots on arms and rashy ankles and spots on legs, rash on both knees
Hi Sisters, I looking for advice or tips that may have worked for you. I'm on weekly Paclitaxel and have hot spotty hands since week 2 (have completed 7 of the 12 Paclitaxel), which looks like sunburn. I bought cotton gloves to wear for protection at Priceline. My big toe nails have lifted but not fallen off completely and are manky looking and funky smelling (have tried condy's crystals for toes on my GPs recommendation and what a disaster with stained feet and nails, I've swapped to soaking/washing in a dilution of Dettol and Espsom salts). My feet, ankles and legs have now developed spots and a rashy look. Oncologist didn't say much but recommended cortisone cream for spots and anti fungal treatment for toes (I haven't tried that yet, but intend too). I started chemo in July and I've completed 11 out of 16 rounds - every three weeks I also have Carboplatin with Paclitaxel, which seems to give me more side affects. I have lost 99% of eyebrows and lashes and of course I'm bald. thank you, Bron
