April 2010 starting chemo
Comments
-
Just wanted to share a funny story. Was going into the grocery tonight to get DH a birthday cake and as I passed thru the crosswalk at the entrance a man drove by me in his car and almost ran over another pedestrian trying to stare at me. Now I had on one of my hats so it's not like I was running around with a bald (or almost bald) head. I watched him continue to try and look at me in his rearview mirror and side mirror almost swerving into a brick column. Now really, am I THAT interesting to look at? I kind of felt like a freak of nature but I had to laugh because he apparently couldn't quite believe that I was walking around in public with no hair and couldn't quite figure out why I didn't have any.
I'm getting ready for #4 of 6 on Thursday. Still have about 10-15% of my hair. Did not lose any more with #2 or #3-all of it was with #1. Still have major muscle aches in my legs-not sure if that's from the Taxotere or the Herceptin. If I have to deal with that until March when I'm done with the Herceptin I may lose my mind. Not looking forward to this weekend and the nasty nausea and metal mouth but AM looking forward to saying "only 2 left!". Best of luck to everyone with treatments this week and wishing everyone as few SE as possible!!!
Have a great week!
Jennifer
-
Sara- I'm so sorry you got sick! I have yet to vomit but with the last treatment on days #3-4 EVERYTHING I ate or drank made me gag. I'm worried that with the next one I won't be able to keep anything down. I don't notice any taste changes with my saline or heparin flushes but I've heard some people have to have lemon drops or mints in their mouths while it's being done to avoid just what happened to you. I'm glad you're feeling better and I hope you don't have any new SE's with your new drugs!
Jennifer
-
Marcy- Sorry to hear your having so many reactions...I hope they find the right cocktail for you. It must wear your nerves away...I hope they resolve this for you soon. Keep the faith.
Sara- Sorry to hear of your bad reaction too! That is so unpleasant. Are you taking Emend? It helped me tremendously!
I am having a SE from the AC....last tx around day 10 I developed a sore throat. When I was seeing my Onc. prior to the next Tx I mentioned this...and that it lasted a few days and went away..(I was afraid that I was getting strep). My Onc. said that it was a SE from the Adriamycin...This time it feels different. It feels like I have a huge lump in my throat...I can't keep from thinking that it is my throat closing up...It is just such a strange sensation...I might call the Dr. tomorrow just to run it by him, and to set my mind at ease.
Karen-
I hope your tx went well today. Do the steroids keep you up?
I am having my LAST AC on Friday....I went in the pharmacy to order my prescriptions today in anticipation of friday's tx. I told the pharmacist not to order any more neupogen for me because it is my last tx...and all of the pharmacist and techs yelled 'YEAHHHH"..they made my day!
Is anyone just having herceptin alone?
Big Hugs to everyone...and remember to FIGHT like a girl!!!
Emme
I
-
Kad22 - I am a TN and going to be receiving DD Tx4 so I dont think that is it but not really sure what it is either.
-
Toughmom38 - I have also had people stare when I am wearing a hat, not really sure what is running through their mind but I have inquired
... I was in Rite Aid picking up a prescription and a woman kept looking at me and every time I would look at her she turned her head. Well finally I said "can I help you?" and all she could say was "I was just admiring your hat.." PLEASE...... I said "thank you, I have cancer" and walked away, her face hit the floor while I giggled all the way out the door. Just thought I would share the humor...
-
JenC- Oh that is the greatest!!! You said what I have wanted to say to so many people! Good for you!!! She could have come up with something better than that. Why do they think we can't see them looking? Does cancer also make us blind?
Jennifer
-
Marcy, my heart goes out to you, how frustrating it must be to react to everything that they have given to you so far. I hope that they can find a cocktail that works, that you can tolerate, and that you can start soon, so that you can put this behind you and move on!
Saralmom, I'm sorry tha you were so sick with your last infusion. I hope that they can get on top of it, it can be such a tiring thing to be vomiting like that.
I also have a kind of funny pharmacy story to share. I was there to pick up my montlhy supply of heparin (which I am self injecting) and the woman in front of me was picking up her prescription of pills. She commented to the cashier that she hated taking pills "Isn't it the most awful thing to have to take pills" The cashier was sympathetic, and then she told the woman that she takes insulin. It just went right over the woman's head, and again she complained about having to take pills. The cashier just shook her head, and when she was ready to help me, I said "I would much rather take pills" She smiled and said "Some people jjust don't get it, do they" So true.
Have a good week all, third FEC for me tomorrow.
-
marcy4: I'm sorry to hear you're having such problems with reacting to the drugs. I hope they find the right combo for you (or a way to prevent the reactions) real soon.
saralmom: Vomiting because of the saline is a bummer. You get those at every treatment. I'm sorry to hear about that because vomiting is just the worse--no control, it's ugly, and it just feels bad.
My first Taxol today was also a marathon. Normally, I go in for my usual pre-chemo blood tests on Sundays since my infusions are on Mondays. This first time, I needed to have extra tests done for the acetyl L-carnitine study, so I had to be accompanied by one of the research assistants and thus needed to go on a weekday. I met her at 8:30 and we went over to the hospital building to get my tests done--and she did say "stat!" just like on TV. Then we went back to the onco department, where I waited for my 10:10 appointment with the oncologist. There wasn't much point in going back home in rush hour traffic, just to come back again shortly. Luckily, I always take a book with me to doctor's appointments.By the way, it's just the best knowing that I'll see the oncologist before every treatment to talk about side effects from the last time and what's expected for the current one, to make sure prescriptions are in order, and to go over my latest blood tests.
Then after seeing the onco, waited a bit more for infusion at 11. So I'd been there 2 1/2 hours already and hadn't started treatment yet. There was the usual time spent getting the IV in, but it went fine. My pre-meds were benedryl, pepcid, and dexamethasone. (I'd also had dexamethasone the day before, but I slept somewhat OK. Emme, I was expecting to be up all night but wasn't. I had to wake at 5 to take the second dose and just decided to stay up after not dropping back off right away.) We had to wait for the pre-meds to kick in, then we started the Taxol on a slow drip and would gradually build up to the full speed drip (titrating). She took my blood pressure a couple of times while we were building up to speed to make sure it wasn't getting high and indicating a start to a reaction. No problem (well, it was higher than normal, but so was the pressure measurement before it all started). I had no side effects other than the usual slight burning I get with almost any kind of IV. It was very manageable. Yay! Unlike some, the benedryl didn't knock me out, but I was sleepy later. The Taxol was a big bag (I'm getting dose dense amounts), so it took about 2 1/2 hours for the full bag to run through. So altogether, the infusion portion of the day took 4 1/2 hours.Luckily, I'd been warned it would be a long one, so I brought the laptop and watched a movie. That helped the time pass better.
Emme, congrats on your upcoming final AC.Yay! Have you already done your Taxol?
I have to take my study meds 3 times a day, so I've been trying to stay up until 10pm for the last dose. It's about there, so good night to all.
Karen
-
Karen - I am officially in the study as well. It's hard to remember to take meds 3 times a day! I hope I don't blow it.
Emme - I did have Emend during the AC part but not for this Taxol part. I think b/c my nausea was short lived and not a reaction to the actual drugs it doesn't warrant the big guns. My nurse did tell me to take 1-2 Ativan before I come again next week to try to prevent it. I can't imagine not being nauseous from it again, and I get the dang saline like 5 times during the tx. Nothing worse than vomiting in a crowded room full of people - so embarrassing, and I felt guilty b/c I know they don't feel well either. Even with my curtain drawn around me, I know the sound of someone vomiting is so gross. Ugh!
-
Sara, I'm worried about remembering the take the study meds 3x per day also. Morning and evening won't be a problem, since I ordinarily take something then anyway. But mid-day will be a challenge, at least until I get into a routine. At least while I'm still at home during the day, I'm never in the same place every day at that time (probably 2-3pm, depending on when I took the morning dose). Once I'm at work, I'll be at my computer all the time and can put it on my calendar to remind me. I almost missed a dose yesterday, and it was just Day 1!
Karen
-
So sorry to hear about problems with chemo - that really sucks!
Sara, I hate to vomit I did the first treatment but at least I was at home - I say don't worry about the others they totally understand! I hope it goes better for you next time.
Well - I have my last AC this Friday like Emme! Yay for us! Although, I am really nervous to start the weekly Taxol.
I am also done for the school year and now my summer starts - I actually don't like being off of work those kiddos really helped to keep my mind off of stuff! Plus it's bad that I am wishing it was next June - just wishing the time away, don't want that - but want to be done with this crap!
I put a new avatar in - finally one of me with my wig! I like it although it seems after a day of wear ing it - it gives me a headache like wearing a cap or ponytail!
Well it's raining here and my daughter is babysitting, husband at work maybe I will go see Sex and the City 2! Good luck to everyone and HUGS!
-
Marcy4 and Saralmom, I too, am sorry you're both having problems. Marcy I really hope they can find something that you are not allergic to - that must be so frustrating.
I have a couple of questions for you ladies today and I'm hoping someone can help me out. Is anyone taking Zometa (for osteoporosis prevention) yet? I had requested it but not sure of the side effects (if any).
Also, I am suffering from annoying hot flashes and have them every hour in the night that can last up to 15 mins. Consequently, my sleep is being disrupted constantly and I can be up for hours throwing the covers off and then putting them back on again once the heat subsides. Is anyone else experiencing these? I am hoping that they end with the end of chemo but I hear that Tamoxifen causes hot flashes too, so I'm not happy about that.
-
For all you brave ladies gagging during the saline flushes and infusions. I read a post somewhere here from a repeat chemo lady. She said if she pinches her nose shut when she gets the flush, she never tastes it. I don't know if it works (starting chemo 6/11) but it's worth a try. I can tell you it helped me gag down that gross glucose drink I had to take before my PET scan yesterday! Blessings to you all!
-
Sorry to hear that so many of you are having a hard time. I hope that it gets better soon. We have enough to deal with without having to deal with extra stuff during treatment. (((HUGS))) to you all and best of luck. I am scheduled for my third AC next friday the 18th. Hopefully no other set backs and no more stitch abses. They tested the last one to see what the bacteria was that was causing the infection and there was nothing. Kinda strange to me but I guess it was just like a pocket of yuck but not really an infection. Would have been nice to know then so I was not waiting 4 weeks between treatments but what can you do, gata do what the doctors say right:) Heading off for vacation in maine on saturday cant wait for a get away, really need a change of scenery...
-
I am finally done with AC. The 4th was the worst for me. I had no energy and felt like I had been run over by a truck. Today is day 7 and I might be human again. At least it was the last one!!!
Now onto Taxol and Herceptin for 12 weeks. I'm nervous about my first go round. I hope it is easier than AC like they say. I would like to attempt to work during the 12 weeks but if it is anything like AC there is NO WAY. I admire all of you that were able to work during AC. Ugh.
I hate hearing so many of you are having SE. I wish there was a button to make all of those go away. Of course if that were the case we would make cancer go away and skip chemo all together!
I received an email today that made me shake my head. A lady was trying to make me feel good (?) about my upcoming bi-lat and compared it to her breast reduction...a little different I think. I know she means well but it caught me off guard. lol
I haven't noticed people staring so much. If I do I am going to take Jen's line!
-
Raeann - Glad you are done with AC! I have one more next Thursday and I will be on to Taxol. I will be following you to see how your Taxol goes. I am wishing you minimum side affects.
Jen C - All of my suture abscesses have been infection free. I have had about 15 of them so far. My doc explain it more as an allergy than an infection. I hope you are done with them. Mine are finally getting better.
Good luck to everyone else getting ready to have their last AC this week.
-
Hello April-ers. I had my last FEC yesterday, no more red devil, yay!! I start docetaxel in three weeks, so I am preparing myself for a whole different regime and possible side effects. But, I am now halfway through, and it feels good.
JenC, enjoy your holiday, Maine is so pretty. I have driven through the state a couple of times, and always thought that it would be a lovely place to kick back for a while.
Have a good day everyone, hopefully SE free.
-
I finally heard about my chemo today. I had one FEC and one AC as I mentioned before and reacted to both the E and the A. They are going to start me on the weekly Taxol and skip the remainder of the other drugs since I reacted to them. On Tuesday I will get the my first taxol and one more dose of just the "C". It is not ideal, but it is the best they can offer. The herceptin will start after a month of the Taxol. I am hoping I can tolerate these drugs, but must say I am skeptical at this point. It has been very frustrating to be ready for my Chemo and find out that my body will not take the drugs. It is really limiting what they are able to offer me in terms of treatment.
Glad to hear so many of you are half way through. Before we know it it will be behind us.
-
Well what a day!! Had my 3rd round of TC today - and it nearly didn't happen! (after staying down last night and having a 3 hour drive!)
Started off with my 9:00 appointment with my Onc being 20 mins late getting in (what the hell - first appointment of the day???). By the time we discussed what needed to be discussed and I got out of there and up to the 5th floor Chemo Day unit I was 30 mins late for my appoinment up there. So I sat there waiting....waiting.....waiting.... it got to 11:15 and I asked how much longer as my appoinment was supposed to 9:30 and heaps of others that got there after me were going in before me. Finally at 11:30 got in there. Started off with extra pre meds to avoid a reaction to the taxotere (phenergen AND extra steroid) waited 1/2 hour for them to kick in. Then they started the T and guess what? Yep had a reaction for the 3rd time - I've officially been labelled a trouble maker by the nurses haha. So they stopped it gave me MORE phenregen and steroid and then while i settled down I heard them discussing me behind me - saying that they didn't want to proceed with it! Even though I'd told them that both times before once it restarted I was absolutely fine.
SO they ring my Onc who came up to talk to me. Basically they don't know why I keep reacting as today they did absolutely everything to Prevent the reaction and it still didn't work. However, she was happy to restart it (which I was fine for the remainder of thankfully) but now she wants me to change regime to AC instead of TC (so only changing the T to A but keeping the C). As funny as it sounds I dont' really want to change as I only have 1 more round so figure I know what to expect and what side effects I geneally have and don't really want to stuff the system up by chanigng now. If I still had 3 left or somehting I'd go with it but I'm really in two minds! She said to think about it and gave me thie information so that I can read about and we'll make a decision when I see her next.
So all in all a frustrating day - didn't leave hospital until 4:15 then had to face peak hour traffic and long weekend traffic so the trip home took a lot longer. Such a long day and now I don't know what to do about my last treatment
-
Question - Has anyone out there had problems with blisters on their feet? I have been having cracked heals, cracked area's between my big toe where flip flops would go and then a few blisters on my feet. Today my feet are very achy, even if I am sitting around they throb. I usually try to walk every day and the last two days the walks have been very painful. I hate to quit exercising but achy feet make me cranky! I called my onc today and I am waiting on a call back to see what they say. I really hate all these side effects!!!
-
marcy4 and DancerMel28, I'm sorry you've had such a rough time getting your chemo cocktails figured out.
LauraM: I haven't had blisters (knock on wood), but my heels are cracked. I do try to moisturize them when I'm doing my arms, but usually I forget.
Those of you who have already done Taxol, have you had bone and muscle pains? That's one of the side effects the onco warned me about (which I thought was just great, since I already get plenty of that, thank you very much, from the Neupogen). I had my first Taxol on Monday and did pretty well for a couple of days, then yesterday started feeling really achy. It feels more like a bad version of the overall body aches you get with the flu than the usual deep pain from the Neupogen. And I didn't start this round's shots until today. I needed to take some pain stuff in order to sleep last night. And here I thought I was going to get off easy with few SEs.
Karen
-
Hi Dancer,
I am on four rounds of TC as well. Had three so far and an allergic reaction to each one. Final one is next Friday and as far as I know we are sticking with iTC. Good luck to you.
-
today I had my first Taxol treament, thanks for all of the encouraging words leading up to this......
It was a long day (about 5 hours), but it went really smooth. Some of the time delay was due to the chemo area being one nurse short today (my nurse said this may happen again due to summer events, vacations, etc.). First I had my blood counts done, which were fine. Then I met with my oncologist. Earlier this week I had an EKG and MUGA test (no reason just a check after finishing AC). Both tests came back good, there was no change in the MUGA test from the inital test prior to chemo.
On to chemo, I was given my premeds.....the steroids and Benadryl have to be infused separately . (they also gave me a nurse call button for today's cycle since it was a new med.) When the Benadryl started I started feeling fairly anxious (I did not expect this) so, as instructed called the nurse over, we discussed it.......could it be anticipation, would I want to take something, wait and see, etc.. She was very calming, we decided to just monitor it, eventually it went away (I think it was anticipation). Then the Taxol was started (very slowly), I really didn't feel anything (at one point I felt the flutter of anxiety, but then it quickly went away.) After a time, the infusion was sped up, then with no reaction, sped up one more time. After Taxol, I had my Avastin/placebo infusion and then I was finished. I felt better at the end of this than at the end of my AC infusions.
so, now I'm home, I took a nap and ate a good dinner. It's kind of wierd knowing that I haven't had any anti-nausea meds and I feel fine. I actually feel pretty good. I know that this is only day 1 so we'll have to see how the next few days go but at least I'm off to a good start. My second cycle will be next Friday, the nurse said it should go much faster (plus I only receive Avasin every 3 weeks now)
good luck to all, and thanks for your support
-
Hi Ladies,
My last AC was postponed Friday. My white counts were low and my Onc. wanted me to wait until next Friday for treatment. Hopefully, by then my counts will be up a little bit. Surprisingly I wasn't that upset. I certainly didn't want to get the tx then end up in the hospital. This week is my sons's eighth grade graduation, and I don't want to miss it. So next Friday it is.
I am also having trouble with hot flashes. It feels like I spend my hole night taking the covers on and off. It's all part of the SE of tx. Menopause fun! My hope is that it doesn't last too long. I would love a decent night's sleep
-
Emme - sorry but also glad for you I guess! ;-) Enjoy the graduation!
I am done with my AC treatments!! Whoop Whoop! The nurse had to stick me three times to get a vein though and I am really worried about starting my weekly Taxol because of this! Hate being stuck but really don't want a picc line! I am feeling ok this time around - tired and a little naseau but so far not too bad.
Hope everyone else is having a good weekend!
-
LauraM - re: blisters/cracked heels - yes, yes! I have. It started somewhat during the last four weeks or so of A/C, but seemed to get markedly worse just after the first Taxol - there was a couple of days I could barely walk. Am curious what your onc said, because mine said he didn't think it was related to the chemo - oh come ON...all of my skin is much more dry and flaky than normal, of COURSE it's related to the chemo...LOL In any case, they told me not to put anything on blisters, and call them back on Monday if it was worse (this was a Friday). After looking at my feet closely I decided it wasn't so much blisters per se as just some very, very dry and cracked areas - but yes, very painful. I'm now using 'Bag Balm' bought at Rite-Aid on them, and it seems to help a lot.
-
raerae7074
Be my guest. I do notice that as soon as I look at someone who is staring they turn their heads. I just walk by now sometimes and say "HI" and keep going. drives me insain. Sorry you are all having a hard time. I got lucky I guess since I had the stitch abses which turns out after the path report not to be an infecction it will be 4 weeks between ACs. My next one #3 is this comming Friday but until then I am enjoying a week at Old Orchard Beach ME with the family.
Good luck to all having treatment this week. Stay strong...
-
Hi all. Going for my second weekly Taxol today. No Herceptin this time, which I am glad about because it made the appointment sooooo long last week, and also I had the annoying SE of crazy drippy nose that I heard Herceptin causes - it seems to be going away in the last couple of days. I'm going to take an ativan before I go to try to fend off the nausea from the saline this time too. Wish me luck.
Regarding dry feet - I have had dry skin on my fingers which actually itches and is somewhat painful. The skin peels away and it's gross. And my heels at one point were really sore - even when resting on the sheets of my bed. My onc called it Hand and Foot Syndrome caused by the AC. I googled it and it is real. I have been putting lotion on my hands and it's helping. And the pain in both has mostly subsided. Hoping that it's gone for good... She said it's often confused with neuropathy but I started having it with AC and before the Taxol. Still crossing my fingers that I won't get neuropathy...
Hope you're all having a good day and feeling well.
Sara
-
JenC - OOB is my old stomping grounds! I grew up in Brunswick, ME and every summer I would head down to OOB and see concerts and just have a great time. Oh how I miss that place!
-
Julia123 & Sara - I hate that you too have had issues with the feet, but glad to know that I am not alone. I called my onc and when they called me back, they left a message that this is not a usual side affect with AC chemo and pretty much said if I have any other questions to call them back. I was pretty annoyed with them and didn't feel like calling them back. I mean...come on, I didn't have this prior to chemo and now I have it, it must be related. On Saturday my feet hurt so bad that just walking to my kids sports games was so painful and at one point I just sat in my car and cried. I felt so stupid, but it made me feel better in the end. I have found that taking 2 aleve every 12 hours makes the discomfort manageable but I have to be proactive in taking it because it takes about 2 hours for it to start working. It is really putting a damper on my daily walking routine...ugh! I will have to try the Bag Balm, hopefully that will help me too.
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