My (perhaps controversial) thoughts as a "newbie" to CA.
Comments
-
Hi Lori-- I'm also getting dental work done--at the U of MD Dental School...need a crown and maybe a root canal...the dental school is great and a TON cheaper--the crown at my old regular dentist would have been at least $1400, not counting X-ray and cleaning prior.....at the school the crown will be $451. Can't beat that. They also spend hours and hours with you--something I'm not at all used to!
So glad your port is out and hope you do well and are soon bruise-free.
When I need to cheer myself up I look at your latest raccoon photo--I do so love it!
t
-
Trill, I'm glad you get as much enjoyment out of my critters as I do. There's a big female raccoon that sits at the patio door begging for her marshmallows, last night we watched as she tried to pull the door open. I'll get pictures of her tonight. It was adorable that she wanted in so badly. The possum I've been giving marshmallows to has been coming every night to be hand fed her marshmallows too. Hubby says "great now I have to call you raccoon and possum lady" I think I'd be lost if I didn't have my 2 hours of down time with my critters every night. All this because I saw those babies on my window sill staring at me 1.5 years ago, who'd have thunk it? lol
Praying everyone is as blessed as I am with all of your kitties and puppies and other critters 🙏💜
Sending out hugs and kisses for all two and four legged friends and families!
-
Lori, so glad you spied them----I, too, think you'd be lost without them--and THEY'D be lost without you--at least your marshmallows!
-
Lori - Keep sending your critter pics and stories. No inside critters at this time, so we enjoy whatever is lurking around in the neighborhood. We have backyard bunnies, along with chipmunks, and squirrels. Once in a while a trash panda can be seen going in and out of the storm drains, and occasionally grazing deer roam the neighborhood front yards. Hardly ever see possums, but know they are around. Of course, there are lots of birds, too. All of this in a well populated suburban area. Never ceases to amaze me!
-
Celia-- You've GOT to tell me: what is a trash panda?
-
Trill, a trash panda is a raccoon as they have a mask like a panda and they get into the trash lol
-
Can you find Bob the stray cat?
-
Mama raccoon finding marshmallows yummy! I wish she'd bring her babies for a visit!
-
Lori- Yes, I see Bob in there! So cute! And love mamma raccoon...I'm sure one day her young ones will want to try a marshmallow or two...I would think they could smell them on her when she returns home...marshmallows have that distinctive sweet smell...
Thanks for posting these~so great!
-
And I love that one shot of the marshmallow in her paws!!!!
-
The babies are here!!
-
Whhhheeeeeeeeeeeee! I love it!
Lori, you must be so proud! Are you ready for Godmother-hood??? Huh??? It's a big job! You have to see that they scamper for food, seek out the marshmallows, and the rest of the time sleep or pose for pictures.....
-
I'd be lying if I said I hadn't thought about "doing nothing". I think it has a lot to do with me just not believing any of this is happening to me. I feel 100% normal - how can I have cancer? That thought runs through my head over and over. Last night I had a dream that I was walking naked through a huge mri tube and screaming "You're wrong!"
I realized today that I am angry - angry that this is happening, angry that on one hand the doctors say I should have a mastectomy but then schedule it 6 weeks out. I'm sorry does the fact that it's called Invasive breast cancer not make you want to act quicker? They didn't call it resting breast cancer! When I think of invasive I picture little cells with army hats on - making their way through my breasts...that damn dense forest...and angry that my 9 year old now has a mother with cancer. Angry that I spend hours thinking about what I might have done to deserve this and knowing that I did nothing to deserve this.
And then I come back to reality and tell myself of course I'm moving forward with my treatment - because that's what has to be done....but the thought has been there...
-
Trill, the little guy couldn't get the marshmallow down fast enough! It was so cute to watch it lick all the sugar off the outside then shove the whole thing in his mouth! The possum that comes to the door for her marshmallows was cute tonight too. I opened the door but pulled the curtain closed to keep the bugs out. After a second marshmallow thru the curtain she just came in the house thru the curtain to get her marshmallows. Just to funny how they trust us sometimes or we them!
Hi Candyapple and welcome! I'm sorry you landed here but your in the right place for support from some pretty awesome, sweet, loving gals! It's hard to believe when we're first told those three horrible words "You have cancer." Your diagnosis is almost the same as mine, your tumor is a little bigger. We are here to help you get through everything that's going to be thrown at you over the next couple of months. It's very scary but you can do this! It will be ok. I had to wait 5 months before I had my DBMX due to insurance screw ups ugh! My BC went from stage 1 to stage 2 in that short time. I said the same thing... invasive means invasive! I was originally told my cancer was slow growing. NOT! I got rid of that BS I don't need someone taking care of me that will lie so easily to my face. We are here for you, feel free to pm me with any questions you may have. I'll help in any way that I can. (((((Candyapple))))
-
Hi Candyapple1--- I so understand what you're going through. Yes, it IS unbelievable....as you read in my initial posting, I just "happened" on my lump on my birthday--completely out of the blue--but of course I felt perfectly fine.
Cancer?
ME?
And the word "invasive" is chilling. No doubt about it. I love the appropriateness of your little army of cells. But I don't think they necessarily mean aggressive--just that the cancer cells have moved out of one area into the next--like out of a ductal cell and into the adjacent one or something. The doctors and nurses do seem quite calm. I had surgery almost 6 weeks to the day after diagnosis and wondered how they were so calm and cool about everything--here I thought they'd hurry me up and have me in the operating room within days of the diagnosis. But no.
That's hard that you have a youngster. I'm on my own--it's just me and Miss Pantaloon (pictured here the day she came to her new home)--but they are all little loved ones and dependent on us and that means so much in the big picture. We worry for them and equally depend on them. They can keep us going sometimes!
As you can see from the stream of postings while I made up my mind what to do, I went through a lot of soul-searching but was finally decided when my therapist, who is so very, very conservative about these things, looked up my cell type and where before she'd said she thought a lumpectomy and then a "wait and see" and no chemo or radiation would do, called me and said my cell type IS an aggressive one (all three negatives--no progesterone receptors, called a triple negative) and that I shouldn't do a wait and see but go ahead and have that boob taken off. Then I decided to have both--I didn't want to deal with a lopsided body and knew I wouldn't miss the 'dangling fruit' bothering me as I went, bra-less, about my artwork.
But I elected not to have chemo or radiation after the double mastectomy. I would have gained 6 months and 10 days additional life after undergoing a rough regimen of chemo for 4 months--no deal. That was an easy call.
I asked my breast surgeon when I went for my post-op,
"Doctor Jacobs, I'm not doing chemo but what are the chances a few cancer cells from this are floating around in me somewhere?"
And she said, very simply,
"It's highly unlikely."
I was happy to have a doctor who would not beat about the bush and would tell me straight out. And I trusted this 100%.
I didn't have any cells in the sentinel lymph node, nor vascular invasion, and the margins were clear. The tumor itself was small. So I was lucky. Not in the cell type, but in the other stuff.
You're a "positive" and I think your cell type CAN be treated with hormonal drugs, which is a good thing!
I hope you'll feel free to reach out and I'll be more than happy to offer you what I can. And there are great, great topics and threads here--more than you will ever be able to cover!
Take care. You will get through this. A dear friend of mine that I went to grad school with and who is much younger than I developed bc when she was 42. Four kids under the age of 12. She had both taken off and had chemo and did fine--and that was going on 15 years ago.
bye!
Trill
-
Lori, I am totally jealous of you!!!!!!!
Waaaaaaa! I want a raccoon baby tooooooo!
-
Candyapple:
I get very upset when all we hear is 'early detection saves lives' and here I am, still waiting for treatment, 12 weeks after lumpectomy. I want to scream, early detection might save me but you slow pokes are going to kill me for sure!
I got a breast cancer diagnosis and suddenly my head, which used to be mostly empty, apparently, is filled with thoughts and concerns I've never really had before. I feel like I was dumped into a club called 'People Who Know They Are Going to Die'. It is not a fun club and the refreshments suck. Of course the truth is that we are all members in this uncomfortable club, but we don't know it. But when you get a cancer diagnosis it's like someone writes a big old name tag with your name in it and slaps it on your chest NEW MEMBER and there is no way to pretend that this isn't your reality. It is exhausting, isolating and terrifying. Fills up space in my head that used to be filled with ocean wave noises or other fluff.
Deciding what to do, how many treatments to endure, do you throw your lot in with modern medicine or do you sacrifice a chicken and eat a boiled toad? From every corner someone is giving you advice, offering you cures, telling you about their aunt's neighbour's cousin's daughter who had breast cancer and she either a) lived without any treatment at all, a miracle! or b) did it all, suffered and died. I began to fear what would come out of someone's mouth! I felt assaulted by everything most people said. Yesterday I told someone I was apprehensive about my upcoming radiation and she said, well it's better than being sick. What? Why do you think I'm having radiation? To glow in the dark? I am having radiation because I AM sick !! What the hell ?!?!
When I was told I had a low Oncotype score (11) and would not need chemo I was happy. Then I wasn't. Then I felt stupid. So many women have suffered so much through chemo and the lingering effects, I was spared that. But am I missing out on one of the few chances I have to live out my life? Am I exposed to more cancer because I didn't blast it with chemo? I hate how a cancer diagnosis has made everything uncertain. Everything.
One thing that I find we have to consider with a critical eye are the statistics that say "if you skip chemo it will shorten your life by 14 days". And you think," pfft, 14 days, that's no big deal. I would happily cut my long life 14 days shorter at the end to avoid chemo now. " But the trick is that the statistics do not tell you WHEN those14 days are going to be yanked out of your life. Will you live 30 years, minus 14 days at the very end? Or will you be bopping along 2 years from now when those 14 days get taken out? Because there is no coming back from that. For me the question is not how much longer / shorter will I live with / without treatment, but WHEN does this come back? How long do I have BEFORE the effects of skipping chemo show up? So far I have not found much to answer that question. If I pop off 14 days earlier than planned, 30 years from now, no worries. If I pop off 14 days earlier than planned 2 years from now, THAT is not going to make me happy!
This is angering, maddening, feels unreal. At first I fell into a black hole where everything I did, every breath I took felt like doom and wet concrete. That passed. I just said to Hub, it's easy to forget that I have a life threatening illness. But a week ago a dear friend's husband who had routine hernia surgery came home from surgery, ate some soup, got in his recliner and died. No chance to fight. No chance to get his affairs in order or say goodbye. And it made me realize that the real threat to my life is life itself. I try to find perspective and grace and wisdom. Nope. Not there yet. Don't know if I'll ever be. Candyapple, everything you feel and think is absolutely valid, normal and miserable as hell. I am so sorry for all of it.
-
Hi runor,
Read your letter and am moved by how WELL you put it. You nailed the whole psychological conundrum we live in.
I don't know how old you are but I think a lot of it has to do with age. I'm 73--turned 72 the day I found the lump--nice birthday gift from mother nature--and since I led a pretty raucous time back when I was a hippie and didn't think I'd make it to 25 feel I'm in bonus land. So it was a pretty easy thing to say no to chemo and radiation once I learned that going through four months of it only to have six months and ten days added to my life. I'm glad you got to skip chemo as THAT was the one that freaked me out the most. I didn't want it AT ALL. I didn't want radiation either but electing to have both beasts removed precluded that.
But it's a far different matter if you're, say, 45 or 55--or even in your 60's--and this strikes and I honestly don't know what I would have done had this disease happened much earlier. My therapist was--is--so opposed to chemotherapy and radiation and is so persuasive that had I known her then I might have steered clear and stopped at surgery. I've heard too many bad stories about chemo since I opted out and people opened up to me--as they didn't want to do while I was still in the deciding stage--that I'm all the happier not to have gone for it. But it's just a fruitless guessing game.
During that thinking stage, someone said to me, what if you decide not to go through with chemo and it re-occurs--how are you going to deal with that? And for a long time I thought of that.
Then I met with the oncologist and got those numbers and it was an easy call. When the oncologist called me to get my final decision and I told her I'd decided not to go for it, she also said that to me--what if you don't and it recurs--have you thought of that? Can you live with that? ec etc.
And I said to her, well, what if I go through the chemo and the cancer returns--what then? I'll have done all that and messed myself up, perhaps permanently, and STILL have the damned thing. How will I live with myself THEN?
Uncertainly is part of life.There are no warranty tags attached to us when our mothers push us out. Someone told me there are cancer cells in all of us, held at bay by our immune systems. I keep telling myself that my own is strengthened by an increased respect for the time I've been given knowing that a silent, invisible, un-touchable, odorless, tasteless presence is probably in me now, lying low. We're none of us getting out of this alive and, paradoxically, life is sweeter--for me, anyway--knowing that.
-
Trill1943, I am 53 years old. I would like to update the bio at the end of my posts but can't figure out how!
Breast cancer seems like a game show with two doors.
Behind door Number One is all the treatments you could take, all the side effects you could experience and the cancer comes back!
Door Number Two has no treatment, no side effects, and the cancer comes back!
You look at the game show host and doubt his sanity because frankly, this game show sucks bad. And you say, both of those doors are crappy prizes. I want the door where I do everything and it never comes back or I do nothing and it never comes back. And while smiling into the camera he tells you those two doors are not part of the show, not something you can choose, you can choose to do everything (and wait for it to come back) or do nothing (and wait for it to come back) Hurry up and pick one, the cameras are rolling.
As I see it, those are the choices we have. We throw our dice and hope. We choose our treatment and hope. Do the right thing, do the wrong thing? Sincee no one can guarantee what the outcome will be, there is actually no right or wrong thing. There is just a choice. Not a great one either way. And hoping like hell you win.
-
Trill, I'll see if I can get one of the baby raccoons in a box and ship it to you. I don't think Miss Pantaloons will agree to having two cute fur babies in your apartment.
Runor, I love the way you sum this crappy game of BC up! Where's door #3? Which is the door the MO, RO and BS is standing behind to say "Ooops we made a mistake and you don't have BC!" It gets easier for a lot of us and I pray it gets easier for you and they hurry the hell up and get your treatments started!
Trill, here's an updated picture of my straw bale garden. It's gone crazy!!
-
runor, my oncotype Dx was 13. I had two positive nodes and extensive lvi. Still two oncologists really recommended against chemo. So I had mastectomy followed by radiation. I take exemestane and hope for the best because I want to live to see my grandson grow up. I am on 56, 54 at diagnosis. But even without cancer there's no guarantee of a long life.
Lori, fun pictures!
-
Runor, I'd rather go for the door where I do nothing beyond the surgical removal of the tumor and just go on living as long as I have.
And I think I would have chosen this were I younger.
I just didn't want chemo. No way.
I'm sharing these thoughts and feelings that JUST APPLY TO ME AND MY CASE. I hope they help you in a good way to come to a decision. I'd rather be frank than coy and non-committal.
Partially I say this with a lot of gusto because my tumor was small and there was no invasion into the lymph node that would have been the first to catch them as the cells moved out of the breast, there was no vascular invasion, the margins were clear--and I got a thumbs-up from my breast surgeon. AND I had both breasts removed.
(Johns Hopkins has a thing called My Chart, where you register online to access info about appointments, tests, all kinds of things with your doctor and hospital. It was there that I read my three-page detailed path report. That's where I learned of the vascular aspect--meaning ca cells into, or not into, the vascular (blood) areas, and of the margins.
Do you have access to your path report like this--where you can see about the tumor you had removed and the node? Or could you get a copy?)
My therapist's 79-year-old mom had a lump in her breast and all she did was to have the breast removed. It left her lopsided, but that was no big deal to her. She turned down chemo and radiation and has been fine ever since (I think this was roughly five years ago), just one boob short of a whole human. Karen--my therapist--is a detail-oriented, facts-oriented critical thinker who dotes on reading about all things tests and test results-wise and advised me against chemo and radiation because of my age, my stats re the tumor, and what she's read of chemo and radiation side effects.
I hate being nauseous. I think I hate that more than anything. I'm allergic to narcotic analgesics and have been so violently ill after surgery where it's been given that I'm rendered a thrashing crazy woman on the stretcher in the Recovery Room.
When I told my breast surgeon about this, my worst fear facing surgery, she was the one who pinpointed that I'm allergic to narcotic analgesics--first person in 73 years to tell me this! All those knock-outs for wisdom tooth extractions, D & C, hysterectomy, sinus surgery--all followed by sheer unadulterated HELL! She said she'd have the anesthesiologist use propofol--which was great--no side effects, no thrashing, no nausea!
No way could I take four months of nausea. Even though they said they have new drugs for that--I didn't want it. And the ACT regimen that the oncologist recommended for my case is an especially tough one--the adriamycin is bad for the heart.
The day I met with my oncologist she went to the computer and brought up a website where you punch in all the stats and it shows various outcomes, life span of people who fit this group, etc. There were several screens that could be opened when this data was entered. I came home from that appointment and opened that website myself and went through it, then got my therapist on the phone and she and I looked at the site together--she on her computer at home--and went over everything. That site was great as far as giving outcomes and stats and answering some general info that helped me.
Did an oncologist go over things like this with you? Offer a chemo protocol and then show you results for women who fit you cell type and other things? It was invaluable to me. I'd ask about it if I were you.
Yeah, it's a crap shoot either way. I think it depends on your feelings about side effects, your tolerances, your mindset regarding taking powerful drugs (I didn't wanna! ) etc.The whole shebang. Many, many women on this site have had chemo and sailed through it. My best friend from grad school with four kids under twelve had a double mastectomy and had chemo and it was, she said, no big deal. She felt flu-like symptoms for a day or so--then she was fine. And still is--all those kids now out of college...
As far as adding stats here on the site, etc--well, I also had to hunt, hunt, hunt. I think that I went to the bio section and there was the teeny tiny little word "settings" in blue embedded in one of the paragraphs. It was hard to locate but that's what I clicked to be able to change the picture that goes beside your name. Look for "settings" in pale blue and click that.
OK-- hope this rambling chatter from me helps a little....t
-
Lori- -I'll be on the lookout for that box. Now don't let me down! Pantaloon is ready with a little bed for him to sleep on...and she said she'd share the Iams but not the Fancy Feast.
And I have plenty of marshmallows...
Love your garden! Wowza! It's so neat and everything! And colorful!
OK, have the Thousand Island all ready and waiting...
-
Trill, I tried to put the smallest, fattest and fuzziest baby raccy in a box but there was no way to hold him in and get the lid to the box closed! I'll keep on trying! Thank you on my garden. It turned out better than I thought it would and I'm definitely doing it again next year!
Molly, I called my MO and asked why I didn't have the onco score test done? I want to know what it is? I was told with my diagnosis they knew I was having chemo and didn't need to have it done. Enquiring mnds want to know! lol
-
Lori, thanks for trying to get the baby in the box....A+ for effort......
Yes, you definitely have to make an annual thing of your garden....really great.....!!
-
Here in Chicago, raccoons are rabid—and definitely a hazard in the home, especially if you have pets. Had a huge raccoon break through my office ceiling—she had pried open the aluminum soffit, crawled into the attic, and had her babies up there before she fell through the masonite ceiling on to my eMac (killing the computer, which was obsolete anyway). Scared the crap out of my cats before she scurried back up into the ceiling. Tried Havaheart traps baited with peanut butter, but she was wily—ate the bait and then left the house after giving birth. The babies were in the closet wall and we had to have the urban trapper cut through it with a keyhole saw. They were adorable and we wanted them released in a county forest preserve, but city ordinance gave us only two choices: turn them loose on your own property or let the trapper euthanize them. We realized that the death they’d suffer at the hands of predators (dogs, feral cats, coyotes, cars and gangbangers with guns) would be far worse than the gas that put them to sleep in the back of the trapper’s truck. Broke my heart, but what else could I do? Fixed & reinforced the soffits so it wouldn’t happen again.
I’m 66.5. I did the math and realized that Letrozole is giving me a grand total of 6 extra months. Cancermath’s tool says that w/o treatment I’d live to age 85. With chemo & letrozole…86. With Letrozole alone…85.5. So I have a lot of thinking to do. Thus far my SEs have been pretty mild. But if they become unbearable I may throw in the towel (especially if the cells were going to develop estrogen-independence anyway).
-
We had raccoons break into our old office building through the "moveable" ceiling panels - they had a good nosh on donuts someone left in a bag on their desk and trashed that person's office. Thankfully, our offices have moved to a different building as we also had numerous mouse sightings as well.
Sandy - I also "ran the numbers" on various calculators and discussed the extra 6 months results if taking AIs with MO at length as I was extremely hesitant to start in. However, he convinced me that with 100% ER+, I should at least give them a try. SEs thus far pretty mild, but will also reconsider if they worsen. Bone scan done in Nov 2016, just before BC diagnosis showed mild osteopenia in spine, Biggest concern now is bones, but not due for a bone scan until Nov 2018.
-
Sandy--- Your tale of raccoons in your ceiling had me pondering their so skillful ways. They are pretty adept with those little hands. I love how they wash their fish catches--or at least I grew up hearing that. Sorry it cost you a 'puter--even an old one....ah, but a good excuse to invest in a new one, eh? Love when that happens (and IF I can afford it!).
What are you going through---I didn't know you were undergoing chemo now.....think I'm out of the loop....
Celia--I feel left out of the raccoon stories you all are sharing. They're funny....I have to say that but of course not from your perspective....the most troublesome critter invasion that I recall was the bat that got in the upstairs...don't know how he got in. Of course I jumped in bed and pulled the covers over me and my father came upstairs and said, "Girlie, they won't HIT you!" I protested and sqealed...he said that, "Of all things in the whole world of living things a bat's the LAST thing you should be worried about. Sooner have a DC-7 hit you," he said, beginning the search for the bat. I think it somehow got in the cellar. An upended peach basket trapped him and out her/she went....
-
LOL I'm loving all the raccoon and bat stories. Racoons are such silly and skillful critters.
Trill, I had a bat get tangled in my hair when I was about 7 or 8... I think? From the way my brothers and sitter tell the story it was such a hilarious thing to watch. Me running and screaming all the way home!! It was quite a job getting it untangled and lucky for me I had enough hair so it could be cut out of my hair! My baby brother went out onto our porch one night after being told to stay in the house as there were all kinds of critters out and about and he could get hurt. Well, he just got out the door when he came back in screaming MONSTER!! MONSTER!! The monster was a bat hanging from the overhang on the roof above the porch. My brother never went outside at dark ever again and I never heard my mom and dad laugh so hard! Us youngins couldn't figure out what was so funny about a monster hanging from the porch roof?!
-
Hi Lori--- Have been ailing with the flu for the past few days....it's a weird thing--today after getting the Safeway grocery order--there was no way I could tackle 90 degree heat with the flu, even though it's tapering off--I put things away, made up some Jell-O, and was feeling like my old self...voila, I thought, I'm over it! Then suddenly I just had to lie down...I felt all queasy and almost nauseous and just stunned with bad feelings.....I got up and put on my two Sea Bands, one per wrist, to press the pressure point related to nausea--and that seemed to help... But it struck me, that, o, no, it's not gone yet! So I just put the computer to the side....
There is one little tale that's sad about critters I want to share. I think you'll probably get a lump in your throat.
I guess I was five or six or maybe even younger. My brother Dick had a pet raccoon he called Jody. One day relatives were visiting us from DC, including my grandfather. Very proudly my brother brought out Jody. They were outside and he let Jody climb a lamp post, which got everybody giggling and laughing it was so cute. But Jody fell. And perished. So an otherwise so joyful sweet time was made tragic. I'm still so thankful that I was too young to be aware of what was happening--I just was told about it. (Or maybe I blocked it?) Well, we all have a sad story or two about our pets and other creatures, I know--since we tend to outlive them all.
Ever since, Dick has had this overwhelming love of critters. They drive him nuts! I'm gonna gather some of your best shots and send them to him to let him see what YOU have got going out there--I know he will love them like I do.
Keep cool! t
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