Ask the Expert: Managing side effects of hormone blocking treatment with Dr Michelle White
Hello everyone! We will be hosting our next Ask the Expert Digital Event on Managing side effects of hormone blocking treatment with Dr Michelle White. Click here to register for the event. Approximately two thirds of all breast cancers are a type called hormone receptor positive. This means they use the hormones oestrogen and/or progesterone to grow. The recommended treatment for people with hormone receptor positive early breast cancer usually includes hormone-blocking therapy, a tablet taken daily for between five and 10 years. For people with metastatic breast cancer, hormone-blocking treatments can provide long term disease control. The side effects of these treatments may be mild and easily managed, but for some people they can significantly impact their quality of life. At this Ask the Expert event, we will hear from medical oncologist Dr Michelle White and BCNA Consumer Representative Kym Berchtenbreiter. Michelle specialises in treating women diagnosed with breast cancer and is the lead investigator for several local research studies and the development and conduct of clinical trials. Kym was diagnosed with early breast cancer in 2009 and will discuss the side effects she experienced from hormone-blocking treatment, her strategies to manage them and her advice for others. This session will address what you need to know about hormone-blocking treatment, including common side effects and how you can manage them, and how to ensure a good balance between quality of life, risk of recurrence and control of disease progression. During this event you will be able to ask Michelle and Kym questions. Please share your questions prior to the event via the question box on the registration page or email events@bcna.org.au. During the event you can submit questions via the discussion box on your screen. If you have any other questions prior to the event, please email events@bcna.org.au. For any technical difficulties on the evening, please contact Redback Studios on 1800 733 416. Event Details Date: Wednesday 29 June 2022 Time: 6.30pm - 7.45pm AEST Where: Online – from your computer, tablet or laptop Your Local Time: WA: 4.30pm NT, SA: 6.00pm QLD, ACT, NSW, TAS, VIC: 6.30pm
Anastrozole and autoimmune hepatitis
Has anyone had this? My liver was perfect until I started Anastrozole and my liver enzymes went up. Stopped it and they went down. Started Tamoxifen and they went up again so onco stopped them completely. Now after a few months, an incidental finding of really weird liver enzymes has the doctor scratching his head. He said hormone blockers can trigger autoimmune hepatitis if you are susceptible. CT is fine but bloods are weirdly out of whack.
Ribociclib and Anastrozole
Hi everyone, I started this combo in January 2019 for Mets lung diagnosed in December 2018. My oncologist told me that results are usually 12 to 18 months and then another line of treatment would need to be considered. Has anyone got any feedback on this combo. Feeling a bit apprehensive at the moment.
Do the aches and pains go away after Arimidex?
Afternoon lovelies, Wondered if anyone has come off Arimidex (anastrozole) and noticed if aches persisted or went away? I was on tamoxifen for 4 and a half years but was then switched to Arimidex because of ongoing gynae issues. I have been on arimidex for almost 8 months now and am having some fairly uncomfortable aches and stiffness, particularly in hands but also in hips and ankles. Feel like 59 going on 89!! As I had osteoporosis in my lumbar spine before starting this, the plan is I will probably come off it in March. My question is, does anyone know if aches will subside then, or am I stuck with them?? Hope everyone is going along the best they can be. Michele xx
Arimidex, radiation and neuropathy
I was diagnosed with BC nearly three years ago and have been taking arimidex for nearly 2.5 years. Over the past couple of weeks, I have been experiencing PN which is starting to get worse with a severe burning sensation after walking. Is anyone else suffering with PN and if so, have you been able to link it back to either radiation and/arimidex? Thanks in advance for your help....
