HR+ HER2-

Has anyone tried DHEA or testosterone for vaginal dryness with ER+ cancer?

I have er+ her2- with a micromet and I want to know if anyone has had any experience with dhea vaginal inserts to help with dryness or testosterone for vaginal dryness. I’ve been reading more about vaginal estrogen and I’m a little confused about it

What radiation options did you choose after lumpectomy for stage 0 breast cancer?

I recently had a lumpectomy for stage 0 breast cancer and am now looking at radiation options. My doctor explained three choices: whole breast radiation (which treats the entire breast), accelerated partial breast irradiation or APBI (which focuses on just the area where cancer was removed), or potentially skipping radiation entirely since I'm over 50 with a small, low-grade tumor and clear margins. I'm trying to understand what each option might mean for my daily life and recovery. If you've been in a similar situation with stage 0 breast cancer after lumpectomy, I'd really appreciate hearing about your experience. • What type of radiation did you choose and how did it fit into your routine? • What factors helped you make your decision between the different radiation options?

I had a lumpectomy 2 and a half months ago and had 5 radiation treatments and started taking Anastrozole yesterday. Two weeks ago I started spotting after 10 years of menopause so my Oncologist had me get a transvaginal ultrasound and it showed I had 5.3 mm endometrial thickness and it's suppose to be 4 or lower. In two weeks I have outpatient surgery having a hysteroscopy/D&C/ Biopsy I also had a 2.3 cm fibroid that's on top of my uterus. I sure hope I didn't go from Breast Cancer to Endometrial Cancer within 3 months. My gynecologist was glad for me to start taking Anastrozole as it may shrink the fibroid. I'm really taking the Anastrozole for breast cancer. Has anyone had new Cancers pop up while treating the first one?

Should I try Enhertu or clinical trial for bone mets after Truqap?

Oncotype score in 2013 was 7. In 2022, new tumor on top of breast implant. Metastasis to bone. 1st line, Ibrance plus fulvestrant. In 2025, cancer mutated toPIK3ca. Changed to truqap plus fulvestrant in Feb 25. Was NED in August 25. Just had petscan Feb26. Cancer back in illead bone in right and back upper pelvis. Considering Enhurtu or a clinical trial at Ohio State. Only God can led my decisions

Should I push for Signatera test despite oncologist's concerns about stage 1 cancer?

I am almost 1.5 years past my stage 1, IDC diagnosis, initial DMX surgery, and chemotherapy treatments. My final reconstruction surgery was June 2025. I have a follow up appointment with my oncologist this week. At previous appointments , asking her about follow up scans and testing, her opinion has been she didn’t recommend them due to, my stage 1 diagnosis, and the percentage of false positives. However, the more I read about the Signatera test, the stronger I feel about wanting this test. I know she will give me pushback. Medicare will pay only if you were diagnosed at stage two or higher. . I am looking into the out-of-pocket cost/cash price for this test. Has anyone had experience with their oncologist being firm with not recommending this test and the reasons why? Did you go ahead with it and are you satisfied with your decision…. any false positive results? I want it for my peace of mind… it’s my body ….. reading it can catch molecular cancer cells 8 to 10 months prior than normal detection. I appreciate any input… thank you in advance.

What is radiation therapy like after lumpectomy for breast cancer?

I had a lumpectomy and my doctor says radiation therapy is the next step in my treatment plan. They explained that it uses high-energy beams to target any remaining cancer cells in my breast area and help reduce the chance of cancer returning in that location. I'm trying to learn more about what this experience might be like from people who have been through it. If you've had radiation therapy after breast-conserving surgery, I'd really appreciate hearing about your journey. • What was your daily routine like during radiation treatments? • What helped you prepare for or manage the treatment period? Thanks for sharing your experiences - it means a lot to connect with others who understand this path.

Has anyone else had mixed mucinous breast carcinoma?

I’m 78. I had invasive mixed mucinous carcinoma with DCIS. - ER positive, 95.0% - PR positive, 98.8% - Her-2 negative, 0 - Ki-67: 10.10% 👉Has anyone else here had Mixed Mucinous carcinoma? I Had double mastectomy July 1, 2024. No radiation no chemo…was on Letrozole nine months. pain was so bad she put me on Anastrozole for six months. had anxiety attacks, depression, extreme mood, emotional changes. Took a break for one month started tamoxifen February 1, 2026. Mucinous carcinoma is rare. It’s hard to find anyone that has had it with their breast cancer. Thanks.

Anyone else get a seroma after sentinel lymph node biopsy surgery?

Anyone develop a seroma at sentinel lymph node biopsy site? Took two nodes during surgery almost 3 weeks ago and last week I got a seroma just under the incision site. The incision is healed and my surgeon aspirated 18 cc of fluid on Tuesday but it’s still painful and some fluid has returned. Seroma is very tender and surrounding area still has nerve related pain: burning, chaffing etc. I’ve got an ace compression bandage around the area as advised. Doesn’t seem to be improving. I see surgeon again this coming Tuesday.

What are some natural remedies for joint pain without prescription meds?

Any recommendations for joint pain, I don’t want to take any thing prescribed.

How can I reduce the cost of Kisqali after breast cancer treatment?

I'm 67 years young. I started anastrazole this week after a lumpectomy (stage 2a) with 1 of 3 lymph nodes positive. I finished 33 radiation treatments 2 weeks ago. The Oncotype biologic tumor recurrence score is 11, 2% Distant Recurrence with AI, <1% Benefit of Chemotherapy. After researching Kisqali as directed by my oncologist, my cost after Medicare if approved is $4700/month for. 3 years is prohibitive. If anyone knows of a way to bring the cost down from $56k per year, please share.