Anyone.Starting Chemo in October 2016?
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well, even though the fingernail thing isn't supposed to start before taxol, last night I noticed that three of my nails really look darker clear up at the top where they grow out from. My husband says I'm dreaming but my son sees it clearly. I think my husband is attempting to prevent me from losing it because I feel right on the edge of a major pity party.
Thanksgiving was tough here. We had a nontraditional dinner Thurs. which was fine. But Friday one son and John fixed a traditional dinner and invited my parents and brother visiting from Chicago. My other son had gone for a bike ride trip with a friend and is returning today. He doesn't like any Thanksgiving food so this worked out well. These 2 sons came without families so I wouldn't catch kid germs. This would have been fine but I just seemed to be incapable of totally staying out of the kitchen. By the time it was over, I had hit a wall of exhaustion and collapsed. To top it all off, i have developed a tremendous sore throat.
The total crowning glory to all of this was that John had given Molly a steak bone. I TOLD him not to do this. I reminded him quite clearly what happened when he did this before. During the night, she had 4 accidents which NEVER happens. Fortunately, I had turned on a light in the bathroom to be able to find the Tylenol bottle and saw 2 of them. I had no problem going in, waking him up, an letting him deal with it. I might have had some guilt if the dr hadn't specifically said no picking up of doggy do without even knowing we had a dog. The other 2 gifts weren't found until morning and he dealt with that too.
The house is empty today with them all gone. I have had one nap and am about to have another. I really have discovered that if I don't pace myself, I am going to pay for it big time. Now, to actually do it
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Agreed VLH on where to break the plates, usually do on my drive way next to my garbage can and sweep up immediately. Thanks for the reminder.
KLNiss on the mouth, I noted mine was more sensitive the last days, but had backed off of the baking soda rinse ( of 3 -5 times a day ), to less. Now back to rinsing more and occasionally the biotene. Wondering if diet and foods might contribute. Onco noted no proven effect of the baking soda rinse, so backed off . And now a few more sensitive spots.
Charlene1 understand joint pain. Somewhat feel the lower activity level contributes. So really pay attention to getting up and moving more often as can loose track of time of being still and lethargic. More movement and lots of water helps.
Luwusu yes, being just days behind you appreciate your updates. My number 6 (Taxol only ) would have been Thanksgiving Friday, infusion center closed, so it's added to the end finishing up on Friday Jan. 13th instead. ( seems appropriate - LOL ) . On the red rash, my onco follow up appt. revealed he felt it lasts about 4 weeks , if it worsens I am to get in touch with him. Boom, 4 weeks plus 3 days, they are fading and far less raw. Still moisturizing with Aquaphor. Added a few more hats, turbans at my hair bussing gathering.
PHOTO : a buzzing party with the loving support of friends
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( had to be goofy, it released some tension).
Laying more makeup ( especially eyes ) on. Gotten lots of comments on it. And Al12 went and bought colorful cheaters, bigger frames, red, black, and blue. Your photo with your 3 amigos gave me the idea. Like them so much, thinking about some dollar store 1.00 to wear to pull more attention to the eyes.
Really enjoying Thanksgiving holiday.....Wonderful family time on Thursday, and more ... ( one a break from Friday infusion regiment) did Houston Zoo Lights instead with the granddaughter and daughter. Tomorrow it's Barbara Streisand concert with my thriver / survivor team - mom, sister, and friend of 28 yrs. Weather is fabulous. Yes, always something to be thankful for. My cup runneth over.
train ride @ Houston Zoo .....
Keep up the great work ladies. You / We've Got this....!
Terry ( aka whistlestop )
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Connie - Cancer sure doesn't make holidays any easier, does it!? Glad you were able to have a Thanksgiving event with family, despite the ups and downs. So true that we just can't run at normal speed these days, but this too will pass! Hope Molly is doing ok.
I also had doggie drama last night ... after I finally fell asleep, my son came banging on my bedroom door around midnight because our old dog Max was having a big seizure! We wound up taking Max to the emergency 24 hour vet clinic ... very scary. They kept him overnight, and we're waiting to see what happens next. Here's the thing ... Max is almost 15 years old, and they are offering tests like MRIs ($2400) etc which are not in our budget. We want Max to be comfortable and well, but I think that difficult decisions will soon be upon us.
I'm trying to stay calm and hoping that all will turn out for the best. (Whatever that means!).
Barb
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Good morning ladies,
I had lots of energy on Thanksgiving, but little on Friday and Saturday. Hope today's a winner. The good news is the bad, inflamed , itchy area on my right arm is better. The bad news is that it has taken up residence on the right side of my hand and arm. I am using a steroid cream that was prescribed.ive had a rash/redness on my hands and arm for about 5 weeks, with varying severity.There is nevertheless a dull moment in chemo-ville. My nose continues to be an issue, too, I know things could be a lot worse, but just feel like complaining.
Barb, I hope your dog is doing better. Having to make tough decisions at this time is even harder than usual. We went through that 3 weeks ago with Rosie. I feel your pain. Hopefully Max has rallied around and is doing okay.
Whistlestop, I love the pics. Looks like you had a very good group with you. One of the good things that has come about is that I no longer need to pluck any stray hairs from my eyebrows (which I still have) or anywhere else.
Happy Sunday to all
Nancie
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Hi Nancie, Max is home ... he seems better, thank goodness. We're crossing our fingers that things will settle down! So sorry to hear about your rash ... things like that are crazy, because they're "relatively" minor (in the grand scheme of things), but such a nuisance! Hope that you find some relief ...5 weeks is a lot of scratching.
So tomorrow I'm finally going to get a port ... anyone have any words of advice? I'm looking forward to having it, since it will help preserve my veins, but the procedure is just one more thing to get through. Onward and upward!
Barb
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Nancie Luwusu feel free to vent here and complain a little as needed. I was just telling someone this morning how this is such a great place to be able to speak your mind without being a drain to others in your support group.
We all need to release.
Barb Abracadabra… so glad to hear Max is home. Portwise for me it was a breeze compared to access full IV the first time. I feel it's the only way to go. I have an auto - reflex mechanism that my hand goes up to protect the area of the port each time I hug someone, or the granddaughter gets near in playing. Another idea, get a fair number of bandages and dressings for changing as you do the first few times. Once you have done it will go fairly ease. For me the main thing is my skin and padding a the port location is thin and you can actually see the line pretty well. I changed some of the tops I typically wear as in the beginning it was very visible.
Here's a photo of how it looks during infusion..... Find tank tops work well. under a button down layering shirt. I am sure you will do well. yes onward and upward...
Keep the faith ladies. Appreciate you and this outlet.
Terry ( aka Whistlestop )
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Barb,
I resisted getting a port in the beginning. I didn't want another procedure and was worried how it would feel. People said it would be a positive thing, and that proved to be true.
* the procedure to install it was smooth and easy
* it has made the infusions very easy. I have lidocaine cream to put on it before port access but there's not much of a difference with or without the cream. There is a one second jab when the port is accessed and it goes away immediately.
* you have complete use of your hands and arms (and use of the bathroom) while being infused with a port
* I asked the radiologist to try to place it to the side a bit so that it wouldn't show with V neck tops. He acted like he had never been asked this before, but happily complied.
* it took a solid three weeks for me to be able to sleep on that side (my right) again. I wish someone had told me that, but that it would be eventually doable
* there was tenderness at the port site while it healed. Three weeks. Your skin has to stretch to accommodate it, plus the incision has to heal.
* don't pull off the steri strips even if you want to. Just sayin.....
* I had "twilight sleep" and was given an Ativan before the port procedure. Extra strength Tylenol that night.
* I am aware of the port but it doesn't show when I have clothes on nor is it painful
I am very glad that I got the port, even though I was hoping to do without one. With weekly infusions, it was a good decision.
Good to hear Max is going okay! Way to go, Mac.
Nancie
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Terry and Nancie - Thanks so much for all the port info. I'm looking forward to getting it over and done ... I really appreciate the advice about things like extra dressings, and not touching the steri-strips, and having the port placed to the side. These types of tips help me to feel more prepared!!
Barb
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I am new to the group and I also have one more infusion of AC on 12/6. Them four rounds of taxol along with Herceptin for a year.
AC has been rough on me but so glad only one more to go. My nurses say that Taxol is a piece of cake compared to AC.
I really wanted the cancer tumor out of me before chemo but my oncologist recommended chemo first.
I want the surgery ASAP after chemo to get this out of my body.
Fight fierce ladies ✝️
Queeny
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Hello 😀 I have been mia for quite a bit! I'm sorry for that.. so much going on! I felt myself falling into a depression and it has been a struggle. Although I am still keeping the faith and dealing with everything well considering.
I had my 3rd infusion on the 21st, YAY to reaching the halfway mark! To say I'm tired would be an understatement, I am literally just so dang tired all the time. I take lots of naps these days!
My daughter still hasn't had her baby, she is a week past due! If she hasn't gone into labor on her own by Wednesday the dr will schedule an induction.. so either way Miss Charlotte will be here by next weekend! I'm so excited!
At my last infusion when my lab work came back my blood sugar was 301.. they're assuming it was related to the steroids since I have never had an issue before but I'm going to my primary car dr this week to have an A1c just to be sure. I've checked it every morning since and it has been between 100- 118 every morning so I'm hoping it has everything to do with the steroids. My mo cut my dosage in half so we shall see.
I tried to read all the posts but I'm not sure I will ever really catch up. I sure hate to come here and dump all of my emotions but this is really the only place to do just that! And I appreciate each and every one of you for listening!! I hope you all have a good Thanksgiving (we did!) and hope this finds everyone doing well and with a little SE's as possible! ❤️ Jenn
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Hi Queeny - welcome to the gang! I'm also down to one more AC (Dec 12), then it's 12 weekly Taxol for me. Here's to getting it done! Looking forward to hearing more from you!!
Jenn - welcome back. I'm sorry to hear you've had a rough time of it. Hang in there ... you are getting through this, and soon it will be behind you. Here's to happier days ahead ... and speaking of which, the coming arrival of Miss Charlotte must be such a source of excitement!!! Nothing like a cute little baby to make the world bright and shiny!!!!!!!
And on the topic of using the forum to vent ... lady, that is what we are here for. We all have our moments/days/weeks where things happen (or don't happen), (or don't happen the way they are supposed do, etc.!). Drop it off here, and hopefully you'll leave a little lighter ...
All the best,
Barb
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Connie: My nail beds are turning darker too, so did my tongue and some of my gums. I'm really looking like HOT mess these days! I can't wait til the day I can say I'm a month PFC (post final chemo)
Whistlestop: Love the buzz party photos, you look GREAT!
Abracadabra: I hope Max is feeling better and that all went well with your port placement today but agree with Luwusu, I wish someone how have told me I would be able to sleep on that side again.
Queeny: Welcome to our sisterhood, sorry you're here but glad you came across us and I hope we can be the support you need. I'm slightly ahead of you I'll have my last AC on Thursday Dec 1 and then starting on 4 rounds of Taxol. I too I'm having chemo before surgery.
JR74: Welcome back, you've been missed. Don't be silly please vent as much as you need that's what we're all here for.
Maybe I asked already (chemo brain) but has anyone else been packing on the pounds? Ughhhh it took me 4 years to lose 75lbs and in a matter of 30 days I've gained 15lbs I figured out why. 1) I stopped working out, I go to the local YMCA (kind of like cheers, everybody knows your name) and I didn't/don't want ppl looking at me differently or treating me differently 2) I have ZERO taste buds. I literally lost all my taste buds so I eat and eat in hopes that I can savor what I once did L (playing the world's smallest violin) so now that I've figured it out I'm being more careful about my eating choices and I've been checking craigslist for an affordable elliptical machine where I can workout at home until this ordeal is OVER with. I'm cold capping so I'm very limited to what I can do to this mane on my head, discolored nail beds, tongue, gums and packing on the pounds Jeezus I'm really starting to look like a bad bad version of Diana Ross.
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I'm glad to hear (well, no, not really) that someone else has trouble with the nail beds Deemendoza just so I can show my husband that I'm not paranoid.
This has been a very rough few days. I started with a sore throat Fri. evening that turned into a major event with high fever. I called the emergency number and they told me to go ahead and start taking the emergency antibiotics they had prescribed in the beginning for just this event since I live I 1/2 hrs away. So a great deal of my time with 2 of our boys was spent with me sleeping and trying not to vomit. John's taking them back to the airport as I type. The only salvation is that he took them out for some seafood a few times and they enjoyed the weather. I didn't even consider going as I was sleeping constantly. I don't know how anyone can sleep as much as I have lately. I am white as a sheet and for the first time, I really FEEL like what I expected a cancer patient to feel like....and that just makes me cry.
Deemendoza, how is the hair holding up? I am so anxious to hear how well the coldcapping is working.
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It sounds like many of us have had a less than stellar week. I don't wish this on anyone, but in a weird way it makes me feel better that I'm not alone in this. I have felt out of it for the past several days. Yesterday I slept for 3 hours in the afternoon which i never do. Then slept 9 hours
last night.
So far, my fingernails and toenails look okay. My redness continues, and I'm not going to bore anyone with it again. I have no taste, either, deemendoza, except for things that are sweet. It hasn't stopped me from eating.
Jenn, the thought of a grandchild being born so soon- that is extremely exciting. Something to look forward to. Keep us posted.
Barb, how did the port installation go? Hope you're recouping and doing well.
Does anyone else feel like the week (I'm on weekly chemo) centers around the chemo day? Waiting for it, having it, waiting for side effects, dealing with side effects? This is the rut I'm in
The photo I s me in my wig on the way to chemo. I don't wear it too often.
Hope a good night is had by all. Nanci
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Cute wig, Nanci!
Connie, I'm sorry Tootsie! Hopefully your fatigue will lighten up.
Barb, how'd your port placement go?
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Hey hey, ladies! I have been upgraded ... I am now "port"able, s"port"y, and I speak fluent "port"ugese (ok ... that last one is a complete lie, but I'm feeling frisky!).
The port placement went very well ... the male radiologist was very open to my requests about avoiding bra straps etc. and he even called over a nurse for another woman's point of view (she was very clever ... she noted that she could see my T-shirt tan line, and had him adjust the mark a smidge over to make sure it would be out of view!).
They gave me a nice mixture of IV sedative and warm blankets, and I was so comfy that I told a nurse it was like a spa-day (she burst out laughing and asked what spa I went to! I admitted that I don't get out much!) No steri-strips ... they used surgical glue to close, and it's covered by a dressing which I'm not supposed to remove or get wet for 7 days. Fell asleep really early but, as you have noted, had some difficulty sleeping through the night due to soreness and twinges. That's OK ... I'm so excited that it's finally done. Progress!!!!!
Thanks again for your support and concern to all.
Nfullblume - big kisses! I felt like you were there holding my hand!!
(((Connie))) - I really hope that you're feeling better soon.
Nancie - What a nice picture ... your wig is so pretty, and what gorgeous blue eyes you have! You look great!
(I realize that this post is maybe a little over the top for something you guys already went through, but it's so much fun to have something to be happy about. Yahoo!!!!!! Have a great day all.)
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I'm ecstatic that it went so well for you, Barb. That little contraption definitely makes things easier!!
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I'm actually looking forward to my next chemo, to try it out (does that sound weird?).
This is going to make a huge difference for me ... my surgeries were on the right side, so all IVs, needle sticks and bp measures etc have been happening on my left arm. The problem is that I'm a lefty, so during treatment my 'good' arm has been taken out of play. You should have seen me during my hospital stay, trying to feed myself soup (yes, they served it daily!) with 'righty' ... I solved the problem by drinking it straight from the bowl! LOL
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Barb, that's so great about your port. In a week or so it will just be a part of you--mine doesn't bother me at all any more.
I had a rough Thanksgiving week--AC #3 on Monday, and I was feeling ok-ish until Thursday morning, when nausea (mild, but making itself known enough for me to back away from cooking) took over as I was baking. I managed to eat a tiny bit of Thanksgiving dinner with my daughter and housemates, but it was a struggle. On Friday I had a fever that ALMOST got high enough to call the clinic (which then, of course, means a trip to the ER) but it just stayed under so I stayed home...but felt icky and had had a headache since Monday. Hovered on Saturday around 99.9, and in the afternoon my right eyelid started to swell up and droop over my eye. I'm sure it was an allergic reaction to something; we contemplated calling in in case it was something neurological, but after a Benadryl it started to shrink back up. I barely got out of bed on Sunday, although by then my appetite was back so I managed some leftovers.
My daughter went back to NYC yesterday and I went to a regularly scheduled checkup with my surgeon; when I told her about the eye droop she sent me right down to my PCP to really make sure I hadn't had a neurological event--which I'm quite sure I didn't. It's almost back to normal today, and there were no other symptoms of anything like a stroke.
This week, I'm going to stay away from pubic spaces pretty much completely. Last time, the day before chemo, I did end up in the ER with a "fever of unknown origin" and I don't want that to happen again--if I can avoid it by hibernating, I will.
My homemade turbans (thanks to those who posted YouTube links) are getting a lot of attention and compliments--as a completely non-crafty person, it's nice to hear (and of course they are so easy to make even I can make one.) My housemates have donated some of their T-shirts since I find that my own are just too tight on my head.
One more AC and then I'm on to 4 rounds of Taxol, then, because of the BRCA 2, bilateral mastectomy with reconstruction (temporary filler), then radiation, then surgery to put in the permanent boobs, then surgery to remove the ovaries and fallopian tubes, then, finally, just hormonal therapy. It's a long haul but on days when I'm feeling ok, like today, I can almost believe that it will someday be over. I'm really trying to take things a day at a time. I'm glad winter is coming on--being shut in is much less emotionally draining when it's too cold to go outside anyway. I have a few can-be-made-warm-and-cozy spots in this very drafty house so I will move from one to the other over the course of these next months...
Lots of love to everyone,
Kate
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Kate - I'm glad that the eye-thing settled down ... isn't it crazy how things just appear out of nowhere, leaving us to try to figure out what the heck is going on?!
I'm with you on the 'avoiding germs' thing ... when I was at the hospital yesterday for the port-affair, I was horrified when a man sitting beside me started coughing. I felt like leaping up and fleeing down the hallway (where there would only be more germs lurking, no doubt). We do what we can, and cross our fingers for the rest of it. Stay cozy!!!
Barb (also seeking cozy spots in chilly Montreal!)
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Kate, I'm sorry that you had such a tough time. Given my quest to find humor even in this challenging time, I had to chuckle at you staying away from pubic spaces. Having not had a date for years, I, too, avoid 'em!
I'm heading to the shower to prepare for AC #4 and that laugh was exactly what I needed. Thank you!
Yay to Barb on being port-ified! Since my port looked so wonky, the nurse had to use an IV in my dominant arm when I had fluids and I hated it. That darned thing beeped every time I moved my arm more than an inch or two. Very annoying!
Lyn
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VLH, worst typo ever, right? I used to be a producer for public television in Boston, and so many times pubic got sent out instead of public, and not just in my correspondence.
And yes, my public/private areas have been private for quite a long time too!
Kate
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Kate- might have been a typo but it made me smile. Thank you! There does always seem to be something new going on.
Barb- hallelujah on the port placement! You will be very happy that you have it now. And I understand about you wanting to try it out. You won't know what to do with your hand now during your infusion! Not true. You will. Be patient with the healing and know it will be something you don't think about much in several weeks. Your description of it being like a spa day was cute. When I was in recovery from my port placement, they gave me one of those tiny containers of canned peaches and I thought they were the best thing I had ever tasted.
Lyn- hope infusion 4 goes well today. I have three important "Lynn/Lynne's in my life right now- my best friend, my therapist, and my oncology nurse. All really good people.
I am decorating our Christmas tree today, slowly. A touch of normalcy. Here in New Hampshire, it is drizzly, cold, raw and gray. The trees are bare. I'm making turkey vegetable soup for dinner and bought a loaf of homemade whole wheat bread. A hunker-down day.
One of my close, wonderful friends is English. She has a saying, "Keep your pecker up!" Which doesn't mean what one would think- it means keep your spirits up. But it's fun enough to say. So I say to all you ladies, "Keep your pecker up!"
Nancie
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What has worked for you when your mouth tastes like something died in there? I've lost 13 lbs in 4 days because everything tastes horrid to the point that it makes me gag.
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Hi everyone, Ive missed so much! Barb and Betty are my cheerleaders! Thanks for all the support! Im having 3 round tomorrow! My ankles are so swelled! Will discuss it with my Dr tomorrow. I've been reading all the post and saying lots of prayer for my fellow ladies! Hugs and Prayers
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Hi Ella! Great to hear from you ... good luck tomorrow. I'll be sending good thoughts your way!! Hope your doctor has helpful suggestions for your ankles ...
Have a good night, and let us know how tomorrow's treatment goes!
Barb
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Hey ladies! I wanted to introduce my precious granddaughter! Charlotte Davis (Davis was my great grandmother's middle name and also my youngest daughter's🙂)
She was born today at 12:05 pm weighing a whopping 8lbs 11ozs, and 20.5 in! And she is precious! Mommy and baby are doing great!
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JR74, she is precious....and such a big girl too. Love the name! Is this your first grandchild
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Jenn - She is beautiful! She looks like she's thinking deep and mysterious thoughts! Thank you for starting my day with such a lovely image. Enjoy your day, Grandma Jenn!!
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Ella - Good luck today. In your last post, you mentioned that I'm one of your cheerleaders, and so I thought I should come up with an official cheer for you. Here it is:
It's treatment day, I've gotta say
I'm feeling really strong today.
Let's get it done, let's move on through,
I'm doing what I need to do!
My B.C. sisters hold my hand
My B.C. sisters understand
We can do this, we are strong,
We'll get through this, we'll move on!
Love, Barb
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