continued Tissue expander pain!!
Comments
-
and i'm just wondering if anyone has had the implants after radiation?
does the back pain ever go away?
-
Traci, I had major back surgery when I was 11 for double scolosis and I lived with pinched nerves for a while prior to the surgery. I don't know if that has anything to do with the ease of my present surgery (high pain tolerance). My sister said that before my back surgery, I would lay in bed and say, I am not going to say it but my back hurts. They did not give pain medicine to me at that time, I just lived with it.
Sheila
-
Hello M,
I hope you continue to explore all your options- I wanted Diep, but didn't have enough tissue, so am going through expansion for implants. It started out painful the first week, but I seem to be breezing through the fills well and w/o pain (knock on wood/my head!) Try to gather more stories as Traci suggested- they may help you decide. I went for about a year w/o one boob, and survived pretty well, although swimsuits were traumatic. I know I could make it w/o reconstruction if I needed to. I have to say though, I love my expanded boobie, and can't wait for my implant! I wish you the very best- I know it's all overwhelming. I am sending you warm wishes that you work out a plan that works wonders for you,
Jill
-
Hi, I had back pain thru expander too. I had the implant put in in early august and still get back pain. My ps said this happens to some people, but will eventually go away. It took me 3 months to be able to lay down and not sleep in a recliner after the expander was put in,
but now it seems to SLOWLY be getting less painful in my back.
Hopefully he is right and it will be gone sooner or later. Standing under the shower massage helps my back sometimes. Also laying on my side does too. I wish you luck and hopefully your pain will ease up too....
-
Ok Urbie,
This is my first time using this site and after reading yours, Katie's and the other brave women's letters I am scared. I had 6 rounds of chemo, a lumpectomy and lymph node removeal, then 8 weks of radiation. Since then I had genetic testing because my mom came down with ovarian cancer and I am positive for the BRAC1 mutation. I am having a hysterectomy in Nov then double mastectomy and reconstruction so I wanted to hear what others are going through and I have to say all of your pain is scarring me into questioning if I want to go through with that. Has it been worth it to you? Would you still make the choice if you had to do it again? Please help me feel safe in the decision I am making!
Thanks, Mamalu
-
Mamalu,
Each person is different in regards to their pain level. I had bilat mast with expander recon on June 1. I have had only mild discomfort with each fill, feels like a too tight bra, for a day or two. Only once did I take pain med after a fill and that is when he put 100cc in and not the 60cc he had done previously. I made sure that I would rotate my shoulders and hold them back (push out chest) to help stretch out the muscles. I am scheduled for my exchange surgery Nov 4 when I will get better shape than I have with the expanders (look like hamburger buns on my chest).
My cancer was caught early so I am not doing the chemo or rads, but I have read on this site that if you can make it through chemo you can make it through expansions.
Should have done it sooner but would do it again.
Sheila
-
Hey guys,
Finally.....relief. No pain pills yesterday or today!! Only took 12 days.
Mamlu, I'm afraid I'm not the right one to ask about expanders because I have had a real hard time.
I saw your other post. I have the brca gene too. Had bi-mast and was suppose to have hyst this past Wed but...it got delayed.
Anyway, if you look through all these posts, there are girls that have pain and girls that don't. Either way, I'm soooo glad you found this site. It has made going thru all of this so much easier. Friends and family are great but this place is real.
Sheila, I am so sorry to hear about your early surgery and probs but, I'm glad it made your expander experience easy. How much did you get filled?
I'm gonna call my ps and schedule an appt for more. I was thinking about getting 100 cc's and then calling it quits. What do y'all think about that idea??? Think I can handle 100 when I've been crying about 50 for 12 days?????
Traci
-
Traci, I had 500cc expanders placed with a total of 600cc filled. He stopped filling me at 540cc and let me live with them 2 weeks before I decided I wanted a little more for projection and had another 60 put in August 16. Right now I feel like I have 2 turtles on my chest (or the coconut hula bra on). I don't know what size expanders I am getting but they are teardrop saline. He said that I will loose the turtle shape with the perm implants and I will actually match and have cleavage. Prior to my surgery I had an small A-cup and a large C-cup. I told him at my first meeting I just wanted to have a pair that matched somewhere between the sizes I was. I think that I am going to end up a large b-small c size. I will be abel to look at new bra's for Christmas - whoo hoo!!.
Sheila
-
Hi Ladies,
I have a pain question for you all, but first wanted to say that I continue to keep you in my thoughts Traci, and believe you could handle just about anything after what you've been through. I haven't attempted more than 50 ccs, but others seem to be able to cruise through it- good luck with your next step.
Here's my question- after reassuring Mamhop that I'm not in much pain, I apparently jinxed myself. Has anyone had sharp, stabbing pains out of the blue??? I'm really comfortable most of the time now that the fills are underway, but just started having this searing pain on the bottom part of my expander- down low, feels like underneath it by my ribs. Then after a few minutes it fades. Bending over seems to trigger it, but it's happened a few other times too. Anyone else have something like that?? M, I hope you're not reading this dear! I'll call my ps Monday, but just wanted to check in with you all- this is scary,
Jill
-
good morning everyone. I have been reading comments for a few days but this is the first time I have posted. Bilateral mastectomy in July. DCIS in left breast and went ahead and took the right for safe measure since I have family history. I am scheduled to have my expanders put in on 10/18 and am quite nervous after hearing all the pain most of you are in!! LOL I was just told yesterday I would need to see a thoracic surgeon since my sternum is apparently bowed....and it will affect how the implants sit. Oh great. Another surgery...more pain.
My ps told me yesterday that his plan was a fill up once or twice weekly! He didn't tell me the amounts though. He said the whole process from the first surgery for the expanders til the surgery for the implants will be about 3 months. What time frame have you ladies been looking at? I sure hope this is all worth it. I am really happy to have stumbled onto this message board!! Finally! Someone who understands!! Hang in there ladies. Nice to meet you all.
-
Hi Gals
I too have been reading your posts for a couple of days- you are all so strong. I had a bi lat mast last october with immediate tissue expanders. I went through chemo and wound up losing one of the expanders due to infection. I had both expanders replaced in May -the non infected side had migrated up to my neck and it was so uncomfortable-I had to restart my fill schedule but now I have stopped the fills and I am going to wait until next year for the exchange, for two reasons, one because my PS says that the longer you wait the better, because the scar tissue creates a better position for the implant, and the other reason is that there is new silicon implants on the horizon-and I am hopeful that my PS will be experienced enough to use them.
I still have pain and the feeling that I am wearing a bullet proof vest all the time-I have not worked since last October because my job is very physical and I did not think I could handle it..
I am not sure that I would do implants if I had to do it all over-but I am making the best of it, even though I feel like Annette Funicello sometimes-remember her boobs never moved-even when she was riding a horse!
-
Oh I just wanted to caution Traci-
I too was taking oxycodone for the pain-I found that I could function okay with the pain in the background especially during chemo-(nuelasta shots kicked my but). Following my chemo I also had a hysterectomy-which actully wasn't so bad compared to chemo-I took the oxy then too. But guess what I found out, one of the side effects of oxy and hydro codone-is hearing loss!!!WHAT!!! I thought I was going crazy everything sounded so fuzzy. I thought it was chemo brain . So be careful and watch for side effects. who knew
-
Jill......
I was so happy to see I'm not the only one with an occasional sharp, stabbling pain! I am 3 weeks out from bilat w/expanders (DCIS). I had my 2nd fill of 50cc's (I'm now at 250) on Wednesday, then Friday night, I couldn't lay down or I'd get this sharp pain on the left side. It hurt most of the day yesterday, only when moving certain ways. Then last night going to bed was better, I could lay down. Now this morning, I've had a couple of episodes of it, but not like yesterday. So I'm hoping it's going away, but it sounds the same as you. Almost like someone stabbing with a knife (not that I know what that feels like!), but that's the only way I can describe it. My PS out of town this weekend, and I have appt on Wednesday. I hope I can stick it out!
I took 5mg of Flexiral (muscle relaxer) last night. Maybe that helped?? I'm not really sure.
Hope yours goes away! It's not fun!
Leslie
-
Hi Mamlu:
I started this thread after my bilat.mastec. & reconstruction which I had July 31st. I felt like I was alone with the pain and discomfort. I found out I clearly wasn't. Some do better than others, that's for sure. There's just no way to know ahead of time. The only thing I can say, now that I'm almost done, is it was worth it. I would do it again. I can't even imagine how difficult chemo and radiation would have been, and you've been through it, like so many of these other women have. That's courage!
I don't know what I would have done if I had found this site before my surgery. I probably would have been so much more scared. On the other hand, no one really prepared me for the experience and of what to possibly expect afterwards. Now I think I would rather have known more than not enough and been prepared. I'm so grateful to have found this web site because everyone truly understands and can share valuable knowledge, care and empathy.
If you decide on the expanders, you'll get through it. Just take all the time you need from work and from stress. I was fortunate to be able to take two months off and just returned last week. I had my 3rd and last fill last week (I started w/ 200cc in each at surgery. I'm at 500cc in each now and will get 420 silicone gel implants at exchange) and will get the exchange in 4 wks. This whole process took 3 months. NOW I can say it was worth it. Athough 4-6 wks ago was a different story, I got through it. I just wanted you to know the roller coaster ride is coming to an end for me and it will for you too. Just keep asking questions and know we all care about what you're experiencing. Hang in there.
Take care,
Katie
-
Katie, I just wanted to thank you for starting this thread. I too was having a hard time in the beginning of this process, now I am a little over halfway thru. I am just taking the fills slow and easy and it is doable. It is true some just breeze thru and some have a more difficult time with it- it is very individual.
As for me I think the first fill I had was just too many cc's for me(150 cc), plus I was just still sore, weak from the surgery and just traumatized from the whole ordeal in general.
I was so glad this site was here cause I was scared in the beginning, but realized there were others out there feeling just like me.
As for the ones of you having the stabbing type pains at the ribcage and under this area, I spoke with my PS nurse about this on fri- when i had my last fill, she told me as the expander gets larger it pulls on the muscles in this area too- and these muscles are very resistant and will cause pain ,tenderness and sharp pains to this area. I too hurt in this area, also it hurts when I take a deep breath (in the ribcage area) since my last fill. I have been taking advil , warm showers and gentle light stretching exercises do help. I only take the flexeril and percocet if I really need them. Everyone take care, I keep telling myself this is temporary, and looking forward of getting rid of these weird looking things off my chest. Susan
-
Hey fellow turtle chest girls!
Sheila, August 16 was my last chemo treatment!! So, you've been waiting since then for your exchange? When are you having that done??
Jill, thank you for your kind words. I am feeling a lot better...however, I do have sharp pains. Mine feel like they are right in my scars though. It's really weird. One day, I had that knife go in about every 5 minutes for about an hour in my right breast. Then, the next day...the same thing happened in my left breast!! It's very strange and very painful.
I have decided to call my ps tomorrow and get another 50 cc's. I feel o.k. now and figure I can handle it again and.....I do not want to be smaller than I was after this!
I'm still worried about how far apart mine are though. I can literally lay my four fingers flat on my chest between the expanders and the one on the left seems to be bigger and is under my armpit and is making me crazy. I have to put powder there otherwise the skin of my arm would rub against it and I can see myself getting a rash over it.
Teribear...sorry to hear about your other probs. I hope you don't have my pain and everything goes o.k. for you. BTW...you look EXACTLY.....like my ex boyfriends ex wife. I mean...it is unreal. When I first saw your pic I gasped thinking Lisa was on here! (We are good friends...they have kids....)
Davisfamily, thanks for the warning on the hearing loss. However, if I have pain again like I did....I'll learn sign language before I don't take pain pills!!!!!
I wish you all well and I'll check in after my fill......deep sigh.....
Hugs, Traci
-
Good Morning Ladies,
Haven't been posting since Friday when I GOT MY LAST FILL!!!!!! I'm now at 760cc's and that's it. When the PS was removing the needle from the fill, a bit of saline shot 6 feet across the room landing on my hubby (he nearly passed out!).
Jill-I have that sharp, stabbing pain on a daily basis. It's worse right after the fill and tends to ease a bit after a week. It never goes away totally but hopefully it will now I have no more fills to look forward to.
Mamalu-I'm with Traci in that I've had a very difficult time with the expansion and probably am the last person that should comment on the expanders. I wish I had known how painful it would be though. I didn't stumble onto the boards until after my mast and I think I would have been more prepared for what was to come. All that said, I think it will be worth it in the end.
I'm having the swap December 18th which is giving me 2 months with the booblet and hopefully she'll settle down a bit. This last fill was the worst one because it's fully expanded. The muscle is really stretched across my back on the mast side and it continues across the expander.
The PS did say he's going to tweak the right side a bit (where he did the lift) and will out the implant in it's proper place. Traci-I have my entire hand between mine. When I asked him if they'd end up a bit closer he said not really but he'd make sure the implant wasn't under my arm. How's everything going with rescheduling the hysterectomy (and is the insurance agent still alive)? How's your sister doing? Hope all's going well.
For all of the newer posters, welcome to the site! We all have stories to tell about how things are and did go for us. Everyone is unique in how they handle things and I think we all have to do what works for us as individuals. Since bc isn't a one-size-fits-all disease, we have to look at it in different ways. It's always important to keep in mind that you have to do what is best for you and your individual circumstances. I think you're all doing the right thing in investigating all of your options. Whatever your choices are, they are right for you.
Have a good one!
Margaret
-
Margaret, I know you are so happy to get your last fill, now just sit back and wait for your exchange- I know that must be a good feeling!! I sent you a private message a week or so ago. We live just across the pond from each other. I know your hubby freaked when that saline flew across the room at him- that was a sure sign you were done with your fills!!! Hang in there, dec. is just around the corner... Hugs, Susan
-
Tracy, I went back to the PS 6 weeks after my final fill (Sept 27) and he scheduled my exchange for November 2. He likes to wait "a couple of months after final fill for everything to settle down to a good stretch". He is going to 'tweak' the left side to get a better shape with the perm tear drop. He told me that 'The good Lord took 13 years to make your first boobs, you have to give me at least 8 months'. I am not trying to push too fast but I want them complete.
In looking back and reading some of the more recent posts, I have had on occasion a sharp pain right under the right expander but nothing I need pain meds for. It seemed to occur after I had eaten a large meal or stretched the wrong way for something, but would go away quickly.
Sheila
-
Mamalu,
Sorry that I didn't see your message until today, but I have been in the chemo threads and my reconstruction has been a bit "on hold" until today!!! I got my white counts taken today - one week post first tx of cytoxan/taxotere and they were great (9.2). I go into my ps tomorrow for a fill and I am going for another 100!
I have had almost no pain with my fills so far (at 300cc now) and I know that it can change, but I have NO REGRETS about the bilateral surgery and reconstruction with tissue expanders. Everyone is different, but I am very happy with the results so far. I experienced more pain with the surgery than most (take pain meds) and almost no pain with the tissue expanders. I am 8 weeks post surgery and I feel really good (other than the chemo part) and strong. I don't have fear that I will have recurrence in my breasts at all and I did what I felt was the right thing to do for me. You will too. Good luck in your decision.
-
Hey Urbie! Haven't seen you in awhile! I'm happy to hear you are doing so well and hope you continue to do so!!
Margaret, your post made me spit my drink. lol! I'm so happy you are done! Woo Hoo!!! I'm so jealous. What a Christmas present for you!
I sent my insurance "conversion" papers overnight to Aetna today. So, we'll see. I haven't called my ps yet. I had an appt sch for Tues of next week so, I might as well wait. Sheila had a good point....by next Tues this last fill pain should be completely gone and maybe, just maybe....the next one won't be so bad.
How are you feeling now? And, what are you doing awake at 5 am??
Katie, is your exchange surgery scheduled?
Have a good night girls!
Traci
-
Hey Traci:
You sounded a lot better in your last post. I'm so glad to hear that the pain has subsided. I'm with Sheila, why not wait and feel more comfortable. My fills got less painful, just tighter!
I can handle tight and uncomfortable better than the pain crap! I have my exchange actually scheduled for Nov. 6th and I'm counting the days.
I know the insurance situation you're going through is going to work out. I'm just sorry you've had to deal with this on top of everything else. You are one tough lady, I have to tell you! You are always so upbeat for everyone on this site and it helps us all so much. Your posts always put a smile on my face! Thank you for that. We're all going to get through this, just not as quickly as we'd like. Please keep us all informed on what's going on with you. You'll be in my thoughts and prayers. I think I might just have a glass of wine in your honor....The sacrifices I make, I tell ya!
Take care for now,
Katie
-
Hello to all from Gail in Michigan. I don't like the sounds of all the pain you ladies have gone through. I have DCIS left breast and am having a bilateral with the tissue expanders next Thursday. I'm scared to death and having bad nightmares about the surgery. I'm really a wimp when it comes to pain. The Women's Center here had me meet with a lady who also had bilateral with the tissue expanders and she told me it was a piece of cake and she only took tylenol. I know I'll never be that lucky. By the way, I also have Aetna insurance and have had some trouble with them too. I had to have a predetermination to have the right side removed because no cancer in that breast. Problem is that I have been doctoring (MRI's, mammograms, ultrasounds) for 2 years for nipple discharge (oh also biopsys) and the cancer was not found until I forced Dr's to remove the duct because I was tired of dealing with the problem. Medical community seems to think that's a good enough reason for insurance to pay. I'm ready to get off this emotional rollercoaster though and get on with my life. It sounds like I'll have to have chemo too because there were cancer cells in one of my lymph nodes. They are removing more and checking them also during surgery. This Cancer thing sure sucks. I had my family Dr. put me back on Zoloft today as all this has been bringing me down and feeling like I just want to go to bed and pull the covers over my head. If I didn't have a boyfriend I sure would never have bothered with the reconstruction as it sounds like the pits.
Gail
-
hi all, i'm new here. typing one handed - left arm in sling because of a seroma, so pls forgive the inelegant typing! i'm 46 & had bilat w/lat flap & expanders 5 wks ago; had some fill at surgery but don't know how much -- i'd guess 120 ccs. took a month for that fourth drain to come out & then came this seroma, so i still haven't had another fill... scheduled for tues. pretty nervous about it.
i've taken something for pain around the clock since surgery -- darvoset or advil plus sometimes valium -- and after 5 wks, this is starting to freak me out. i've always been a natural health nut, but i'm beginning to wonder if i'm destined to be one of those glassy valium women because of perpetual discomfort.
can someone tell me -- will i ever be comfortable in my body again, or is that just a luxury we give up in exchange for getting to live thru thus?
-
hi all, i'm new here. typing one handed - left arm in sling because of a seroma, so pls forgive the inelegant typing! i'm 46 & had bilat w/lat flap & expanders 5 wks ago; had some fill at surgery but don't know how much -- i'd guess 120 ccs. took a month for that fourth drain to come out & then came this seroma, so i still haven't had another fill... scheduled for tues. pretty nervous about it.
i've taken something for pain around the clock since surgery -- darvoset or advil plus sometimes valium -- and after 5 wks, this is starting to freak me out. i've always been a natural health nut, but i'm beginning to wonder if i'm destined to be one of those glassy valium women because of perpetual discomfort.
can someone tell me -- will i ever be comfortable in my body again, or is that just a luxury we give up in exchange for getting to live thru thus?
-
Traci,
I am probably the one who mentioned the cracked rib with my expansion. I had a pretty terrible experience with my expanders and the ps only injected 60cc's every two weeks. Just wanted to mention that I only had a total of 300cc's injected but at my exchange my implants (smooth, medium profile, round saline) were 575cc's which makes me a D cup.
I don't understand why the doctors expand so much more than the size of the implants but I didn't have any problems with my exchange.
So sorry you all are suffering so with the expanders. Just keep your eyes on the prize and remember it will all be just a memory very soon!
huggs, Sherry
-
Gail - please know that the reconstruction is not painful for everyone. I too am a MAJOR pain wimp and I have had almost no pain with mine. I had EMPTY tissue expanders placed at the time of my bilateral because I was told that it is more painful it they put anything in them at the time of surgery. I had my first fill at about 4 weeks after - 100 cc and had no pain at all other than minor muscle soreness that first night. I think that sore muscles from doing sit ups is worse. I have had three more fills at 100cc each and again have had no real discomfort to speak of. I am very pleased with how it looks so far and can really see that my chest will look better than it did before! I found the surgery recovery much more painful and you will be given an ample supply of pain meds for that. I took them when needed and actually have a bunch left over that I never needed to take. Go into this facing it head-on and strong and you will do great. Good luck!
-
Hi Lulu and Gail,
I am one of those people who chose to use this forum to whine, sorry there is nothing that feels better than to have people that know what you are going through. I guess I did not give any thought to people who were just starting and panicked. I remember that feeling. In fact I remember reading that book "Why I wore lipstick to my mastectomy" I was so intent on getting information, but I had to put it down for self preservation, she described such a horrific chemo experience, I was sure that I wouldn't live through it.
But I did. And I celebrated Thanksgiving, and Christmas, went to my kid's school functions, I didn't work because I was blessed with a generous disability program, but life went on.
Keep a couple of things in mind as you go on this journey, even though most of us are using this forum to vent, I would lay odds that our families and our friends are not even aware of how we are feeling. Maybe a little but not in the graphic detail we reserve for our sisters on this board. Also when you are feeling GREAT you are probably least likely to post.
So having said that, I am choosing to keep these really uncomfortable, expanders in until next year. I can live with it.
Lulu-I also had seroma, and believe it or not the doctor filled that side more, he felt that it would allow my body to better absorb the fluid. That time it worked after about a week.
Good luck guys and remember we are here for you.
-
Hi all! I'm new to this site and appreciate everyone's comments. I had a mast. 2 weeks ago with tissue expander. They put in 50cc's at time of surgery and did skin sparing mast. I went in for my first fill yesterday. He asked me how I was after 100cc's and I was totally fine so he tried for another 100 and then stopped at a total of 180ccs since I told him it was feeling tight. Well, I was fine til about 5 minutes after I left. I started having throbbing pain that came and went. I took some vicodin when I got home and the pain was manageable. I slep through the night fine. This morning I only took Advil and the pain is horrible! Worse than yesterday but not sure if it's because of less drugs. Do you think I just had too many cc's put in and should have some taken out or is the pain temporary and I should wait it out? Any advice is appreciated!
-
Valerie,
Call your PS. They may want to remove some to make you feel more comfortable. I will bet that it will feel better in a couple of days-if you can stand it. Try to do some shoulder rolls see if maybe you can adjust things to become more comfortable. The pain will probably go down to manageable levels soon. Good luck
Julie
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