June 2007 Chemo
Options
Comments
-
Joanne Elizabeth, my oncologist says different doctors have a preference for one or the other treatments although both are thought to be about equal if their effectiveness.
Terry, I am so sorry to hear about your trouble today. I sure hope the antibiotics work quickly on the infection! This disease seems to have more than normal roadblocks in the treatment. So frustrating....
We had a wonderful weekend, I hated to come back for treatment today, but I will be glad to get another one under my belt. I noticed by hair is starting to leave my body. Oh well, the sooner gone, the sooner it can grow back.
Take care everyone! Debbi -
Hi Terry, heck don't worry about the attitude adjustment, you have alot on your plate right now so being crabby sounds normal to me. I hope you get some relief when you
get your US today, keep us posted.
I've been pretty crabby myself but when you don't feel good or are worrying about things it just happens.
The vertigo could possibly have been in connection w/your infection. It's so hard to tell sometimes. I know I had vertigo before my infection set in but figured it was from the chemo.
Let us know what you find out about your son, -
Terry, I think you have the right attitude considering what you are dealing with. It's got to be horribly frustrating and to be worrying about your son at the same time is just the worst. Hopefully you son's MRI will have good results and the antibiotics will get you back on track shortly. Best of luck this week. My prayers are with you.
xoxo
Kathleen -
Terry - I'm glad two appointments are out of the way at least. Take a nap now or a bubble bath or something to make you feel better before the US. You know we are all hoping for a positive (as in ALL IS WELL) call for your son's mri and then you can worry about dueling doctors offices.
One step at a time...........................
Dawn -
Thanks everyone for your sympathetic ears. My son's MRI results were negative, woohoo!! They said it was a contusion and nothing needed to be removed, best news we've had in a long time.
As for me, they drained 40 cc out yesterday and while I feel some better, still not 100%. I need to be fever-free for 48 hours before the onc will administer my second tx. So far, so good. Still a lot of tenderness so quite sore yet.
I'm supposed to hear from the surgeon's office this morning as to the next step. He's got to figure out why I'm still draining....or not draining as the case may be.
I don't want to get too behind on my chemo schedule but my onc nurse said the dr likes to take a very conservative approach when dealing with infections. I certainly understand his concerns and am thankful. I just want to get the whole process over with though so it is frustrating to say the least.
Hope everyone is doing well today! -
Terry,
So glad to hear your news - good on all fronts!
Linda -
Terry, am so glad they were able to drain that for you, and thrilled that your son's MRI was good. Now just take it easy, and never apologize for how you feel, even if it's grumpy. I think we all have such ups and downs going through this, and it's normal to have days where you don't fell well and simply need to vent, and what better place than here, where everyone else has been where you are.
I did my first chemo yesterday. It went pretty well...my port got kind of kinked up during the A, so they had to stop it and get the port working again, get blood, then started the C...they had to stop about half way through as I had that headache, sinuses, then the whole back of my head. They gave me three tylenol, and waited a bit, then started it again. I got it finished, but was already having some mild nausea. Was really nauseas last night, all night, the Zofran just isn't working well. I go back today for IV fluids, more anti-nausea meds and a Neulasta shot. My nurse said I could take two motrin at bedtime tonight if I need it and two in the morning when I get up if I need it. I started the Decodron by mouth this morning, with Ativan, 1/2 to 1 every 6 to 8 hours, as well as the Zofran, and Lortab for pain...I thinking...gosh...I hope I don't overdose from all of this Scary thought I'm very nervous about taking alot of drugs anyway, and drug interactions, becuase I'm VERY sensitive to drugs of any kind....so hopefully this will all be ok.
Still nauseuas this morning, nagging headache. BUT if this is all there is, I can do this. It won't be fun, but I can do it. I'm right UNDER the line where I start throwing up, but at least I'm not throwing up. No appetite at all...I tried everything last night, crackers, applesauce, toast, chicken nooodle soup....YUCK...couldn't take more than two bites of anything. Even popsickles....they were WAY WAY WAY too sweet. Sigh.
One down, seven to go. Let go and let God.
I think I'm going to get proactive and cut my hair off before it even STARTS falling out. That way it's in my nands, NOT the chemo's.
Talk to you all soon.
Blessings,
Gracie
IDC, Grade 3, Stage 2, er/pr + her2-, 1.7 cm, 1 node -
Great news Terry!! I know you are so relieved about your son!
40cc's - ugh!! Hope they figure that out soon so you can get on with treatment.
Gracie - sounds like you had a bit of a rough time yesterday - talk to your onc - they'll let you try other drugs and get it right for the next treatment!! Glad you feel a little better today.
My almost 17 year old son (my baby) buzzed my head last night! He had a lot of fun - guess it's paybacks for all the buzzes I've given him over the years! Lots of bald spots under what hair was left! Feels weird wearing a turban with a scarf tied around it but fairly coordinated today! Can' say I'll be tomorrow!! Oh well.
Have a good day everyone!!
Dawn -
Good Morning Ladies,
I just read the last few days postings. Wow what a busy bunch we are! I haven't been spending much time lurking because I have been feeling GREAT!!!!!! I go in for tx 3 this Thursday. I spend the first three days feeling a little queazy, and then get progressively better each day following. I went to Look good feel better yesterday and had a wonderful time. The women took such good care of us, and talk about good products! Mostly, it was just nice spending time with others that are in the same boat.
Terry, I'm thinking that it is your turn to start feeling better! My good positive thoughts are going out to you! What a relief knowing that your son is ok.
Dawn, did you also razor your scalp? I have been shaving my head every couple of days as I still have hair growing. I like the smooth feel vs. the cats tongue feel. My girls were very emotional when they clippered my hair. I can't help but think that my boys would have had a much better time "de-hairing" me. I know that every day that passes, I become more comfortable with my looks. Actually, wearing a cap has allowed me to meet some very nice people.
Gracie, I know what you mean about the overdose worry. I find that using a pill keeper works really well. I fill it, then double and triple check each day. After that, no more worries. It sounds as though you had a rough indoctrination into this chemo trip. I am sorry to hear that. Dawn was right, talk to your onc or the infusion nurses. They want to make you comfortable! My first treatment went well however, I didn't take my compazine often enough to thwart off the nausea. Now I take it every six hours the first week! What a difference that makes. Well, time to get back to work! Have a great day everyone!
Peace,
Terri -
Terry whoohoo is right regarding your son's test!
Gracie I'm so sorry you are having a hard time w/your chemo. All the pills, I know, isn't it something? My Onc wanted to give me another pill last week and I said no thank you. lol
My first time I too thought just about everything tasted terrible. Ended up eating mostly oranges and popcorn.
I hope after a few days things will settle down for you.
I shaved my head over the week-end and it feels so much better not to have hair everywhere.
I'm going in for treatment #2 Thursday and really not looking forward to it, having an awful time w/this Taxotere. I am in my third week and still feel awful.
Well I'd love to work on this house, I'll give it a try but not sure how much will get done,
Hugs everyone, -
I'm so bald, but I'm loving the scarves and have not worn my wig one single time. I even just go bald at home in front of my 17 year old son's friends--heck, they sure as heck don't care as long as there are cokes in the fridge!
---I just wanted to remind everyone who is just starting their chemo and about to lose their hair that:
Hair loss is not a sign of our illess, but rather a sign of our RECOVERY!!!!
I hope everyone is having a good week!
Kathy -
Good reminder Kathy as I'm feeling a tad bit alien today in a turban w/a scarf decorating it. I am not a fashion plate - never have been and I'm going to get tired of trying to coordinate colors!!
Gracie - maybe your onc will switch meds instead of just adding more to your list. Let us know what they say.
Terri - just a buzz last night - w/the shortest clip, no razor yet. I was hoping it would just fall out but if yours is still growing I guess I may have to razor it. Sounds really weird moving around on my pillow but it's nice not to have hair everywhere!!! I need to vacuum every single room in my house still!!
Pam - I'm in for #2 on Thursday also! Doing the a/c right now. Hoping not to get a migraine this time! and trying to figure out what else I can get done while I'm feeling good cuz I hear the fatique is cumulative and like everyone else here - I just don't have time for that!!
Have a great day everyone!
Dawn -
Bummer! I have to put my chemo on hold for at least two weeks, it'll be three by the time this is all over. Not happy about this turn of events!
The surgeon finally worked me in today and he had to reopen part of the incision, drain some more out, pack it up and sent me home. For the next two weeks a nurse will come and change the packing and bandages and hopefully this will clear it up so I CAN continue chemo. Still on antibiotics so that should help too. This is certainly a double-edged sword, good that the infection will soon be gone but blasted on the chemo front. :-(
Am I still considered a Junie? LOL
Gracie, I'm sorry that food doesn't appeal to you right now. The only thing I felt like eating that first couple of days was chicken broth with saltines. It tasted SO good to me. I also drank a lot of fluids. If I think of anything that might appeal to you, I'll post it. Hang in there!
Pam, sorry to hear you're having a tough time on the taxotere. And to all the ladies who've shaved their heads in anticipation of hair loss, you're my heroes! I haven't had the courage to do so yet. Now I'm thinking it'll be awhile before I lose my hair anyway.
Ah, this too shall pass. -
Hello All!
Terry great news about your son; SORRY your tx is on hold
!
I just got back from my first tx of AC..... 1 down and seven to go!! I feel okay I think right now, a little tired, probably from the "anxiety letdown" I think. My hubby will pick my anti-nausea perscriptions up after dinner. I'm trying to push the fluids....flavored water seems to taste really good. I have to go back tomorrow for my Nuelesta shot; I asked about bringing it home to administer myself, said they have to check with the insurance company!!! Oh well....
I hope everyone is feeling as well as can be expected, remember girls..... WE WILL GET THROUGH THIS!!!!
Bonnie -
Terry - that is a bummer! You had your first a/c on 6/4 right? All the comments I've read said they started losing their hair at about two weeks - I sure did and that would put you at 2 weeks yesterday - got any coming out yet?
Of course you are still a Junie!! Little bumps in the road can't change that you still started treatment in June!
Bonnie - that "new" anxiety sure hits hard doesn't it? Not knowing how something is going to go is almost as bad as waiting for results. UGH. Glad you are done with the first and feeling well so far!
Hope everyone has a good evening!
Dawn -
Hi all,
Terry, I am so happy to hear your son's results were good. What a relief. But what a bummer about putting off the chemo. But it sounds like it's necessary and I guess we just deal with whatever comes our way. As you said, this too shall pass!
Gracie and Bonnie, I had tx 2 yesterday, and although, if I remember right, days 3, 4 and 5 were my worst, the one thing I am doing this time which I didn't do before was brush my teeth at least 4 to 6 times a day with Biotene toothpaste and use the Biotene mouthwash, and I am also using salt/baking soda (1/2 tsp. each) mixed with a 1/2 cup of water and swishing it around and gargling with it about 3 times a day or more. I'm trying to avoid a horrible taste in my mouth that I got last time and also the thrush. I don't know if I'll avoid either this time, as I'm just at day 2, but my appetite seems to be a little better this time around. Maybe it's just easier the second time, but just thought I'd mention those things as I wish I had done them last time. Also, stool softeners, Senacot or Milk of Magnesa if you are at all constipated. I waited from Monday until Friday to do anything about that, and as you can imagine it became very painful! I'm on top of it this time for sure.
Good luck this week to everyone!
xoxo
Kathleen -
Oh, one more thing. The hair thing. I am also avoiding the head shave. I'm not sure why. I had it all arranged with my hairdresser and then I cancelled. At exactly day 13 my hair started coming out everytime I touched it. But there is still enough there for now. I hope I get the courage up in the next few days. I want to be more like Kathy and remember the sooner the hair is gone the closer I am to recovery. Thanks Kathy for your positive encouragement!
xoxo
Kathleen -
Good Morning!
Well the ant-nausea meds they gave me IV didn't last as long as I thought they would! I started to feel a little queasy right at dinner time, needless to say I couldn't eat anything. I took a compazine and that really didn't help; the pukes started around 9 or so.....yuk! And then again at 11, took another compazine around 12 along with a xanex and finally got to sleep for a few hours. Now I'm trying to get down my cup of coffee.... otherwise I'll get a caffiene headache. Then I'll try and eat some toast or something so I can take my Regelen (sp?) and Decadron.I know I also have to push the fluids! Then this afternoon is back to the center for my Nuelesta!
Hope everyone has a descent day!!
Bonnie -
After I had tx 1 of AC, says 4 and 5 were my worst. Then, after tx #2, days 5 and 6 were the worst. I have tx 3 on Tuesday the 26th, so we'll see what happens. After the second tx my mouth has stayed sore--no thrush--but little, what my granma called--liebumps and stuff. I've started rinsing my mouth with a half benadryl-half maylox concontion. My sense of taste is still shot--I got it back during the 3rd week after tx 1....so now I'm either eating everything in sight to try to 'taste' something, or I'm not eating anything becasue I think 'what's the point?'. I will be very curious how I react to tx 3 next week.
I haven't have the nerve to update my caringbridge page with a new pic of me in a scarf, but I guess I'll try to do that before next week.
My boyfriend is bring over some of the best pizza in town tonight and I have planned him an impromptu party of sorts for his birthday on Friday after work. His birthday is Sun, he'll be 40!! I figure and fun night out with friends is exactly what I need going to next week. I have a really great boyfriend!
You women keep having a good week and Bonnie I hope you get to feeling better. I've not thrown up at all so far (knock on wood). -
Bonnie,
I'm sorry you are having nausea and throwing up. That is rough. Next time ask for state of the art antinausea meds in your IV. I got one which I can't remember that name of (dang! something like z or x something)but was good for three days then I used compazine at night. Hope things level out for you soon.
Terry, once a Junie always a Junie. After all we are only talking about one cycle or so that you will miss plus we continue on into July and beyond..... Anyway take care of the infection.
Pam what's taxotere doing? I take it in combination with cytoxan and so far OK. I can imagine it is very strong alone. The only good thing I've noticed (aside from cancer fighting effects) is that mosquitos and chiggers won't bite! You have those in Oklahoma, too!
Went to Look Good Feel Better last night. Great class. Got a blonde wig. Cancer is such a leveling agent. Many different women were there all with the same affliction.
Wild.
Keep your chin up and the rest will follow,
Linda -
Hi everyone,
Sorry I seemed to drop off for a bit but.....
Friday past I got a fever. It ended up being 102.6F. Off to the hospital we went, and I didn't see the light of day till Monday. White count was .7, by the time I was discharged it went up to 1.3, but because I didn't have a fever for 48hrs, he said he would release me if I promised to take my antibiotics and come back if it reach 101. It was a great deal considering I didn't want to be there. As for the garage sale it didn't happen, but my neighbour is great she kept all the signs and is going to help me this Saturday. Got my head shaved yesterday and have my wig on now. I wish I had taped my son's reaction when I took my wig off... it was priceless, he was so excited and I told him it was our little secret, so he asked me if I was going to show my friends my short hair. I told him no and he said good only me and daddy. I am so glad he is 5 he gets so excited about things, and makes me see the good in it.
TerryNY - GREAT news about your son, and I am sorry your teatments are being delayed. It will work out in the end!!
I am heading to the family doctor today again. Yesterday, everytime I ate or swallowed something it was like a huge lump going down and then I would get the worst pain in my side. It even got to the point I couldn't drink. This morning I had a cup of tea and it was fine. I went to eat some toast and the pain came back. I have not ate since Monday night I am SOOOOO HUNGRY!!
Anyway, hope everyone else is doing well, and I will chat later
Keep Smiling -
Oh Terry that is good news about your sons MRI! I hear you on the delayed treatment....here's where I'm at. As you know after my MRI, they found a lesion. So I went yesterday for an u/s and more mammos. I got to talk with the radiologist first that said the lesion is very round, very smalland has characteristics of it NOT being another cancer. She said she's 95% sure the calcs are benign as well. So, off to the new breast surgeon (who was wow, pretty easy on the eyes and I had no problem showing him my chest, ha, ha,)...anyway, he thinks they are "nothing to worry about" and to have the biopsies and then I can put this behind me and start tx finally! He seemed so confident and I would think surgeon's don't like to be wrong. So, next Wed, 6/27, I have to have TWO biopsies, the core biopsy via u/s on the lesion and then the stereotactic on the calcs. I remember that core biopsy all to well and it hurt something awful. I just couldn't get numb and this sterotactic contraption is freaking me out a bit. They did perscribe some valium for me so I sure hope it works.
Of course, if it comes back malignant, then I will have to have the mast but since I've already had two surgeries, the surgeon thinks definitely biopsy and I should continue on.
At this rate, my first tx will not be until July.
Hugs,
Susan -
Tomorrow morning I go in for my first AC treatment. I am bit nervous since last weeks reaction to Taxomere. The nurse really looked at my veins. I hope I am ok without a port. The only thing I have to do is take Emend one hour before and I am trying to drink a bunch of water today. Anything I am missing? Oh I just can't think.. This weekend I was very tired and felt nausea I wonder if it was from the 6 drops of taxomere I got last week. I slept all day on Sunday. How is everyone else doing with there chemo?
-
Got compazine yesterday instead of zofran. I'm still nauseated. Have been searching most of the day for something I can eat. Not only am I nauseated, but food seems to actually hurt in my stomach ...yuck. Small headache, feel like I have the flu, but then I got my nuelasta shot yesterday too. Hvaen't had constipation, one bright spot in all of this, but man my gut hurts.
Gracie -
HI, all,
A quick update, the home health nurse came yesterday and changed my packing and bandages, whoa, this is going to be a fun time...NOT. She told me to take some Advil or Tylenol before she comes back today. I wish I had thought of that yesterday. My boob is sooo sore this morning.
On the hair front, I did start losing it Tuesday night, that wasn't a banner day for me! Went yesterday to a salon and they took me to a private room and cut it really short. Not as short as I wanted but I figure I can shave it easier at this length, maybe this weekend. I am finding hair everywhere and keep blaming the dog, poor girl.
Allgone, I'm so sorry to hear of your infection. Hope it's smooth sailing for you here on out. Too cute about your son! He's mommy's co-conspirator in this fight!
Litig8or, I'm sorry I can't remember your name, but I wanted to wish your BF a Happy Birthday! Enjoy that pizza.
Gracie, have you tried Emend for the nausea? It really worked for me.
Linda, too funny about the mosquitos and chiggers Hey, they don't want this poison in their system either! LOL I don't think it would find a market though.....
I'm glad you were able to attend a class. The ones in my area are booked up for the summer and I"m on a cancellation list.
Susan, Good luck next Wed. I'll be thinking of you. I know the xanax works for me, just takes the edge off. Take the valium, it will help. Hugs to you. And cute drs make the whole process somewhat easier to handle, no? LOL
Kiddlegirl. good luck today with your first a/c treatment. Just make sure you take the Emend on each successive day, it worked fine for me. Check in and let us know how you're doing. -
Terry , great , great news about your Son! Sorry though to her of your delay in treatment. Also sorry about your "boob" and all the pain there. Man , it seems like one hurdle after the other with this bc. I had my second treatment yesterday , but almost didn't. My white blood count wasn't coming up fast enough and the previous days blood work showed it to be boarderline. The onc said I'd have to wait till Friday. Which upset me and he said , well we could have you go take it now and see if it had come up so I did and it had. Today , I have to go back for my neulasta shot. I had it scheduled after my work hours , but I was so sick this am that I didn't make it to work. The nausea and heartburn hit about 2am. I couldn't sleep and took to rolaids for the heartburn. Which eased it off. I am going to see if they can give me something more for the nausea. I am taking Kytril and Compazine. It just gets so bad.
Well good luck to all who are having problems. Your all in my prayers. Melody -
Hi girls,
Still feeling a little pukey, can't seem to keep much down, If it doesn't let up soon I'm gonna call and get something else for the nausea. I'm trying to keep the fluids going tho. Went for my nuelesta shot yesterday.Have any of you heard that this shot costs around $4 thousand dollars???? Just the price of meds is enough to make a person sick! What do people without health insurance do!!!??
Hope everyone has a good day!
Bonnie -
Linda oh boy do we have chiggers, mosquitos and ticks here! I do manage to find a tick now and then sad to say,
the itch stays w/me for years sometimes, I just react badly but I have a small dog who goes in and out. Hubby is going to spray this week-end.
The Taxotere is just knocking my socks off. I'm sooo tired, bone pain, weak, the first few days I was staggering and then course had the low blood count which landed me in the hospital. I try to get up and do something or run an errand, if I can but only good for about half an hour if that long and I want to go back to bed. Here it is day of 2nd treatment and I don't feel any better. One of the docs hubby and I talked too said having already gotten chemo in 03 may make this round harder on me.
Bonnie, I'm so sorry to hear about the nausea, tell them go give you something else. Hopefully it will pass quickly for you.
Allgone, so sorry to hear about your hospital stay. Having just gone thru that myself I so understand. I hope your counts continue to go up and you do better.
Susan good luck on your biopsies, sounds good though and fingers crossed they will be b9!!
Honeygirl I'm so sorry to hear you have been sick w/nausea and heartburn. Please do ask them for something else, surely they have something to work better.
Kiddlegirl I hope your first treatment goes smoothly, good luck to you and keep us posted, -
I am back from my second attempt at my first treatment. I took Emend before and they gave me some other stuff and I have eaten and feel fine. I do feel a little doppy and went back to work today. I think I will leave at 3:30 and go home for a nap.
1 down 3 to go -
Hey Gang, I haven't been posting much either. I have been keeping up with y'all though.
I feel like crap. I'm on day 9 of TAC. That Taxotere is some nasty stuff. No energy, still slightly nauseous, major indigestion, mild headache. I don't EVEN want to go to work, but I tried today, and lasted two hours. I walked the store twice and felt like I had run a marathon.
Anybody else have tubular carcinoma? I've been reading online, and I'm finding that there are some oncs who believe there is a small subset of women that don't benefit substantially from chemo. I think I'm in that subset, and I'm thinking seriously about being done with this. It's gonna take everything I have to go back to his office and let them do this to me again.
I had NO idea the Neulasta shot was so expensive! I joked with sis today that if anything was to happen and I didn't have insurance, I'd find someway to land myself in jail so the system would have to take care of the illness!
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