2012 sisters
Comments
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I got nail issues from AC i suspect, although the brown pigment around nails came first, then the lunates disappeared and then some redness and tenderness occurred while on taxol. It has made it hard to do several simple tasks. They ache now, dont seem to be loose and none have fallen off.
I was clued into the nail issues on this site, so wasnt surprised. I can see some normal nail growing also. Others have had nails fall off, so you may want to baby them a bit. -
Wow bev...sorry I seemed to have struck a nerve; and I totally agree that out health care (or lack thereof) is crap! I have a PILE of copays, etc my table and honestly just don't give a fuck right now. They will get paid slowly over time. There is no interest and they aren't going to put the cancer back in me.
I know you've had a totally horrible time since your surgery and the fact that you have to go bankrupt to pay for this glorious experience just adds insult to injury...literally!! I am sending you some BIG HUGS and keep my 2 cents to myself. What the heck do I know anyway. I'm not a Dr (who had to go bankrupt to pay for their education!). You're right our system sucks!
(btw just because written words dont always come across as spoken in my mind FYI I am not being sarcastic in any way.) -
OMG, juneau, you mistook MY words.... If I came off as sounding pissed at you, I 100% absolutely was not. If anything, I was pissed off at our insurance system that makes someone have to worry if they might have to wait a month longer for surgery. I was pissed off because my PS, who saved my life not once, but twice (with the emergency surgeries) and who I love dearly, does not take my GHI insurance but they do submit, then I get the checks and give them to him but I'm in to him for $1,050 as of now and because of my open scar more than 2 months after surgery, I still have to go to him all the time and the latest is I'll probably have to go to a wound doctor and get a wound vac. So, if I sounded pissed off, it was just me venting and letting off steam and getting all political which I'm known to do all the time (you should see my facebook page).... You had a definite point. Get the surgery and fuck the bills. I was just saying a lot of doctors don't seem to be in a big rush and if she could avoid the aggrevation of the bills, maybe she should look into it. I was NOT NOT NOT NOT mad at anything you said. Please, you're going through enough crap on your own. I was just giving another perspective and venting at our insurance situation here and my situation in general. I am extremely sorry I made you feel bad for even one minute. xoxoxoxoxo
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Bev: it's all good. I knew it wasn't directed at me personally. :-) we are ALL going through enough crap... And that's what we are all here for, to go through it together so by all means vent anytime you may need (I sure will)!
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Bev the friend of your son with the testicular cancer, that is so sad to me that a young man like that has to go through the spread and now chemo. It really struck a cord with me because he's close to my sons age. They think they are so invinsible at that age.I could see where they might even ignore symptoms. Dang I'll say a little prayer for him.
Juneau Nice to see you on a little more this week ranting or not-lol Damn chemo you have reason to rant and whew-there is no way to sleep comfortably with the coconut shell is there!
Hope everyone has a nice weekend-try to take a mini mental vacation from this friggin BC !!!
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Hey everyone. Welcome another woman to the fold: diagnosed July 19.
I've written a lot about my story on my blog, but speaking out isn't the same thing as speaking with. I hate that we have this thing in common, but there it is.
I've just started the journey and the game plan is to take Tamoxifen for 16 weeks, have the lumpectomy, and them chemo. I could have reversed and moved the pieces around, but my surgeon believes that once the tumor shrinks he will be able to offer me a much better cosmetic result with the lumpectomy. You know, on one hand I say "I dont care," but on the other hand I say, "Eff you cancer. You're not going to make me wonkier than I need to be."
Choices. Always choices. I just keep thinking: a year from now this will be behind me. And I sincerely hope behind me forever.
Wishing you all nothing but the very, very best.
Scorchy
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Bev, get the wound vac. It worked miracles and there is no packing involved as the medical staff has to do it. Only had it 3 weeks and it was amazing home much I healed. My incision opened completed up due to a hematoma.
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Welcome Solteria and Scorchy, sorry you are joining us
Ramols - I smiled when you described rescuing your kids from your father who was teaching them to fly paper airplanes out second story windows. How was your MO visit?
Tazzy - sorry to hear about the infection and that drains are still in, glad you have your Zen spot to retreat to, hope you have a good weekend in spite
Juneaubug - I feel like you are just a few days ahead of me in your chemo journey, good to see that things are getting better for you.
McCook - hope you can relax and enjoy the weekend, never thought I'd say this but most of the time don't give the missing boob a second thought, too busy dealing with everything else and know that eventually, if I choose to, that I can have reconstruction. Thinking of you.
Bev - hope all things wound related resolve quickly, sounds like the wound vac may be the way to go
Jpmomof3 - I was thinking of you during your shift yesterday, hope it wasn't too busy or exhausting for you
I found myself exhausted yesterday and finally succumbed to it. Tried a walk with my husband and only did about a third of the normal route, yawning frequently throughout. Went to bed at 08:30 and only up for bathroom breaks twice, slept to 08:30 a.m. Feeling a little less tired this a.m. but not looking to jump any buildings in a single bound. This afternoon we have been invited to a neighbourhood barbeque so I will pace myself this a.m.
Hope you guys realize how much your posts mean on both the good days and the not so good days.
Take care, everyone -
Websister, I just have to say I love your posts. They read like stories, and bring me peace. I did not have chemo, only radiation, but the pictures you paint apply to all of us. Hope you have a great time at the barbecue, and that your fatigue lifts.
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I agree, we have amazing stories and great writers here.
I am doing ok healing wise, still weirded out that I look so ....I guess the weird is wiped out when I wake up. Al,ost 2 weeks post exchange. Hard tI think my body will be my real partner ever again. Sigh. Well, my new wig looks better than my old one that had a Crisis. Off for a walk to get coffee and try to perk up. -
PS took off nail polish, and boy do my nails still look all the colors of the rainbow. Put a coat back on! Sensitivity comes and goes: example cannot put necklace on this morning, can't do the clasp./p>
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Hi Everyone
Been lurking for a few days. Some good info some that is scary to me. My readers digest story... dx dec 2011, ovectomy then mastectomy with TE installed this past March. then a break until quite a few weeks of radiation, didn't know that radiation could have such a bad effect on the final results.Finished the radiation, making regular visits to the ps for expansion,ps wants to make sure he has plenty of material to work with, so hopefully I will only have one more fill then will have the implants put in. I am really looking forward to getting the bricks off my chest. Currently on tamoxifen and going thru my second round of hot flashes and night sweats. Took a day off from everything yesterday and went to the beach, that was the best treatment I have had since this thing started.
So glad I found you guys.
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Soltiana, Scorchy, sorry you have to be here, but welcome. So much going on in this thread, hugs tovall. Much love.
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Ditto, welcome. If we have to do this at least we can share here.
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SO MANY NEW 'FACES'... That just SUCKS!!! I hate this fucking disease; but welcome one and all.
Websister; I had the same thought regarding our chemo start dates; but you're already sleeping... How I envy you. :-) get some extra for me would you?
CharlotteNY; I feel you.... Literally (damn coconut) and holy shit in the night sweats from chemo!! I have changed my shirt THREE times per night since I started last week. I used to get them when I had my period but never this badly!! My pillow, clothing, hair (which won't be an issue soon) SOAKED! Shit, SHIT!! 44 years old with night sweats and Tomoxifen induced hot flashes to look forward to. Did I say SHIT!?
(if cursing offends you then you should not read my posts btw. Sorry but it's just how I express myself, I'm not always a gutter mouth but I find this disease brings out the best in me!).
Scorchy; I hold in to the year from now thought too... In fact I was trying to explain how I've been feeling to a very close friend today and said I look in the mirror with my one breast gone big, hard and round and other sagging happily one the left; my short hair ( I cut it off 2 weeks ago from below my bra strap) and feel butchered up by this experience and I just want to Look on the outside like the me I still feel on the inside.
A year from now I know I will hopefully start feeling like that woman (although forever changed) that I used to see in the mirror. Sexy, beautiful and serene. Right now I feel like transsexuals must... The outside and inside just don't match. I want to be able to walk confidently that I'm beautiful and smart.... Yadda Yadda Yadda, BUT I'm just not feeling it when I look in the mirror and see a strange body staring back at me.
So anyway, I didn't think I was explaining my feelings to her very well, but she said I had explained it beautifully.
I too and am to a BBQ now. Try to enjoy some of my life. That is why I am fighting this BC with everything I've got; so I can LIVE not just exist. I forget that somedays. So Just for Today I am going to go out there and live and laugh and love. Just for Today I will try to get a better perspective on things. Just for Today I will not let cancer fucking win.
Hugs to you all! -
2fried - you cracked me up with the visual of braiding your arm hairs. We went to a pool party today and I had my hubby try to help me out with the electric razor to see if he could make any more progress than me. No go... I'll just have to wait for it to all fall out during chemo.
Mcook - hope you're having a good time this weekend and can forget some about what is coming up. Not sure if you're opting for any kind of reconstruction as part of your surgery. But I can tell you that I debuted my TEs (with 3 fills now) in a bathing suit this afternoon and felt pretty darn good. I could see the scar from my left side peeking out a bit from the side of my bathing suit top - but I think I'm the only one who would have noticed it. And while I felt slightly self conscious - because I knew what was really going on under my suit - I didn't really spend any time thinking about what was really missing under there. I don't think I'm explaining it too well... But I think the point I'm trying to make is that as much as I thought I would miss them - I don't. They were cancerous. So good riddance I say. I know we are all different and have different levels of
attachment though. So I hope you can find some peace before Thursday arrives.Tazzy - sorry to hear about the infection and the drains remaining. Hopefully that will all clear up for you sooner rather than later. Try to enjoy your weekend!
Bevg49 - every time you share more of your story I want to reach out and hug you (and smack your doctors - even though you say you like them). I hope things start getting better soon!
Jpmom - hopefully you get some good rest after your long work shifts, and are feeling good!
Websister and Juneau - hope you're feeling a bit better. I won't be too far behind you. Have to wait for the schedule to be finalized, but it's looking like 8/29 will be my start date. 4 rounds of AC, followed by 4 rounds of taxol, with the herceptin
worked into the taxol rounds. I loved my MO and her nurse - both lovely. Lots of info to absorb - but nothing I wasn't expecting to hear. Will hopefully get my MUGA scan done this coming week, and get this show on the road the following
week. My anxiety level seems to have calmed a bit and I feel oddly energized. Ready to grab this next phase by the horns and obliterate any troublesome, sneaky bastards that might have escaped my surgeons reaches.Oh - and the nurse confirmed I do in fact have cording and gave me a prescription for some physical therapy. Argh! Just what I need - more appointments to eat into my days... This cancer crap is so darn time consuming!!!
To all of you new ladies who have joined us - everyone says it, because it's true: I'm sorry you have to be here but we welcome you with open arms. You've come to the right place. Here's to hoping for a restful night sleep for everyone and one more lovely day this weekend. Sending bigs hugs to all of you!
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ramols -- boy do I second the "cancer is time consuming" I swear I've spent more time working on my freedom from cancer project than I did on my masters degree.
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ramols, thanks so much for what you said.... I need a hug
.... lol.... I sound pathetic and feel that way some time. It's funny you say yoiu wanna smack my docs. I have friends who say the same thing, like there has to be someone to blame for all this. Truth is, I don't know if there is or isn't. PS was there for me every second. During the 2 emergency surgeries, I believe I came close to "the other side" once or twice... He was there every morning at 7:30 like clockwork. He was there within 20 mins. both times I needed the surgery. He was in recovery at 10 p.m. after the surgery when I was soo very bad off. He was ther 2:30 A.M. to check then 7:30 for rounds. Did he do something wrong? Did the BS? I'll never be able to figure it out but shit happens and mistakes are made and I can't let myself think about it. Before I stopped working I worked in law offices as a paralegal. People are too litigious. That's why docs can't get malpractice insurance and part of the reason why we pay through the nose for our insurance. I don't know what caused me to bleed and I don't know why my scar opened and won't close. I do know it sucks a lot and I'm just trying to be patient...Oh, and I also have an appt. this Tuesday for PT. No LE thank God and no cording but range of motion sucks according to BS.... Well, she didn't exactly use the word "it sucks" but you get the drift hahaha....One more thing, have you noticed that we have so many New Yorkers here? Scorchy and charlotte both new ones... Welcome to the club no one wants to join, ladies. Where in NY if I may ask and where are you being treated? I live on the Queens/Nassau County border and had all my surgeries (haha) at North Shore Hospital.... My BS, PS, now PT are all in Great Neck, NY....
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Bevg49,
Cancer is such a punch in the throat. Throw in some complications as a garnish and it's a party! Lordy, I hope things settle down for you and soon. I can empathize with your desire to be patient and not necessarily assign blame. It's a difficult time.
I'm being treated through the Comprehensive Breast Center out of St. Luke's-Roosevelt on 10th and 59th. Paul Tartter is my surgeon and came highly recommended across the board. I'm impressed with his record and I like his no-nonsense yet friendly manner.
When I moved to Manhattan from Southern New Jersey (Haddonfield) I worried about health care. I figured with so many people here getting a doctor would be a nightmare. But I have the best health care I've EVER had here in the city. My internist, gynecologist, et. al. And when I learned that the boob was askew I counted my lucky stars that I was in NYC with some of the best physicians in the world here. I wish everyone had this access.
Now that all of the initial insanity of diagnoses, tests, etc. is behind me, I find that it's been a lot of hurry up and wait. Now I wait for the Tamoxifen to start working. An exercise in patience if there ever was one.
Scorch
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Juneau ,ramois,Bev, Cindy - yes to all you said. I was feeling waa waa tonight, my incision had a tiny bit of pinkness above it tonight, I did wear a diff (and awful) bra I will never wear again (sports bra post exchange 24/7 but I only had one so I bought another one, turned out to be too tight and flat but it is hard to find something that fits.) i called my PS. He said probably just surface irritation from bra but to start antibiotics again. I called pharmacy, they are closed!!!So I hope it us nothing and tomorrow is soon enough. DH out of town.
I went to a b-day party of someone from work. First party since summer started, me and the wig. It was fun but there us that underlying surreal feeling. Is this me? Where did my body go?
I think Ativan will be my friend tonight. -
lisa, hopefully it's just an irritation. I have something like that under the scar site. It's pink/reddish and very painful. The BS says it's probably from the tape since I have to be bandaged every day. I also wear a sports bra over the bandage so it could be that too. I hope yours turns out to be nothing serious. My doc told me to use bacitracin on it for now. I know what you mean about the surreal feeling. I look in the mirror and I just wonder what the hell happened? I know so much I didn't know at all a mere 5 months ago - stuff I wish I didn't know. Ignorance is bliss -- until you get cancer....
Scorch - you are so right. There is no better care anywhere than what you get in Manhattan. I just wish it was available to all but that's another story. I get pretty good health care out here at North Shore/LIJ but it doesn't match what you guys get in the city. It's funny, before my original surgery, a friend said I should go to Sloan to get the best of the best care. I figured this was just a very routine mastectomy/reconstrution so I'd be fine at North Shore.... Ha Ha.... Was I fooled.... There's been nothing routine so far.....
Sending good vibes to all of you good ladies !!
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Yeah California, it's hard to find bras that work... and other clothing too. Basically, nothing that I wore before cancer fits well now. I've lost about 25 lbs, a good thing, but, all of my weight is coming off my waist and but. I've lost 2-3 pants sizes. Again a good thing, but I need to replace everything. My top half is another story. Bras that I wore before my lx are still 2-3 inches too small. I'm still so swollen on the surgery side. Both front and back. As for the tops, well, they are tight on the surgery side, and loose on the non-surgery side. If they have sleeves, the sleeves are too tight, especially on the surgery side, but also on the non-surgery side. Gah. I need all new bras and compression type garments to try to get the swelling under control... I'm hoping cooler weather will help with that.
Then there's all the emotional stuff, including stuff that has nothing to do with cancer. We are in the midst of a dispute with a newly former employee. Ordinarily, I'd leave that sort of thing at work, but he's been on my mind all weekend and it's really torking me off. Must put him out of my mind or, I'll never get to sleep tonight.
Bah.
Well I'm headed for bed, it's late here, almost 9:30! Yawn.
Rest well everyone!
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bev - I'm glad to hear you're at northshore (truth be told i was afraid you were going to say you were at Flushing hospital...
. I had my first son at northshore LIJ and was really happy with our care there. I feel really fortunate that my Dad works at Sloan and that I live close enough to access them - not to mention being only 20 minutes away from their Commack center where you can do all your follow-up post-surgery. Where in Queens are you? We lived in Whitestone for about 5 or 6 years and had our first son there. Not sure how my husband managed to get me out to Suffolk County - Jersey girl that I am. But I have to admit, I really love our little pocket of LI out here in St. James. And the former City girl in me can still walk to the supermarket and local drug store, as well as the LIRR for the days I trek into the City for work. Yet I have all the wonders of suburbia at my fingertips. Nice middle-ground. Although - ever since I got the BC, I joke with him all the time that he moved me out to LI and bam - I got breast cancer...
lisa2012 - heres to hoping that irritation goes bye bye real fast. Enjoy that Ativan. I might dip into my xanax bottle tonight...
And to those of you who have been pondering the medical alert bracelet - mine finally arrived in the mail today. I have to say - I actually really like it. And it kind of feels like a badge of honor.
Nighty night beautiful ladies!
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Juneaubugg you crack me up! I'm a born again Christian, and I try
not to cuss, but who wouldn't going thru all this crap?!?!
I went to the Ohio Concealed Carry Course today. IM CERTIFIED!!! Just wish I could shoot cancer's ass!!!
I read that the most common age at diagnosis is 61, which I am, but most of the ladies on this site are so much younger than me. Even some in there 20s.
We've been praying for the brother of a man in our church. His name is Jim. Family kept telling him to get the spot on his face checked out, but he kept putting it off. It turned out to be cancer. He has surgery on aug. 31, and they have to remove one whole side of his face. I was looking in the mirror a week or 2 ago, thinking about mastectomy, and I told GOD, " I'm feeling down because Im about to lose a breast and this poor man is about to lose half of his identity." I grieve for him, but I still grieve for my breast too.
Have a restful night ladies. Thanks for caring.
Paula -
Wow, we need an Greater NYC get together by Christmas. I'm one hour west of the city. Not sure how I ended up this far west. I grew up 20 miles further east in Parsippany... Just go over the George and kept going. I spent almost all my nights in the village from 16-19 then moved to London and Boston. Yet here I am in West Bumblefuck! LOL! I thought about going into the city for care and like Bev thought it would be simple. Glad I didn't now. Id be drained financially, emotionally and physically from the commute!
Morristown has a pretty new cancer center and they've been amazing. My friends father is a recently retired RO and hes directed to the best of the best their. I'm really happy with my care. Isn't that the mist important part?
But I got my education HERE. All the experience and information we share empowered me to ask the right questions to MANAGE MY OWN HEALTH CARE. This disease gives us so many damn choices... It's a gift to have so much information and support as I have found right here in this "room".
I have grown to count on each of you to be there when I check my phone and need to vent or know that someone out there is struggling too and it's not just me that has been selected to travel through this.
So I'll just say goodnight, I am grateful to you all...
Hugs... -
And Cindy, the last thing I feel like doing is shopping!! Hugs to my east coast buddies!
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To Soteria and any one else who takes offense at curse words for religious or any other reason, like Juneau, I get relief and even pleasure out of talking like a truck driver now and then, especially when it refers to something as disgusting and distasteful as the freaking (I controlled myself there, typed the rea but was thinking u) trials and tribulations of breast cancer. I apologize in advance for offending....
Ramols, I live RIGHT on the Nassau County border, 11 blocks from LIJ, in Bellerose which is partly in Nassau and partly in Queens. I live on the Queens side. I've been out your way a ton of times, Ramols... One of my very best friends lives in Commack and my son lives in Plainview (west of you, I know, but Lon Giland is Lon Giland....Juneau, I'm very familiar with Jersey too.. Lived in Toms River during my first marriage many moons ago. Have cousins in Marlboro and Teaneck.... I spent a good part of my misspent youth in the village also. Those were the days! Way before you girls, in the '60s.... Oh, to go back to the '60s now.......
I had my original mastectomy at Long Island Jewish then when I was rushed back with the emergency stuff it was to North Shore because my surgeon just happened to be doing a surgery there at the time I needed him. So I was at both places recently and I do say, the care was good. Knowing what I know now with all the stuff that's happened, I think I'd have gone to Sloan but hindsight is 20-20 as they say....
Have a great night, you good ladies..... sending those healing vibes....
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Loading dose of Herceptin at first TCH took an hour and forty five minutes. I have Herceptin weekly for the first 18 weeks. They say 45 minute infusion when it is Herceptin alone. Thats not bad. Just enough time for a catnap!
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This is a great website! I was just diagnosed about 3 weeks ago and I am sure I will be on this board a lot.
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Welcome to all the new folks here! Sorry for the reason but know this is a great bunch to share, vent and kick cancer's ass (KCA) together! I am up at 4:30 AM with allergies for second night..sneezing my head off, waiting for the zyrtec to work. First place I head is to these boards...SO GLAD I HAVE YOU ALL HERE!
Soteria25..I'm a fellow Buckeye...son graduated from OSU last year. O..H..
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