Implant Reconstruction After Radiation
Hi, this is my first post. I had a lumpectomy with radiation 10 years ago at 44, and I've recently undergone my 2nd lumpectomy on the same side due to the return of this hormone ER and PR+ BC. Due to having my lifetime exposure of RADS on my left breast 10 years ago, my option is mastectomy. I'm battling with my options (of which I'm blessed to have) and tossing between a double mastectomy with reconstruction using first tissue expanders and later implants, or going flat on my left side. My right breast is healthy. I only have enough fat for one very small breast, about half the size of my healthy breast. My main concern is having implants after radiation. The aspect of capsular contracture, skin or nipple death has thrown me for a sixer, and I would love to hear from you beautiful survivors about your stories of reconstruction after radiation. I have a wonderful breast surgeon who I have been blessed to have 2nd time around. She highly recommended the PC who has been transparent in the risks. Stories?Inquiry
Had left hand side mastectomy with sentinel lymph biopsy 3 weeks ago and results showed 4mm on the node and dcis 19mm and invasive ca 22mm found hence surgeon suggested axillary clearance which i have done a last week and still recovering. I dont get enough sleep as i kept waking up in the middle of the night. I have not book my post review as still processing all the information.Hormone Therapy
I had a double mastectomy two weeks ago and need to take letrizole. I have also been told to have a bone scan and PET scan. I have a few questions, firstly, when should I begin taking letrizole, do I wait till I heal more or start now? I am worried about the side effects while I am still recovering from the surgery. I have the same question with the two scans, (bone density & PET) should I do those now or wait till I have recovered more from the surgery? I know I should have asked my surgeon at my last visit, but I was concentrating on her explanation of the pathology results and didn't think of it. The last 5 weeks since my diagnosis has been a rollercoaster of emotions and I still shake my head that I am where I am! I know that I tend to worry about the 'what ifs?' too much, and probably delaying all the inevitable instead of just getting on with it. Thank you for your advice.
To take Tamoxifen or not to take it.
Hi, Im awaiting my oncology appointment which will clarify if I need to take tamoxifen for my situation : Grade 1 tumours, bilateral masectomy recently done, less than 7mm tumours each in size (multifocal) no lymph. Hormone receptive cancer. Does anyone have a similar profile above and been told they won’t need tamoxifen? I am dreading taking this drug. If I have grade one tumours and a bilateral mastectomy my chances are already so low of recurrence…🤞
Telling my toddler and child I have breast cancer
Hi All, Last month I was diagnosed with IDC and 2 weeks ago I had a single mastectomy. I have a 3 and 5 yr old who I am struggling on how to discuss this with them. So far for all the surgeries and appointments we have told them 'Mummy has a sore booby' which has been enough for them. However I am likely to need chemotherapy and I with the likelyhood of hair loss I will need tell them more about what is going on. I have done reading online into how to do this however it seems to all be directed at older age groups. My children I dont think would understand cancer or even cells. We tell them to brush their teeth so they doing get bugs eating their teeth so I am worried to say I have a bug in my booby to them and scare them of bugs! Any advice or suggestions would be greatly appreciated. I was wondering if anyone had found a good little video or book to help them understand what cancer is?
Expander to implant surgery
Hi, I’m looking for feedback on how long everyone had to wait to have their second surgery to replace the tissue expander with an implant. I’m being told that I’m now on a waitlist for ‘elective surgery’ that could take 12 months. Is this normal? I feel like I’m living in limbo and can’t even begin to recover or move forward until the second surgery takes place. I’m in NSW. This is my second breast cancer after my lumpectomy and radiation in 2018. Both times DCIS
A-cup surgery options
I have very small breasts and I do a lot of running. My surgeon says she can easily do a silicon implant reconstruction for my unilateral mastectomy, but she didn’t have a sample of an implant that was small enough to match my size in her collection of samples or in recent patient images. I’m concerned that the end result will be annoying when I’m running and whether an aesthetic flat closure would be a simpler option for someone with such small breasts to start with. Can anyone relate and what did you decide?
Mental health and new diagnosis.
Hi all, been struggling really bad finding out i have cancer in my right breast early diagnosis. I dont know what sort as i cant cope with the details of it all. I have seen the doctors and waiting MRI appointment and surgery date. I am really struggling with the anxiety and the moving forward bit. I suffer with anxiety and depression quite badly. I was given the option of just having the two lumps removed or the whole breast. I cant decide which option will help me move forward better. So firstly is there any mental health accept to this organisation? I only have my hubby to rely on who is also classed as my career. I am unsure which option to go with as my mental health plays a big part in my descion. I need to make a descion that i can be happy with and wont make my anxiety worse. Unsure of who to talk to or where to go for help.
