Newly diagnosed with DCIS - starting the rollecoaster
Hi all, I live in Geelong. I'm 41. Single mum to a 13yo son, co-parent 50%. I was diagnosed with DCIS estrogen+ on the 14th Feb. Luckily is stage 0, which eases my worries a bit. My mum and sister had stage 2, and they are in remission. So this gives me hope and keeps me positive. I am not scared of the surgery or radiotherapy...but just have lots of doubts of how is the process going to affect my ability to concentrate on my phd and thesis writing and my ability to work (part time teacher, looking for change in career). I'm considering taking an intermission from my phd, but I don't know for how long, and how I am going to support myself financially. Did anyone kept working or studying through the treatment? I'm a planner....but this doesn't have a timeline...and I think I just have to take a day at the time. I don't have a date for surgery and radiotherapy yet...I don't know how long is going to go for and how I am going to feel.....My guess is just go with the flow.....
How long should you keep working.
Hi everyone, I was diagnosed with Mets in December 2018 and am having pleasing results to date, however I’ve been told that Ribociclib is only effective for a year, I’m hoping my Oncologist is wrong. I am working full time in a senior management position and feeling the effects of fatigue from the treatment. My work is my life and a distraction from the reality of this shit disease. I’m 57 and financially could consider dropping my hours and stepping down from my role. My fear is am I giving into this shit disease or is it time to start easing up and smelling the roses. The unknown of how much time I have and the quality of time is weighing me down and causing anxiety. I’m so tired of the uncertainty and inability to concentrate and even make decisions because of this shit disease... it’s hard work and it’s been a f... hard day 😩. Is there any hope out there, if so send it my way xxx
time gap from surgery to starting of Radiation therapy
Hello everyone, I have a super quick question, from the time that you had your surgery, how long was it till you started your radiation therapy? and if the dates didn't a line with your life and needs, and how long was it before you could start, like 2 months etc before your treatment started, I'm asking as I'm looking for advice, as I'm struggling with so many things, thanks
Working - radiation and hormone treatment
Hi everyone - I feel a bit slack complaining that I am about to start radiation and I don't know how I will manage to continue to work when I hear of people working and having chemo. I feel overwhelmed by the thought of managing. How have other people managed? I am run down after surgery, working and day to day living. I am a widow and I am alone in this. Thank you for listening
Did you miss the Webcast: Managing long-term side effects of breast cancer treatment?
Hi all, If you missed the webcast on Tuesday night, you can now watch on-demand via the following link https://kapara.rdbk.com.au/landers/73f44c.html The webcast was well received and a topic that is relevant to many people navigating the side effects of breast. This webcast addressed common long-term side effects of breast cancer treatment and how you can manage them, explain why ongoing support and follow-up care is important, explore the role of survivorship care plans and why you might need one, and let you know about support and resources available to you. Registrations exceeded 3,000 and more than 1,000 people watched the webcast live. We welcome feedback from those who have already watched the session.
