-
What do you wish you had known when you (or your loved one) were first diagnosed?
Share words of wisdom, unique tips, self-care, and coping advice for our newbies here! It will make a difference for all those joining us this year. Thank you!
-
How well do you feel your family understands your diagnosis?
Please take our poll and share your experiences below on navigating a breast cancer diagnosis at any stage with your family!
-
Share your stories of online support friends here: From the forums or zoom meetups
Hi All, We'd love to hear about the supportive relationships that have formed at Breastcancer.org. Thank you All for sharing! 💜 Your Mods
-
MBC Caregiving Partners Virtual Zoom Meetups every other Tues at 4pm, ET
Hi All, Reminding you that we offer a free caregivers meetup for partners of someone with MBC every other Tuesday. If you are a caregiver, or have a partner who you think could benefit, please share. We meet every other Tuesday at 4pm, ET. People need to register here to participate:…
-
How to fill out your Profile to let others know more about you!
Our community is built on connections and shared experiences. So, we’re excited to announce we’ve made it easier for you to learn much more about each other with our NEW Member Profile! Filling out your profile benefits you and others by allowing registered members to compare your information with theirs and create a…
-
In Treatment? Join us on Zoom, Tues & Thurs weekly!
Hi Everyone, We have created a weekly virtual support group for all who are planning or going through active treatment. If you've just been diagnosed and are planning surgery, chemo, or radiation, join our weekly Zoom Meetups. We have two meetings for you to register for: Register here: Tuesdays at 1:00 PM…
-
Anyone experienced numbness and tingling on one side of your body?
My bc diagnosis was in 2021 and I had a lumpectomy and lymph node biopsy 12/21, followed by radiation 3/22. I was 71 at the time. My diagnosis was pure mucinous, clear margins, no lymph node spread, grade 2, stage 1.About a month ago I experienced complete numbness of my right leg and foot from the groin down. It lasted…
-
My Husband, My Life, My Love, My Family, My Cancer
As I go through this forced path I have been thrown down, I have come to realize the love I have always had for my husband was strong. He is amazing and I love him with my very soul and entire heart. Never would I ever imagine the thought of dying and him being alone. Then the worst part hit me!! I can't seem to shake the…
-
Implant reconstruction after radiation
I have a recurrence of DCIS in my right breast. In 2017 I had a lumpectomy and radiation. I now need to have a mastectomy and I’m hoping to have an implant reconstruction, rather than the DIEP flap. Most of the conversations I’ve found on the success of an implant reconstruction years after having radiation are pretty old.…
-
FAST Foward radiation treatment schedule option
Hi, this is my first post. I’m also not sure if my dx signature/details automatically attaches to my post. But I’ll add those details if I need to. I’m in Canada. The radiation oncologist gave me the option of the Fast Forward dosing schedule of treatment. It’s not first in line protocol here yet because it hasn’t been…
-
Primary endocrine resistance
hello. I was dx with stage IV de novo in July 2023. ER/PR+, Her2 - small Mets to pelvis Treatment was Letrozole with Ribociclib. First scan after 4 months showed reduction. Second scan 3 months later showed bone mets reduced but small spots on liver. Told I was primary endocrine resistant. Moved on to capacetabine. On…
-
Lets Post our Daily Exercise
I'm doing the Firm Cardio Step mix and will walk the dog for a mile later today. Lorrie
-
So...whats for dinner?
I thought it might be fun to start a thread on what we are having, making or had for dinner. Sometimes it is the best tuna steak you ever had, sometimes it's a can of soup. But we all do it every night in some form or another. Maybe we can give each other ideas on what to make, or bitch about what we had, or the fact that…
-
Can we have a forum for "older" people with bc?
I am an "older" woman with breast cancer (I was diagnosed at 65 and am now 66). I notice that most of the posts seem to be from people younger than I am (often by quite a bit...). I'd love to "talk" with others my age, exchange info about their diagnoses, effects on their lives, etc. I see that there is a forum for young…
-
4 Letter Word Game
Hi Ladies, It is time to add a four letter word game. I received an email of a forwarded scrabble game. The game started with a four letter word and kept changing by one letter. I like playing here much better. Get your 4 letter words ready. First word: Word
-
De Novo Stage IV
I'm wondering if there is a topic just for de novo Stage IV. I'd like to know how people found out. Did you have symptoms that led you to the doctor for an answer? Was it found out of the blue when you had another issue and how was it found? Are there others like me who have never shown it in your breast but only where it…
-
March/April 2024 Surgery Support Thread
Please gather here to get and give support. Feel free to share your type of surgery, date, and let us know how you're preparing and how you're doing post-surgery. We're all here for you!
-
10 years after BC diagnosis, I have mets in lung which are BC
Hi All My oncologist called this morning to confirm that the node in my lung is indeed breast cancer, it took them a few days to figure out but they knew it wasn't lung cancer. I'm so shocked. I had stage I, HER2+ breast cancer diagnosed 10 years ago and had a lumpectomy, lymph node removal (which was clear for cancer),…
-
Kisqali/ribociclib, Faslodex/fluvestrant & Xgeva combo - Anyone?
I've been on this combo since Nov 2019. Since all treatment combos seem to offer their own side effects and challenges, I'd like to hear from others taking these drugs. Especially your experiences, duration of success and how you deal with the fatigue, itchiness, etc that goes along with this treatment.
-
STEAM ROOM FOR ANGER
This thread is meant to be for RANTS and RANTING. Then Rant again. We need a place to simply get rid of the anger. Write it here. Unleash it all. Get it out. This isn't meant for the Stupid comments(great thread). This is for the gut wrenching, tell them off anger. IMPORTANT: When done ranting don't necessarily stick…
-
Pain Before Diagnosis
Hi everyone. I’m hoping you guys can give me some information or ideas. I have seen my ob and I have a diagnostic mammogram and ultrasound scheduled in 4 days. I’m wondering about the pain. It is my biggest symptom. The pain started out like I was cold. It wasn’t very painful, but my nipple hurt like I stepped into very…
-
Ribociclib/Kisqali with Letrozole - Any one on this combo?
I am starting this new forum for all those who are on this newly approved drug combo. I started on Kisqali/Letrozole combo 6 weeks ago and so far it has been tolerable. Letrozole gives me joint pain and low back pain. My oncologist has asked me to take this on alternate days. Would love to hear from others about their…
-
how about drinking?
Where did our thread go? Is anyone out there from our drinking group? Did I miss something - like we became too offesive or ...well, drunk? I would love to hear from you gals! Janie
-
Zometa side effects
I will be having my first infusion of Zometa this week. Has anyone had any side effects from Zometa? I hope to be able to travel a few days after and to go to work the next day and wonder if this is a reasonable plan.
-
How long have you been Stage IV?
We have a thread of what age you were diagnosed at Stage IV, so how about "How long have you lived with Stage IV". Also please state if you were Stage IV from the get go. I'm asking for this information in hoping to have MANY more years than the 2-3 I was given and to give hope to those newly diagnosed with Stage IV. 1…
-
Starting Chemo April 2024 Support Thread
Gather here to support one another, ask questions, and share experiences. We're all here for you. What is the type of chemo and regimen you'll be doing? When do you start? Share your thoughts and get support!
-
Pathology Report- how long?
May I ask how long typically does it take before you receive your pathology report from surgery? I am through week one starting week two. I’m anxious because those results are what will give me more info as to my treatment plan and what to expect going forward. I know waiting is THE WORST.
-
Calling all triple negative breast cancer patients in the UK
With so many forums and threads on this site to go through for information, I thought it would be a good idea for all of us in the UK to form a forum specifically for us, and to give our details and experiences in a compact manner. Anyone else in the world is welcome to join in. I was diagnosed with a very large tumour,…
-
Illinois ladies facing bc
I'm very curious about all the Illinois ladies who are making this breast cancer journey or who have finished it. Where are you located? What's your diagnosis? Where are you in your treatment plan? How's it going for you? I thought we might be surprised to find somebody right in our own back yard that could use some…
-
Comfort dogs
Okay, I am just throwing this out there: does anyone else feel closer to their dog than to humans through this roller coaster journey? I have a wonderful life and great support, but my little blind shelter dog Lewie (a white poodle mix) has been constantly by my side- whether I am sleeping on the couch after chemo or in…
-
Gemcitabine / Carboplatin
Anyone have any experience or tips on this combo. I’m starting this combo on the 19th Nov since Ibrance/Falsodex and Xeloda failed after 11 months in. Thank you in advance for any tips or suggestions. I got my port placed Wednesday. Thanks so much, Karen
-
Breaking Research News from sources other than Breastcancer.org
I watch for research news on breast cancer, treatments, etc., and frequently see interesting articles. There is a topic on BCO called "Breaking Research News from Breastcancer.org." One of the moderators suggested that another topic might be appropriate for posting links and synopses of reports on research found elsewhere.…
-
Bone Mets Thread
I've started this thread after suggestions that it would be useful. Mod Note: We have removed the original link as it is no longer viable. At one of our member's' recommendation we are offering this link as a resource for you. https://youtu.be/YpFfLrITfEI
-
mets to lung
hello. i got scan rusults yesterday. looks like abraxane is not working, since cancer is spreading. i am going on navelbine now. any words of encouragement? thanks. i am new to the boards, happy to find you all barb
-
Did your doctor talk about your Ki67 %
Hello - I have IDC Stage 2 (++-), and I am one week out from my bilateral mastectomy. My lymph Node pathology reports were posted online, and from what I can read, there is no cancer in my lymph nodes. However, my Ki67% - was reported at 43%. so I have a Ki67: 43%. Is that bad? Did your doctor put much stock into your Ki67…
-
HIgh ALP and very concerned. Please help
I posted a few weeks ago that my ALP levels were rising and had been since starting letrozole and officially entering menopause. I just took another blood test and the high normal for them was 121. I am now at 129. So now I'm officially high instead of at the high end of normal. I don't want a bone scan but something is…