Starting Chemo in JAN 2007
Comments
-
Mizsissy, Missed you last night. I was wondering how Mena is doing?
So glad to hear Mel is ok.
Loved our chat, really nice to have a chance to ask questions. Which brings me to ....
I found the little we discussed telling people (timing of) interesting. Anyone who wants to share that ... when and whom did you tell?
I had my biopsy the day before TG. The radiologist told me the tumor was "highly suggestive of cancer" based on what she was seeing on the mri/scan. So I knew.
I told my husband who accused me of overreacting. I shut up and didn't discuss it with him or anyone over the weekend. Had a houseful for TG.
The Sunday after TG a dear cousin died unexpectedly. The funeral was that Tues after TG. I had a business trip and knew I would get the results while out of town, so went on the trip, and dh went to the funeral. Sure enough I was alone in a hotel room when the call came. Couldn't call Steve b/c he was at the funeral. He called that night, asked and I told him.
I came home the next night. I called each of our adult kids. They were all shocked. Thurs I went back to work, told my boss who told his wife and son, also very involved in the business. I made the decision, which they supported, not to tell anyone else at work or in the industry.
On that friday, Dec 1, I had my surgeon appt. STeve came with me. We scheduled the mast for Dec 11. I was meeting my best friend for coffee that afternoon, told her, called my brother. As far as I was concerned, that was it. Steve needed his family's support, so I agreed to have him tell his parents, who told his verrrrrry large extended fam. They have been, as I have whined before, very disinterested in the whole thing. It really makes me feel hurt.
Looking back, I would not have told his family, but am glad about everyone else. I am glad not everyone knows as I am so private (you wouldn't know that from the board).
Caya, still amazed you could keep it quiet for 7 wks. What did everyone else do, and would you do it again?
Melia -
Hi Melia,
Sorry I missed chat...sounds interesting!!!!
I've been trying to call Mena but she's not answering. No one has heard from her for a while. I'm worried. Several of her friends have gotten some very bad health news recently. I hope she's OK.
Mizsissy -
Melia,
Believe me, it wa very hard for me to keep in quiet for about 7 weeks, but I can give you the timeline for it all.
On Jan. 30, 2006, after weeks of various "episodes', my husband Allan was finally diagnosed with a brain aneurysm. He had a coiling procedure done, which means the dr. goes through the groin and stuffs the aneurysm with tiny platinum coils - endoscopic surgery. He could have died in the weeks preceeding this, also could have died from the procedure (2 - 3% chance), or had severe mental complications, again low risk of that, but possible. To make a long story short, I had to take over our entire business, comfort our two very scared daughters, worry about DH, - thank God for my mother, who came home from Florida (she winters there with my stepfather) to take charge and stay at my house when I had to travel for business. To make a long story short, DH recuperated fine with therapy, and was well enough by June 2006 to go to NY for business. I went with him, and travelled with home during the summer of 2006 to help him.
I had the infamous mammogram and breast ultrasound on June 29, 2006, showing nothing LOL - and DH was feeling good, so I scheduled my breast reduction for Oct. 16, 2006. In Ontario the government will pay for a BR if the plastic surgeon deems you big enough as to be physically challenged with your boobs ( I was a 34 DDDD) - I had had the initial consultation with the PS in Dec. of 2005, and the government gives you one year to have the surgery - so I wanted to do it before the one year expired.
Went in on Oct. 16, 2006 - my surgeon saw the cancer, cut it out separately (essentially performed a lumpectomy) and did not say anything to us right away as he was hoping the pathology would come back ok and did not want to worry us unnecessarily.
The path. came back BC - I will continue with part 2 so I don't lose this post. -
Mary, when I start rads next Monday it will be 7 weeks out so I barely made it within the range. I was VERY frustrated as they took their sweet time and kept reminding them there was a window or I would probably still be waiting. Don't be afraid to keep checking on them! - Skye
-
Hey ladies,
Chat was a riot as usual. I was a little dismayed that a student came in with a survey question about how a comic strip might have affected our cancer decisions???? The rules are very clear that these chat rooms are for us only, and students and researchers are directed elsewhere, but not everyone reads the rules. I think we need to feel free to talk among ourselves without worrying we are ending up part of someone's term paper. Although if someone wanted to misrepresent themselves that could happen. Also, I always notice there are x number of "anonymous" people viewing this board at any given time. Hopefully most are survivors like us but you never know.
Anyway, thanks Mr. Mel for the update, and Caya looking forward to as Paul Harvey says, the rest of the story. Roofers are here in force again today but a different crew. - Skye -
So I went to the PS office for a post op check up, and he tells me - I was so shocked, I nearly fainted. No history of BC, and I had just had the stupid mammo and ultrasound. He called in DH, who had to lie down. We were distraught - Allan was still not 100% from the aneurysm - very sensitive and this new pressure was not what he needed. I came home and called my GP who saw us the next day, already had set up appointments to see the onc. and breast surgeon.
Allan and I decided not to tell anyone until we knew what we were dealing with - remember, the plastic surgeon is a plastic surgeon - and although he was great, he couldn't tell us much about my prognosis - I mean he knew the basics from the pathology report, but I needed to see the BC big guns to know what I was dealing with. And my mother and stepfather were leaving the next day to drive to Florida for the winter. - So we get home at 3:00 p.m., at 6:00 p.m. my mother is standing in my kitchen saying good bye, telling us that all she wants is "everyone to be healthy this year". Of course I was dying inside, but what was the point of having everyone else be miserable until I had seen the onc.? ( I didn't win the best actress award in my senior year of high school for nothing gals).
We also did not want to upset our girls, who had been through enough with their father. So we went to see the onc. and breast surgeon over the following weeks, had scans done to see if the cancer had spread ( it hadn't), and the surgery was scheduled for Dec. 18th - but still I didn't tell - why? because my right breast was not healing well from the reduction surgery, and the breast surgeon said he could not operate on it unless it had healed better, and wouldn't know until a week before - so I'm shlepping back and forth to the plastic surgeon, who had prescribed a special gel to help heal the scar faster, and he's trimming the scar tissue, and the BS is checking it all. In the meantime the onc. is getting good results back from the scans, and the final path report comes in.
I finally got the okay from the BS that he would do the surgery, but we held off telling my mother, our DDs and the rest of the world until the Friday before the Monday surgery - I held off because my oldest daughter Amanda had final exams for first semester that would be over by then, and I didn't want to upset her.
It was very hard, but I saw a great shrink and lived on Ativan - once it was out, of course I had great relief. My mother flew home immediately of course. At first she was upset that I had not told her right away, but then she understood why I didn't - again, what was the point of having my entire family get all crazy upset again when we had been through so much with Allan only months before?
And did I mention that 5 days after my BC diagnosis I got shingles on my neck and face - everybody thought it was because of the stress of the year with Allan's aneurysm and the breast reduction operation - but of course DH and I knew it was the cancer diagnosis.
So that is why we didn't tell - I was trying to keep it quiet so that everyone else could get on with their lives, and then the surgery would be done just before the XMAS holidays, when we could all be together - and I recuperated very well from the mastectomy, better than from the reduction.
My girls took it very well, my mother was very brave, my brothers etc. and my best friends were all great - yes, a bit peeved that I held it in, but understood why I had to do it.
And here I am, almost 8 months out from diagnosis, and starting herceptin tomorrow.
BTW my onc. nurse called this morning, and said barring some unforseen reaction, I should be home well before 4:00 p.m. to attend DDs senior prom pix party.
sorry this was so long, but there was a lot of unusual background info to know about my case.
love you guys, had a great time on the chat last night
caya -
Whew!!!! So glad to hear. Our best to Mel.
-
Mr. Mel, THANKS!!! for letting us know Mel did okay.
Send her our love!
Cindy -
Melia,
It was indeed fun last night.
Being alone in a hotel room when you got the call must have been very hard. Do your neighbors or your other friends know?
I found out about the same time as you. I had a mammogram on Monday before Thanksgiving. The radiologist told me she was very concerned, and was able to do a biopsy later that day. After the biopsy, she repeated that she was very concerned, gave me a big hug and told me hat I saved my life by having a digital mammography. Needless to say, I was stunned.
I told my dh right away and told my kids that weekend, before I got the biopsy results. I got them on the Tuesday after TG. My primary care doctor told me its not that bad. IDC- not that bad I changed doctors.
I didnt tell my mom until after the surgery in December. She is 90 and I didnt want to worry her. I have not told her that I now need a mastectomy because they misdiagnosed me. I know I have to tell her, but I will wait until right before the surgery, or after. I havent decided yet.
My second opinion at Dana Farber found another piece of bc on another area of the same breast. My original pathologist did not catch that. His report showed only the original IDC and my surgeon told me he got everything out when he did the lumpectomy. My original surgeon biopsied that other suspicious area, but he and pathologist diagnosed it as benign, and as a result, was not concerned that he did not get clear margins on that area. I did not find this out until after I started chemotherapy. I fired him also.
Now I am getting a bilateral mastectomy with Diep reconstruction after my taxol ends, in August.
That about wraps it up for me.
Caya,
You have been through a lot. Getting diagnosed just as your dh is feeling better must have been very hard on both of you. I can totally understand why you didnt tell anyone right away, especially your mom who was on her way to Florida. Even so, it must have been very hard to keep it all to yourselves.
Skye,
I agree that is was inappropriate and uncomfortable for that student researcher to have been there, nevermind asking us about a comic strip. Next time, if she dares to enter again, we can just ignore her. It was a lot of fun. I was laughing so hard. I am slow, so I had a little trouble keeping up- my first time- virgin as you call it. Next time I will get faster. Lol
Viddie -
Melia When I got the biopsy results over the phone I was at home alone. At the time DH was finishing up his MBA and was in class all day but he knew Id be calling good or bad when I got the results. When he answered his phone (he had to duck into the hall during class) I was so upset that I couldnt talk. When he asked if I was OK I just started crying. So he left school and rushed right home (he left so quickly he didnt even tell anyone). By the time he got here about 20 minutes later Id already called my OB/Gyns office to get a referral for a breast surgeon, called my mom (she knew about the biopsy), my mom had talked to the dr. in her dept about who I should go to for surgery, and Id put in the first call to the surgeons office. DH stayed with me all afternoon and we went together to pick up DD from school. Thats where I saw my good friend who also knew I was waiting for biopsy results. Id only told my husband, mom and the one friend about the biopsy. The friend I had told because we carpool and I had needed her to take the kids to school so that I could make it to the appointment. Anyway, when I saw my friend in the pick up line at school I told her about the results. I also gave her permission to spread the news to whoever she wanted to. That way I didnt have to deal with telling the other moms at school and our neighbors. You know all those people that would eventually find out but that I dont know all that well. Well, turns out shes a darn good gossip so I really didnt have to tell anyone else after that point! My mom took care of telling the rest of the family.
-
I was at work teaching a class when I got the news. Up until then, I'd heard from everyone that it didn't look like anything to be too concerned about. I always wondered if they told that to everyone so they wouldn't worry. I guess not. Up until then, I didn't tell my parents or brother. Just good friends who knew I was worried.
I told my boss at work because I had to leave right after finding out. She blabbed to everyone so I had to tell very few folks at work. That was good and bad. I very quickly turned into the go to person for all things breast. And honestly, if you were waiting for biopsy results, why the F would you want to talk to me about my experience. People want the good results, not the cancer results.
Mother told the relatives and everyone else she met. I guess that made her feel better. DH told everyone as well. I finally told them to cut it out as I couldn't go anywhere without the turtle faces. -
I found out on October 27, when I went to mammogram. I had thought...OK, here's my 2 year test, I'm outta here in ten minutes. Then the tech found the lump; it was large, hard & easy to feel. I was frightened.
DH had come with me because we'd gone shopping. He wanted to know how it went and I debated whether to tell him or not because I didn't want to worry him. So I just told him they'd found a lump, but that 80% of lumps are benign and not to worry. But I knew I was in trouble.
The next week was miserable, waiting for the second mammogram and a definitive diagnosis. The second time I went by myself to Ann Arbor. The nurse who did the mammo was a very, warm caring young woman. She felt the lump,and she said, you're probably OK. I asked when I would find out, and she said, not today, they won't tell you today.
Then I went across for the ultrasound, and the tech worked very, very slowly, spent a long time under my arm, so I knew then the results weren't normal. It took a long, long time, then they had me sit in the waiting room.
The mammogram tech came and got and brought me in to meet the Radiologist...by now I knew it was serious. We sat in a darkened room as he looked at my films, explaining that he was very concerned. I asked him if it could be a cyst, and he turned around and looked back at me with consternation on his face, thinking she's just not getting it, and repeated "I am very, very concerned."
Then the nurse took me by the hand and took me to a small room with a table, held my hand. I asked her if I was going to die, and she said NO, it was just a little bump in the road that I'd be fine. That she'd had a lump 4 times as big when she was 8 months pregnant.
I told her I didn't want to wait anymore in the dark while the tumor got bigger. She spent an hour on the phone trying to get me for a biopsy the next day, and then gave me the name of surgeon, and told me to make an appointment immediately, not to wait for the biopsy.
I called my husband from the parking lot & gave him the news, sugar coating it as best I could. After that he came with me to all my appointments.
The biopsy happened the next day. On a Friday, I met the surgeon, and we said, well, what is it?!! And he said, you mean you don't know, it's cancer all right. But we got right on the fast track. He was a wonderful, concerned, caring surgeon. By Monday I was in the operating room, and the damn thing was out!!! Three days after diagnosis. What a relief!!
We didn't tell any of our family for a while, except I told my mother in the early stages. She's very old and frail, blind and deaf, but I really regretted telling her because it worried her to death. She would call at all hours, angry and upset, because the diagnosis was taking too long...
Fortunately things worked out OK...!!!
Mizsissy -
Had fun in the chat last nite. Good to hear that you are doing well Mel, hopefully you'll be there Thursday nite for chatting.
Lynn, my hair and eyebrows are growing in, but I still don't have any eyelashes. Yours will start growing back in really quickly, and it sounds like yours grows faster than most, so you'll have a head of hair in no time.
Dan came with me to the doctor the day I got the results of the biopsy. I was a basket case, but he asked all the right questions, and made sure we had all the right answers. My doctor set up the surgeon's appt and has helped me all along.
I only had to tell my sisters, and they told everyone. At first it was a bit embarasssing, as I live in a small town, and everyone knows everyone. My sister told a bunch of people at curling, and from there it escalated around. Then I was a bit hurt, but my sister's must have felt it helped them to tell everyone. Oh well you can't change the diagnosis. -
I had noticed my right breast seemed to be shrinking for about a year. In August '06, I went for my yearly gyn appt and told the doc. He spent extra time searching for lump but couldn't feel anything. It had been 2 years since my last mammo so he said I should definitly make the appt.
Fast forward to Oct '06 when I finally got my mammo. They called me back because they compared to the last one and noticed my breast was smaller. Went for 2nd mammo and they still see the breast is smaller, but nothing is showing as a problem. A week later they called me back because the chief radiologist saw my mammo and wants to do ultrasound just to be safe. Well, he actually did the mammo, not the tech and spent a long time. Did the core biopsy right then (they usually need to schedule these things). This was a Friday. I told DH and my sister (she is a nurse), my boss and a co-worker. What a long weekend that was. Went into the office (I stay over night) and got the call about 6pm on Nov. 7th when I was at still at work. My gyn was really sensitive and said he could call the next day when I was home, I said no, find out the results and call me back. He did with the positive for ILC. Then I had the 2 hour drive home by myself. I called my sister for part of the drive. DH had a nice fire in the fireplace and a glass of wine waiting for me. I didn't tell my mom until after the surgeon appt. which was later that week. Told kids that weekend. Since ILC can mirror in the other breast, I needed an MRI before surgery and that couldn't be scheduled for over 2 weeks, then was Thanksgiving. Ended up having to wait until Dec. 4th, almost a month after dx before I finally got the surgery.
And then I met all my sisters here! -
Either I still have serious chemo brain or I've been spending entirely too much time online (or both). This morning I asked my 3 year old if she wanted "some more e-mail." I meant oatmeal. Ooops. She looked at me like I'd just sprouted another head.
-
I don't know if you guys remember me when I first was diagnosed. August 31, 2006. Didn't get my surgery until Dec 5th, 2006.
I had no insurance and no doctors would see me.. .remember? I sat at home crying for almost 3 months with cancer and no doctor.
My lump was found by accident at my regular yearly gyno viset during a breast exam. (I almost didn't go that day) She was all, "Your 41 and have never had a mammogram? Get your butt down there for a mammogram."
Then, when I had my ultrasound the tech told me, "If I had to make a bet.... ..... I would need someone to come in here and PROVE to me that this is not a cancer." (This was his exact words!) I knew then, it was cancer. Even though everyone else told me it's not for sure until you have a biopsy. I just knew. No family history, nothing. I didn't even know what cancer was, just something you heard about with other people. But now, I could write a book on breast cancer.
I have a feeling that stress and worry has a lot to do with your immune system and that's what happened to me. Now, I tell myself, "Do not stress over the little shit in life!!" and I'm sticking to it.
Thank you guys again for being so wonderful!!! I am still in SHOCK!!! I can never thank you all enough!!!
I love you,
your chemo sister....RobbinJaye -
RobbinJaye - I remember very well your posts from October. I didn't know you from this group, but I remember reading your posts about not being able to get surgery scheduled and then when you finally did get a date.
-
Robbin Jaye,
I didn't join up here until about December, and then I wasn't part of a group, so I didn't know how awful it was for you all that time, waiting for surgery. What a trip!!! But you have survived, and you've done well.
Maybe you should write a book!!!!
xxxoooo Mizsissy -
Caya, wow, I didn't realize you'd gone in for a reduction only to discover this. One of my best friends from FL, a teacher who now lives in Atlanta, had a reduction last week. She was very worried about her pathology. I now see why. That wouldn't have occured to me. And it does run in her family.
Herceptin went smoothly this am. Well, took two sticks to get it going but turned out it was the machine and not my vein. I was down 2 lbs. from 3 weeks ago, so that's another bonus.
Sitting here waiting for my hair to "process". I got more Loreal color yesterday. I just can't justify a salon color w/so litle hair. I got dark ash brown this time... you'll hear me screaming all over the country if it turns out like Elvira. But the lighter ones were turning reddish too fast on me, so I got bold...
Yeah, Jan, sad group we are when we think of the perks of being in the hospital: extra sleep. -
Yeah, I didn't join here until, I want to say Feb... so I didn't know about Robbins tough road either.
-
LOL, Jan on offering your daughter more email. I was doing a lot of that a few months back...
Boy, can I tell the diff. now btw. feeling good and not so good. The Taxol wipes you out so gradually, over a 12 week period, that half the time I didn't know if I was imagining it or what... or maybe I was in denial. I hate to give in to feeling down. But I feel so full of energy again. Back to the real me. -
OK...last post. I feel like a "board hog". I read that link about adriamycin and if I read it correct, it's saying that it's only eff. for approx. 8% of women...those that are "topo II" positive...for which there is no test. Most topo II+ women are also HER2/neu+. So, not that I want to be topo II+ because I have no idea what that implies, but maybe I didn't do adriamycin for nothing. It blows my mind that they can come up with this stuff after we've all been put on the drug for yeaaaaaaarrrrrrrrrrrsssss....
-
Really, TPPJ, you feel good again?! I am leaving in 30 mins for taxol 8. I am so tired of feeling achy and tired. Not awful, just not myself. How many weeks out are you? Do you really feel normal? Right now walking down the hall to put in a load of laundry is an act of will! I don't say much to my husband, but inside I sometimes feel so discouraged at how much effort everything is.
Melia
Melia -
Isn't it amazing the bond we have here? Yesterday, while Mel was in the OR, I felt as if I were in the waiting room with Larry. I don't know him at all, but was there beside him waiting for word.
I feel closer to you girls than to some of my good friends now. This place is very appreciated by me. -
Of course, I remember you! You got your diagnosis soon after my surgery. I was ready to march on Washington because you couldn't get a doctor. The only problem was, I didn't have the energy to march to my mailbox. I'm so glad for you that you got it all worked out.
-
I seriously thought my head was on straight lately. No incidents to speak of for a month or so. Then, a couple of days ago as I prepared a meal, I asked DH to hand me a clean dish towel. He opened the drawer (small drawer, nothing but dishtowels). He started laughing. There sat my freshly washed and peeled red onion. So much for feeling okay again.
-
I found a lump one day during a self-exam in the shower. I spent a few days considering the implications of it before I told ANYONE, even DH. When I told him that I thought I had found a lump he said oh yeah I know. DUH .important info! I called for an appt at my general practictioner, and they made me wait 6 agonizing weeks, because it qualified as a well visit. (I am going to be getting a new Dr, of course). I finally got in to see the Dr in early November, and she sent me for a mammogram. I called as soon as I got home for an appointment, but the earliest they could give me was in 4 weeks. ANOTHER agonizing wait and I went for my mammo on Dec 6. Up to this point, the only person who knew anything was cooking was DH, and my best girlfriend. I had my Mammo, and I knew something was up when they called me back in for more images. I was sent down the hall for a sonogram. I was watching the screen during the exam, and the image started turning colors as different things were enhanced. I could see a large black hole surrounded by a halo of shimmering colors. Conversationally I asked the tech what she was looking at. When she said blood supply I knew that it was a tumor. The Radiologist came in and confirmed it .and even without a biopsy said that I better find myself a surgeon. Before I knew it I was crying in the arms of the technologist, and they shunted me off to a room to meet with one of their nurses, whose job (apparently) is to break the news to people. She was awesome .but I have to say that it was a bit surreal she told me I very likely had cancer, and gave me all these glossy pamplets and so on like I was going on a cruise. I was at the Breast center for 3 hours .They did not want me to leave because I was there alone and I was pretty hysterical (imagine that). I finally overrode them and left. By the time I got home it was 9PM or so. At that point I called my mother, father and sister, but told NOBODY else and instructed them to keep it quiet as well. I made the news generally known when I had the surgery date for my Mastectomy. I did not tell my children until the two days before my actual surgery because I did not want them to have a long anticipatory freakout.
The whole thing was awful there are so many different right ways to do this. -
Ok, my kids just walked in and called me a Goth. Note to self: do not buy Dark Ash Brown again. Medium is sufficient. I do look like Elvira, but it's funny...I really don't care because I'm not doing topless anyway. I've always got a hat or scarf on and I know, "this too shall fade". Ha-ha! I guess after you've done "no hair", it's all relative...
Melia, I do feel good. Normal again. April 4 was my last taxol, so I'm 2 mos. out. I've felt good for quite a while now too. I did Herceptin today too and again, no s/e's at all. You will feel good too...you just have to remind yourself that it's strictly the taxol and it will be a few rough weeks ahead. When you feel down, remember that... say it's not me...it's the drugs...
Rebecca, my story is identical to yours with the exception that my primary dr. saw me immed. I was sent straight over to a breast center and they knew right from looking, what it was. The tech was a young girl and she said something like "oh, my sister has leukemia"....she left out "too". It was like she was saying "my sister has cancer too". That gave me my first inkling that this wasn't going well. That, and the fact that they were studying it so intently for so long. The doctor came in and she was great. She was so good at breaking bad news, I feel like writing her a t.y. card now, all this time later. I got the brochures, like you... the talk about contacting a surgeon... all before pathology came back. It just looked like classic BC on the screen. I don't even RECALL how my kids found out. I think I've blocked out a lot of that time in my mind. I'm sure I told them asap and said "oh, I'm so lucky we found this early..." -
Goldnmom, I hear you on being attached to this board. I've been highly absent on regular email w/my five or so girlfriends in Boston that I talk w/regularly.
-
Quote:
Either I still have serious chemo brain or I've been spending entirely too much time online (or both). This morning I asked my 3 year old if she wanted "some more e-mail." I meant oatmeal. Ooops. She looked at me like I'd just sprouted another head.
That is hilarious!
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team