Starting Chemo in JAN 2007
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Hi,
Melia,
I am so glad you had such a great time. My oncologist told me I could get a rash. I started taxol on Thursday, one day after you. I will let you know if I get a rash.
Lynn,
I know what you mean about that "full" feeling. I have that also. I feel like I ate a Thanksgiving meal and wake up full also. I am also gaining weight now and did not before. I am even eating less than before. I do not get it- it is frustrating.
Rebecca,
Sounds like you had a great time last night. Today's barb-e-que sounds awesome also.
Skye,
Good luck with your last taxol tomorrow.
Phone is ringing- catch you all later,
Viddie -
Good Morning all:
Well it is really foggy here today, but hopefully the sun will come out and burn it off.
Melia, glad to hear you had a nice trip. It does sound like a s/e, but if the bendryl doesn't work, I would give the onc's office a call, they probably have something that can take it away pronto. No need to suffer.
TLC, I have been suffering with a bit of a fever since Friday, at least today it is gone, and now I'm back to normal. I have had this from the beginning of chemo, and I usually get it betweeen 5 and 10 days after chemo. They prescribed CIPRO for me. Skye, I think you are right about home thermometers, mine seems to register higher than the hospitals...by a few degrees....38.8 on mine 38.3 on theirs.
MizSissy, jealous of your eyebrows...that is what I want to come back soon.
Viddie, your comment on keeping in shape and now not enough to make the plastic surgery work, sure makes a person think.
I took different drugs to try to get pregnant, even tried the in vitro route to see if I could have kids, but all to no avail. Sometimes I wonder if I caused my own problems. The one drug I took 'danazol' put me into a pseudo menopause, and now they are saying HRT drugs also can cause BC. At the time, I thought I was doing the right thing. Also, sometimes I wonder if over the years I've had too many glasses of wine or one too many beers, but you know what, it doesn't do me any good now to go back and think like that, because I can't change it. Just have to keep plodding forward, and hope that my doctors now, know what they are doing.
Mary if find out the answer to the sun...let me know, especially what we are more prone to. PS...darn Red Wings.
Amera, I hear you on the comments from people. The florist lady at the Safeways here is one of my neighbours, and is always saying what an inspiration I am...gees...I'm here to get carrots, not conquer the world!!
Tina, sorry about your weekend. 12 years old is a tough age, and they actually expect everything nowadays, I think because in most cases they get it.
Nancy maybe your "loafer" stepson could help you with the garden, or run some errands for you, as all he is doing is laying around. Maybe you should take him one day to chemo so he can see how tough it is.
Rebecca...bbqs sound like fun, and you sound like you're up for it....have a great time.
Lynn, along with my dry mouth, I do have a bit of sinus problems, and it does sound like a clicking.
Hope everyone has a great day.
Hugs to all.
Joni
ps: Tae...I now have shiny red toes!! Hope you are feeling better!! -
Viddie,
Did your dr think a rash would be a concern? Obviously, since I am such a doomsdayer, I am worried that they won't let me finish the taxol. Oh, I just want all this behind me! Grrr ...
Melia -
Melia,
She just mentioned that a rash could be a s/e. I asked her so many other questions, I forgot to ask her what to do if I got a rash. I would call tomorrow anyway if you still have a rash just to let them know. They might be able to give you something stronger to get rid of it.
Joni and TLC,
I was told that we can get fevers when our WBC are at their lowest. My oncologist also puts me on an antibiotic also if I have a fever to prevent an infection.
Joni:
Hmmm: If I gain enough weight, perhaps I can have a DIEP procedure. But what if all my weight goes to my boobs instead of my stomach!!! LOL
Have a nice day everyone,
Viddie -
Melia, I can't remember when I got the rash, but I definitely got it from the Taxol - about halfway through, I think. So later than you. They just watched it for a few weeks - well, all the time, actually. It didn't itch except for one week, when I had intense itching and had to leave work it was so bad - that week they gave me a medrol dosepack and told me to take benadryl. Otherwise, nobody seemed to be too concerned. I had it on my arms, and then after the very last taxol I also noticed it on my legs too. No itching now, it just feels like I have dry skin that is irritated from the inside instead of the outside - that's the best I can describe it. My point is, I think the rash is fairly common with taxol, so don't lose any sleep worrying that they won't let you take your next treatment. They'll manage it if it becomes a problem.
Mel -
It's me again. Lynn, I wanted to tell you that I've also had the exact same feeling of waking up full (but hungry), and getting more uncomfortable when I eat. I don't know if it's just a sensation, or if I'm actually bigger, but I do have the feeling that I've just eaten a large meal. Of course, my weight is up a bit, but I think that is the swelling from the taxol. I'm certainly not eating much right now - if I'm gaining weight, I'm going to be really upset! I got all the way through to #11 taxol without gaining any weight at all - it wouldn't be fair to gain weight now that I'm done.
Viddie, I've heard two schools of thought on this, but some docs say there is no sense in gaining weight in order to qualify for a diep procedure because what ends up happening is that they grow and shrink as your body gains and loses weight. So if you gain weight so that you can have bigger diep breasts, and then lose it afterward, you will just lose the volume in your breasts at that time. Then again, other surgeons will have patients try to gain weight before the surgery, so who knows... I have a friend who is trying to gain now for her surgery.
Skye, congrats on having your last Taxol tomorrow - it's a great feeling to be done with chemo. As far as supplements go, I was taking a number of things before diagnosis, but even though my oncologist didn't make a big deal about it, I cut out everything except my calcium/vitamin D/magnesium when I started chemo, and added B6 in because I was worried about neuropathy - that was 100 mg. My onc said not to bother with the glutamine, so I didn't, although I bought some. I even stopped my multivitamin because it was a fairly high potency multi and I was concerned about the number of things in it which had antioxidant effects. I guess in a week or so I'll start back up on that, if it's ok with my PS, but honestly, I feel like I've gotten so many drugs poured into my system the past six months, and I don't want to take anything that isn't absolutely necessary.
Rebecca, I had to laugh at your comment about the word Ativan not even being WHISPERED in your oncologists office. It's not whispered in mine either! I must admit I've been a little jealous of the girls who got it, but it's probably better that I didn't have it because I would have taken it for sure.
Your comment about how we have had to cope with being diagnosed with cancer, and then on top of that had to cope with the end of treatment and all that goes with that was right on. I hadn't thought of it that way, but I have had a bit of an issue with that. It seems like I was just getting accustomed to thinking of myself as a *cancer patient,* and now suddenly I'm cut loose. Now what am I? I'm not getting treatment anymore - but when the wig comes off, and the makeup, I sure as hell look like a cancer patient! And finally, I FEEL like one, too. It's just confusing.
I seem to be talking too much this afternoon, but I'm not done so I'm going to post and then finish later. -
Ok, part three, then I'll shut up. Amera, I'm so impressed that you're doing step class. I know you've been trying to exercise all along...I did too, until the last few weeks, but from where I am right here right now, step class seems like a giant, huge accomplishment. Shuffling across the street to the mailbox sounds like a huge accomplishment. I hope one day soon I can do regular exercise again - but it seems so far away. Who knows, though - I may be feeling lots better by the end of the week, now that I'm off the taxol.
I also notice that the fact that I wore my wig all the time has changed my perception of my cancer journey, and also changed people's perceptions of me. I got very few of the pity looks, and not so much of the "you're an inspiration" type comments. I still looked like me, only the hair was a bit better. Now it's getting hotter, and I may be just wearing my scarves - guess I will have to be prepared for that.
Dar, I've also had more dark thoughts this weekend, all the what ifs have been visiting me. I think it's because this is the first time I've had a weekend to myself, and I haven't felt like doing anything. Working really saved me in a lot of ways - I was too busy during the week and then on the weekends I was both trying to rest up, and getting all my weekend chores done. I didn't have much time to worry. Obviously now I'm going to have to keep myself busy. Hope you're feeling better.
Joni, you and I finished chemo at about the same time. How are you feeling by now? I'm impatient to be better, I guess.
Mizsissy, even though I just wrote something above about not wanting to take ANY more medication, I think we have to realize that this is a very disruptive process we're going through, and we may need meds to get us through it. The crying and all that is normal, but it seems to me that this wouldn't be a good time to stop your antidepressants, and maybe you even need to be back on the Ativan, or something similar to replace it. I think this is what you would probably say to someone else if you were advising them, right? Maybe you're just expecting too much of yourself - you've been through a lot and have been strong for a lot of people. It's not so easy to just stop everything because treatment's over. Be good to yourself.
Well, I have to be at the surgery center at 6:00AM to get those *&%^$# tubes put in my eyes. I have a feeling I'm going to hate them, and I hate the thought of another anesthesia and surgical procedure (not to mention going in with no makeup or eyebrows or lashes) but I am SO ready to be done with this constant tearing. So, wish me luck.
Hugs,
Mel -
Amera, I finished chemo Mar.7. I don't have a full head of hair - just some of it is 1/2" long! Still tired too - good for you with the step class.
I go back to work May 9, and we're going to BC May 1-5, so really, I only have this week. My daughter, grandaughter and I are going to the zoo on Wed. A year from now (right before our Canadian tax deadline of April 30) I'll be telling a different story!
I guess that some days are just darker than others. Can't change the past or see the future, today is all we have. The sun has come out and I feel better - makes me wonder how much of my mood is determined by hormones and the sun! -
Hey Ladies,
Taxol rash: taxol can definitely cause rash, I didn't get one though til last week when I had Herceptin alone. Either way the docs want to know about it.
On the supplements, I just checked out a bunch of different papers on an NIH sub-page. Turns out there are conflicting studies on the use of antioxidants with chemo, but I think most now are leaning against using them. Most of the things I'm taking are not antioxidant so I'm not too worried (I'm going to cut out the C again however). However they seem to agree that antixodants gotten from the diet are not detrimental and there is no food that should be avoided (we can have chocolate!). It's the specific concentration in a pill that concerns them. So I'm going to keep drinking my cup or 2 of green tea as well. The antioxidant supplements that were specifically mentioned in most of the studies were vitamins A,C and E taken in pill form.
Interestingly, a woman I knew from college had bc a few years ago and she is married to a chiropractor who injected her with a LARGE dose of vitamin C every day. I thought this was excessive at the time and would never have wanted it for myself. But she's 3 years w/o recurrence so far.
Rebecca, Ativan, what's that? (tongue in cheek). It was never offered to me or mentioned at all. My onc said he preferred I take tylenol p.m. if I could get by on it so that is what I've done.
Dar, hang in there, remember you've got all of us, all in the same boat so we can take turns paddling. The dark thoughts always pass.... - Skye -
Quote:
right?
Well, I have to be at the surgery center at 6:00AM to get those *&%^$# tubes put in my eyes. I have a feeling I'm going to hate them, and I hate the thought of another anesthesia and surgical procedure (not to mention going in with no makeup or eyebrows or lashes) but I am SO ready to be done with this constant tearing. So, wish me luck.
Hugs,
Mel
Mel good luck with that operation! Is that for tearing you got from chemo, or a pre-existing condition? -
Mel, Tubes in your eyes? That's sounds awful! Is the tearing you are getting from the chemo? I've been lucky and not had any tearing at all. Hope all goes well tomorrow, we'll be thinking about you. Check in when you can and let us know how you are doing.
Regarding DIEP and weight gain. I asked the PS about this the other day. After my active treatment is done, I'd like to get back in shape. He did say that the fat the will become my boobs keeps it's memory, so if my loss of weight historically happened in my belly, then it would happen in my boobs as well. It also would mean the same if I gained weight. So after my treatment, I will work on getting back into shape, but not focus too much on losing tons of weight. Sounds like a plan to me.
I was working in my front yard today and one of my neighbors came over. We aren't really close and don't have much interaction except for the casual hello and chat when we're both in our yards. She found out about my bc from my other neighbor a few weeks ago and sent a card. I thanked her for the card and she couldn't get the 'you look great' and 'you'll be fine because of your positive attitude' out fast enough. So I'm standing there trying to chat with her, my nose is running like crazy and all I can do is wipe my nose with my wrist and arm hoping it's not too noticable and what is she doing the entire time? RUNNING HER FINGERS THROUGH HER HAIR..NICE!
We decided to watch the SOX/YANKS tonight and watch Sopranos tomorrow On Demand. A sweep would be nice, GO SOX! -
Oh and regarding the Ativan. My Onc didn't offer it to me either. I did ask for it to supplement with the Ambien I already had prescribed for sleep. He only prescribed me 20 tablets with 1 refill. Right before tx #4, I had to see a different Onc in his office because mine was on vacation. We were discussing my bad nausea from #3 and he asked if I was taking Ativan. I said yes, but only at night. So he goes on his computer and sends a script to the pharmacy for 30 pills with 5 refills. A bit different than what my Onc gave me. Different opinions not only in different offices but within the same.
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Quote:
I took different drugs to try to get pregnant, even tried the in vitro route to see if I could have kids, but all to no avail. Sometimes I wonder if I caused my own problems. The one drug I took 'danazol' put me into a pseudo menopause, and now they are saying HRT drugs also can cause BC. At the time, I thought I was doing the right thing. Also, sometimes I wonder if over the years I've had too many glasses of wine or one too many beers, but you know what, it doesn't do me any good now to go back and think like that, because I can't change it. Just have to keep plodding forward, and hope that my doctors now, know what they are doing.
I feel the same way. I took birth control pills early in my life and then later when I had problems with my period. Now they say lobular cancer is related to HRT. I also took fertility pills for a month to have my second son (although I don't regret that) and I have been known to enjoy a drink or two! So I feel the same guilt but all we can do is go on. I just wish drs would let their patients know the possible harm of the drugs they are taking.
P.S. Going to try to stay up for the Flames/Red Wings tonight but it's going to be hard getting up tom for work if I do. -
Hi all,
Thanks for the info/reassurance on the taxol rash. I just want this over with, don't want treatments delayed!
Re what we could have done differently: this is the way I look at it. It's like car maintenance. You check tires, brakes, get it regularly serviced. Then one day you are driving along minding your own business, and there is a rock or piece of glass in the road and your tire blows out. That's what happened to us. We need to make the repairs and move on. We didn't do this to ourselves, we were just living our lives the best we knew how. Sure, maybe we coulda, woulda, shoulda. But who knows if it would have made a difference?
Melia -
I never got a rash on Taxotere but in the last 4 days my upper chest and lower neck have darkened. My daughter was over and accused me of being dirty from playing in the yard with the dogs.
I can't quite tell what's happened. I think it's happened over an area where I had some sun last summer. It's pretty noticeable. I'll have to show the onc. when I see her on Friday.
Cindy -
"Your comment about how we have had to cope with being diagnosed with cancer, and then on top of that had to cope with the end of treatment and all that goes with that was right on. I hadn't thought of it that way, but I have had a bit of an issue with that. It seems like I was just getting accustomed to thinking of myself as a *cancer patient,* and now suddenly I'm cut loose. Now what am I? I'm not getting treatment anymore - but when the wig comes off, and the makeup, I sure as hell look like a cancer patient! And finally, I FEEL like one, too. It's just confusing."
I think you ladies are singing my song. We need to start a choir!
Having a foot in both worlds is so difficult. I wonder which way I'm going to slip. The good Lord knows I don't want to go backwards but it is a quandary how to claim a new position.
I never dreamed ending chemo treatment would start these questions in my mind.
Cindy -
May your last treatments be smooth and uneventful!
Cindy -
Hi Gals,
Checkin' in for the evening. Most of you are getting close to end of your treatment and on to the next phase, and wondering about the transition. Before I became a member of this group I posted all over the support site and got responses from women who were much further along than we are, and they said they liked being "in treatment." It made them feel safe, like they were doing something.
I took a Zyrtec last night and slept like a log...but it was kind of a drugged, foggy sleep. I think it helped break the pattern. I didn't dream as much as I needed to..I think what is really necessary in sleep is to dream and let your mind drift illogically, which my mind just won't do lately. But I feel very tired and relaxed like I'll get a good sleep tonite w/o drugs.
Spent part of the day outside raking and doing spring cleanup which is amazingly exhausting. I kept on having to take breaks from the heat and come down here to the basement to cool off...my hands were trembling very strongly, is this a taxotere SE? After I cooled off the shaking would go away.
Mary, I don't know about you but I have no doubt my cancer was the result of taking synthetic hormones. I was really overexposed, (1) to DES in the womb, which my mother said she took by the handful, (2) to lots of infertility hormones in a vain effort to get pregnant, and (3) birth control pills, early and late in life, to control periods (4) HRT up until the time of my dx, which included testerone, estrogen WITHOUT progesterone for a few years (which I found out is a no no). This is good & bad, because I wonder if all I needed to do what get off all the phony hormones to disable the cancer.
Skye...I am not very up-to-date so I don't know why you are getting tubes in your eyes at 6 am tomorrow but it probably sounds a lot worse than it is!! Good luck!!
Mel...I do think I need the antidepressants now..I hate to give up my prozac for tamoxifen. Maybe I should consider the AIs, though I hate the thought of dealing with bone loss.
Mizsissy -
Quote:
I took different drugs to try to get pregnant, even tried the in vitro route to see if I could have kids, but all to no avail. Sometimes I wonder if I caused my own problems. The one drug I took 'danazol' put me into a pseudo menopause, and now they are saying HRT drugs also can cause BC. At the time, I thought I was doing the right thing. Also, sometimes I wonder if over the years I've had too many glasses of wine or one too many beers, but you know what, it doesn't do me any good now to go back and think like that, because I can't change it. Just have to keep plodding forward, and hope that my doctors now, know what they are doing.
I did everything right and still got cancer, so don't beat yourself up for what you might have done, it's all really what's meant to be I figure. I have never done drugs, no birth control pills, very little occasional drinking, eat healthy, no smoking, no family history, have a child, stared my period at 16, etc. Whoda thunk I would get cancer?? Not me!! But it was my spin in the game of life, so here I am. I do find it ironic though, that the one thing I did do was HRT after a hysterectomy at 41, and I ended up being triple neg, so that's not even a factor.
I guess my point is we can't beat ourselves up for what we may have done to contribute to our situation. We do however need to get better and pay attention to the knowledge we've gained in our journey.
It's not the "what" that matters as much as the "what now?"
Peace to you all,
tlc -
Hi Guys,
So many posts. I think I'll get up tomorrow am w/a big cup of coffee and see what you've all been up to. -
good evening ladies-
I've been in chemo fog for most of the day - wow, it hit me hard this afternoon - slept for about 2 hours this afternoon, woke up a bit dizzy - and I think my tastebuds are finished - YUCH!! I've been laying on the couch for about 4 hours, watching some old movie musicals - hokey, but about all I can handle today.
I hope everyone is doing okay, just glanced through the posts, too out of it to really comprehend much... I'll try tomorrow... -
The eye tubes are called Crawford tubes - they are usually put in babies. My tear ducts are almost totally blocked from the taxol, to the point that if they aren't opened up now I could be stuck with the tearing problem for the rest of my life. So, I have no choice but to do the tubes - they'll stay in for a while and then be removed in the office, or possibly they can fall out unintentionally (but I hope not). Anyway, I'll take all your wishes for good luck tomorrow.:)
Hugs,
Mel -
Mel, a friend of mine, non-cancer, had those tubes put in last year so it isn't just us. I still have that tearing with the Taxol but it's better than it was with the AC. At least it stops sometimes. I just assumed it would go away after the Taxol ended. Do let us know how that goes.
I'm another one of those who figured I should not have gotten cancer but Melia's comparison to car maintenance and then hitting a rock is a good one. Whatever thing we can think of that we may have done to blame ourselves, whether birth control or having a few drinks or whatever, think of all the millions of women who took more pills or drank harder and never got cancer. There just isn't an obvious rhyme or reason, hard as that is to accept. The only risk factor I had was age, although recently a study came out saying "dense" breasts (which I had) increase your risk. But that was just my body design, nothing I did to make them that way. One of my neighbors sort of smugly informed me she wouldn't get breast cancer because she had breast fed her last child for a while. I felt bad telling her I nursed my two for 11 and 6 months, respectively. Evidently someone forgot to tell the tumor!
Heading to bed soon so I'm well rested for my four-hour Benadryl snooze tomorrow. At least I'll know the onc staff is well fed on fruit and cheesecake while I snore through my final Taxol infusion. - Skye -
THank you for your kind words, ladies - you are awesome. My daughter and grandaughter were here for a few hours - nothing like a 2 year old to keep you in the present.
As to the "why" we got bc, we may each have our theories that apply to us personally, but many others with the same risk factors - be they fertility drugs, hormone treatments, weight, drinking, etc - do NOT get bc, so who knew? I had my first child at 19 - that should have reduced my risk, but apparently not enough. Maybe if I would have had a child every 2 years for 30 years like my great-grandmothers...
Good luck tomorrow Mel - hope it helps.
Rebecca, you are right on about it being a big transition at the end of treatment. Being diagnosed was much worse, but this transition at the end may take awhile. -
Quote: Maybe if I would have had a child every 2 years for 30 years like my great-grandmothers...
No that wouldn't be the answer. My SIL had 10 children, 1 to 2 years apart and 16 years ago had breast cancer. She is still alive and well! And she breastfed her chldren. I agree, there is no rhyme or reason for this. My point is though that the drs should tell us that birth control pills or infertility drugs CAN increase our risk.
Off to work, 8 more days to my surgery - but who's counting?
Joni, sorry the Flames lost, I couldn't stay up but I heard it was a good game.
Good luck Skye and Shorti. Hope you feel better today Caya. Jan - where are you? -
Skye,
Congrats on your big day today!!! -
Post deleted by TPPJ
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Quote:
With my thin light eyebrows and the few lashes I really remind myself of Lord Voldemort from the first Harry Potter movie.
MY SIL PUT COLOR ON MY BROWS YESTERDAY TOO...I WAS A LITTLE AFRAID THAT IT'D BE TOO HEAVY. WRONG. APPARENTLY NOT ONLY ARE MY BROWS JUST SUPER LIGHT/FADED COLORWISE, BUT THEY ARE A LOT MORE "GONE" THAN I REALIZED. WHEN I PUT THE COLOR ON THEM I COULD SEE ALL THE BARE PATCHES. NOW I HAVE TO FILL THOSE IN W/PENCIL. -
Lynn,
Had a massive sinus thing going on while on Taxol. Blew my nose for weeks. It would be bloody. Constant drip too. Happy to say that's gone.
And the fullness thing. If I ate just one bite more than I probably should have, I'd feel like I'd explode. I attributed that to my TRAM flap scar though. That fees like I have a rope tied tightly around my middle...and if you eat too much....you just feel awful. -
Mel, good luck with the eye tubes; I will be thinking of you. And Skye, the LAST ONE. Good for you. We will all get there. Have a good day ...oh, and by the way, re the antivan. I had thought that I would ration them, cut back, etc, then decided one each evening is maybe what is getting me through this. I rarely have trouble sleeping. When it's all over, I will deal with any withdrawal, weaning off issues. Right now I need a crutch!
Melia
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