Starting chemo Dec 2007
Comments
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I'm ALLLL done!!!!!!!!!!!!!!!!
The onc dr decided to change my last dose to Taxotere (KMK & Jeannie had/have), which is in the same family as Taxol but doesn't have the problem with neuropathy... he was concerned about that. Since this dr seemed pretty "Everything's fine. No problems" about other things, I felt very comfortable going along with his opinion on this. I feel the tiniest bit queasy, so popped a Compazine when I got home. Other than that, I'm ok. Hoping that's my only glitch. Plus side is it only took an hour, so I got home about 3 hours early!
My nurses threw me a little party... they had sliced fruit and cookies for everyone in the clinic. They passed ginger ale out to everyone, and they all toasted me and my last chemo. And they gave me a teddy bear and a rock that says "Hope" on it.
I cried.
But below is me BEFORE that happened. I look pretty goofy because I wore/brought something from all the people who have supported me in my family/friends, including the faux diamond necklace that used to belong to my birth mom.
(sorry abou7t the size. I tried to reduce it twice but it refuses. Oh well)
Yeah, yeah, I know the sun is positioned in a rather odd place... I had no idea at the time and my husband didn't say anything. Gave me a good chuckle when I saw it.
It's over. Let the healing begin! Hugs to everyone.
-Sal
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Cute pic! Sunshine or setting too!
CONGRATS on being done! You look like so young and sweet! Too pretty to have been through all you have! Hope you continue to feel great!
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Congratulations Sal and Suz!!! I'm so happy for you!! One more for me. Today was chemo day so I probably wont be posting for a few days. Talk to you all later.
Kate
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Kate, Congratulations!!!! Only one more, your on the home stretch girl. We're all cheering you on and hope you have little or no se's. Big {{{hugs}}} your on the home stretch now. Much love, Suz
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Sal, you are completely adorable. (The sunshine made me laugh out loud.) You look so happy and relieved. And clearly a lot of people were wishing you well!
How's everybody feeling? That last week or two of feeling crummy was harder for me than I thought--I was so impatient to feel better, and it was just as hard--if not harder--than before. The only thing that helped was knowing it was the LAST TIME!!
Wishiwere, I'm so sorry you have to go through another scare so soon. A couple other ladies here have found things and had them checked and everything was ok--hopefully that will be your story, too. Let us know what happens--I'll be thinking about you.
I've been having a real up-and-down week...seems like the sunshine (which used to affect me a lot before all of this) is a complete maker-or-breaker now. Sunny days, I'm like SuperWoman--I painted the rest of the living room, rearranged the furniture, sewed curtains...then the sun went away yesterday and I could barely get off the couch!! So weird!! I really should haul my light box out of the basement. But it's spring!!!
How's everybody doing in the hair dept.? (Suz, in your picture, I didn't notice your lack of eyelashes at all!) I'm seeing some "real" hair growing now, under my white fuzz. I had another dream last night that my hair grew back in a day, a thick luscious auburn mop (ha ha--my natural color is nothing like that!)...I'm really curious to see what I get! I haven't seen my real hair color in years! I never lost all my hair...I think only about 60-70%? Enough that it would have looked awful if I hadn't buzzed it...
love to all.
A
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Hi all!
First of all...A big YAHOO! to Sal, Suz and Laura! You did! You are all done! Can you hardly believe it?!! It took a bit for it to sink in for me and really I can't wait till next Friday which would have been a chemo day for me (if I was not done) Gee, that's gonna feel great!! What cute pictures and stories you had! Suz, your picture made me cry! How thoughtful that was!! You're really something special!!
I had some rough body aches again Monday evening and took Tuesday off work. Glad that's over with now too!! So, tomorrow I have my MRI and am anxious to see the results! Hopefully, the lymph node tumor is all but gone now (like the one in the breast). Last ultrasound it was under 1 cm and I had another tx after that! I'm starting to get a bit "anxious" (I guess that's what it is) about surgery...Not the actual surgery but how many lymph nodes we will find out are involved. Obviously hoping its 3 or under so I can stay stage II but preparing myself for more than that as report from mam & ultrasound say "several". Staying positive though with the knowledge that I responded so well to the chemo or should I say my tumor responded so well...of course I'm sure the tumor was not happy about it since the chemo KICKED IT"S ASS!!
Amy, Glad you are having some great days! The sunshine helps so much! I feel the same way! I'm ready to start walking (and I like it better outside than the treadmill) so I can lose my new 20 pounds plus a little more, hopefully!! I am really digging my hair right now....mostly for the fact that there is some there! It's the white fuzz but it really feels like it's getting longer each day! Crazy, I know! I'm curious to see if the current white color will change since I was so grey to begin with! Actually there was still a bit of dark at the nape of the neck so maybe some will come back! The wait to color is going to be VERY hard for me! I'm way to young for as much grey as I have and it makes me feel terrible!! I'll have to start with the ammonia free "Loving Care" since I know I can't wait the recommended 6 months!
We sure all finished in a pile, didn't we! And to the few with 1 or 2 more to go....hang in there, your day is coming very soon!!
WishIwere, Keeping you in my thoughts and prayers! Hope your news is good! Please let us know!!
Hope everyone has a terrific Easter!! Oh, and Happy Spring! It's official today!! Now, just bring on the warmth!! Lori
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Wishiwere, sending you prayers and hugs for your latest scare. I echo the others... hoping it turns out to nothing serious.
Suz I glanced at the pink balloons and thought they were your family/friends... what a sweet and touching addition to your last day to have us with you.
Lori, good luck with your lumph nodes. Got my fingers crossed!
Hang in there, Jeannie and Kate... your days will come and OHHH, how sweet they will be. Not a feeling in the world to knowing it's your LAST one.
Thank you all for your good wishes. I'm still a tiny queasy this morning-- reminds me of AC-- but other than that I feel simply marvelous. I'm ready for whatever SE's come because I know they are the last round.
I don't have to start Tamoxifen for another few weeks. They already set up my appointment to have my port removed in 3 weeks. And I'll see my plastic surgeon mid-April to set up my surgery to have the tissue expanders removed and the implants put in. My sciatica is slowly but surely getting better: I've been (on my own decision) exercising twice a day, and that really seems to be helping... I can sit pretty much anytime I want (although it's still a little sensitive). Gittin better, one day at a time.
I'm not going anywhere, but did want to thank all you ladies for all your support through the chemo. I had quite a few whiny days, but you ladies pulled me through them all. You are all blessings.
-Sal
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Wishiwere, Hope all went well with the mammogram today.. were all hoping its nothing to worry about. You are in my thoughts and prayers today.
Sal, Loved your pic, and was that ever sweet for all the nurses giving you a send off party. Your right, now its time to heal.
Lori, Good luck with your MRI and keeping it to 3 or less. No matter what you kicked their but big time. I also hope your surgery will be a breeze.
Amy, LOL... You probably had no energy the next day due to how much you did on the sunny day
. Try to take it easy on yourself, your body is still healing.... baby steps for a little while longer. But that said, what color did you go with. I am itching to tackle my living room/dining room and hallway. Not so happy about needing to do the ceiling (I hate painting or spraying ceilings)
Hmmmmm, Hair department.. I went smooth bald when I started the taxol
so far I have the really short white fuzz about 1/16 of an inch long, but I hope its the start. Ive read that our hair can come in white then change color later. I have no idea how much grey I'll have. My eyebrows are real sparse but I can touch them up with a bit of blurred eyeshadow, looks more natural than brow pencil on me. I do the same for my eyes (and hide behind my tinted glasses) A thin layer of dark eyeshadow around the rim gives a bit of an eyelash effect and doesn't run quite as much with the tearing eyes. BUT... I noticed yesterday a tiny bit of fringe starting to poke through. I cant wait to feel and look healthy. I feel & look like I aged at least 10 years through all this. But with summer coming and some healthy living I plan to take back those ten years and get on with work, play time and life!
A big yea to all who are now done and hang in there for all who have only one or two to go. We haven't heard from Joy in quite some time
not sure what her finish date was.
Much love and big hugs ,Suz
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Ladies, thanks for hopes. I'm supposed to call in the morning to talk to one of the nurse coordinators to see if she can put a stat on the report. I lost it in the little rooms they have for those getting mammos. They were so sweet (too sweet) and my strength I'd gone in there with crumbled when one too many ladies asked why I was there. Just lost it! I've not done that yet and was afraid I'd never gain control. I just felt so stupid, you know? After all I've done to fight to NOW lose control of my emotions and cry? WHY?
Anyway........ the coord nurse said that the MRI in oct showed B9 stuff so it's probably just that. Also that it's possible if they see something they'll call me in for an US just to be sure. Whether cyst or other, so IF they do, not to panic. SURE, Don't panic. Easy to say huh? I saw the pics (well 3 of the 4) as she closed it too quickly after the 4th one and that bothered me. I think I saw a cyst amongst it, but who knows. There was a lot of white, but that 'could' be what she was talking about in the old mri. I'm just anxious, ready to lose it again and feeling so danged mad, I could spit!
Then I remember all that others before me and currently are going through and think....it's going to be okay.
I told dd the first go around, 1:8 meant I was getting it rather than my sisters, mom or dd's or such. Fine with me if they didn't! So does this mean, then that my nieces and so on won't get it too! I surely hope so if it's come back! D*#& it! I'm just so sick of being sick, as we all are! IT's just maddening and disheartening!
Okay....that's my rant, now I'm going to say that I'm going to move on tonight and not think about it and just send up prayers that NO one on this board has to go this crap again! NEVER!
Love and {{hugs}}
me
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Congratulations to Sal! Yippeee!!!
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Wishiwere, here's hoping that this will turn out to be nothing! Both Sal and I went through finding lumps that turned out to be B9 and I sincerely hope this will be the case for you as well.
Love and hugs
FUBC
Laura
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Happy Easter, everyone
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Yes, FUBC!!!!!!!!!!
Thank Laura, I appreaciate the thoughts!
I'm hoping like hell-0 too, but my mind just can't get around it not being something as you well know. It's just too much right now! Between the pap yesterday and I know I'll get called back on that by his looks and then the UTI they found and my hands are started back up and now this crap! I am just freaking tired of being down.
I want spring NOW!!!!!!!!!!!!!!!!!! So i can out and DECAPITATE & MURDER SOME weeds!
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thank you for the chuckle! I needed that! Hope it made everyone else chuckle too! Love the bunny comics especially!
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Thanks Laura, Happy Easter to you to! LOL, love the cartons
Suz
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wiw--I see no mystery in you breaking down at this point--there's only so much stress a gal can take. And those nurses have seen worse, I'm sure. It was probably good for you, in a way, to let it out a little (not to get all psycho-babbly on ya). Sometimes for me, the thing that puts me over the top is kindness or sympathy--I can hold it together, but then somebody says something nice, and that's it--flood gates are open.
Anyway, it sounds like they're doing the right thing by putting a "stat" on it, and it also sounds like there may be good explanations for the lumps other than bc. I know you won't feel better til you KNOW, but there's so many ways it could go--try to just deal with what's right in front of you. That's what you did up to now, so you know it can be done. I know, way easier said than done. We're thinking of you.
I just have to RAVE about my yoga teacher for a minute (I just got back from class #2). She is awesome!! You'll be in some weird position, and straining and sweating, and she'll look at you and say, "just try to move your back inner armpit forwards", and -- wallah!-- it's like a whole new world of comfort and relaxation. Who knew I HAD a back inner armpit!? AND that it had such awesome powers!? Ahhh...every week I come back trying not to move ANYTHING because I don't want to mess up whatever alignment I manage to achieve... Anyway. Yoga is good.
Suz, I wimped out on the living room and did a pearl white, which is actually like a parchment color. It's very nice, and I have a lot of color in the room otherwise, so it's good to be neutral. I should warn you, though--it's still a little hard to do that stuff! Moving the bookshelf in particular! I'm working on baby steps. It means learning to do things over the long term, rather than in big bursts. It is the mature way to do things, so it's a fine goal, even though I have no choice.
Laura, I love those bunnies!! "what?" bwa ha ha ha ha ha!!!
A
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Thank You ladies! Seriously, those rants help every time, don't they! And yes, A, those sweet things they say or do are the time bombs ignitions! I would have been safer had they been nonchalant or even B*tches to me, I know that! I appreciated all their concerns, but it was just a melt down I didn't want to have in front of anyone, let alone people I don't know!
But yes, I've decided I can't do anything tonight, so I'm going to take one of the xanax that the BS gave (8 of 10 pills left) me before surgery last fall, and try to get a good nights sleep so I don't fall into hysteria when I get that call that all is fine tomorrow! Buck up and beat the turds back again if I have to!
Thanks sweeties!
A, I'm really close to jumping into a class of yoga, piletes (sp?) or something to learn more too! Sounds wonderful. Hopefully I don't get twisted up and never come out of the knot!
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I'm praying for you this morning, Wiw. Hoping all turns out ok.
-Sal
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I called the breast coordinator this morning and she promised to put a stat on it and said SHE would call me back this afternoon, not to worry! HA! Sure, I'll just forget it all!
Anyway, I'm sure she'll get on it as she mentioned there is no reason to have to sit all weekend worrying! I love this group, just not my onco
Thank s for th pray Sal. I'm keeping them up for everyone here too, believe me! We can use all the good thoughts and prayers we can get!
I really wished I'd asked more questions or looked closer at those images yesterday. I was/am hoping those white spots are just fibro stuff and nothing to worry about. I can't imagine how women get through this that must wait week or month to get their results! I'd be taking more than that the xanax I took last night!
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Congrats to all who are finished now.. a big huge woohooo!!!! Sal you look great! what a wonderful picture. I am having my last infusion next thursday and cannot wait.. i cannot post this enough...LOL
Question ... did you ladies do something special for your onc. nurses?? I am trying to think of something to do. Perhaps just bake something or bring in some other food items???
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Kimbly - I, too, am thinking of doing something for the onc nurses. I have an appointment at the clinic on April 4 which, I believe, would have been my labs to prepare for next chemo the following Monday. I know I certainly will be celebrating that day, knowing that I don't have to have chemo again! I was thinking of taking them a platter of fruits and pastries or something like that.
Some of my ramblings.....
It's interesting how in some ways having cancer puts things in perspective. Here in our hospital they give you a plastic card with your details on it, and you are supposed to use this card to identify yourself any time you come for treatment, labs, etc. Well there was a woman there last week who was a recurrence (after 10 years) and was complaining bitterly about having to show this card twice in the same morning in different parts of the hospital. I dunno, but I just said to her - well, it beats the alternative. After all, if they have some picky rule to ensure they give the right tests/treatments to patients that can't be all bad. Apparently they implemented this rule to eliminate confusion with patients who have the same names (cancer is booming!) Things that may have irritated me/got me totally worked up no longer bug me a bit.
Now this is worth getting upset about - this has happened here in Canada:
108 women died after botched cancer tests, Newfoundland says The province prepares to open an inquiry into a medical scandal that has raised doubts about quality control in laboratories across Canada CARLY WEEKS From Wednesday's Globe and MailMarch 19, 2008 at 5:00 AM EDTMore than 100 women have died after receiving inaccurate results on a critical breast cancer screening test, health authorities in Newfoundland revealed yesterday as the province prepares to open an inquiry into a serious medical scandal that has rocked the province and cast doubt on the quality of medical testing across Canada.The judicial inquiry, set to begin today in St. John's, will examine how hundreds of breast cancer patients received questionable results over an eight-year period on a hormone receptor test, used to determine which course of treatment a woman should receive.Yesterday's announcement marked the first time the government has revealed how many women who received faulty results have since died, but no one will ever know how many would have lived if their results had been right the first time. The government said 275 women who received inaccurate test results are still alive, and many patients involved in the scandal say receiving faulty results has had devastating consequences on their lives.
I can't imagine how devastating this would be for women with cancer and their families/survivors!
Two days ago I was working on my computer in the dining room. It is still a bit cold here but very dry and sunny. My son came running down in a panic and rushed out into the back alley. He had smelled smoke through his bedroom window and when he looked out he saw that our fence was on fire. I think someone walking in the alley may have thrown a cigarette or something into the dry grass along the fence and it all went up like tinder. This poor cedar fence is relative new (2 yrs) after being rebuilt due to our neighbours crashing into it twice previously. Now about half of it will need to be replaced. I just threw water on it, shrugged my shoulders and went back to work, unfazed. I guess when hubby gets here he will have another project waiting for him, lol.
I can't stop thinking about how happy I am to not have any more chemo. On my last tx Monday as they were injecting the Epirubicin into the IV the nurse noticed some leakage and steaming under the plastic tape at the IV site. It is like a T-joint on the IV tube and where the joint was it wasn't sealed, so the fluid was escaping onto my arm from this. Well, that was quite a bit of excitement for the nurses. This stuff is so toxic that it MUSTN'T touch your skin. I wanted to laugh hysterically like a crazy person. Imagine what it has done to my veins, heart, etc. if it is so dangerous to even get it on my skin! Anyway, they (with their protective eyewear and gloves) mopped up the stuff as if it really were a toxic waste spill, disposing of all the towels and wipes in the toxic waste and then told me to scrub my arm thoroughly after the tx was done. After they pulled the needle out they put the cotton puff on it and asked me to put pressure on it, as usual. Then they taped me up and off I went. I realized a couple of minutes later when I went to the washroom to scrub the arm that the hole where the IV had been hadn't sealed up and I was bleeding freely, with my shirt soaked with blood. Fortunately it stopped bleeding as soon as I noticed it. I felt a bit of a wreck when I got home. Let's just say I am beyond happy to think I don't have to deal with any of this stuff again. My nausea is gone today and I believe yesterday I ate the last MacDonald's breakfast I will eat for a long, long time. Now I will start back on the highly nutritious diet (I did NOT buy chocolate for Easter!) and getting some more exercise.
Amy, you inspiring soul! I still have cans of paint stacked up in the corner of my dining room - they've been there since my dx in September when I was in the process of repainting my house. I'll get back to that soon...One thing at a time.....
Cheers to Kimbly, Jeannie Bell and Kate on the countdown towards the end of chemo.....Hugs to WIW, and prayers that everything will be ok. And a happy Spring and Easter to everyone....
Love
Laura
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Pretty good news!!!! Well, at least I can relax till monday. Maybe???
IT seems when I had the MRI guided biopsy last fall (In a town nearby) after the US biopsy in the BS town, the Mammo's and MRI were NOT sent back to the BS. Soooooooo..... the radiologists had nothing to compare the one done yesterday. GREAT! Did I mention my middle name is MURPHY!!!!!!!!!!!!!!! UGH! Always something.
Anyway... the radiologists does NOT see anything he would consider a cancer. I did remind them that last fall the Mammo and the US did not see the second lump which was in fact a 1 cm ILC with LCIS. And she said that's why they have scheduled an US for Monday at the health center there. Not sure what to think really, b/c as I said, the US didn't show this 2nd lump I had before either. BTW, both myslef and my reg doc had felt it. Only when he did the MRI did they find that.. I'm going to think positive and say it's nothing till monday. Okay, I'm going to TRY to think positive and say it's nothing till Monday.
Thanks for letting me steam off ladies! Love and ((hugs)) to you all!
Laura! EIther you are on good drugs or you've learned to not get excited about the small things, but I bet your ds was surprised you didn't get upset!
SOrry it happened! Your poor dh must feel horrible to not be home and have to think of you all doing all that yourselves! When is he supposed to be home?
Ladies in the final weeks of chemo and those moving on the rads! GO GET THEM GIRLS! Many, many {{hugs}}, prayers for those who want them and most off, a hand and arm extended to wrap tight in while you get through these final weeks of treatments! Wishiwere there in person to help!
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Wiw, What a frustrating thing to have to wait AGAIN. But I'm still pluggin for ya.
Laura, I read your story about not letting the chemicals touch your skin.. that was morbidly amusing... you can't help but laugh eventhough it isn't funny to think of what it's doing to your insides. Kinda like how my onc described one of the SE's of Tamoxifen as an increased chance of uterine cancer... cure one cancer and create another?
Kimbly, counting down the days. Woohoo!!
Regarding your question, I sent an "edible arrangement" to my entire onc dept. The arrangement is made out of fruit, some of it chocolate covered. They are pretty pricey, but I wanted to do something and my energy/creativity level is still pretty low. I also, seperately, sent a card to my nurse to personally thank her.
My hubby is pestering me for the computer, so away I go. Big hugs to everyone out there.
-Sal
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I got an ad in the mail for one of those the other day and mentioned this to dh thinking it might be a good idea. My kids are home from school this week and although they are teens they do distract me LOL We have a local place called Incredible Edibles perhaps I will try them. The nurses have been so good to me and I plan on buying a card for each of my chemo nurses and then the arrangements for the entire dept if I do that. Thanks for the idea....
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Laura-- Holy moly. First your fence burns down and then your arm starts disintigrating!? I'm with WIW, either you've got some good drugs, or you've found some kind of shaman-level inner peace, because that's not exactly what I would call "the small stuff"...even though I guess it is, in a way. For me, the small stuff is like, a pile of laundry, a pile of dishes, a pile of papers...(there are a lot of neglected piles around here...) Anyway, you have a great way of telling stories! I laughed, albeit in horror, at both!
WIW, I hope you got your results yesterday, and I really hope they were reassuring--let us know when you get a chance.
Hey, Sal. I hate those kinds of mix-ups. Did they not have any kind of marker for where to look for the comparison? When I had my US/core biopsy, they put a little marker in the "area of concern"--apparently shaped like a little bc ribbon (weird)... anyway, at least it's better news than if they COULD see something! Hope they get their act together and give you some all-the-way good news soon!
I continue to overestimate my abilities--yesterday my older son had a day off and my younger son's school was open, so I took the big guy out--we went to a big thrift store (he loves cheap junk, like his mom), then bowling, then out to lunch, and then had a Guitar Hero showdown (yeah, ok, I really like Guitar Hero. I know.). Then I had to lie prostrate for 6 hours. Grrr. Oh well. I'll work it out eventually.
love to all--
A
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Yeah Sal, I think we share the same kind of morbid sense of humour.
Amy, yesterday I was thinking about you ladies with younger kids. I know I have felt incapable of doing much other than working and cooking and doing a bit of laundry and housework. The rest of the things on the list I have just let them slide. I don't know how you have managed to get through chemo with younger kids. I can certainly understand the desire to jump back in and do so many things in a day, and I definitely know how that can bite back. I have great ideas daily about all the stuff I want to do but am still struggling to stay out of bed past 8 pm. I can go out at night but it really wipes me out the next day. I got tired just reading about your busy day with your kids!
Hugs
Laura
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Sal! -- Congratulations on being through with your treatment....Way to go!!!!
I went to have my next to last treatment yesterday (Friday)... but because my Platlet count was down too low, they have postponed it another week... Bummmmer!!!! I still had my Herceptin yesterday, just not the Taxotere/Carboplatin....Also, I started getting Procrit shots 3 weeks ago because my Red Blood Cells are down...Anyone else had to have their treatment postponed? Or had low Platlet counts or Red blood counts?... I was soooo disappointed... Never thought I'd be sad because I couldn't have chemo...hmmmmm? On a good note though, I wont be sick for Easter.... But now my finish date looks like April 18th if everything gets back on track... Who else finishes in April? Am I the last one?
Happy Easter Everybody!!!!
Love and Kisses to All!
Jeannie
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I aplogize--I was confused when I wrote my last message--I thought wiw's message was from sal--they were right in a row or something...
I thought my brain was improving, but apparenly not.
love
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Hello friends !
Just got back from NYC! We celebrated my oldest (16) daughter's and my youngest (9) birthday by taking the whole family to see The Little Mermaid. It was AWESOME ! Even my son loved it !
I have been so emotional today. I think it is the birthdays and the Easter holiday that have made me more sensitive than usual. I have so much to be grateful for.....and now that spring is around the corner, OMG, watch out world ! Rebirth, and all of it's Glory...
I wish each of you a wonderful weekend........xoxoxoxo cindy.
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Hope Everyone has a Happy Easter today! LOL, these bald heads look a little familiar. Love & Hugs, Suz
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- 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