anyone starting chemo in Nov 2005
Comments
-
ONE MORE THING . . .Last night at my support group, there was a new person who had started A/C on on 11/7. She reported that she was fine for 2 days and then spent three days throwing up, not eating or drinking anything and wound up in emergency Saturday night because of dehydration. She was not drinking any water (before or after) and did not call the doctor during the week. She stated she thought she had been told about water, but forgot and she hadn't read any of the material the oncologist gave here. OK then. I hate to see anyone have such a miserable time of it when it isn't necessary. I also realize that we were are dx we are in shock, bombarded with information and decisions that have to be made, and overwhelmed by the uncertainty of what lies ahead. I was thinking that we could help our new sisters by putting together a list of Do's/Don't During Chemo. Just a quick reminder list based on your experiences. Some things might be drink lots of water before and during, wear comfortable clothing, Biotene, popsicles, meds, etc.
If you think there is some value in this, please send me your tips and I will compile a list for all of us.
I am off, see you Friday night or Saturday.
Nancy -
Hi Kaye-
If you're results come back Her2 neg as well as ER/PR neg, its called a triple negative and you might want to take a look at this thread: Receptors Negative and HER2-Negative in the Recurring and Metestatic forum. I'm not familiar with CAF. I'm triple negative, had a lumpectomy with clear margins and neg nodes, Grade 3, Stage 1. I got three oncologist's opinions on treatment options -- 2 said go as aggressive as possible (4 A/C, 4 Taxol all dose dense), one said not so aggressive (4 A/C only). All said follow up with radiation. I'm taking the aggressive approach as insurance against recurrence.
Sorry you have to join our club, but you will find strong and inspirational women here!
Take care,
A day at a time!
Lana -
I posted my story yesterday for the first time but wanted to add for those who like to keep track of such things that I live in Maryland and work for the Department of Defense. I see my oncologist on Monday for the first time and anticipate starting chemo on the 28th or 30th. It's nice meeting all you wonderful ladies. I just watched the survivor video. Thanks so much for posting the link. I think I will add the video to my daily routine along with listening to Melissa Etheridge's I Run for Life single to keep myself focused and positive.
-
I will be starting on Nov 30th. I regretted the decision after I got home, thinking I should have started sooner. My husband thought we should enjoy thanksgiving first.
I will be doing 4 cycles of Cytoxanand and Adriamycin. I am not looking forward to this but I know it is necessary. -
Hi Everyone, Lynn you will do just fine! And yes I'm ok still a lttle fuzzy. No side effects from the meds (thank God) Welcome all newbies glad you could join us, all of us together helps build our strength, "WE CAN DO IT". And Nancy you are incredible....so extraordinary, glad you are feel well.
One of my co-workers brought over loads of food today, kinda of unexpected and it was great (fruit, soup, variety of bagels, spreads, spiral ham) and no I'm not fat but may get there (smile) My mom also came over and brought juices, paper plates, cleanning supplies and she vacumed the carpet and moped my tile big help and pluse we visited she is precious, 71 years old and don't know what I would do without her.
Nancy I too worked very many hours a week before BC and I had to slow down. I am a Real Estate agent and also an administrative assitant for a local company of 20 years both full time jobs and work fast and fierce. My medical doctor told me that I may never get 6 months off of my job again so relax and enjoy this experience as if I'm having a baby and when my husband and I go to Chemo is like a lamaze class.LOL right!
For now.....
Blessings to All, take one step at a time we will get there.
Grace05 -
Hi there, everyone. I see some newcomers tonight..welcome. Well, my first AC was today. I had to be at the hospital for the RVG scan at 9am. I never heard the word MUGA scan before, so I asked the nuclear medical gorgeous guy, if the tests were similar, he said EXACTLY. just differnt names. That went fine, was done by 10:30. then had to wait around until my 2pm appt with the oncologist. ugh, that ran late. 3pm finally got in her office. she told me what to expect from the chemo, and the drugs she is giving me to counteract the nausea. Then we talked about my pathology from the quadrantectomy/lymphnode dissection. A complete pathological response to the herceptin. No sign of any invasive cancer left. She feels we can do the 4 rounds of AC, and skip the Taxol. WOOHOO..... , That cuts 12 weeks out of my treatment, I am excited! I will get to the radiation, then the remaining 39 herceptins. So my bi-lateral/reconstruction can be done sooner, than I thought. Yippee,,,,get that DCIS off of me, that is left!!! Got up to the infusion floor by 4pm, had saline for a while, then the Adriamycin push, then more saline, then the Cytoxan drip for an hour, then more saline to flush good. It didnt bother me at all going in, and i havent felt funny or sick. i wouldnt want to drive though, because of the decadron and zofran, i am a little spacey. i was told to stay on top of the zofran, decadron 2 times a day, morning and night, even if i feel good, for 3 days. and use companzine in between, if i get any periods of nausea. and the ativan to sleep, if i am jittery from the decadron. I just spent $67 at the pharmacy getting the 4 prescriptions, plus senecot and colace. the over the counter stuff is for constipation, which the decadron causes. so this day is behind me, and i am glad it went so well so far, except for the long waits. I hope the next few days go as well, I will stay ahead of the meds, so as not to get sick. water water water, constantly, to flush the stuff out. she told me the cytoxan causes irritation to the bladder, and no bladder infections allowed!! the adriamycin makes you pee red/pink/orangey. and yes it has started already! recommended to gargle with warm water and salt. to keep mouth sores away. so much to learn!! so that is my story of my first day on A/C. looking forward to hearing the other reports! Rhonda, where are you??? Miss seeing your smiling photo! Take care, LynnZ
-
Well, thanks to everyone for such a great welcome. I had my port placed yesterday, piece of cake!!! Then on to treatment. After treatment, my Husband took me home. I felt kind of weird. They injected so many anti nausea pills. (emend and 2 others) I did not feel nauseous. I felt like my legs were tree stumps. I did eat some dinner. A very small amount, but I still felt like I had eaten way too much. I had heart burn and still do. My nurse said to take a prevacid.
As for the kids, they are great. My job has let me pick my schedule for now. (Escrow clsr for Title Company) So I will take care of me. I agree with the above mentioned "tombstone" saying.
This morning I am going in for a CT/PET scan, so I do not remember if I am supposed to eat or drink before???
Oh well, LynnZ, hope you did as well.
Wendy -
Lynn-
You got great news!! How wonderful -- much shorter treatment! Hope you're still feeling well today after your first treatment!
Wendy- Sounds like you did well with your first treatment too!
Chins up!!
;-) Lana -
Hi there, everyone,
I fell like i did great after treatment #1, I took my Ativan at 10pm, and fell asleep during ER. I woke up with the girls for school, and took Decadron, Zofran, went back to bed, and slept til 11am! Then I took a compazine. Not because I felt ill, just because the doctor told me to take that in between. I have been sucking down flavored bottled water, and a few saltines today. nothing heavy, and i am not hungry anyways.
Wendy, how did you feel getting up today, and going out for testing, after your first treatment? I am going no where today. I just want to play it safe, and lay low. -
Hey Everyone, I'm back!! I'm sorry I haven't been back on here since I got home from my first treatment. I can't believe how much I need to catch up on in just a few days!!
First off welcome to Liz, Stacey,Wendy and Kaye.
Liz your dx and treatment are almost identical to mine.
Stacey, I hope you are doing well. I know how hard it is having young kids I have 3 of my own (girls 9 6 and 6) I think this is the hardest part of it all. They are actually doing really well I haven't lost my hair yet I think my oldest will have a hard time about that. They know I'm going to but I don't think it has really sunkin in with them.
Grace I'm glad to hear your treatment went well and you were able to keep your appetite!!
Lynne, That is so AWESOME that you get to cut out the Taxol. I am so happy for you. I am glad you are feeling good too.
I have actually been doing pretty good. My friend was here for the first few days that was nice she kept me company if it wasn't for her I probably would have stayed in bed and felt sorry for myself wondering and waiting to see if I would get sick.
Well I never got sick I am on day 5. On day 3 and 4 I was a little tired. I went to get my WBC shot Wed. Morning I was a little tired when I got home so I took a 2 hour nap. Stayed up till around 5 then layed back down when Martha Stewart came on my hubby came up and turned the tv on so I would watch it. He knows thats one of my favorite shows. I thought that was nice of him.
Thursday my oldest daughter was being recognized for being an A honor Roll student and was also preforming in a jump rope dance in front of the 3rd grade classes. And the school was having Thanksgiving Lunches for the students,parents and grandparents so I stayed and did all of that. I was pretty worn out when i got home.
Today I went and did some x-mass shopping. I wanted to get some of that done before I loose my hair. I swear I think that is going to be so hard to go out the first few times!!!
Kim and Debbie, I will probably be loosing my hair on Thanksgiving too. Have you guys cut your hair at all?? I haven't. I just feel like I want to look like me for as long as I can. Not sure if that s the right thing or not??
I think the worst thing for me so far has been headaches!! Has anyone else had them? The only medicine I have had to take so far is Sennokot (sp) My onc never gave me meds to take before treatment and only gave my Zofran for after so far I haven't had to use it. Iv'e been eating fine maybe not as much as usual. I heve been munching on Oyster crackes alot.I craved cheese pizza yesterday. Ate 4 slices I know it's not healthy but it tasted good!! And drinking water.YUCK!!! Oh, I have had a little bit of the medal taste in my throat. And I noticed today I think my head is feeling a little tingly is that normal does that mean it is getting ready to fall out???
I am glad to here everyone is doing good. And I will go back and read more of the post that I missed this week.
Lynne, I love your picture and will send you my reconstruction photo right now.
Talk to you all soon
Rhonda -
Graycie,
the Xanax has helped a bit, particularly when I get up in the middle of the night. I notice it is not helping as much as before and plan to discuss with Onc. this week. he did tell me the way I am taking it WILL NOT be addictive and we can wean me off easily when this journey is complete.
good luck
susan -
HI Nov ladies, Here is my update for the week
1. Be prepared for the depression after the steroids- I had a few VERY BLUE days. while understandable my onc also blamed on steroids!
2. Had 2nd A/C on thursday- went much smoother than first- I had streaking first time, so we slowed it down, gave me 1/2 decadron before 1nd second half after. I get woozy when they finish Cytoxin and remove needle- had to wait 1/2 hour for BP to go back up.
3. My chemo reaction is complete crash that night- no phones, no remote, just veg and sleep- next days are tired but better
4. Day 14 hair started to shed- I already had a wig, so went to my salon, had him buzz my scalp (GI Jane look now) and trim my wig- I AM READY TO FACE THE WORLD- I get my 2nd wig on Wenesday and also have losts of scarves, caps, etc to wear around. I am very proud of myself, since when I forst picked out my wig I had a complete anxiety attack and could not get out of bathroom of the salon!
I am doing OK- people keep asking me "really?" like they want to hear the horror stories. I think I may make some up just so they feel better- JK!
Praying for a smooth journey for all of you
Susan -
Bosom Buddies, you all sound like you are doing GREAT! Lynn, I am so pleased with your news. By the way, can I have one of those -- "nuclear medicine gorgeous guy." Susan, tell me more about "streaking"--what is it? what causes it? what is the effect? etc. For those new or waiting for first treatment, you can see that we're doing well and so will you. By the way, Lana sent me a message that there is already a great thread called "Chemo Checklist" under "Help Me Through Treatment". She's right, it is great and I encourage you to check it out. I know I will need a reminder before #2 and will use that site.
Yesterday at a business meeting, my 9 managers-in-training did a presentation entitled "Nancy". Each of them was wearing a different colored neoprene bracelet that represented an attribube "Love" "Long Life" "Friendship" "Courage" "Hope" "Patience", etc. They gave me a pink one and said they will wear theirs in my honor as long as I am in treatment. You should have seen all the people in the room, (some very tough old birds) crying. It was an incredibly moving and loving thing to do. Grace, its like someone bringing food or Rhonda's friend staying, or all the other acts of comfort, kindness and love that we all have experienced since our dx. Puts a whole new meaning on Thanksgiving, doesn't it.
Hugs to all of you.
Nancy -
Hi nancy,
Streaking is when you have a bit of an alergic or skin reaction to the adriamyacin. I do not have a port, so we use a vein. The area around the vein and up my arm had red marks and was a little itchy. they changed the Adria push from 10 minutes to 30 minutes and it really helped.
Not very common- I guess, I am just sensitive. good news was they used the same vein both times and was still good.
Take care
susan -
When i was in chemo this week, my nurse gave me a little plastic bag from "Sanofi aventis" they make Taxotere and have website "livingwithit.org"
In side the bag were seven necklaces each with a letter from the word "journey" It also included a card with a quote and a little note card-
Join me.....
I've sent you one of seven letters of the word journey as a simple reminder that you and six others will form the circle of support I will need. Knowing, as I travel the road ahed, I will never be alone.
I had a hard time with picking just 7, but what a lovely thought.
Perhaps some of you can find a way to make your own JOURNEY circle
Susan -
Glad to hear...so many of you are doing fine with the chemo. I still dread my first day. I am a real baby when it comes to this kind of stuff, especially when I am so sensitive to drugs like Vicodin and Percocet. I only seem to be able to tolerate plain old Aspirin. I do take Xanax, have for quite a few years, always had anxiety. I am a high stress person.
Well the 29th is creeping up fast....so will let you all know how it goes.
Thanks for letting me know about the triple negative thread. I did check it out, and thanks also for the survivor movie.
Kaye -
Good afternoon, November girls. This is day 2 past first A/C. i woke up to drive my daughter to work, and took my Decadron and Zofran, and back to bed til 11am. Took the companzine at noon. I feel fine. i have been eating very light. Chicken soup last night, nothing so far today. i dont feel hungry. i am drinking plenty of water, and the red/orangey pee has stopped, so I imagine that is a good sign of plenty of flushing. The hospital pharmacy called a little bit ago, and just wanted to check in on how i was feeling. I thought that was nice. They are very concerned about keeping the nausea at bay, and it is working. She said to expect to feel the most tired by next week, when my blood levels drop. That will be Thanksgiving weekend, and I am having a few people here. Hopefully lots of help, and no germs!!! I am glad everyone is reporting in on there details, it is good to know we are all doing what we are told, and feeling the best we can. Hang in there ladies....lynnz
-
Kaye, I just wanted to mention to you, that I too am unable to take most narcotics. this was a big concern for me, having the surgery. My mother and I dont tolerate things, and end up throwing up all the time on them. I opted for a paravertebral block for the surgery, and it worked great. My surgeon found a great narcotic, that typically doesnt cause problems for nausea, Dilaudid, it is considered very strong, but in small doses works great. i was apprehensive using it after surgery, but did fine with it. No sickness at all. of course I couldnt drive,and had to just lay low, but it was a great thing for me. Maybe you could mention this your team, and it could be something for you. good luck. LynnZ
-
Hi Lynne,
Glad to hear you are feeling well!!! You mentioned about feeling bad next week. I was wondering that. I have actually felt pretty good this week. I thought it was the first week you felt your worst and then the 2nd you start feeling better. Now I'm starting to get worried again. I hope I don't feel bad next week. I am actually thinking about driving to Indy to see some family memebers (5hrs)but now I'm not sure if I should. i would hate to feel sick while driving alone or when I get there and might have a hard time getting home. I'm so confussed.
On day 4 and 5 I started eating like crazy. I am trying to drink all the water I don't think I have made it to 8 glasses in one day I am at 6. I saw your post about the flavored water. I'm going to try that.
Thinking of you and everyone on the board.
Rhonda -
Hi to everyone. I have read each post concerning your experiences with chemo and found lots of information. I found a lump in July 05, while my husband was recoperating from heart attack # 4 and open heart surgery #2. I went through with biopsies alone, because I couldn't tell him and didn't want to worry my sons. The diagnosis was multifocal ILC 8/05. Mastectomy was 9/05 with 7.5 cm tumor and 1 lymph node positive, stage IIIa. Had to wait longer than I wanted to get my treatment started, but the oncologist that I wanted was on vacation. My chemo finally started 11/7 and I must say it was not as bad as I had anticipated. No nausea thanks to emend, a little queasy, and fatigue. I had a neulasta shot 11/8. The nurse said I could have some bone pain, but didn't notice anything different. I have eaten everything thats not nailed down and been able to work most days. I am very fortunate as far as work in that I can lay down in my office and rest during the day. Chemo #2 is Monday and next week maybe a different story. My scalp has been tingling, but the hair hasn't gone south yet. Hope everyone has a good weekend.
-
Hi Rhonda, I hope I didnt scare you regarding your holiday plans. My doctors told me, that by day 7-10, my blood levels will be the lowest, due to the chemo attacking the cells. And I would be more fatigued and susceptible to germs. SO to just be careful around crowds with the holiday. Not that I would be sick, nauseous. That is being controlled nicely with the decadron and zofran for 3 full days, then the companzine. today is day 3 for me, and i feel fine. tired, but not sick. I rest a lot. I am getting ready for church now, then will take my daughter to the mall, and come home and cook pot roast for dinner. today looks like a good day, for me. Yesterday I did NOTHING! hope this clears things up, I wouldnt want you to change plans on going to Indy, based on mixed info. have a great day.....LynnZ
-
Hi Lynne,
I think I've decided not to go to Indy. Unfortunatly my mom is a smoker. My little sister and her 3 kids will be there so I think it would be best if i just stay away. The smoke grosses me out and she smokes like a chimney. It makes me sick!! I could stay with my oldest sister who I am best friends with but the whole purpose of me going is to see my younger sister (long soap opera story)My oldest I think is planning on coming here for my next treatment.
I'm also nervous about Thanksgiving we will be going to Alabama and there will be 2 other kids besides my own.
One of my twins is starting to get sick right now. UGH!!
They only go to school 2 days this week so hopefully we all won't get sick.
I also think i might be getting a bladder infection it is kindof hurting when I pee. Could that be from the Chemo??
I put up our X-mass lights outside the week before my treatment. I'm going to put up the rest of the decorations today and take the girls to get some new tennis shoes. Then come home and watch the COLTS!!! GO COLTS!! We always have family dinner with the inlaws on Sunday so we will be going to there house for dinner. Yummy I think shes making a Thanksgiving type dinner since we won't be here.
Enyoy your day today.
Oh, Are headaches and blurry vision normal
Rhonda
BTW I do have expanders and that is the sguare look. They are starting to be real uncomfortable I went to PS on Friday and he said it's just all the swelling is going away now and I can feel them more. I wish I could just get the implants now!!! -
LynnZ~ thanks for letting me know that you also are sensitive to drugs. That just took a whole LOT of weight off my shoulders.
Now maybe I can get through this with a much better state of mind.
Kaye -
Rhonda, I was told that Cytoxan, can really wreak havoc with your bladder. I am not sure if you are on AC or not, I am . So i have been drinking 16oz bottles of flavored water all day long. the worst thing you can let happen is an infection. Try to pump the water, it is definately a bladder flusher. I hope that is all you have going on, and can fix it on your own. Good luck. i am not a sports fan, but if the Colts are your thing, then GO COLTS!!! Good for you gettin up the xmas lights. i havent even thought of it yet.
Kaye, glad to put your mind at ease about the sensitivity to narcotics. nothing is worse than throwing up, when feeling so poorly otherwise. Ask your doctor about decadron and zofran, neither are narcotic, and shouldnt upset you. if you are having pain, the dilaudid, 1mg, worked well for me, and didnt cause any sickness. it is a 3rd cousin to morphine, my doctor said, so it is addictive in long term use, but at a low dose should not be a problem. good luck.. have a good sunday evening everyone...hugs, prayers, LynnZ -
Hey Lynne,
Iv'e been drinking the 16oz size bottles too. I have made it to 3 a day somedays I have probably had an extra glass of water.
I have never been a water drinker I read in one of my books that cancer thrieves on dehydrated bodies.
I am on AC. I'm just surprised I would get this as much water that i am drinking. I have cranberry juice so I'm going to drink some of that.
Have a great night
Rhonda -
Hello bosom buddies. Ronda, drink, drink, drink. My onc also rec cranberry juice. Lynn is right, a common side effect of A/C is bladder infections, so we have to flush it out of our systems as quickly as possible. You all sound so good. I am at the end of my second week and don't feel any nausea, but am very tired. Went to a 10 Tenors concert yesterday (Debbie, you would have loved them) and slept through part of it (at 2 p.m. matinee). Oh well. My son and grandson both have a cold, so may not go for Thanksgiving--we'll celebrate another day if we must. I don't want to do anything to delay my next treatment on the 30th.
Kaye, I'm another one who is sensitive to anything and so avoid medications. But, I have learned that our bodies need these and the doctors have a lot of tricks up their sleeves if we don't respond well to one.
Looks like no one is starting Thanksgiving week--anyone on another round this week? Does that mean we'll all be enjoying turkey or whatever. The next week looks busy, we have 3 of us starting (Kaye, Laura, and Suave--did I miss anyone?)
Hugs to all of you.
Nancy -
I start treatment #2 tomorrow (Monday) morning 9:00. Don't know what my Thanksgiving will be like.
-
Hey Ladies-
I have a learning session on Wednesday this week, then start my first AC on Monday the 28th....just want to get this rolling!!
All of your posts have really helped me to know a little about what to expect and really to see that everyone reacts a little differently!
Chins up!!
Lana -
Good Luck on your treatment tomorrow . I hope everything goes smoothly for you.
BTW Where is Maryville Tn.? I'm in Spring Hill thats 30 minutes
south of Nashville. We've only been here for a year. It's beautiful here.
Rhonda -
Hi ladies!! This is Sidney Rhonda's daughter. I hope you all
are feeling okay. Have a fun week. I think you all will hang in there. I wish you guy's didn't have cancer.
Stay strong !!
Love,
Sidney
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