Cold cap size
I'm under going 4 rounds of AC and have used the cold cap medium size First round didn't lose any hair and had a hair cut in between rounds and lost allot of hair from my crown in the second round. I'm wanted some advise on whether I should go to the small size as does the firmness of the fit impact success?
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:
Scalp cooling - tips on cap size and forehead pressure?
Hi all, I'm about to start my first of 12 x weekly paclitaxel treatments on Monday (combined with trastuzumab infusions every three weeks). I am keen to try scalp cooling to try to reduce hair loss and had gotten my mind around the cold factor (I think!). However, I had my chemo education session yesterday and got to try on a cap. I discovered that the cap alone for just a few minutes was very uncomfortable/slightly painful on my forehead and am now not sure how I'll go with this for several hours! The nurse did get me to then try the next cap size up, but this didn't seem to be as good a fit and had a gap at the back of my head - hence may not be effective. I also didn't have a headband on when I tried the first cap - so possibly this might also help a little. Just wondering if this tightness/pressure/forehead pain is normal or if anyone else has experience and tips on dealing with this? I noticed from other posts about scalp cooling that these seem to suggest the hardest period is the first 15-20 mins and then your head acclimatises/becomes numb. Just wondering if this also applies to the feeling of tightness of the cap? Or if there are any other tips on reducing pain/pressure on your forehead during the cooling process? I figure I'll give it a go anyway on Monday as I can always stop the scalp cooling if it is too much for me, but any advice would be very welcome!
Ice Caps to prevent hair loss
Are you worried about losing your hair during chemo treatments? For me keeping my hair was very important. I am a private person and the thought of people seeing me hairless felt very intimidating and public. I wanted to choose who I would like to tell I had breast cancer and not just be on display everywhere I went for everyone and anyone to diagnose. I decided to give ice caps a try and it was absolutely successful. Keeping my hair gave me a sense of control over the chemotherapy and its nasty side effects. For me it became an uplifting and very positive experience, giving me something satisfying to focus on, instead of on the cancer.
Cold Capping and hair loss experience with TC chemo
I went for my first TC chemo session with cold capping on a Paxman. I've got wavy coarse hair, that's not particularly thick. Conditioner and water was applied with a focus on the top of the head. I was expecting a brain freeze but came nowhere near that in the 2.5 hours of the cold capping. I'm a skier so I'm comparing it to having damp hair on the snowfieds. The nurse said only about 20% of his patients keep their hair. I'm now paranoid it was ineffective and am sitting at home with a bag of ice in a large ziplock affixed to my head, which feels colder than the cap. Has anyone had a similar experience with cold cap not being as cold as you expected, but still had reasonable hair retention after that session?
Caps with 'fake hair' to wear , during/post chemo
On Xmas Day, I was at a restaurant for lunch with friends & one person was wearing the 'middle' cap below - and it looked really cool!! They are available on ebay & Temu etc I am sure there are more 'styles' too. Here's a couple more - would you consider wearing one? take care
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?
Tender scalp 5 months post chemo
Hi all, did anyone experience a tender scalp post chemo. I noticed it happens if I brush my hair back perhaps. Is it perhaps a sign of growth. My hair is still very short , back and sides are longer than the top and very curly. My natural is curly but it's curlier now which iama very common I understand. Wondering if there is a reason why it feels tender at times and what best to do, to handle it? Thank you.Chemo almost done...next is surgery. Hair growth questions.
Hi all, it's been a little while, hope you all doing well and this year brings you all good health and happiness. I am almost done with my chemo (AC and 12 weeks paclitaxel, 4 perjeta and another one (not sure of name), 2 more infusions of paclitaxel. Did anyone find bits of fluffy hair starting to grow already? I don't want to get too excited but am starting to notice some growth. Anxious and excited about my appointment tomorrow with the surgeon to discuss surgery options and how the tumors have responded to the chemo. Any advice would be appreciated. Still awaiting genetic testing results. Now the fun part. We have a family wedding in October this year and some other events and I am very excited for my hair to start growing. Any tips or advice. Scalp treatment or oils etc vitamins. Should I have a shave after chemo so the hair grows evenly and also what kind of length can I expect in 6 months or so. How did you hair grow? Lastly. If anyone is based in Sydney and would want to meet for a chat, support, pray , let me know. Would love to meet some ladies, we can encourage each other. Can direct message me if you like. Thanks and look forward to hearing your progress xxx
