Starting Chemo October 2009
Comments
-
Mary, my port is acting much the same. I think as long as it isn't hot and inflamed, doesn't hurt, and you're not running a fever, it's probably ok. Just point it out to the doc next time you see him/her.
Juannelle, I think the idea to watch funny movies is a great one! Here's to high WBC!
Michele, I read the book "My Sister's Keeper" and loved it! But I have to admit, I am a little scared to watch it - i read the book long before my dx.
I found my wedding dress today! It's really pretty, but I do need some alterations on it. I go back to pick it up next week. I hope they do a good job, because I won't have much time to fix it again after next week! My girls also found really cute dresses to wear. So, that's one more thing I can check off my list!
Peace to all...
-
Always a relief when wedding planning to have the dress taken care of! Congratulations!
My port seems to be protruding, and has stayed irritated looking for two months. I tell myself it is protruding more because there was probably some swelling that hung around for a bit after it was put in. The color? I compare it to my scar tissue and it isn't any more red, so I figure it is just tissue that will take time to heal. How do I know? I don't, but that's what I'm going with!
The nurses and doctor have seen it and don't seem concerned.
-
Marilou, Yes indeed fiber one is here in Canada. I am in Ottawa, but I lived my life in NB.
-
Could the bruising be from your platlets being low? I thought that bruises lasted longer during chemo?
-
Hi All!
I'm just popping in for a quick hello!
I'm glad to read that everyone is getting through their days as best they can and moving right along with treatment.
1L - I'm sorry to hear about your low WBC and being confined to home BUT better home than hospital I say!
I've been busy running around this week getting as much done as I can (finished my Christmas shopping) and tonight I am beat. It's not even 9 pm yet and I'm wishing for bed!
I am on day #5 post #3 TX of FEC. This week went very well as far as escaping SEs for me and the only complaint I have is this "full" feeling. I'm not really constipated because I have had some success (I feel like I"m toilet training again) but I'm feeling full, bloated, with a bit of heartburn.
The grapes are not working for me this time so I'll pick up the Fibre 1 cereal tomorrow. Thanks for tips!
I had the PICC line dressing changed again on Friday and the blisters are dry and healing! I'm so happy with how the nurses kept on top of this and didn't let it progress into something more messy (like a full blown infection) or jeopardize my PICC line.
I'm looking forward to a pajama day tomorrow and maybe (I said maybe) do some laundry!
Good night all!
Marie
-
I can not believe I am still having sleep issues. It is 5:47am and I am wide awake.
Marie - glad to hear that PICC is doing better and the blisters are healing! That is awesome. You have been struggling with the PICC since you gotten it and I am glad to hear things are finally better.
1L- I sure hope your WBC gets better so you can do your Thanksgiving shopping. Neupogen worked great for me and I am sure by your next blood test your WBC count will be in the good range.
Congrats txstardust on finding the perfect wedding dress. That is half the battle. I am sure you will be a beautiful bride.
To those ladies joining the anal fissure club...I am so sorry to hear that. The only way the fissure can heal is for you to have regular soft bowel movements, along with frequent warm sitz baths. Take advil for pain, I found that that was the only thing that helped with pain. For those of us without fissures, keep up the water, fiber, stool softners and Phillips Milk of Magnesium to keep us regular. There is notihng more painful then a fissure.
Okay enough of the fissure talk.
Yesterday was my best day yet. I felt so good. LIke I was not on chemo. Of course not as good as before chemo. I went to the movies to see Blindside....great movie. I took DD to get her eyebrows waxed. And I just enjoyed time with my family. Thankfully my next tx is the day after Thanksgiving, so I will be able to cook the meal and enjoy it with my family. I am not looking forward to my next tx, because I had such great bone pain last time. And I have slight numbness in the heels of my feet.
I am definitely praying for all of you ladies and hoping we all have a wonderful Thanksgiving with minimal to no SEs.
Anita
-
Hi, I am day 5 after tx of T/C. I have been so wiped out since Friday. All I do is sleep, can't stay awake more than 1 1/2 hour and asleep I am again. It is driving me nuts, I feel like a shell of a person.
I get up, eat something (nothing tastes good), can't focus --then sleep again. Is this just the yucky days of 3-6 phase? is it coming off steroids??? Is my body adjusting to the port? I can't stand the thought of another day like this ...it is only 8 am on Sunday.
sorry - it feels a bit like a lonely pity party, Jean
-
jean, you can whine all you want, we are here for you.
My husband is much better and I think I will go home today. My cousin has taken excellent care of me and I think that is why I have done so well have my last tx. But I am ready to go home, it has been over a week and I miss my puppies, my bed and my DH. I really don't know what I would do without my cousin, she goes to all my appointments, gives me my shots, goes to chemo, fixes all my favorite foods, does my laundry, you name it and she is right there.
I have to go on Monday and get another Neupogen and then on Tuesday I will get a blood test. My WBC had better be up. Of course, the Neulasta should be kicking in about now, so I should be super charged.
Everyone have a relaxing and recharging day. Watch a movie or a football game, what ever you do to relax. Have a great day.
Juannelle
-
TXStardust ~ how exciting you found your dress and your girls too.
Juanelle ~ glad DH is feeling better. I am sure it will be nice to go home. So hoping your WBC is up on TUESDAY!
Jean ~ I am sorry you aren't feeling good. Just do what your body is asking and if sleep is it, then sleep... your body heals when you are sleeping.
I am Day 6 post TX #2 of A/C I feel pretty crappy.......... but hanging in there.
Have a great Sunday girls !
Alicia
-
Juanelle glad you are going home. You are lucky to have such a supportive cousin.
Jean I am on TAC so I get all of them at once. I felt lousy days 5-7 after my first round. I also had some stomach issues, but basically had more enerygy and felt good days 9 until the next round. I am doing acupuncture so that may have helped as well. I am going for acupuncture tomorrow which will be day #5 for my second round. I am hoping it helps.
Marie glad things are going better for you.
A low SE day for us all!
-
Well, I did not make the wedding last night. We came home from the dance competition and I just seemed to hit a wall. (BTW - Em got a gold in her solo, and her group routines received a high gold and 3 more golds). I told the kids to let me sleep for an hour, but I just couldn't do it. DH came home from Dubai (he's been gone about 2 weeks?) around 400 in the afternoon, so I sent him to the wedding with the card.
I think I missed a Claritin somewhere because I am having some hip pain. I am going to force myself to stay home today and rest. I know I have so much to do for Thanksgiving and Christmas, but I have to get passed this. I know its bad, but I'm thinking of just getting a bird from Honey Baked Ham or Harry & David's. Heck, we're going to be camping (in motorhomes) out in the sand dunes. I don't think anyone will notice that I didn't home cook my turkey.
I just want things to be back to normal and this is making me cry. Sometimes I wonder if it will be this way for the rest of my life.
Waah. Pity Party over. Hopefully.
Love ya!
Laura
-
Oh, I forgot . . . My tongue feels like its almost too big for my mouth, and my neck glands are sore (not really swollen). Has anyone had this? Or do I have some new mutant disease? Great . . .
L
-
Azdiva ~ I am sorry you are feeling crappy. I too had that pain/sore feeling from my earlobes to my hips from the Neulasta this week. I was so bad Friday night I had to call the dr. on call for something for pain, tylenol or motrin weren't doing it. The neck glands were the worst, DH couldn't even touch me. The dr. said 3 motrin seems to work, well it didn't for me. Hope you feel better. And next year we will be stuffing that big ass bird in the oven with so much to be thankful for. Especially that this will be behind us and we can forge ahead.
HUGS !
Alicia
-
Hi Jean and Azdiva, I can tell you both I have had all of what you describe - extreme fatigue, "hitting the wall", can't stay awake, feel like this will be the reality of my life. It is awful, sad and scary. But it feels so good when it stops. And it does! And then we move on........YAY! You'll be your peppy selves again - til then don't fight it. Love, Valerie
Oh and I have swollen glands and a slight cold and sometime a slight sore throat X2 txs- I think its just a dormant little illness that kicks up when the WBC r low (or something like that) but it goes away w/o going out of control.
-
Marie, Glad to see you again. Happy to hear your PICC is doing well...I am thankful that my PICC has given me not trouble...I would hate to do chemowithout it.
I always worry a little when I don't see someone on the thread for a few days. I prey theyare doing well...funny how this group can get you connected with strangers and make you friends.
Anita, I am like you for the first 5-6 days after chemo...I am tired but can't always sleep. At least I know my schedule now. TX, no poo, no sleep, yes poo, not taste buds, loopy,,,sleep
Jean, Sleep as much as you need...your body needs rest after being injected with poison. Remember injecting poison into a lesser person would kill them, you are STRONG, and you can take it like a lady.
Juanelle, Glad the old man is feeling better. You are luck to have a cousin as great as you have. You need all the support you can get at a time like this...When you are better you can do something great for her to say thank you...a day at the spa, a special gals weekend away..just a few ideas. Give your pups a hug.
Laura, I have driven by those sand dunes you mention. Amazing...I couldn't believe people actually camped in the sand...If I were you I would buy the turkey, open the can of cranberry, buy the pies, and open two boxes of stuffing...Remember is is about being together and celebrating, not about how hard you have to work to get a turkey meal on the table...Next year you can go all out...That goes for all of us this year. We can all pull out our cancer cards and lay them on the table beside the boxing (stuffing in a box, which by the way is good).
Txstar, glad you found your dress, I am sure you will look beautiful in it...we want to see pictures.
Great day to all, Michele
-
Hi chemo sisters! I hope everyone is doing ok on this lazy Sunday. I know I should check in with you guys more but I'm always a little afraid that you guys might hate me because I've been having an easy time of it. (Knocking on wood as I write this). The only thing I have to complain about is a slight "burnt feeling" on my tongue. It doesn't hurt but it feels like when you have burned your tongue with a food or drink that is too hot. It makes me a little more sensitive to temperature and spices when I eat but nothing much other than that. It usually goes away after the first week or so so not a huge deal. I'm still working full time and only miss the Thursdays when I have my infusions. That being said, I have stooped to using the cancer card to get out of hosting any holiday dinners and parties this year. I could do it but I just don't want to. Not being Scrooge or anything, just don't feel like going all out and the work that goes along with it all.
The one thing I am looking forward to is our annual Thanksgiving morning flag football game. A huge group of friends (about 30 of us) all get together early in the morning and play flag football in the park for a couple of hours before all of the cooking starts. It's so much fun. I'm not missing that because of cancer. In fact, I'm trying hard not to miss out on anything I want to do because of cancer. My DH and I also went and saw The Blindside yesterday and can't recommend it enough. We went with a group of friends and we all enjoyed it. We needed a great "feel good" movie and this one did the trick. The rest of today will be spent watching pro football. I love this time of year. I actually get depressed when football season is over. I'm weird, I know. Everybody have a great day and hope your treatments are as SE free as can be. Go Raiders!
-
Today I woke up from a deep sleep feeling like I've been hit by a truck. My back is aching (probably from Neupogen), my eyes & mouth are dried (from chemo), and my upper body is stiff & sore.
All of these can be explained and there is nothing to worry about. It's just a constant reminder that I'm fighting BC.
I'm sure I'm tired because I'm coming off the steroid high (and maybe doing too much) and the upper body is because I haven't been able to properly use my arms for weeks now. Between the cording on my left and the PICC on my right I'm losing strength & muscle in my arms. I can't even make my bed anymore - I don't have the strength.
So I'm just going to stay in my pjs today and crawl back into bed (after my shot) and not worry about it.
Have a great day ladies!
ps. I have the sore neck glands too but I agree it's probably some low grade virus that we're fighting off. There is so much going around right now we just need to be more careful!
Marie
-
Ladies, my heart goes out to all of you that are having SEs and all this weekend. I am 10 days post tx and I just have no stamina. Is it because I have slowed down so much that I am just weak, or is it from the tx? I did get out and walk a couple of days, but I know I am not doing much. But I get so tired, I get up to do a few things and then have to sit and relax before I can do anything else.
michele, I will do something special for my cousin. I don't think a day at the spa will do for her. She wants a table saw and that is what I am going to get her for Christmas. When she mentions something that she wants that she can't afford, then I go and buy it for her.
Juannelle
-
Hi ladies, I'm pulling myself a little out of the post-chemo haze to come in and say hi. I just took a short (maybe 8 minute) walk with DH. The fresh air was nice, but I'm still totally drained. Last night was the first Neupogen shot of this treatment cycle, and I can already feel the aching starting. Last cycle Tylenol and Vicodin didn't touch it, but Percocet helped, so I got a big bottle of it for this go-around.
Juannele, I think the table saw is a great idea...sounds like your cousin will love it!
-
3new4dee ~ your flag football sounds like fun on Thanksgiving. Somehow makes me think of The Fockers/Meet the Parents movie.
Michelle ~ Hope you are feeling good. Is your stubble falling out? My hair HURTS it is getting really sparse and stubble all over my pillow.
Juanelle ~ The table saw sounds like a nice gift if that is something she is looking for and cannot afford.
Meredith and Marie ~ Hope you feel better. OH that aching is simply the worst. I was thankful for a Vicoden on Friday that the Dr. called in for me. Rest and I hope tomorrow is a better day.
Goodnight girls !!!
Going to watch Will Ferrell in Land of the Lost with my kids and DH now ~
GIANTS won woo HOO... (barely)
-
Now I have to put my 2 cents in-GO PATRIOTS!!!!!! I will love them tomorrow - they make me forget all this sh#t.
I am glad 2 say that after being bald for a while - my head (stubble) doesn't hurt anymore. three of the men at work shaved their heads so last friday I went hatless. felt great.
Have my next tx on Tuesday - my sympathy w/ all who are suffering now.
Good night-Valerie
-
meredith, glad you had a little bottle of relief. I have been there this week also taking my hydrocodone.
My cousin is always doing something around the house and has started doing mosaics and she has been wanting a table saw for awhile. She lives in an older house and there is always something that needs to be done. The table saw is something that she has said she wants, so that is what I will get her. I am not sure that she would ever spend that much on herself. She is retired and is on a fixed income and has enough to get by and live a good life but not lots of extras.
She is the greatest person. She lived out of Texas until her mother got sick about 15 years ago, then she quit her job and moved back to Texas to take care of her mother. Her mother lived about 2 years, after that she found a job and decided to stay in Texas. When she retired she moved to the same town that I live in so she could be closer to me. Earlier this year, my niece was diagnosed with cervical cancer and in my niece's last weeks of life my cousin went to stay with my sister to help take care of my niece. That was about the hardest thing that she has ever had to do, it is hard to watch a 40 year old woman die of a horrible cancer. Then, came my dx and she has been my rock. I wish I could do more for her, but she will not take money, and I do lots for her when I can, but I will never be able to repay her for her help through all of this.
Juannelle
-
Oh, I discovered some magic today. I was despairing with my constipation issue so called the onc's office. I spoke to the doctor on call. I told her I was completely bunged up and need some resolution before my next chemo treatment tomorrow. I listed all the things I'd tried - Senokot, Colace, Milk of Magnesia, lots of fruit, fiber, hot drinks, water - with no good end result. She called in an Rx for lactulose. It produced satisfactory results in two and a half hours. What a relief! Maybe if anyone else is having this issue they might want to try this too.
Juanelle, maybe the tiredness is because of your low blood count. You probably need to take it easy for a while. You are so lucky to have a cousin who has been so good to you.
Re sore neck. I got that after both treatments. I think it happened on day 4 or day 5. I presumed it was the lymph nodes in my neck. Since there are so many white cells in the nodes, my theory is that the chemo drugs were doing a massive kill off of those cells and then it takes another couple of days for the Neulasta to build up the number of white cells again. So I figured the pain/soreness was because that is one of the war zones. A number of you have mentioned the sore neck but when I mentioned it to the oncology nurse she said no-one had ever mentioned that SE before. She made me think I was imagining it.
Marie, sorry you are feeling so tired and sore today. Remember it will pass just like the last time.
Dee, it's good to hear that someone is doing well. It gives the rest of us hope. Don't feel guilty.
Jean, with Tx #1 of AC, day 4-5 were the worst, then I started to feel better. But with #2, just like you, the bad days seemed to be extended. I really didn't feel well until day 10.
-
My hair started to fall out nine days ago. I still have a few strands left. But my head hurts and itches. How soon will that feeling go away? Is there something I should be rubbing on my scalp to help?
-
Dear Mary,
The head hurts mostly because the strands are tugging on the hair root which is now weakened. Best to buzz it down real short now.
-
yes I am getting close to being a skin head. I buzzed it really short (crew cut). It hurts a bit. God forbid you rub it in the opposite direction of the hair follicles. OUCH ! I can rub my head over the sink and what seems like TONS of little hairs fall out. I should be done in a day or two. I won't miss this uncomfortable feeling. I asked DH if he has any Alien Abduction fantasies I can fill. LOL TMI ~
-
Hello All,
Just checking in after hovering for a while. I'm gearing up for tx3 on Friday. I'm almost looking forward to it just to get it over with. I had the swollen neck gland thing too and my onc prescribed an antibiotic (thought it might be tooth related), but after I started taking it, my cheeks started itching and swelling and I developed a painful rash on the lower part of my face. It's wierd because I've never had any allergy to penecillin before but the on-call nurse at the cancer center said to stop taking the antibiotic and take some benadryl, which has helped immensely. But it just figures that the rash would be on my face. I feel so ugly that I hate seeing my own reflection just from losing the hair, and now I have red splotches on my face along with that.
As for energy, I hit a wall pretty quickly after 45 minutes shopping at Target. I'm not very good at resting and I always push to do just "one more thing" before I stop and by then I'm shaking and ready to fall down. DH gets really upset with me when I do that.
Be well, and love to all getting treatments this week, Sido
-
HI EVERYONE
I'M feeling good again now had a lovely weekend with my family stayed at my sisters all weekend , great .My husband had the weekend of from me as well which gave him a well deserved break ,but he said he missed me too much ,oh, how nice ,.
The food thing is just great isn't it, i love really spicy things i did like then before but even more now , the best is KFC a spicy breast fillet with mashed potato and gravy on it , then a ice cream after ,YUMMMMMY ,Sam takes me there when I'm starting to come out of ground hog week its a special treat .
BUDOMI
You are right i was a big smoker many years ago haven't had anything for around 10 yrs exp for about 3 smokes inbetween , my sister has arthritis badly and does chemo as well she is a big smoker and has been given the ok from her doc ,she only has the stuff that is totally chem free so she gave me some Ive had a few smokes and it does help I'm not a drinker, hate wine so every now and then its nice to go and chill .
Well hope all is good with every one
JOJO
-
Dee, Don't feel guilt about not having a tough time with treatment...That is great. I too have had little problems. Enjoy your football game, but don't hurt yourself.
Marie, Who needs to make their bed anyhow. You are just going to get back in tonight..Wish I could spend my day in my pj's..sounds heavenly.
Juanelle, A table saw sounds like a agreat gift. Your cousin sounds amazing. Will she adopt me, do you think. I have no family close to me. So my Dh and my kids are my support team. I myself will be asking for rubber floor mats for my new van floors...My DH thinks this is a bad idea to get me this...as everyone will think it is a sucky gift for a wife...I just want my van to stay clean...I like practical gifts..
Mary, congrats on passing the mass...Go Mary...
Alicia, What ever fantasies you and the DH use, way to go...Gotta keep the sex life going in between, the nausea, constipation, fatigue, what is left of our periods, joint pain, baldness and what is left of out breasts...it is hard to get in the mood, so what ever floats your boat, us it.
Sido, I am doing #3 on Friday as well. Good luck to you sister. I as well hit a wall shopping on Saturday. The DH and I spent far to long at Home Depot looking at floors, moulding, lights and everything else in between. I know HD on a Sat. must be nuts. Meanwhile I am wearing my wig and my head is getting hot. The minute I walked outside I thought I would pass out. Just hitting the wall of cool air...I was ok, but in the car I ripped my wig off and enjoyed the feeling. Taking that thing off is much like removing your ski boots after a day of skiing....the best feeling in the world.
Jojo, Thanks, now I am craving KFC...I would skip the potatoes and go straight for the frys....mmmm..The first time I had KFC in the states I nearly cried when I got mashed potatoes and not fries...sorry..That is just not right...
Well I guess I should go to bed, tomorrow is a school day..
Michele
-
mary, hope the head is feeling better. I have some hair that is just going to hang in there and my cousin buzzed it my electric razor and it felt so much better. I know what you mean about rubbing it in the opposit direction.
alicia, keep those fantasies going.
jojo, glad you had a relaxing weekend with your sister. It is good to have a place to go and just let your hair down. lol Even our families need a rest from us.
michele, I decided last year, that I would only give practical gifts. No more, just buying to buy and giving to give. One lady at work has what ever she needs, but she has dogs, so for her Christmas present, I gave her all sorts of things for her pets. She thought that was the coolest gift. So much money is spent on things that are never used. Now that is not to say that I don't buy any fun gifts, but you know what I mean. This year with my kids I think I will just give them money and let them pick what they want. I just don't know if I will feel like getting out and fighting the crowds. I will guy for my grandkids, but I don't buy a lot for them and I put money in their savings account, kids have way too much these days.
Good luck to all of you that will have a tx this week, wishing you mild ses.
Juannelle
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team