Starting Chemo July 2013
Comments
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Wow aaoaao,you are awesome and an inspiration.Lark they are going to give me 4mg vs 6mg,i quess the nurse just squirts some out?Or maybe it comes in different doses?Ang
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Aaoaao
Morning ... You are a b$&@/y inspiration - so strong !!!
I am pretty positive usually so thank you you really made me smile this morning - you go girl
2 Hobbs. I feel I can see the finish line for chemo but just can't quite touch it - apprehensive like #1 all over again - who knows why
Post more later
Soriya, Angela, Hanna, Marsha, lark, HB, R50 ( as opposed to R2D2hehe), of course JeriG and anyone i have missed hope you are all feeling stronger- u all rock
Xx -
Hi All,
I loved reading all the inspirational stories. So many things to be thankful for, and yes, even though we may feel bad or don't look like ourselves we are alive and will get through all of this when some are not so lucky. When I used to walk in the cancer center I felt like a cancer "victim". Now I take a look around and speak with other people who have thing so far worse and am thankful that I am a cancer "survivor". I will be forever changed, and even though the treatments are hard sometimes life lessons are hard. I have so much to be thankful for and am truly blessed. I never knew the depths of love from my family and friends and strangers that I have received, and some people will never know that until it is too late. If that all makes sense. Peace and love to all...........
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Angelanature and Nocompromise2013 thanks for the complements. I agree with Hannariggs, this disease does give you the insight into how much you're loved and how much your family/friends mean to you. Most people don't realized this until it's too late. Now I remember to say I love you before I leave someone or finish talking to them on the phone. I never want my last words to them to be anything else.
Hang in there everyone, although the treatments are difficult, you will get through them. I hope for the best for you all. You will be forever changed but there will be good changes along with the bad ones.
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Hello everyone...am back. My yeast infection is getting bad, no discharge but its red and sore. Applied the doc given by doc but it is not working as fast as I want it to be. I am jumping up and down after every pee. Anyone to share on this? Any medication? Doc said he will not want to give me anti-biotics, since chemo med is already bad enough for the body.
Hi Sue, hope you get your chemo done without a glitch.
Hi Angela, glad that I am normal! I started to get worried if I am going blind with the teary eyes. Sorry to know about your son's accident but I am sure you have gained a new perspective of life after BC, just like me.
Hi Twohobbies, talking about anxiety. I am eating lorenzepam to calm myself down. Especially with the yeast infection now, the pain is so unbearbale
It heightens my anxiety badly. I cried so loudly, hugging my mum yesterday. Bald or hair, we are all warriors and will be survivors.
Hi Lynn, enjoy the game.
Hi Marsha, not sure if I can get aquaphor in Singapore. Let me try.
Hi Lark, there is always a rainbow after the storm. Your daughter is lucky to have a great mother. I want to be alive for my daughter. She just turned 11 months two days ago.
Talking about white and red blood count, I am not a promoter but the only health supplement which I have been eating is papaya leaf in capsules form. It was by chance that I spoke to a friend and she sweared by it. It is her life-saver, she have blood disorder and blood transfusions are normal for her. Until she found out about papaya leaf and started consuming, she no longer need any blood transfusions. Her doc and her had a small test, she stopped for a week...and her blood palettes went very low and dangerous. She consumed again, went back for aother test, her blood palettes are normal.
I will not do any advertisement here. But if anyone is keen, please pm me. I am giving one bottle to an colon cancer patient, she has been missing her chemo due to low WBC. I met her during one of my chemo and chatted. She said she would like to try. I am meeting her on Monday. I will update here if it works on her.
Cheers to all... and big hugs.
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Cherri, I was told today to have a bath and add vinegar to it and soak. This will help with the ph to help that yeast infection. It can't hurt. Maybe google it to see how much to add to a tub?
Hannarigs, so glad you sound do good. You were in my thoughts as Taxol 2 went down the drain.
My first dose wasn't too bad, except I was out cold that first day. Wow. Chemo at 9 am and I slept till 5 pm and even went to bed that night. I'm hoping I'm a little more coherent tomorrow. I guess I'm good to go, as I never got a call to say I had to wait a week. Never thought to be excited about this! Another one bites the dust.... Tomorrow thay is.
So I better get sleep. It's an early appointment tomorrow. Ughhhh. LOL but say it with me now.... Another one bites the dust. That's right.. I know your all singing with me..
Sleep well warriors!!! And keep kicking butt. -
Hi Honeybunny, thanks. I will hang on and hope the cream works. Its already stinging pain and I am jumping up and down after each pee. Not sure if the vinegar will bite more into the soreness.
I am singing with you
Good luck!
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Cherri what about plain old zinc oxide bappy rash cream to act as a barrier when you pee ??
DONE DONE DONE. All chemo Tx FINISHED. Yay. Yay and yay
My son had his 18th yesterday so we celebrated late night
Whilst sitting in the BGC at midday today I get a call from him.
Where are you mum?
Having chemo Ben where r u?
I went 4WD and got bogged mum
Can a mate go and get u out ?
No mum all at work or TAFE
So post chemo good old mum picks up his cousin and we drive 1hr out of Perth in DH work ute (OOPPs). To pull him out. Which they succeeded to do after about half an hr of digging, and jacking up etc great. Takes my mind of chemo hey !!
Roll on day 7.)))))
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Hi Sue, I tried using it before I went to the doc and the patch got bigger! My gal's nappy cream... thanks for the suggestion. Glad that you finished one round of chemo!
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Aaoaao- just read your post (how did I miss it???) Your courage and strength are amazing!!! Each day is truly a gift, for anyone, but somehow cancer puts life in a new perspective. We can choose to let it swallow us whole and sap our will, or take the bull by the horns and ride on, as you've so gracefully done. Thank you for sharing
I needed a positive start to my day - very little sleep last night (likely due to the far-too-large grass-fed steak I ate last night ;-)
Sue- So you're DONE??? Big hugs and congratulations!!! I'm jealous, of course ;-)
Cherri- hope the diaper cream helps! I've had a couple of yeast infections since starting this mess, but both have been more manageable than my stinkin' hemorrhoids!!! I used Desitin for a couple of days - don't know if it helped, but it can't hurt to try! What about sitz baths with Epsom salt? It doesn't sting. The papaya is interesting! I've been anemic for years (take injected B12), and chemo has made my hemoglobin counts ever lower... Will have to explore ;-)
Taxol folks- have you all experienced tiredness worse on the day of chemo with this than AC? Just wondering - I start teaching a class on the evenings of my chemo mid-October, hmmm.
B/T/W, I'm going to the Braves game tomorrow as a SURVIVOR!!! Kickin' cancer's butt!
Happy Friday, Firecrackers!!!
Lynn -
Rambo-Taxol for me has been like the AC in the respect that the side effects hit about the third day. I get bone pain and fatigue. Definitely easier than AC but brings its own side effects to the table. I see where alot of people are having fatigue the day of infusion due to the benedryl. This didn't affect me at all. I get a little drowsy but it wears off quickly. The only problem I have is on the day of infusion due to taking steroids the night before and the day of infusion I only get a couple hours of sleep that night. Next infusion they are taking me off of them the night before and will only receive the day of. Hopefully that will help. Bottom line is every person is different so you will just have see how you react. Tomorrow is my day 3 of taxol 2 so will have more to report then. I did a full days work yesterday and today and am feeling good. So I guess we will see what tomorrow brings.......Happy Friday to all !!!!
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So today is first Taxol! Took the steroids at 9:30 last night and 3:30 this morning (apptmt is 9:30 this morning & they said steroids should be taken 12 hrs and 6 hrs before T). Onco said steroids would cause havoc with my diabetes (type 2) and said we'd have to do something if fasting BC went above 180 - I just tested & it was 233!! Not sure what they'll do - it was 95 yesterday morning! Ugh. Good luck to 2bluestars and all warriors starting T with me today! Lana
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Cherri- when I had a yeast infection one of the lovely ladies here suggested keeping a spray bottle filled with water in the bathroom. Then after you pee spray yourself like crazy to cleanse. I found that it did help while I was waiting for the med to kick in. The sitz bath and vinegar in bath water sound like good ideas. If you're worried about it burning try dabbing a tiny bit of the diluted solution on yourself first then have the spray bottle handy just in case you need to wash it off. Hope you get relief soon!
Aaoaao - you're my hero. I pray that I can handle this with some of your grace and wisdom.
Sue - I guess I lost track and didnt realize you were so close to the finish line!! Congrats, thats awesome! Funny story about your son. Im surprised you weren't muscling the truck out of the mud yourself!
Rambo - glad you're feeling up for going to game! Hope that means the hemorrhoids are better. (How strange that I'm talking to strangers about yeast infections and hemorroids!) With my first taxol I was very sleepy for a couple hours from the benedryl, then got wired later that evening and the next day from steroids. So for me that night was ok, but see what others say.
It's day 9 after the first taxol and I'm still soooo tired! I drive my kids to school which takes about 45 minutes round trip then I have to come home and lay down. Thought I was going to faint in the grocery store a couple days ago. Still achy and not sleeping well. I thought it would be better by now. Admire all of you who are able to work and do fun stuff! -
Cherri I had the same problem with my last infusion and it did last longer than normal. Do you have an external medicated cream you are using? I rinsed with water only throughout the day. Then apply the medicated cream or petroleum jelly or baby rash cream as a barrier.
NC being mom doesn't stop just cause you're in chemo. Sometimes I want my teen to be more independent but it is nice to be needed!
Stay strong warriors -
Lana, I also have crazy blood sugar problems with the steroids. Before my last infusion it went up to 500! I had never seen a number like that before! My endo prescribed an injection of NPH (Humulin) each time I take the steroids. I also give myself an injection when they hang the bag of Decadron during the infusion. I try not to worry too much because I know the steroids are temporary and things will go back to normal. Good luck!
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Hi ladies, started chemo July 31st. So far my cocktail is AC for 4 rounds and then I will start on weekly TH for 12 weeks. Anyone else on AC? Ever since I started chemo I have on/off lightheaded ness and spacey feeling. Completely annoying!!!! Anyone else experiencing this?
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Welcome Girlstrong! Many on this forum/thread have done or are doing 4 rounds of AC. Everyone is so different - some have had very few SE's and others have had many. I think general "fatigue" and lightheaded/foggyness (chemo brain!) are very common. Personally I did very well with AC and mostly just had fatigue.
I had my 1st Taxol today - pretty uneventful, thankfully! It was a long day - started at 9:30 and finished at 2:30 - was delayed some due to another blood clot in my port -pretty common for me now. I had a little restless legs but that's it! Nurse said to see how my BS count is sat & sun and if it stays high to call my primary next week. First she said it is fairly common for diabetics to need temporary insulin shots during T because of the steroids. I only take one metformin a day because I have been able to control it mostly with diet & exercise so I'm hoping if I need to do something that they just increase me to 2 pills a day vs insulin!
Hope everyone is doing well! I hope I stay SE "free" during T! Stay strong fellow warriors - only positive thoughts! Hugs! Lana -
Good evening alll!
Back from my first taxol. Got there at 9:30 this morning. Didn't get home till six. What a long day. Just the taxol alone took 4 hours. And they changed my pre meds after all. He kept the Emend and Aloxi the same and added Avitan (sp) for nausea, he doubled my steroids from 10 mg to 20mg and he added a small drip bag of pepcid ac, those took almost an hour. Slept on and off the whole time, first time ever. Slept in the car on the way home, first time ever and came in and hit the couch and slept for 2 more hours, yep first time ever. I blaming the avitan. I met with MO before chemo and mentioned the word "worried" about 3 or 4 times, at different times and about different subjects. I guess he thought I was too "worried" because I got a text from Walmart he ordered me zoloft and when I go down stairs, surprise.... there's Avitan added to the mix.
I was just trying to tell him I'm 1) worried about long term se of neurapathy, how is he going to prevent this
2) I'm worried about my cancer being TN, what measures can I take after treatment to prevent it coming back
3) I'm worried about having severe muscle and bone pain from taxol, what do I do if I have it
4) my cancer boob started hurting at the former site of the tumor and I was worried it might be re-growing.
Anyway, I'm not sitting around worrying and stressing all the time. I think we had a mis-communication. He has an Indian accent maybe I didn't understand him entirely and vice versa. Anyway our next visit I will be asking and if that's why he prescribed it, I don't want to take it. I really don't need it. I hate being this sleepy. That's why I don't like to take benedryl either. The nurse really thought it was for nausea. So I said, mo told me that's not supposed to be a se from taxol. She said all chemo drugs have the potential and in her opinion, Taxol is worse than ac regimen. Damn. Didn't want to hear that.
So Lynn/Rambo I am more tired so far. But not sure if it's avitan or taxol. I was looking forward to the double shot of steroids to get a few things done tonight and tomorrow. Usually, my tiredness kicks in on Sunday. Oh well. I only have 3 more to go! So hot damn for that!! Woohoo....I see the tiny flickers of light at the end of the tunnel. :-)
I hope everyone is doing well and have plans to have a fun filled weekend. Can't keep up with everyone individually, but I read each and every post and think of all you ladies often and keep you in my prayers!
Edited to add: It's been 5 hours since I've finished first infusion of taxol and 2 naps, I'm feeling pretty normal. Not any different then when I did the ac. Who knows what I'll feel like in the am...kinda scary waiting for the shoe to drop, so to speak. :-)
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Blue stars. - I would keep off the Ativan as much as poss. Sure if really anxious go for it. But your MO needs to be proactively trying to prophylactically treat your valid concerns re neuropathy, TN etc
Remember Cancer doesn't usually hurt (in early stages at least ) because they are our own body cells I have def had some muscle stiffness around Mx area that I don't recall from the start and have put it down to cumulative chemo effects and chemo is far more effective on TN than other types
Did you have Mx or lump? Will u have rads ? Good margins??
So glad you can see a flickery light
That will only get brighter))
Xx -
Nocompromises, I haven't had surgery yet. That will be after chemo. My lump did hurt. That's one reason why I thought it was just a cyst, it hurt and I was close to starting my period. I will definitely stop the avtivan. I don't think I need it. Too late this time since it was put in my iv. I seem to be "sobering" up a bit now. Thank goodness. :-)
I will have 6 weeks of rads after surgery. If I decide to have recon, bs say's it'll be about a year before I'm healed enough from the rads. By that time I'll be used to prosthetics so may not even bother. Too far out to tell.
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Hi All,lark I'm on day 11 and still have terrible bone pain,especially in my back,I'm dreading tuesday!Chemo really does hit us all differently,i was expecting skin problems,not agony.Taxol is easier my a#@##@.Congrats Sue!!!!I'm so happy for you and can't wait until it's my turn. I'm starting to feel like a drug addict,pain killers around the clock and like they say ,you start to need higher and higher doses. Ugh!!!!2bluestars your concerns are so normal ,not signs of depression,chuck those zolofts but keep the ativan for sleepness nights and it really helps with the nausia.Hi Girlstrong,the lightheadedness is called "chemo brain"i had it with the ac but not so far with taxol.Thinking of all of you,hugs especially to aaoaao and dreadix and my taxol sisters(may you have it better than me).Angela
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Angela, I agree, so I'm not even going to pick up the zoloft. I KNOW I don't need them.
Good news so far...I woke up at 7am feeling NORMAL. Really normal. Woohoo! I'm so exicited about that. I'm pretty sure the extra steriods are the cause, but at least I've slept of the Ativan. I'm gonna run with it and have a fun filled Saturday, after I get my neulasta shot... hopefully I won't have to "pay" for it too much over the next couple of days, if I do, it will be worth it. :-)
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Hi Cherri3
I haven't posted in a while but felt I had to respond to your issue. I started to get the same issue but got a handle on it by going to dollar store and getting a squirt bottle filling it with water and every time you go to pee are the other rinse rinse rinse I got two bottles. That saved me hope it helps you honey hang in there.
HUGS FROM TEXAS
Gma04 -
Hi All,
I hate day three of any treatment. It got me with the AC and now the Taxol. The first two days after infusion are great. Completed a full days work and a little "normalcy", until today. WOW, I feel like I am 90 years old! Every inch of my body hurts! Today is the first time I have taken any pain killers throughout any of my treatments, but today I could not handle it any longer. Even my family members were begging me to take something. Probably because I was a LITTLE bitchy. lol. Its so hard to explain the pain from taxol unless you have gone through it. I have broken bones before that don't hurt as bad as this. The only good thing is, it doesn't last as long as the AC SE did. At least with weekly taxols I have four good days and roughly three bad. Always something to be thankful for............hope everyone else is doing well. Rest well
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Hi All,Hannariggs you explained it perfectly,no other pain i've ever experienced(and i have 2 kids)comes close.I'm so nervous about tuesday and being bitchy too,mine started the next day and was really bad for a week. Maybe because i'm getting a double dose?If this happens again i'm switching to weekly taxol.Hugs to all Angela
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Hello Ladies.
Will someone please help me get this Vice grip off my head? Headaches are back. Have not taken my fiorecet today, trying to fall back asleep.
I only had carboplatin and taxotere this time, no herceptin. My heart function dropped 20 points in the MUGA scan, and while it is still is in normal range we decided to wait for it to come back up before trying again. It's annoying because it pushes the end date out, but at least it's only herceptin and I can get the other stuff out of the way.
I'm planning on returning to work next week. I've been on STD since May for my surgery. I'm so bored at home, and I hope the time will go by faster if I have something to do.
Friday night I started altering clothes, and I stayed up all night until the sun rose to do it. I was feeling the chemo effects starting and I figured I could sleep the day away and maybe not feel them at their worst. I have altered just about every article of clothing I own and purged what will never fit (this is my third purge since my surgery). I took about 6 inches out of all my knit tops and dresses, 3 inches out of pants and shorts. Some dresses were more tailored and had to make bigger darts. Now instead of dumpy and frumpy I have a new wardrobe that is actually flattering. Many of my clothes were an XL or size 14 or 16 and I'm now I'm a medium/large and size 8/10. Some of this change is due to weight loss from the past year when I had IBS and then went gluten free, and the rest is my DIEP surgery where i went from a DD to a B cup and had a tummy tuck. If there is one thing I can't complain about with this latest round of cancer, I love looking at the girl in the mirror. She looks like I did when I was in my 20s. I just wish she felt like her too.
Echocardiogram next week.
Hang in there ladies. -
Has anyone getting taxol had any skin problems? I have tiny little bumps all over the middle of my back that get itchy. Its very hard for me to get a good look at it. My husband thinks its acne which I've never had a problem with in my life. I dont remember them mentioning this as a side effect. Just wondering if its "normal".
Angela and hannarigs - sorry you've had so much pain. I dont think mine has been as severe, but there have been alot more aches than I was hoping for. Still so tired that I'm questioning if I can do another dose dense on thursday. Angela, my prayers will be with you on Tuesday. It seems like there should be a way for them to make this more tolerable for both of you.
Marsha - you were so productive! I'm sure you look great in your "new" clothes and you WILL. FEEL. GOOD. again! I hope you can get some sleep and that that will help relieve your headaches. Let us know how the echo goes next week.
Hope everyone else is feeling good and enjoying the weekend. -
Day 3 of my first taxol and getting some pains - mostly my hips and my back - hope this doesn't get too bad! Getting my neulasta shot tomorrow. Hoping for a good nights sleep tonight. My energy level today is way different thn yesterday! Lana
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Angela-Good luck tuesday. My taxol isn't dose dense. I can't imagine how much pain you must feel. I actually look forward to the infusions as I feel no pain for two days and then WHAM. My weekends are spent hurting. So much so that it is hard to leave the house unless on pain killlers(which I hate taking). They say you always want the things you cant have. I told my husband this weekend I would rather have your dosage as at least you have two weeks that are tolerable. With weekly doses you have 4 our of 7 that are good. It gets really old. 9 more to go after this week. Whoo Hoo!
Congrats on losing weight Marsha! I lost alot before my diagnosis. A good thing as I have gained 15 since my treatments. I figured it was the only time in my life where I could indulge in sinful things. I was and 8-10 and now I am a 14-16. lol. Hope it comes off easily, if not save those clothes I may need them. lol
Lark- Have not had any rashes yet. I do use alot of lotion on my feet, hands and my head. Seems like my skin is dryer than normal.
Has anyone done the "feel good" makeup class through the cancer center? I have signed up for ours and its Sept 30. Really looking forward to it, as I am told I will lose my eyebrows and eyelashes with the Taxol. So far so good, but I am using the Brian Josephs twice daily. I hope it works, if not Tammy Faye here I come.
Lana-Are you doing dd taxol? I am not getting any neulasta shots. Is everyone getting neulasta?
Saw a friends baby today and seems like yesterday she had him. Hes already six weeks! Life is rolling on. I look back at the summer and it seems like so long ago. Yet, each and every day seems so long. We all have come a long way, and still have a way to go. I will always be grateful for the friends I have made here. I Will never forget this past year and hoping for us all a healthy future.
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Hannarigs tried to sign up for that program but cannot get in til Dec. My nurse nav said I can go anytime, so I might go after my rads are done. That way I can concentrate on me.
I too have had lower back pain & knees, ankles. Heating pad was my best friend. I couldn't use it in evening though due to the hot flashes I get . I only get them for an hour or so around supppertime.
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