Is There A September 2011 Chemo Group?
Comments
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Thanks, Belle. Hope your labs come back good and you enjoy the nice day with your DIL.
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Good evening ladies! Hope you are all doing well tonight. Just got off work at the store. Had a great evening and trained a new girl! Whoop! Whoop! Finally I don't have to feel so bad about not working some of my shifts.....we have relief!
Well it's chemo day for me tomorrow. Looking forward to seeing the nurses and lab personnel again. I have such a good time with them! They like to cut up and laugh a lot and that makes me feel so much better. They try to make it a fun time and not so depressing. I fit right in!! Can't wait to see what new friends I will meet tomorrow or maybe see some that I have already met. Will not have to go back to work. Got my route covered for tomorrow. Trained a new sub and she will be driving for me tomorrow. No school Friday and that's a good thing. Will have to go back to the big city to get fluids and my neulasta shot but at least I won't have to worry about rushing back to drive the bus. Yeah!
Hope everyone has a wonderful day tomorrow. I will be back when I can. Carry on my friends! I'm counting on reading some good stuff when I get back here!
Hugs!
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NanaDeb, Maggie, and RJ - I feel like we should throw bon voyage parties before treatment. Safe travels. We will miss you. Come back soon. RJ, glad you have some subs trained to give you a little more wiggle room for taking off for treatment.
Belle - Fashion- challenged. I love that description. Me too. I used to wear a dress every day to work. Now that I work out of my home for the last few years, I haven't been out of my sweats or shorts except for a few occasions. Boobless, hairless, and wearing sweats is not a look anyone is going to want to copy any time soon.
CJRT - So sad to hear about your friend. Weird though, isn't it, two friends and both at such a young age. The two of you are going to have a special bond now I would think. I know I found it helpful to ask my sister a lot of things when I was diagnosed. I'm sure you will be able to be a great help to her, being that little bit ahead of her on this journey.
SCPMadi - Congratulations on living in Canada. There are times I get so disgusted with the way things are run living here that I think "That's it....I'm moving to Canada!" On the subject of BRCA, I did not check into it because my sister had already tested negative, I have no kids, my uterus and ovaries were already out, and I was having both breasts taken off anyway. Obviously, there was no need for me to check BRCA. They used to suggest testing for people based on family history, age of onset, and other risk factors. I think now they are seeing more of a connection between the triple negative cancers and it is becoming more routine to test that subset too. I sure don't know what to make of "undeterminable" aspect of your pathology. Maybe if you gave the whole statement surrounding that it would make more sense.
For me, tonight my sister is dragging me to some breast cancer financial planning seminar I guess you'd call it. I guess it is her way of nagging me to make sure I have some funeral arrangements planned and paid for, will in order, POA, so on and so forth. What fun this is going to be. Can't freaking wait.
I was at the grocery store after labwork and the lady who was packing my groceries sneezed in her hand and then packed all my groceries. Sigh. Thank god my white count is back up per the labs. Can't live in a bubble I guess. I would like a t-shirt that says "I'm on chemo, don't sneeze on me" "Keep your snot to yourself." I don't know how people with kids or working with kids do it without being sick all the time.
Belle - About double mastectomy, the pain was not too bad. Actually I think chemo has been worse for knocking me down pain-wise and fatigue-wise, although I was napping a lot after surgery too. I did have 4 drains that were in forever, 5+ weeks, and these limitations on activity that were hard to live with. I sure hated those drains hanging off me. At least it's cooler now and you can hide them under heavier clothing than I could. BS kept telling me to limit my movement and activity because the drainage wasn't slowing down. I was talking with my hands in their office and they were exasperated with me "See what you're doing? Don't do that." Oy. I should say that my drains were in for an unusually long time, way longer than most people. Chances are good that you would not have the same problem. I also did not have reconstruction, so had less pain than the ladies with flaps or tissue expanders, so your mileage may vary on the pain thing.
Maggie - Glad you're brother-in-law is OK. It's OK to feel resentful at getting cancer when you have been taking care of yourself. Although she never said it out loud, I'm sure it bothered my sister when she got breast cancer and I had way more risk factors than she did. In the long run, despite my smoking, drinking, lack of children, I was diagnosed at the same age as her. She also resented getting cancer before 50 when our parents smoked and drank heavily and lived to their late 60s and early 70s. The way she said it was "I expected to get at least as much time as them, and probably more." I sometimes wonder now if mom would have gotten cancer if she had been using the hormones around menopause that my sister and I did. Well, not something we are ever going to know now is it?
Have a good day ladies
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CJRt: So sorry to here about your friend...I'm sure you are a wonderful support and hopefully she will find more support online here.
SCPMadi: Mine came back indeterminable as well and my doctor explained that the cells had become so primitive that they were not able to tell by looking at the cells what type they were to begin with. They tested negative for every kind of cell they tested it for. However, since it was located in my breast and not elsewhere, they were sure it was breast cancer. He explained that sometimes happens with grade 3 very aggressive cancers. On the BRCA, I was given the option based on family history, triple neg. status and my age and I decided to use it to help me determine what I would do in the long run about mx. I also wanted to know how much of a concern to have for my own children. It was a huge relief to know I am negative.
Kimberly: I feel your pain about the sneezing people....my husband has a terrible cold right now and it is only today that he is finally getting that he needs to stay away and not sit next to me while he is sneezing and coughing....ugh!
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Good afternoon everyone hope you are all doing well today.
LWarstler- Thank-you for sharing the info about why they could not determine you Cancer type. It always helps to get a explaination. I am glad you came back negative, I am hoping I will be as well when I am tested in Nov. You are right it will give me an idea of what I would like to do in the future if I am positive.
I am still laying low fighting off a teribble sinus cold. I went to the Doc today just to make sure it was not more than a cold and he said it was not. Checked my chest said I had a red throat and told me to rest. The hard part is knowing that just as I start to fight it off I will be back in for round three. I did ask about supplements and he confirmed I should not take VIT C or any OTC supplements like Cold FX as they often thin blood. So I am on my own to fight it off. I can take the OTC cold meds at least they help me to sleep.
I was wondering if anyone had had any pains in thier lumpectomy surical site. I have been experencing some sharp pains or sometimes a throbing around my SNB scar and up into my armpit. I am super paraniod right now that it is more than just post surical pain. Onc. checked the breast at last appoint. and said she felt no lumps and was confident it was proably nerve pain I was feeling. I do have numbness in my bicep which has been there since the surgery. I have such high anxiety about it and wonder if I will ever be able to not worry about every ache and pain.
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Good evening ladies. Hope you are all doing well tonight. Everyone that had chemo today, hope you are resting and feeling really good with no SE's coming your way.
I'm telling ya ladies, this kinda stuff only happens to me! It happened again today at lab. Went in to get my port stuck as usual. Everything going great. Had the same lady that broke my "virgin" port in the first time and the second time. She's very good! Needle went in fine. I felt nothing! Then....no blood! WTH? It's worked like a charm every time. She had me move my arm, move my back, raise my arm, still no blood. Puts herceptin (sp?) in it. Leaves and does another patient for a few minutes. Another nurse comes over and tries.....still no blood! I can't believe this stuff! So, they tell me it's working fine. All the cleaning stuff and fluids that put in went in, they just couldn't get anything out! Ended up poking my arm. Really didn't mind cause all them men and ladies up there are really good at finding and sticking your vein the first time. Makes it all better. After that, chemo infusion went off without a hitch.....except.....yeah, only me again. My potassium was a bit high and I had to have extra fluids. So it took a bit longer today that I wanted. Oh, well, back tomorrow for more fluids and a neulasta shot. Please cross your fingers that nothing weird happens to me tomorrow! Only me! LOL!
Madi: Gotta get better girl! Just take what they say you can take and get lots of rest and fluids. Hoping you kick this cold out soon!
CJRT: Really hate to hear that about your friend. I have a friend with a lump under her nipple and Dr. wants to see her in a month to re-evaluate it. Wishing your friend the best. Hope she joins the site. The ladies here will really be able to help her through this.
Kimberly: I wouldn't mind a party!
Been a while for me but I think I might get a little something, something for Halloween. Nothing I like better than not having to worry about driving that bus after I've had treatment. Thank you, subs, for being there for me! Yeah!
All the rest of you ladies, keep rockin' it sistas! Song came on the radio today "Bad to the Bone" and it reminded me of all of you. Just remember we're bad to the bone! We are rockin' it and kickin' it right on out of our lives!
Lots of Hugs and Warm Wishes coming everyone's way!
Hugs!
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RJ - I think you have a better day on chemo day than most of us have on regular days. Rock on sister.
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hi all, saw the mo ,labs came back good except potassium is low so another pill added to the mix.
nurse weighed me on different scale my scale was calibrated with the other and by it i lost 3 lbs by new scale i weighed same, at least i didn't gain by either i guess!
chemo tues 25th, mo appt nov 3 and blood draw for brca test same day.
went to jewelry party with one of my daughters tonite and watched a movie.
bone pain tonite,tho.
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Any advice on dealing with the heartburn? Not enjoying this part at all!
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Nexium works like a charm for me.
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Kimberly: That made me laugh! I don't know about that. Seems like something weird always happens to me on chemo day. Other than that, Onc is pleased with progress and believes only good things are in store for me. I hope and pray he's right.
Belleast: My potassium was high, yours was low, WTH? I got more fluids and you got another pill. Only us my dear!
Pinkshirtnow: I don't really have any heartburn so I'm no help. Sorry. Kimberly has a good idea though.
Well ladies, fluids and shot went fine today. Had to wait on a chair but that's okay. Did a lot of reading while in the chair. Nobody in my group was talkative today. Dang! So I went shopping after I got done. Bought myself a birthday present.....a velour pants suit. Those things are so comfy! And I got myself a new set of sheets. Happy Birthday to me early. I also got my grandson a few shirts for his birthday which is Monday. Party is here Sunday. Please let me feel good! Got my granddaughter some winter clothes. She's gonna be sooooo cute! Can you tell I love to shop? Picked up my repaired stereo and came home. Now I find out that my oldest daughter and the kids are staying with me a couple of days because of strife with the boyfriend. Dang! What can ya do?
Hope you all have a wonderful evening. Will post more as I can. Probably gonna be a little busy these next 2 days.
HUGS!
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Good Evening everyone hope you are doing well.
Spent the night unable to sleep my whole body felt like it was surging heat. I had this same problem on day 14 last cycle, and my hair started falling out the next day. Hopefully tonight will be better. I am hoping to get a little Halloween celebrating in this weekend with the kids. Pumpkin patch and cookie making as next weekend I will be post #3.
PinkshirtNow- My Doctor prescribed Zantac for my heartburn. I find I only need it for the one week after my treatment. In Canada I think you can get this drug OTC. With prescription it was covered. It is not as strong as Nexium though.
rjbaby- Sounds like you had a great time shopping. Nothing like a little retail therapy to brighten a day. Happy Early Birthday.
Belle- Sorry about the bone pain. Was the movie good? I am always looking for new stuff to watch during the day well the kids are at school.
Hope you all have a good weekend.
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UGH! third time is not the charm for me. Wed was my third taxol tx and today I have numbness in my hands and feet
I also got a call from the radiation onc to let me know that now my insurance may not cover the radiation because they consider the treatment at the cancer center as being done in a doc's office and my ins does not cover it there. The problem is that none of the hospitals in the area do radiation treatments and it is only done at the few cancer centers in town so I am going to have to call them on Monday to find out if there is a hospital nearby that does the rad tx's May be having to travel a little to get it covered. Such a pain in the butt. Tucking myself in for the weekend of SE's and can't wait til Monday the turn around day!
Have a great weekend all
Maggie
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hi all, had a good day today took advantage of it and the good labs, had lunch with my sister,then spent the afternoon with her and a friend at their work,i've missed visiting with them. will stay home this weekend and try and catch up with housework.
on the way home my nose started running like a faucet, gonna have to put something on it because already feels raw. one thing after another, at least bone pain is gone for now tho i think now it was a sore muscle pulling on my neck. hope i don't get any bone pain.
scpmadi, we watched green lantern,her boyfriend got to choose,it was good.
dr prescribed pill for 7 days for my low potassium,big ones!
hope all have a good weekend.
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PinkShirtNow, I use Walmart's version of Zantac. It was way cheep and I think it lasted me about 12 hours like it says. I also gargle with a mixture of baking soda and salt. Anything icy and cold feels great since my esophagus must be raw too. The heartburn and mouth situation has been the worst of this whole situation. I'm now on day 12 of tx #2 and I think I am finally getting some of my taste buds back.
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Pinkshirt- I know others are giving the recommendation for the heartburn meds. Today my oncologist also recommended I take a probiotic- Florastor. She said it is good for both diarrhea and acid.
I got thrown a curveball today- my oncologist recommended an MRI to determine possibly sandwiching the surgery in the middle of my chemo. (I've had 3/6 infusions.) She said that it would give my body a break from the beating it is taking from the chemo and that she no longer can feel the lump. I have mixed feelings because I was deadset on a mastectomy and am now being told that a lumpectomy + radiation not only has the same survival rates as the mast. but also the same recurrence rates. My onc. is also suggesting splitting up the meds in my cocktail to be administered in two different combos so that my SE's aren't as severe. Though it seems like good news, but I don't do well with thinking I'm on a certain path and having it switched on me. I was also thinking I'd be done chemo by Christmas and now don't know the timeline until after the MRI and my next appointment.
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CJRT - My sister at one point also had to have a change in treatment because of side effects. She is HER2+ and they wanted her to be on 12 months of Herceptin but she could only tolerate 7 months because she developed cardiac side effects (which thankfully corrected once she was off). I think she was very disappointed at that time, but here she is 6 years later and still NED. Whoohoo!!! I should mention that she started at IIIA.
Maggie - I hate your insurance, whoever they are.
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Thanks, Kimberly. That makes me feel better.
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CJRT - Sorry. I know nobody wants their chemo interrupted. No one wants their cheese moved. No one wants any of this, period.
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CJRT: I just wanted to let you know that I made my surgery decision up. I don't know if this will impact yours or not... but I wanted to share with you because I know we had kind of talked about keeping each other up to date since our doctors had told us similar things. I have been to a few support groups lately, and after talking to many woman I have decided to do a double lumpectomy. I feel like my surgeon is kind of hinting that a lumpectomy would be suffucient. And I do believe that a lumpectomy would take care of the cancer that I have now. BUT - one of my main reasons (and this was supported by the women that I talked to over the last week) is that I want to do everything in my power right now to not give this cancer or a new cancer a place to come back. If it does come back elsewhere in my body - then hey... I can't control that now (other than making sure I am eating well and exercising to reduce the risks). But... as far as my breast goes, I feel like if I leave that tissue there then I will be wondering daily if it was back. Not all but many of the women I spoke to have had breast cancer and then had a recurrence or a 2nd breast cancer and their sentiments matched exactly how I feel. Its a quality of life thing for me. I would just feel more at peace if I know that I have done everything I can to not give this a place to come back.
I have two separate appointments with two separate plastic surgeons over the next two weeks to begin discussions.
This is a very personal decision, I know that. I just wanted to let you know my decision. I am one hundered percent comfortable with it. So if my husband and family.
Just know that this is your decision - and your docotor can try and sway you one way or the other but ultimately - it is up to you.
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Sorry I haven't been posting but I have been so dowwwwnnnnn lately, since my 2nd infusion on Oct 7th. I actually felt better physically after this one, but not mentally. I don't know if it's the bald thing sinking in...the reality of it, or if I'm having some kind of invisible PMS. I was due a few days ago, and although I never got it, i did get cramps and FEEL like I was gonna get it. Does anyone know if thats normal? My onc did tell me it would stop but I didn;t expect to have symptoms.
And the hair thing, I can barely look in the mirror. I feel like, why bother to put makeup on when no matter what I do I will still look awful. The wig is hot and itchy and I hate the feeling of hats and scarves (I know I am a Negative Nellie and I'm sorry). Luckily, I'm not working right now...but I have to go back after Thanksgiving (no more sick days) and I know I will still look be bald by then and will have to wear the wig every day. And who even knows if I will feel better by then.
All I really wanna do is hide out in my house.....anyone else feel like that? I just wish I could blink and have this whole thing over with. Also, I've gained about 5 lbs since I started, I guess it's alll the comfort food after losing a bit of weight after first round. But the weight is just making me feel worse. I need help to try and stay positive.
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I hear you Jersey--today I had to go pick up a prescription and some food and nothing I put on made me feel good about myself. I am packing on weight and I hate the feel of a wig...itchy and gross. We need a fast forward to end this asap! The Neulasta pain set in today so that does not help. The only thing that is keeping me going is knowing that this is what I have to do to save my life. 3 tx down and 5 to go! Keep your chin up my friend and we will all be done with this crap before you know it and back to our luscious selves!
pinkshirt--I take a prilosec during the days surrounding my treatment to stave off the heartburn.
Maggie
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oh and Jersey...I got my period just after my last treatment. I was shocked because I thought it would be gone. It was a bad one too!
Maggie
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Jerseylicious:
so sorry you are feeling bad. I understand the bald thing... My wig is itchy and I have rarely worn it for longer than a few hours at a time. I will have to wear it when I go back to work and I am not sure how I am going to deal. I think as soon as my hair grows out I will be sporting the short do. But - the scarves don't really bother me so much. I would rather wear them with the scarves. One thing that did help... i buzzed my hair as short as I could go without shaving it with a razor. It fell out in patches and was splochy all over. I ended up shaving it with a razor the other day since I was so sick of the splotchiness. The wig feels better like that. I have also gained a few pounds since this started. The damn hormones make me want to eat everything in sight. Its horrible. I have always been a little heavy so resisting the urge is very hard for me. I', going to have to do something to curve this hunger.
I've had one period since I started and it lasted two weeks. I've had a one week break and I just started lightly again. I cannot believe it. I certainly don't want to spend the next two months menstruating. That's all I need. Crazy cycles are all any of us need. I am hoping to keep mine though. My husband and I would like the opportunity to have another child.
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jersey, i'm sorry you are so down, we understand. the physical se have been milder for me too,this go round but have dragged on longer. 1st treatment wk. i was sicker than a dog 1st wk, felt better the 2nd wk. this time i am still having bad days esp today so tired of it already.
now about the headcovering, have you been to the tlc website,they have kerchiefs i got a black on white falling leaves/leaf one so comfy and looks good. i just ordered more a camel one, wh on black,and another design paisley. they have a lightly padded headband so no gaps, have ties sort like an apron, very easy to put on. you can turn them so the knot/tail is the side. you can also get a halo to wear under it so it looks like u have hair. i didn't but i don't work. they have several different kerchiefs to choose from, $16 apiece if you buy 2or more $ 15. do u have an exercise dvd,maybe doing it will or walking will help stave off the lbs and improve your mood of course this comes from someone who has hardly moved off the couch, no energy this go round.
khegidio, are you getting a double masectomy?
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Belleast: Yes I have decided to get a double mastectomy. It won't be until after my chemo treatment so probably the end of January.
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khegidio, are u doing reconstruction or have u decided yet,just curious because if my brca comes back positive, i'll be getting double masectomy,too. trying to think ahead so i'm more prepared this time. even if i have to go that route i'm pretty sure i will have to do radiation because of my chest wall that might limit or eliminate me getting reconstruction.
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Belleeast: I am planning on doing reconstruction at the same time. My bresat surgeon has told me I don't have to do radiation if I do a double mastectomy. What type of reconstruction.... I don't know that yet. I will wait until my meetings with the plastic surgeons over the next few weeks. My BRCA came back negative, but I still do have th family history. I have read many articles and even the genetic dr. told me that just because my BRCA came back negative, doesn't mean that my breast cancer is not hereditary. There are other genes that they just don't have tests for yet. Because of my age and my family history, my gut tells me this is something genetic. I don't want to give it a second chance.
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khegidio, i think you are making the right decision. if you don't mind ,let us/me know what the ps say.
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Khedigio- Thank you so much for updating me about your decision. Because of my oncologist's switching things up on me, I may have to make the surgical decision much sooner than I thought I would. I, too, am leaning toward a double mastectomy, even though my oncologist (who I really do think is great) looked shocked that I would be considering it. Though the medical director at the institute told me that "no one will look at you like you are crazy if that is your decision," I feel like there is pressure to opt for the lumpectomy in my case. The reason that you shared about doing everything in your power to decrease the odds of recurrence is exactly what I am thinking. It's bad enough to fight this once, and I just don't want to ever face it again. I know that the lumpectomy plus radiation might be the same odds, but my head just can't wrap around that idea right now. I know how obsessive I can be and worry that I will constantly be second-guessing myself about a lumpectomy. I go for an MRI on Wednesday and then will see what the surgeon says about lumpectomy versus mastecomy, since we haven't discussed surgery since chemo started. I'm glad that you have made your decision and that you and your family are on the same page. Thanks again for sharing.
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