Bone and join pain side effects of chemotherapy
Hi, I’m new to this group and have only just started chemotherapy. I’m experiencing strong bone and joint pain from the chemo and wondering if anyone could suggest ways to minimise this. I’m taking Panadol but it doesn’t cut through. Im also doing the scalp cooling treatment. I’ve been advised to wash my hair only once a week. Does anyone have any suggestions on how to keep it looking fresh? It looks very greasy and bedraggled.
Neuropathy in feet - any advice? TNBC
Hi everyone I've TNBC and am 6 treatments down with the first Carbo/Taxel/immunotherapy regime. For part of my infusions, they put cold gloves on my hands to reduce the risk of neuropathy there, but didn't offer anything for the feet. They suggested I go online and purchase my own cold socks to wear during treatment. Last week my toes started feeling numb and then yesterday my heels started feeling sore when I walked. I walked a bit at the shops this morning and my feet felt odd the whole time. I'm assuming this is all related to neuropathy and I must admit I'm a little freaked out. I've purchased some cold socks now online and will start wearing them during treatment, but I'm worried what damage has been done already. Be interested to hear what experiences others have had with this, what they've done about it and whether it has resolved after treatment finishes. (NB I'm putting this in the general discussion arena as I thought it may not be simply TNBC related?) Kathy
Starting chemo this week: Doxorubicin, Cyclophosphamide and Pegfilgrastim then Paclitaxel
Hello everyone, this week I start chemo. As I understand it, 4 cycles of Doxorubicin, Cyclophosphamide and Pegfilgrastim then 12 cycles of Paclitaxel. I am looking for any advice and tips on how to get through it. We all know that experience and side effects are all different and individual but it would help to know how others have coped. I haven't had my introduction session with the oncology nurse yet and the fact sheet is a bit scary. I am in Melbourne and will be treated at St Vincent's private in East Melbourne as that is where my medical oncologist works. For the time being I am remaining a private patient as insurance covers it. I am choosing to try the 'cold cap' to see if it will help with not losing hair but as I have fine hair and already experiencing age related hair loss, it may not work. I know it will add about 2 hours to treatment and am willing to give it a go. My plan is to take audiobooks and colouring books with me to pass the time during treatment. I'm aiming to keep busy but not taxing myself too much. At this stage I do not plan to work on treatment days but do plan to work from home other days. A friend has suggested a probiotic as a precaution as a relation and her mother used one during their chemo and found it helpful. Has anyone else found this? With the second treatment and Paclitaxel I am concerned about the possibility of peripheral neuropathy side effects due to a previous condition. I read in another post that some ladies have tried cold gloves and socks - has that worked? I will have to look into it further but am curious and want to be prepared. Thank you all for reading and any advice and tips :heart:BYO Cold Cap?
Hi all, I have just found out that my hospital (Monash) doesn’t offer the cold cap for chemo. The breast care nurse I spoke to was very disparaging of them, saying there was no evidence they worked, which surprises me as they seem relatively common in better hospitals. She said the only option was to BYO frozen caps in an esky - has anyone here tried this? Was it successful? How do you keep the caps cold enough?
Chemo Tablets?
Hi all. I was diagnosed Triple Negative in late Nov 2023. Went straight on to Chemotherapy with lots of negative reactions, including anaphylaxis. Then had Surgery to remove lump and one lymph node which was all clear. Just finished 4 weeks of Radiation. Now my Medical Oncologist wants to put me on Capecitabine tablets for 6 months. I can't seem to get a straight answer as to why I need this as well as everything else. I was just starting to feel a bit more 'normal' and looking forward to life again. Has anyone else used these tablets that can give me an honest opinion. Thank you.
Best skin repair products for chemo and radiotherapy
A friend of mine bought me some Rich Glen Olive balm as part of a lovely Chemo care pack. My hands and nails held up so well during AC does dense and 12 rounds of taxol chemotherapy. I also used this undergoing radiotherapy to both breasts along with Moo Goo Soothing cream and my care team were amazed even with double dose of radio I had no burns no blisters and minimal redness. Links below if you want to add them to your kit... https://moogoo.com.au/collections/moisturise/products/soothing-msm-moisturiser https://richglenoliveoil.com/collections/body/products/rough-hand-balm-100gm
Hair cut before cold cap?
Hello there! I am going to start chemo soon and am going to use a cold cap. I've read your hair may still fall out so I'm wondering if I should still make a hair appointment to get it cut pretty short? Did any ladies with the cold cap get their hair cut short before starting chemo or should I just wait and see how my hair goes before taking drastic measures? And while you're at it, any tips on withstanding the cold cap? xx
Constipation
most of the threads I can find about constipation are quite old so thought I would start a new one . Having just spent a very uncomfortable Friday / night at home, followed by fun Saturday in emergency, and a Saturday night in the short stay unit with the worst constipation ever am looking for some tips advice on how others have managed this going forward Generally I am a good popper , once a day (give or take) and have a faulty good diet. But this round of chemo that went in Monday had upset my whole system So love to hear how others have coped what food to eat / not to eat , drink , drugs etc
Pacletaxil & Peripheral Neuropathy
Hello ladies, I'm wondering if anyone had peripheral neuropathy (PN) whilst having weekly pacletaxil where it became so bad you stopped early? I've completed 4 x AC fortnightly & started weekly pacletaxil on 20/12/23 planned for 12 weeks, post lumpectomy & axillary clearance for PgR & ER+ BC with 4/30 positive lymph nodes. However last Wednesday which should have been no 10 my oncologist graded my PN as a 3 & has paused tx for a week to see if it improves. My nurse coordinator discussed stopping chemo as I also developed a jugular DVT from my PICC, which I had removed. I'm now torn between finishing the last 3 chemo sessions, stopping due to the PN & the potential of some of this being permanent verses what if I don't complete the 12! Obviously I will discuss this with my oncologist & thought someone on this site may have a similar experience. Thank you for reading & happy Sunday to all the pink ladies out there 🩷
