Radiotherapy (5 weeks)
If you haven't been through it yet and are worried, please don't. It sounds much worse than it is. The receptionists, nurses and radiographers are really lovely. It doesn't hurt. It doesn't take long. I was in and out within an hour or less. My boob was a bit itchy throughout the treatment and became redder as the treatment progressed. But it wasn't sore. I felt tired for about 30 minutes after the treatment. The first week after finishing radiotherapy, you could clearly see the area and a clear line where the radio was targeted, it was a bit bumpy but not blisters. From the beginning I put sorbelene on twice a day until my friend told me about Tallow cream, I alternated them at first but after a while just used tallow because I found the sorbelene made me more itchy. Second week after finishing; there where a few changes to my skin. It was the same as the after ejects of sun burn without feeling the burn. My skin turned a darker brown, then peeled back to a nice tan colour. I've had quite a few headaches since finishing radiotherapy but I get migraines anyway so it could just be normal for me. I wish you all the best throughout your journey with breast cancer. I hope I have helped to take some worry out of the whole experience. Think happy thoughts, love Becky
Menopause - It's more than a hot flush! Recording available now
The recording of Menopause - It's more than a hot flush! webcast is now available here. We hope you find it both informative and enjoyable. Please feel free to share feedback, questions or thoughts below in the discussion. ---------------------------------------------------------------------------------------------------------------------------------------------------------- Ask the Expert: Menopause – It’s more than a hot flush! on Wednesday 6 December 2023. Many people experience changes to their sexual wellbeing associated with breast cancer treatment that can be caused by menopause or menopause-like symptoms. These can include vaginal dryness or discomfort, loss of libido (sex drive), changes to self-esteem and fatigue. Topics like these can often be difficult to discuss with your partner or health professional and it can be reassuring to know you are not alone. During this webcast, you will hear from Dr Tonia Mezzini, Sexual Health Physician based in Adelaide. Dr Mezzini is a leader in this area, with her level of expertise, she provides best practice and compassionate medical care. She presents in an open, informative and engaging way about sexual health and wellbeing. The webcast will be facilitated by BCNA Consumer Representative, Naveena Nekkalapudi. Following her diagnosis of triple negative breast cancer and the subsequent treatment, Naveena decided to re-evaluate her life and focus on matters that are important to her. She describes it as changing from being career ambitious to being life ambitious. Naveena is a consumer representative of BCNA, Cancer Council Victoria, Breast Cancer Trials, VCCC, and Walter and Eliza Hall Institute of Medical Research to name a few. This webcast will help to provide you with strategies to manage menopausal symptoms and discuss the support available to assist you with your sexual and emotional wellbeing.
Letrozole - Year 2
I'm six weeks into my second year of Letrozole. The good news is my hands have remained better since I took a one month break after six months. They still hurt, both bone and joint pain, especially with the cold weather, but they've never returned to the earlier level of pain. My ankles have bone ache 24/7. This pain is now spreading up my calves. It's also spreading into my wrists forearms. My elbows remain sore and the inside soft tissue very tender. I've given acupuncture a red hot go. It seemed to help my hands initially but not so much now. It gives me pain relief for my ankles while I'm there, but none when I'm gone. It's had no effect on the hot flushes. All in all I think I'm going to pull the pin on it shortly. It's expensive and I don't think the results justify the cost. So I've moved on to try osteopathy. Many of you here have raved about it, and I've joined your ranks! It just makes my body feel better. The effect lasts for a few days, it's cheaper than acupuncture, and I get some money back from the health insurance. I've accepted that the five to ten years on Letrozole are going to be painful. There's no getting away from it, so now it's about doing what I can to help me cope. For example, the best thing about acupuncture is the heat lamp. It really soothes my ankles, so I'm going to save up and get myself one. The mental health aspect remains challenging. I discussed it with my oncologist. Cancer or menopause or Letrozole or a combination of some or all? So she has asked me to take a two month break, keeping a side effects diary for two months before, and during the break. That way we'll know what is the Letrozole and therefore if we can tweak the AI in some way. I'm going to do that in the summer so I can really enjoy the break. My oncologist was very sympathetic. She said it's often difficult managing the estrogen drop in women like me, who haven't gone through menopause before BC and then go onto an AI. She had some interesting thoughts about estrogen sensitivity. That in her experience the women who develop ER+ BC are very estrogen sensitive and therefore have a hard time on AIs. She said AIs had been tested on women with ER- BC and they don't suffer the side effects anywhere near as much to zero. She said I'm in the 10% risk range so there's no doubt about it, I have to be on it. I'd very much like not to be the woman who cries on the phone when she's talking to her dietician (who she's met face to face six times) and finds out that said dietician is leaving forever to live in London (a romance)... However it seems as if that's who I am now. Hopefully a 'side effect' that stops when I stop taking the little brown pills. Ridiculous! Oh and my oncologist also confirmed that the joint pain is arthralgia, and won't turn into arthritis when I've finished taking Letrozole. This was one of the questions that I put to the webinar doctors that wasn't answered. There was more but I of course can't remember. My right toe joint is very very sore tonight me so I'm going to take a pain killer and go to bed and try to sleep. BS tomorrow for my next check up. Nothing to worry about but I can't help but feel a bit nervous. I think the worst bit is the flashbacks to diagnosis and all the bad news I received in that office. Nothing for it though, has to be done.
Hot flashes and itchy skin!
Hello everyone, I finished my AC a few weeks ago, and will start Taxol this week for 12 weeks. The AC has plunged me into menopause (I was nearly there already). I just cannot regulate my body temperature - I am mostly hot all the time, but sometimes fluctuate between roasting and freezing, and my skin and eyebrows (the only hair I have left) are super itchy! I suspect this is all hormone related. This has been going for weeks. Has anyone else experienced the same, and does it start to settle after awhile? Any helpful tips? :smile:
Menopausal Symptoms
Well I'm coming to the end of my chemotherapy treatment- wasn't as bad as I had anticipated. First I had four rounds of AC followed by 12 weekly doses of TCH (I'm double negative, HER2 positive) and there has been a massive reduction in the tumour and my lymph nodes look pretty clear now too! Yay! I'll be on the Herceptin for a year though. I just wanted to ask a question regarding menopausal symptoms for anyone who's been through them: I am getting hot flashes constantly, like every 1/2 hour to hour. My head gets covered in sweat, I throw everything off, and then a few minutes later I'm cold again and put everything back on. Driving my family crazy turning the a/c on and off all the time lol!! But- here's the weird thing, I've been getting period type cramps, like ovary and uterus pain, and I want to know, is this part of menopause or are my periods getting ready to come back? They've been gone for a few months now but the cramps are intensifying. Also my hair is growing back, it started coming back when I switched from AC to Pacilotaxen. And my surgery is going ahead but they're not doing much in the way of reconstructions because that's not considered "essential" :9 I had been hoping for a double breast reduction and now they're saying they can only do the one breast. And if I have to have a full mastectomy there's no reconstructions on the cards! Anyway thanks if you're reading this, love to all during this scary time! Kylie
Tamoxifen and Periods
Hi just wondering if it is normal for periods to return? I AM 46 I had chemo last April and my periods stopped, I started tamoxifen in August , 2 days ago I started bleeding I assume it is my period returning after 9 months even though I was told the chemo would put me into menopause, I was getting hot flashes etc too..just seeing if anyone had a simular experience, am I normal?
