Taxotere/Cytoxan starting February 2012.
Comments
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RuthieG - Just got mine too a week after the second treatment. 28 days to the day...as usual. What's up with that one??? I also have hair growing - anyone else? I've kept all arm hair, still shaving the legs..altho, not as frequently as before. The hair in the other areas is starting up??? Anyone have a clue on this?
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I have a bit of hair growing back in on my head too, just kind of sparse prickly bits, but enough that I want to shave it again. Leg hair is pretty much gone and haven't had to shave in a while, same with under arms. Eye brows and eye lashes are both hanging on, thining a little bit but not much. Arms, etc seem to be a bit thinner but again not really noticable.
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Bonnie - yes round 3 tomorrow! Yipeee!!!!
Kelly I will be thinking about you!
Well, I haven't asked my MO for Emend samples. Bonnie, thanks for the web site, I will check it out.
Ann - I have marihuana and I was sooo dumb not to take it last time that day after chemo!!! This round I am going to use it right after treatment and for 4 days afterwards and will see what happens! ;-)
I am having terrible hot flashes. I wake up during night soaking wet. I got Lupron shot to shut down the ovaries and so I am not sure if this the cause or if it's Lupron + chemo. I haven't gotten the period so I hope Lupron works!
My hair is growing everywhere. On my head even. I still have plenty of hair. Got me thinking maybe I should not have clipped it just cut it short... but then I wonder if I still would have this much after combing it.
And I have to shave everywhere. Leg hair growing like crazy. I was really looking forward to not to be shaving my legs. Oh well. I still have two more rounds so I am expecting the hair to be falling out more.
Bonnie did you say plenty of exercise was okayed by your onco? I play tennis a lot or I run... good luck with 5K! And it is great to hear you had no SEs!!! I am going to ask them to run Cytoxan slower as well.
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All, I haven't posted for a while, and just read about a week's worth of posts here and on the Feb chemo thread. I'm glad everyone seems to be doing well. I have been exercising and drinking tons of fluids. I am more tired at the end of the second chemo cycle than after the end of the first chemo cycle, but am hanging in. Today was my last day before round three on Thursday, so I took the day off work and took my twin 8-year old daughters to the zoo. DH had to work, but we had a wonderful time. Temperature in D.C. was in the high 70s (unheard of in March). We had a lovely day. A friend of mine who dealt with cancer 30 years ago told me to make sure that I enjoyed the really good days when they came along, and that's what we did today. So nice before the next round of chemo.
I know that at least four of us are having chemo tomorrow. Good luck to all of you. I don't post during chemo because I have to take so many anti-nausea drugs (nausea during chemo has a been a real problem for me, even with Emend and tons of Lorazapam). I even threw up during first chemo but have avoided it since then. Bottom line -- I am just too drugged to be useful on chemo day. On top of that, we are dealing with cold caps, so the entire day is an ordeal. The good news, after tomorrow, just one more to go.
BTW, I asked my MO about 4 versus 6 TCs. She told me there was no evidence that 6 TCs were better than 4, but that there is study comparing 6 TCs to TAC. Results are not yet known.
Wishing little SEs for all. -
ColdenMom, Kim48, Leveled, Silviazara & Mom2JJ: Want to wish you the best today I hope all goes well and you all do well.
DonnaDS,NikkiEliz and woodburns Hope you are all feeling good and have had limited Se,s
Ali68 good luck with the port placement and your treatment tomorrow .
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Good Morning Ladies,
silviazara: My Oncologist said I can continue to exercise. She did recommend I do ONLY one activity a day. I do what I feel I can. If I feel I can do boot camp & run I will. She also mentioned the more exercising done the more toxic the chemo can be (if heart rate is constantly elevated). Hence, why she was recommending only one activity a day.
Mom2JJ: Glad you popped back in...GREAT to hear from you! Wishing you the best today!
Last night I went to listen to a few speakers discuss The Anti-Cancer Diet (Based on Book Anti Cancer A New Way of Life by David Servan-Schreiber). It was pretty good! Here are a couple websites they mentioned, www.helpguide.org/life/healthy_diet_cancer_prevention.htm & www.aicr.org.
Yesterday started with a bit of a runny nose & allergy like symptoms to me. I have no fever and my nose is not bloody yet this time.
XOXO,
Bonnie
When you arise in the morning think of what a privelege it is to be alive, to think, to enjoy, to love... ~ Marcus Aurelius
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Thinking of everybody who is going through a treatment today "with me". Good luck ladies!!!
I had a sleepless nigh filled with anxiety as usual a day before... loading on my steriods now. Round 3 here I come!
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Hope all are having a good day today. Prayers are for all.
Yesterday was a good day. I know this was my first round of chemo and that this is the easiest one. But I am so greatful it was not as bad as I had been expecting. Today I am a little tired, but figure it is because no Dex. today. I have an EN&T appointment tomorrow. The PET scan had showed something at the top part of my throat. They said I could have swallowed during it and that is what they are seeing. Just want to make sure nothing is there. Since I fell asleep a couple of times and woke myself up snoring. LOL!!! Maybe that was it. Maybe I can convice the Dr. to give me a C-Pap for snoring.
Silviazara, Mom2JJ, Leveled - Prayers are going with you today.
Mom2JJ - Glad you had such a good time at the Zoo. Prayers with you too today.
Leveled - For me, now that I finished the first round, I feel more better about all this. Still don't like the idea, but it was not as awful as I had imagined in my mind. It is the unknown that I think got me the most. Not to mention, no control.
AEM47, NikkEliz - Wow, I was looking forward to no underarm and leg hair. To me that was going to be a perk.
Kim48 - Did not have the Neulasta shot. My Doc said she preferrs not to give it unless my count goes way down. It is at 4000 before my tx. Will see how it goes at Labs next Tuesday.
To everyone I have missed mentioning, you are in my prayers too. Thank you all for sharing so honestly. You are all a great comfort to me.
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Thoughs and luck to everyone going in today!
Woodburns: The lack of control was certainly a large part of the nervousness/anxiety for me too. That's why when it came to the hair loss in particular, I took control and chopped it off and buzzed it on my terms instead of letting the chemo 'take it' from me.
I've been a bit more tired this round so far, and a bit of nausea day one which I didn't have last time, but they ran the drugs faster than normal so perhaps that's why but today I feel pretty ok. Crazy hot flashes last two nights with night sweats like CRAZY! Anyone have any suggestions on how to reduce this at all? Like certain types of fabrics for PJs that came help with sweating or something? I dunno. blah. Hehe
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Mom2JJ so glad you were able to make yesterday a wonderful day with your girls.Very good advice to enjoy the days you are feeling good.
AEM47 I do recall someone that is part of my Chemo team telling me that we loose the hair because its timing and interrupts the hair follicle growth.So we would see it start to grow at times but will also fall out during again treatments.More of a tease and aggravation this way.
Myleftboob great you feel liberated after getting rid of the hair.I am struggling with this now and was really hoping to at least get through my 2nd TX before I do this.We will see what happens over the weekend.
RuthieG I was also promised the Chemo-pause and have yet to see it.In fact had it the week before 1st TX and for 2 weeks spotting then a feel another full blown one this week.This was the one good thing I was looking forward to ,besides no more shaving.
Not sure if any of you felt like this but for me other than the hair loss this week I am absolutely normal.If it wasn't for that I would swear it was all a bad dream.
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So I am back from chemo session. Uneventful. But, I already feel little nauseous and my taste is changed already! WTH?? :-( This weekend won't be fun.
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silviazara - My third T/C was not a picnic. The nausea started earlier and I had that yucky taste in my mouth right away. I also was much more tired. Having said that it did pass, except for being tired all the time, the past week has been pretty good. Of course, next week is #4 so I will have to go through this one more time but at least I know it is the last time for all these things. Hope you can rest this weekend and just sleep through all the yuck.
MomtoJJ - Hope today went okay for you and easy SE's
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Today was my second treatment and boy was it a long day! I arrived at 8am, did bloodwork, a fill, MO and then infusion. Unfortunately, infusion was behind three hours!!!! I finally arrived home at 6:45pm. Remember how I was asking people about the rash on my hand where my first infusion site was... Well it's gotten worse and they believe the chemo infiltrated under my skin. My entire hand cannot be used for infusion. They then went to a vein at the base of my thumb, then to the side of the wrist, the inside of my wrist, and on and on... The 6th infusion nurse got it. All my veins were either not good or collapsed. I go for a medi-port on Wednesday! My arm is pretty beat up needless to say.
No reaction this time though to the drugs! Yea! I'm pretty exhausted so I'm tuning in for the night. Silviazara- thinking of you today too! I too have a funky taste going on.
Good night all! -
I was told the treatments get more difficult just didn't want to admit it to myself! But it is true! I feel nauseous, tired and having no taste whatsoever few hours afterwards ... :-(
Gayle - next week you will be all done! GREAT!
Kelly that sounds terrible! Where did they find the vein after all? I am so sorry!!!
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Silvia: I found this third round made me feel more tired, and nauseous too. But now, ending the second day after treatment, I'm starting to feel a bit better. Hopefully It'll continue that way and for you too!
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Silvazara- they ended up getting it in my forearm off to the side... Very awkward. I had to keep my arm straight and flipped up the entire time. They tried my veins on the inside of my wrist - it was less that comfortable and it looks ugly to say the least!
Good night ladies! -
Hi Ladies:
I have had three rounds of T/C so far. Today is day 3 after and I am tired and have no taste buds, a little heartburn, but nothing worse.
Coldenmom - I had the same "rash" where my IV went in and my doctor also said that some of the chemo had leaked out. At first I thought it was an infection and I was very concerned, but he said it was merely an irritation. They did manage to start an IV in a different spot for my 3rd chemo and it went smoothly.
I am 53 years old and I never realized how well I generally feel. When I feel even slightly "off" from the chemo I get very depressed. I can't believe I'm here again after 19 years. And I feel guilty for complaining when some women have it so much worse than I do.
It's a difficult road we tread, isn't it?
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I feel quite bad feeling sorry for myself this morning after reading what everyone has been going through yesterday and today. This was day four after first round and had nausia, dizziness, and all joints aching. Took meds and it helped the neasia, I have no taste though. Lemon wataer seems to be the only thing that tastes good. I am doing better now, but so tired. But getting nervous again about what is ahead.
DH took me to the EN&T today. Very relieved, throat is clear, said probably swallowed during PET test. Told him I fell asleep and woke myself snoring. He said that would do it. On the plus sign he gave me a prescription for a C-Pap. My DH is respiratory and I had one awhile back. Slept like a baby. EN&T doc said no reason not to get another and not have to have a sleep apnea test. So when this is all over will use one again and get some good nights sleep.
Everyone - I am keeping each of you in my prayers. I am so sorry for all the SEs. You are in my thoughts all the time.
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Day 7 after last treatment. Didnt feel well for the first few days but I feel quite good now, and look forward to a couple of good weeks before the next treatment. I really dont have any complaints. I hope each of you are doing well, I read your posts, and wish I had a magic wond and could take away everyones SEs. You are in my thoughts and prayers
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Woodburns, So glad you had good news about scan!! What a relief!!
Joan, I know what you mean. I hope I will never take feeling good for granted kin the future!
Glad that many of you put another treatment behind you this week.
I agree that some SE increase on round 3. I'm on Day 10 after 3rd T/C. I am fighting a terrible cold. Atlanta is in full spring and I have bad allergies which are making it worse. I can't stop coughing. They called in antibiotics on Tues. I'm glad because for the first time my WBC is low. The first time it was 16+ so they gave me 1/2 Neulasta on round 2, it stayed in the normal range so they did 1/2 shot again for round 3, today my WBC was only 3.5. I guess my strong first grade teacher immune system has finally been hit by chemo. I am praying for this not to get worse. Looks like I'm staying home and away from any crowds and out of pollen. It's 80 in Atlanta this weekend! Bummer!
I think of you all each day. *hugs* to all, but not in person! No passing this cold to any of you!!!!!! -
Joan - was wondering how your were doing. I am glad your SE's aren't too bad.
Kim48 - Feel better. It is hard to avoid germs when you work with little ones. I was testing in a third grade room for three days this week and it sounded like an infirmary.
Firstcall -glad you are feeling well.
Silvia - you are 3/4 of the way done - hope the SE's aren't too bad this round - sleep works wonders.
Gayle
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Hello Everyone, I haven't been posting since I have had a bad time of it lately. Had a severe allergic reaction to the T, so now we have had to change for this 3rd tx yesterday. So I got AC instead, aka the Red Devil. Nausea hit in just a couple of hours and pretty much been out of it today. But I am half way through!
Somedays it just seems to be to much. I really appreciate everyone sharing. It helps to keep my going.
Marlene
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Morning Ladies,
lmlola59: Glad yo're feeling absolutel yourself!
ColdeMom: Uuugghh, behind 3 hours! Sorry to hear about your arm as well...Boy, no kidding, about being exhausted!
woodburns: So HAPPY to hear your throat is clear!
SheryIR (#3 Down, Wahoo!) , Ca7tko, & ali68 (Ladies, are you half-way done now?): How did it go yesterday? Thinking of you!
mkgutierrez: Glad you popped back in! Hang in there!
I'm still having some allery issues: sometimes nose dry, then running, & some sneezing. Eyes dry then sometimes watery & scrathcy...
Yesterday was a SUPER long day! After Boot Camp I received a message from my mother who was having to call 911 for chest pains! Needless to say, stinky and all, I drove like a maniac for 20 minutes to the hospital praying to God the paramedics got to my mother in time. I was trying to call her and there was no answer. Thankfully, she was able to call me and she was in the ER. I couldn't tell you how relieveing this was, but yet knew she wasn't out of the woods yet. While in the ER her blood pressure was through the roof 226/100 and in A LOT of pain! It was so sad! I had arrived around 8 am to the ER.
Again, thankfully, it was Day 11 post-treatment. Eventually, we were moved to the Cardiac Cath area. I can not tell you enough how WONDERFUL her nurses were in the Cardiac Cath part of the hospital! I was given warm blankets, hot chocolate, a doctor's/nurse blue type coat/gown, & a mask (plus LOTS of extra to hang on to while mom stays in hospital). When they asked my mom about eating something around 11:30 they asked me as well. Even asked if I had any protein yet. They fed mom & I.
While in the Cardiac Cath area they did a Cardiac Catherization. I'm not sure if any of you are familiar with this, but they sure have come a long way! They used to have to go up through the leg which is clamped and then after procedure you have to lay for hours and not move with a sandbag over your leg. Not anymore, if you're lucky, Mom was lucky
. They went through a vein in the wrist which lead them to the heart. AMAZING!!! Dye is used to look at the heart. In my mom's case there was blockage in two arteries. However, on a good note, her heart is good - no damage! After the procedure, in a nut-shell, she just had a plastic bandage on her wrist with this small balloon (which would represent the old sandbag on the leg) they inflate/deflate when necessary.
Around 1:30 pm she was finally admitted to her hospital room. Hallelujah, it was a private room! My friend came and brought we a change of clothes, lunch, snacks, and things for me to wash up. Friends, how important they are in our lives!
I left mom last night with mom no longer in any pain! I didn't get home till after 7. Finally, I couldn't keep the tears back any longer. The emotions came to the forefront! I didn't even cry like this when diagnosed! It was just that moment, on the way to the hospital, of the unknown whether I had my mom with me or not that finally took it's toll on me.
I know Mom is in good hands right now. So today I am going to attend an event I have been registered for for awhile now. My friend and I are attending a Women of Faith event. I have NEVER been to an event like this. So here's to stepping out of the box
a bit!
To those of you with SE's I'm hoping they subside for you!
I will be thinking of my mother today along with each and every one of you! Lots of prayers & hugs my friends!
XOXO,
Bonnie
Most of all other beautiful things in life come by twos and threes dozens and hundreds. Plenty of roses, stars, sunsets, rainbows, brothers, sisters, aunts and cousins, but only one mother in the whole wide world. ~ Kate Douglas Wiggin
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A_Fighter,
So glad to hear that your mom is not in pain now and it sounds like they are taking wonderful care of her and you. I can relate to how you felt when you got home. I had my lumpectomy on the 23rd of December and suddenly lost my father (3000 miles away) on December 29th. My husband came running in the room cause I hit the floor in tears and pain. I had planned to spend Christmas with him but my diagnosis changed all that. I still feel as though I haven't been able to truly grieve.
I hope you enjoy your event today. I think that stepping outside the box is sometimes necessary for our growth.
I don't know what I would do without my friends. They keep me up when I get down.
Prayers for you, your mother and all of you!
Marlene
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Just checking in... been reading mostly. Sounds like it's not such a great week for most
Hopefully next week will be a much better for everyone. My SE's weren't too bad from last treatment, but I think it was foregoing the neulasta that made it bareable. Now I'm housebound for the weekend, per doc's orders because counts are fairly low. I need to have them checked again over the weekend so that they can get an idea exactly how low it goes. Anyone losing eyelashes yet?...mine are thinning out tremendously and I'm just sooo upset over this.
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Hi All
Congrats to those with another one under their belt! Hope SE's start to get better. Mine have been manageable, a bit worse on the nausea side, but still no bone pain or fever so fingers crossed there!
Bonnie: Sorry to hear about your mom, glad she's getting such good care and is doing better though! *hugs* Thoughts are with you both! Have fun at your event today!
AEM47: My Eyelashes are just lightly thinning, Eyebrows too. Not too bad though, hopefully they'll hang on enough that I don't notice that much, btu I do have to colour in the brows now so that they don't look like a small chunk is missing in one.
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Bonnie so sorry to hear of you mom but glad she is no longer in pain.Now that they know what has caused this they can hopefully get her better soon.Hope you have a great time with your friends today sounds like you deserve it
Gayle56 Wow last treatment next week seems so far away
Coldenmom awful that you had to wait 3 hrs to begin and had a problem with the veins,this also worries me the most going in for my next one.
NikkEliz Glad to hear that you are feeling better I think you have been handling this really well congrats to you
Kim48 Sad to hear you have been sick with a cold please take care of yourself and get well soon
mkgutierrez Sorry you had a bad reaction this go around,has this been the first time?
AEM47 Funny I was just looking at my lashes this AM and was thinking they look a little thinner I have only had 1 TX YIKES.Can hide the hair if you choose ,can fake the eyebrows I think but not anything at this time that you can really do about the lashes BITES.I don't wear a lot of makeup but I have always enjoyed bringing out my eyes
Day 19 took a shower and think I have lost 1/2 of the hair went out with a hat but think I am going to have to make the decision to just get rid of it before the end of the weekend.Expected and excepted but still so sad
Hope evryone feels good and enjoys the weekend
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Hi everyone ---
Feeling great on day 18 -- but treatment #2 is leering at me just around the corner. SO not looking forward to going through the cycle again. 1 down, 3 to go. It will be done.
Imlola -- yes Miracle Mouthwash is prescription. They had me swallow it for sore throat in case it was thrush -- which I did 'ever so slightly'. seemed to work.
AEM47 -- why were you able to avoid the Neulasta shot? Your counts were up that high? I'm told if counts are high enough -- I'll get half the dosage for round 2.
NikkEliz -- LOVE the blue wig! Please let me know if Claritin D works for you. I tried reg 24 and it didn't work for me. I took the 1st pill right after treatment, but some others took it before treatment. I'm going to try that as well.
Bonnie -- sorry to hear about your mom! Glad she's in good hands. Good luck if you run the 5K. You're energy is an inspiration!
I'm going to ask about slower cytoxan since I've had a headache in some form or other (mild or more) everyday since treatment... and I'm on day 18.
Marlene -- do you mean you had severe allergic reaction to T on your SECOND treatment? Damn. I thought if it didn't happen the 1st time, it likely wouldn't happen the second time.
So my hair is shedding -- though it doesn't gross me out, could be that my tolerance is high from having a large breed dog and a hairy boyfriend. I had cut my long hair to chin-length before 1st tx, its now, on day 18, beginning to take on a slight "dread-lock" look. Dread-locks are common where I live and I've always liked the look. So I'm going to let it play out and see what happens. At some point, I expect to buzz it -- but as long as its looking okay as is -- I'll leave it.
Have decided no wig, will just wear hats -- newsboys and beanies -- I have one turbon/scarf combo for fun. I've made a halo from the hair I'd cut off already, which when worn under my hats will work enough when I don't feel like looking like a cancer ad. Otherwise, I'll just wear hats. I think its interesting how we each handle the hair loss in our own individual way. I imagine this summer, when its hot, going "topless", or with just hats, might feel good.
Anyone know -- once treatment is over -- when hair begins growing back? How long until you have about an inch?
Oh -- friend me on facebook if you want to connect over there too: shera delia
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Shera: Thanks! The nurses went crazy about the blue wig and were calling everyone over to check it out haha. Now evertime I call about something or they call me they all ask what I'm 'wearing' on my head today and how diva I look. haha I ended up nt able to get the Claritan D. The didn't have ANY in stock at either of the pharmacies I was able to get to. Plus the pharmacologisy there said that I shouldn't mix Claritin D with Tylenol 3, so if there WAS still pain, i'd be stuck. My MO did however give me something else which I started the day before the bone pain usually starts. It's like a perscription version of Advil instead of tylenol, more of an anti-inflammatory and so far, practically no pain even with full shots! A tad stiff in the morning but not much more than I am when I just sleep in a weird position which might be the case with all the hot flashes making me thrash around at night. Haha. Never been this glad I live/sleep alone!
Had a great day yesterday, first day 4 with no pain, no fever, had about an hour or so of nausea but I'll take that over a 4-5 hour stay in Emerge anyday. My St. Patty's day plans got cancelled cause the guy I've started seeing and was supposed to meetup with was sick, blah. But I ended up just having green ginger ale at a bar and then a friends house after, playing boardgames all night. Hopefully going out to see him tonight though since he feels better! Yay!
Hope everyone who's been having SE's are feeling better, and those who haven't, keep feeling great! *hugs to everyone!*
Nikki
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Hi all,
As those before me I decided to buzz the head this morning I could no longer stand the shedding .This was done alcohol and tear free which I was very proud of. Was able to try the wig on without hair and find the fit will be ok but I think it is to full for me so I am going to go down and see if I can get it thinned a bit this week.But it is good to know that an average fits.Also was very curious to see the shape of my head doesn't seem to have any flat spots so looks like mom did a good job of not leaving me to long in the crib.I think right now I like the halo and hat as my scalp is still a bit sensitive but assume this will pass also. Only problem I have with the hats is they seem to keep falling forward so may have to look for some type of tightener for these.But is done and feels so much better.
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