Has anyone started a forum for Chemo in Dec 2008?
Comments
-
Sherry, I just went by the color swatches in the catalog. They were pretty much right on, in fact my blond wig was prettier than expected. I was afraid it would be gold but it was such pretty beige highlights in a lighter ashy blond. a friend just ordered 2 and the colors were great. I cut them into a short sassy style and she looked awesome.
Artsee
-
Happy Thanksgiving!
I was looking at simvog's list of Dec. chemo ladies....I'm glad that I won't be only only bald one at Christmas! My hair is normally short, I plan to have my head shaved on 12/9. I have not felt in charge ever since I felt the dreaded lump, and this is something that I can control. I can't stand the thought of of my hair coming out in hunks!
No Black Friday for me! We are going to Milwaukee and going to the art museum. Jim and I wanted to do something fun, as I won't know how I'll feel after 12/2.
I hope that everyone had a happy Thanksgiving. I'll touch base after my treatment. Hey 12/2 Ladies! Let's compare notes sometime next week!
Stay strong! Carol
-
Carol, where do you live? Near Sheboygan?
-
Artsee I purchased a wig from a local salon. The American Cancer Society also has a free wig program in the area, but my daughter really liked the one at the salon. Since I am letting her be in charge of the Mom Makeover
, I am letting her be involved in my beauty program! I was concerned about the quality of the Paula Young wigs....... I still haven't gotten a supply of caps yet; I need to get some ordered.
Sue I live near Richmond - not too far from your old Ft Wayne stomping ground. The UP is a special place (must be the iron in the water that we drank that keeps a magnetic hold on us). Do you eat at Borders in Marquette? Our favorite Mexican restaurant in the UP!
Sherry I too am counting the days til the 2nd. But I am ready to get started - sooner to be done. With a house full of company, I'm too busy to think about Tuesday, I just hope I have everything done and prepared. (But I know I don't)
Lisa You will have to give us tips on scarves!
Mary
-
Everyone starting the fight......May Gods healing hands continue to be over you, and may he bless you and give you peace. Artsee
Mary..your DX is (almost like mine)
-
Artsee Did you have an Oncotype score? My score is (31) which put me in the high risk of recurrence category, hence the chemo. I noticed you also post on the HT forum; I'm thinking chemo is a piece of cake compared to the AI SEs.
Thankful all of us are getting to know each other and will be traveling the same road at the same time; therefore, we can guide and encourage each other. Anyone feel like our chemo start dates are like different exits on an interstate highway going to the same town?
PS Friday Night Fish Fry is also in the Upper Peninsula of Michigan.
Mary
-
Oh so true about the fish frys there are none other like them.
I totally get the off ramp idea. We are all heading to the same place at almost the same time. My mom today bought me a new bra. I havent worn one in three years since I was reconstructed after the last time and since they took my implant out on the left I am a little flat on one side
. So I need a bra to hold the gel one I have but dont need support or underwires. I asked the lady for a training bra in a large size. She thought I was nuts until I explained. They threw in a T-shirt that says "Cancer Sucks!!!!" I will have to wear it to the first dose. I asked if they had one that read "I am going to kick cancers a**" but they didnt. I may have one printed up. lol
Hope everyone had a great Thanksgiving.
Sue
-
Mary...My Onco score was 35. My Drs. were very surprised, and gave me no choice. You are right the Ai's are gruesome!!! After six month I don't think there was much in my body that hasn't started to hurt. Can you imagine what happens in 5 years. My midriff can tell that my daily walks have been put on hold. It's tough when we get between a rock and a hard place. Maybe if I hadn't had osteoporosis to begin with it wouldn't be quite so bad. Having an ex-ray of my left knee on Mon.
Artsee
Tonight it's Friday Night Fish Fry!
-
Artsee and All,
I don't live near Sheboygan, I live in the far NW suburbs of Chicago. So Milwaukee is not too far away. It was a beautiful day. Sunny and bright. We did not go to the art museum, but went to the Pabst mansion instead. That was really cool! Then we went for a late lunch, walked around downtown Milwaukee, and then went to the movies to see "Four Christmas's" It was a cute movie. I went to college in Milwaukee 33 yrs. ago! LOL! I couldn't find my way around downtown at all now!
Message on the phone today reminding me that I have an appointment at 10 am on Tuesday, 12/2. As if I could or would forget....but it was fun to forget for a little while today!
{{{{{{{{{{Hugs}}}}}}}}}}}}} Carol
-
Hi my chemo sisters,
I have a problem. My onc. called me tonight. He said he had my oncotype results and wanted to let me know before the end of next week. He said my score was in the high range so he wants to do dose dense TAC for 4 months every other week. When I first saw him and based on my biopsy report he was talking Tamox. only. So this is a big big change from that. He said that when I go back to my surgeon to get my port placed, he's strongly urging me to have a full axillary dissection because there is a micro mets of .2cm. in one of my sentinel nodes. When I saw my surgeon post surgery and on my second meeting with my onc. they both told me that the micro mets doesn't count because there are no stats indicating that there is any difference in recurrance with micro mets and not having micro mets. At that meeting my onc said I could probably get by with a light dose of chemo for 4 treatments mostly based on my age. But now he wants standard chemo and a full axillary dissection. He said the axillary dissection was up to me. He can't really guide me one way or the other. He said that because they don't really know if it makes a difference, oncs tend to over do treatment. I'm terrified to have this done. After doing some research I've found that over 1/3 of women having a full axilla done have sever SEs. I already have some range of motion and grip issues in my right hand due to a screwed up trigger finger surgery. I don't think I can deal with limitations on my left side too. I just don't know what to do. I sure would hate to think that my cancer came back because I didn't do this, but with dose dense chemo for 4 months, what could possibly be left???? If I don't do the full axillary dissection, he might want me to do rads after the chemo. I also don't want to do that. Onc. said that when they do the full ax. dissection, they will probably find no cancer because only one of the two lymph nodes has micro mets. And he's fine with it if I decide not to do it. Does any one have any thoughts on this?
I already don't want to do A. I think I told cebula that I wouldn't do A. So, now here I am looking at it anyway. He reassured me that we would do the heart function tests and A doesn't affect vascular stuff. Only the pumping of the heart. Nice. I'm just sick over all of this tonight. I feel like I'm going to just curl up in a ball and die. I can't think straight. My DH, as helpful as he's been, said ," Well it isn't that much different than what we thought. It's just a month longer." It is very different!! TAC every other week for 4 months is very different than TC for 4 treatments every three weeks. Throw in a full axillary dis. or 6 weeks of rads and yes, virginia, it is very different!!
Than you know what really sucks even more than all of this? I got fired from my job in mid. Aug. Was diagnosed with BC the first week of Sept. I've been trying to get back to work. I knew I'd need time off for the bi mast. Now I'm probably going to need some time off for chemo. Who in the world is going to hire me? My DH has a small cabinet shop that is now in that "no work coming in" time. Besides all of this damn cancer crap, I'm afraid I'm going to lose my house before all of this is done.
How in the hell am I going to make it thru all of this???????????????????
-
Hi Firni,
I am sending you good and positive thoughts today. It does suck to have to worry about your treatment and job. I wish I could say something to comfort you, but just know I am thinking of you.
I am off for a brisk walk.
Hugs to everyone.
Mimi
-
Firni, so sorry, I was under the impression that you were doing chemo, that's sure a lot to diggest in one day. I'm gald you found my other thread comparing both treatment. Hopefully that will be of some help for you.
-
Firni, take deep breaths. You will be ok. I know receiving this new 'not so good' news has thrown you for a loop, just remember that you are strong and you will get through this. You have all of us!
Sue, thank you for some of the tips you posted. I didn't now that yogurt was a 'no no'. I haven't had much a taste for it lately anyway.
Has anyone else noticed their appetite decreased during all of this? I am barely hungry for anything these days so I can't even imagine what it's going to be like once I start treatment! I am getting my hair cut short on Wednesday and I can't wait. My hairdresser is going to give me something really short and cute (I hope!).
To all the ladies starting their chemo tomorrow, I will be thinking of you all day!
Love, Elaine
-
Firni..I will pray that you make all the right decisions. With a 'Grade 2' your Onco score can't be that high? Boy, it sounds like you got the mother load dumped on you...Just remember everything happens for a reason and just because one door is closed, another will open for you.
Berry.....Isin't the Pabst Mansion beautiful? So many things have changed in Milwaukee..at least you got to experience the new 'Marquette Interchange' Yeah, we are happy for that change!
Have a great weekend, Artsee
-
thanks everyone for your thoughts. I just need to keep reading my own signature, huh? One moment to the next. I'm not going to do the full axillary dissection since there is no evidence that it will benefit me. I'm doing some more research on chemo and what will and won't work for ILC and Her2-. It seems that chemo is not very effective with that combo. I don't want just the "standard treatment" if it isn't going to do any good.
Lainey, I haven't been very hungry either. Except for chocolate. I hear sugar stimulates cancer growth. How nice. Someone else posted that you should eat yogurt for the live culture so you don't get yeast infections. I'd ask the Onc about any food limitations. Of course it looks like you'll hear something different depending on which onc you talk to.
-
Fimi, What a burden to bear; I too wish I could comfort you, but you are in my thoughts and prayers. You are right - a month longer and more treatments are a huge deal! I'm sure you are finding out more about treatments and will be able to work with your onc for the best treatment
Don't be too hard on DH, I suspect he is stressing as well and is just trying to be encouraging. Unfortunately this BC just doesn't affect us...... it affects the whole family.
Mary
-
Thanks CindyD! Yes...a big Buffett fan for many years. Many of his songs have become the soundtrack to my life - even this crazy journey. My oncologist is getting used to my follow-up questions. It's actually become a joke with us. I've switched plastic surgeons for my reconstruction because he literally refused to answer questions. I asked him what size tissue expanders he used and how much he put in them at the time of the initial surgery and he said he didn't remember. I asked him to check and he said he let me know at some point duirng my future visits. My chart was in the room with us but he wouldn't take the time to check it out. First of all, we should have discussed it pre-surgery (my bad - just wanted the cancer out and didn't think about the other stuff). Now keep in mind, I travel 2+ hours each way to see this guy...needless to say, when I got home, I called my insurance company and some nurses I know and was referred to the head ps at MD Anderson which is only 45 minutes away from me. So far so good with him! Anyway...thanks for the support!!!!
-
Hey All - Hope everyone had a great thanksgiving. Getting a little scared because Dec is fast approaching. As much as I wanted to start the treatments to get it over with now I can't believe it will happen in 3 days. I got to see my Mom, but she is not really doing that well. We will get all the reports back sometime on Monday. They released her from hosp. on Thurs. but she is still having such are hard time breathing. She basically goes from the bed to the chair. I am just praying for the best. I don't think I can handle anymore bad news.
Firni: I am sorry to hear about all that you are going through. Can you get another onco to read your reports and get a different opinion. When my ocno asked me to do the dense dosage trial I did not know what to do. But I had three diffent onco tell me that I should do it. It made me feel better. They were completely different onco that were not from the same hosp. Regarding your job and house, I will keep you in my thoughts and prayers and hope that you get good news.
Colleen
-
Hi ladies! I just wanted to check in. I got my Christmas tree up today. I wanted to get it done before next week so I wouldn't be sitting around wishing I could do it after my chemo starts. I'm amazed at how fast Tuesday is approaching.
Fimi: I am sorry to hear all you are having to deal with. I hope you can find the answers you are searching for. I agree with Colleen about getting some more opinions. I haven't heard from my oncotype test yet and I still worry about the unknown. I will keep you in my thoughts and prayers and hope things get better for you.
Carol: I haven't gotten my "reminder" call about Tuesday yet, but I know I will. How do they think we could forget???
Colleen: I will be thinking about you and your mother. Sorry to hear she is having such a hard time. Mothers are precious and it is hard to see them be sick. I hope she improves soon and that you get some good news from the reports.
-
Wow Sherry, You're fast with the Christmas tree. I barely have thanksgiving dishes done. LOL. We usually do our tree mid Dec. My DH doesn't like Christmas to last too long.
Thanks again everyone for all your warm thoughts and prayers. It all helps. I know things will work out. They always do. For the life of me tho, I can't see how this time.
I'm almost jealous of all of you who know what you're doing with chemo and are actually starting next week.
Mary, my DH has been great. Sometimes he just doesn't understand. I don't complain much so he naturally thinks everything is fine. He does know how stressed I am about all these decisions and he is trying to be helpful and encouraging. Sometimes he just misses the mark.
-
Dear All,
It is amazing how this BC brings us together. It is a tough situation for all of us and hope GOD will give us patience and resistance against all these chemos and the power to defeat this disease.
I had my BLT Mast on 17 Nov. My surgeon said I had Grade 3 Cancer bigger than 5 cm. He believes I should get chemo and rad. I have an appointment with my Oncologist on 6 Dec. I do not know anything about my HER2, Oncotype test etc. I believe my Oncologist is gone tell me.
I am worried about everything. Especially not knowing what is gone happen. I wanted to put Port already. How long the surgery for port take. I believe it is easier to have it. Anyway, so many things to worry.
All the best to ALL and will check on you.
Hope
-
Sherry - If they don't call with a reminder, can I claim I just forgot that Wed is my first appointment???? *smile*
I also got my tree up and the outside wreaths out. Shopping is mostly done, just wrapping to be done. But I had to because I will be leaving town on next Monday and not back until Dec 22nd. Between that and not knowing how I am going to feel, I figured that I better do it now or Christmas just might not come to my house this year.
Firni - any one of us working women could be in your shoes at any time with the way the economy is going. Don't hesitate to check out every financial resource available, including the American Cancer Society and Susan Komen Foundation -- and the ACS has a program for free wigs for those who can't afford them. Go to the Look Good Feel Better program and get a wonderful kit of (free) makeup. At our meeting they also brought a whole basket of hats/scarves that had been donated by survivors (and washed and pressed) -- again at no cost If you haven't, call your bank and see about refinancing your home for a longer term. But above all, you have to concentrate on you and getting through your treatments and getting well.
For those starting this week, I am sure you are as nervous as I am -- together we can do this!
Brenda
-
Hope: Sorry you are going through this, but glad you found us! We will all get through this together. I had BL MX also. Did you get expanders for reconstruction? That's what I did. Just curious. . . .
Brenda: I haven't thought about that! If I get "chicken" about it and don't get a call, I might try that excuse. . . .
. . . . not! LOL I have mixed emotions about it and sometimes wonder what I will think that day, even though I have just wanted to get on with it and get it over with. There's that "roller coaster" effect again. I want to do it - no I don't - yes I do - no I don't - I have to!
I hope all of us starting our chemo this week and this month have an easier time of it than we are all imagining. Best wishes to everyone!
-
Well, ladies, I have my 1st TAC Tuesday morning. The port goes in Monday morning. Had a wonderful Thanksgiving however, did not get the decorations up as it RAINED RAINED RAINED!!! But we need it. I will eventually get it up. Daughter and I went wig shopping on Wed. This is the one side effect I will have problems with.
Will be thinking of all of you. Linda
-
Brenny, thanks for the suggestions. I will call ACS tomorrow to find out what they can do for me.
I'm feeling a little better as I feel like I have a plan now. I call my onc on Mon. to set an appt for Tues or Wed. to schedule my heart tests and talk with my onc. At that point I'll have the answers I need to decide on my chemo. I'm calling to schedule my port insertion on Monday so when I see my onc, I can find out when I start. More waiting, but things are getting scheduled. I see my PS on Tues for my second fill. I'm actually starting to look like I have something. I'll get to the ACS office this week to find out about LGFB programs here, see about a wig and talk to a councilor about finding a job during chemo. Must be someone there who can guide me. My DH is looking at doing some kind of seasonal work during Dec and Jan when his business typically brings in nothing. (If he can find something. Even those are hard to find this year). I'm going to contact some of the temp agencies here to see if any of them will take me on. I figure temp will be better so if I'm feeling too crappy, I can not work. I might even find a real job that way. So, I'm feeling better with a plan and by the end of this week, I should actually know what's going on.
My brother is coming in from MN on Thurs. I'm so excited. I haven't seen him for almost a year. He'll only be here 5 days but it will be great. My nephew and his wife will be home from Abu Dabi for a week too. Then there will be the chocolate party. We know a lady who orders like 200 lbs of chocolate and makes truffles, bark, coconut balls, just all kinds of chocolate. Then she has a big party for everyone she knows. It's a lot of fun and a good networking opportunity as she tries to connect people. I know I shouldn't eat all that chocolate, but....it's a good networking opportunity. It's going to be a busy 10 days or so and the distractions will do me good until I have to start chemo.
I know we all say it all the time, how much it means to be able to come to this site and just freak out. Everyone understands and rallies. This site is a lifesaver. Thank you, everyone.
Good luck everyone starting chemo this week. I hope everyone has an easy time with mild SEs.
-
Firni - Glad to hear you're feeling better about the situation.
We got our Christmas tree up last night. What a pain!!!! We usually get it a week after Thanksgiving, but knowing I might start chemo next week, I wanted to be able to enjoy our yearly tradition which includes drinking Bailey's & milk while putting up the tree, wouldn't have happened with nausea! LOL! I was so looking forward to getting the tree, well, couldn't find one on Friday night, got one last night, hubby had to mess with the Christmas lights for more than an hour to try to find the burned one, couldn't find it. The whole process took more than 4 hours, never had such a hard time putting up a tree, of all years! But now it's all nice & pretty.
Tonight, we'll be having a really nice dinner with wine, this might be our last one until chemo is done. I don't know how I'll be feeling and what kind of food I'll be able to eat, so I wanted to make sure that we'd have a nice night before this all start.
Dreading tomorrow, I'm suppose to tell onc which chemo I want to do and I'm still not sure! I had decided on TC, but after a few things people have said, I might actually benefit more from AC+T....
Hope y'all have a good week even if your treatment starts
-
Linda, I see that you are doing TAC. That is what my onc is really leaning toward for me. What kind of a schedule are you on? My onc said I would do 8 treatments every other week. Sounds grueling to me. Let me know how it goes for you.
Caroline, I'm glad you were able to enjoy some traditions before chemo. I'm kind of on the fence about getting things done early, or waiting so I have a distraction. Of course if a distraction won't help, my DH will have to do everything. I think we'll be alone for Christmas this year. Our kids live in FL and CA and neither are coming home this year. So, if we don't do a lot that will be ok too.
I know what you mean about not knowing which chemo to do. I'm hoping my onc will go over TAC and TC and tell me exactly why he feels one is better that the other. If it makes sense to me, I'm comfortable going with his preference. Other wise, well, then it will be a more difficult decision. I already am second guessing not doing the full axillary dissection. I'm not going to change my mind, but I feel like that was one treatment I decided not to do. I don't think I want to risk my future health too much more. So, regardless that I said I would never do A, if my onc can show my that it will really benefit me, I will do it.
-
Hello Everyone -
Firni - I'm so glad that you have a plan! I know that the ACS will have some resources for you and your DH. You are not alone! Please come here and Biotch as often as you need to! We're all in this together.
47 hours and counting! You know, I am dreading this whole chemo business even more than the surgery. I'd had surgery before, so I know what was coming, but this chemo is the unknown. You read about all of these SE's, you wonder about the holidays and how you're going to get through it all, especially when your 2nd treatment is 12/23! (and you're bald too!) NICE!!! All these drugs I have, and could possibly have for SE's....I used to be a healthy person, I only took Excedrin for headaches! But if I guess if I didn't have all this crap to look forward to, there possibly wouldn't be a Christmas for next year for me. OK! enough of that!
Tree is going up today. House will be cleaned as Jim's mom is coming to help out next week. Grocery shopping was wierd...what will I eat? I did get some popscicles, but otherwise, I'll just have to play it by ear. Oh guess what I did yesterday!? I went ice skating for the first time in probably 35 years! Haha! It's NOT like riding a bike...you DO forget how to skate! I was a wall-hugger for the first 4 or 5 rounds! And definately could not skate like I used to!
Thanks for listening to me whine. I'll check in on Monday night to hear about how things went for our Monday Ladies! Good Luck Girls!!!!
Carol
-
Good Luck to everyone this week.....I still have not had the onc. appointment yet....it will happen on the 8th...I still have one of my drains in from the BL mastectomy on 11/4. The PS did give me my first fill this past Monday and I should get them every Monday until I'm where I want to be. That felt weird. Does anyone know how many cc's there are in a cup size(c).
Please give me some suggestions on the wigs, my plan was to cut my hair short (about an inch from head) a few days before chemo started. My daughter is a stylist and suggested that so my head wouldn't itch as much.
My thoughts and prayers are with everyone this week and yes this is a wonderful site. Although I have a wonderful support group at home, it is nice to be able to talk to all of you that are going through the same thing and at the same time that I am.
We will get through this together!!!!!
Be strong
Tricia
-
Please come and share your experience in the new topic - Diary - Starting Chemo DECEMBER 2008.
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