Starting Chemo July 2013
Comments
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Hi all,
Soo tired and headache after round 3. Didnt get these symtoms with 1 or 2 until about the 3rd day. I am hoping the sooner they come the sooner they leave. Will keep you alll posted on the dreaded 3. Minimal side effects to all. I am so glad to have someone I can vent to that truly understands. Hang in there sisters....
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Hannariggs, I love the story about your dog. I needed that.
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Hi ladies,
Funny on dog checking our shaved hands- Charley was looking from me to Eric at our shaved heads, wagging his tail slowly that he approved but not sure the reason for short clips!
Hoping as day comes to a close that allot you managed. Getting some king of mouth ulcer along my tongue but at least I had a great omelette for breakfast and late lunch so I can hang with this and find a solution for tomorrow if it continues. Friends came over and I modeled all my new wonderful hats and one friends shared some of her own hats and beautiful scarfs and tied it artfully. I feel beautiful and they were all loving how I was made for wearing great hats! How fun and a confidence booster to be told you look great!! I wish you all such loving visitors. Such a sweet share JerriGace about your classroom angels. May we all be smiling tomorrow. {{{Hugs}}} -
Hello everyone ! Havent been here in a while , struggling with round #2'and the loss of my mom . I miss her terribly
Wishing u all health n se free txs . {{{{{hugs}}}}}, to All of you -
Hi all!
I've been loving week 3 and feeling so good I guess I kind of overdid it. Couldn't even get out of bed his morning I was so tired! But I went to my wig place this afternoon and got a couple more scarves and head coverings. Friday is the big reveal for my wig when I meet my new students and their parents. Hoping it looks natural to them.
This is only day 17 for me and I had my head buzzed on day 15. How much longer is it going to continue falling out? My shower and sink are still full of hair (very short hair) and I'm getting really patchy. Does it eventually stop? Is that when it starts getting itchy? -
Momx2, so glad to hear from you. I know that we can't imagine what you're going through but you have a lot of people supporting you from afar. I hope your side effects pass quickly. It must be so hard to be physically sick and mourning at the same time. Hope you have family and friends around you to help. Hang in there.
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JeriGrace, my hair keeps falling throughout the first resting cycle, after second infusion it falls out even a bit more. Hair usually comes off in a patch at the itchy spots. I got used to mine falling off now, just hate all the vacuuming and cleaning!
Mellie, thanks! It seems what I got in round one was really a hand foot and mouth infection, not the hand and foot syndrome. I am feeling fine except being sleepy all the time
Going to have my Filgrastim shot today, yay. -
Hi All,
2nd chemo today, I was so drowsy. Got hom around 3pm, had early dinner and nap around 4pm, didn't wake up till 7:30pm. I didn't get to exercise today :-(, . SE didn't effect me yet, usually hit me 2 days later. Will get my neulesta shot tomorrow at 11am, claritin here I come. Friday morning my nurse told me to go in for IV fliuds, since I had nausea pretty bad on 1st cycle, so I hope this will help me with my nasusea.
I shaved my head even before starting to fall out, I was afraid I mite get freak out if I see my beautifull hair fall out in clum. So far I noticed some of my hair fell off here n there but no bald spot yet.
Hannarig, I love your dog story, cracked me up, thanks for the laughs.
MomX2, I can't even imagined what you're going thru right now. Please take care of yourself. Be strong!!!
Hugsss to All!!! -
geesh.. I have to scrub my not so bald head with my passion party body scrub because it looks like I have a zillion little black heads. Did anyone else find this?? I also found that my hair/head was hurting today and yesterday too. Is more coming out? Either give me hair.. or make me a solar panel. I mean don't get me wrong.. I love dressing up in my scarfs. It's fun and I have people complimenting me on how great I look. I even had to go buy earings to jazz me up to make me feel better too. I haven't worn earings since highschool, but I must admit... I look good.. hence I feel good! I should start taking more pics when I fell great!
*sigh* Doc appt tomorrow, round 3 AC Friday.. YAY over half way done the "devil"
hannarigs.. that's so funny about puppy. I'm sure my one cat looked at me and ran the first time she saw me. I had to go sooth her and assure her it was me! LOL Now she comes around all the time.
~~healing vibes~~ to all going through their next treatment this week.
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Hi Ladies,
Sorry I haven't been here for a while. I've had a cold that turned into bronchitis and let's just say I couldn't cough without peeing my pants. TMI I'm sure but very annoying! Went to see Primary Doc last week and got an antibiotic and an inhaler. Was feeling so good this past week I have cleaned house, went through a box of photos that I've had laying around and got them into photo albums where they belong. If you knew me you would know I don't just stick a picture in a photo album, I write down occasion, person in photo, date it was taken, etc...I had those old albums where you opened the plastic page and stuck the photo to the white board and closed the clear page, remember those anyone? lol well my updated photo albums have clear plastic photo pages that you just insert picture into and come in different sizes and are easy to take out. So this has what has been keeping my attention lately.
I was just reading about everyone and what they are dealing with in their lives. I send Big Giant Hugs to all of you Ladies!! Hope you are feeling better soon and staying tough to get through the next round of chemo. To the ones losing hair, I have lost mine as of last week, I have some really dark fuzz coming in but figuring in the next couple weeks it too will fall out as my 2nd round of chemo is tomorrow.
If you don't know me I am a Type 1 diabetic and have started my steroids yesterday (Wednesday)...Needless to say blood sugars are over the moon!! Keeping blood sugar watch consistently and because at 2:39 a.m. central time zone my blood sugar was 350 after changing my infusion set in my insulin pump I can't sleep
I have also noticed the steroid is giving me major heartburn, I thought this was a side effect from my first chemo treatment July 18th, I believe now it is the steroid as I haven't had my chemo yet but will in 7 hours or so. I have my tums handy and if they don't help Maalox or Pepto is on my shopping list after chemo treatment today if I am feeling up to it.
Primary Doc says first treatment was nice to me and to be ready to be knocked on my butt with the second one...I hope to prove him wrong. He doesn't know how strong I am and even at my lowest I will not crawl. Just me, just the genes given to me.
Anywho just wanted to check in Ladies and have missed you all. Hope to be here more often in the next couple weeks while laying down resting lol. Heal On Ladies, Heal On!! xoxoxo
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Acid reflux anyone? Ho do you deal?
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Hi All,HVV my onco has me taking otc prilosec,its expensive(16$)but totoally worth it,he has me take 1 a day for one week after chemo infusion.Hannariggs,I got the severe headache immediatly after round#3 too,its still terrible today,this didnt happen right away after first rounds,its keeping me up at night.Ive made an appt with my eye doc ,my onco said the type of chemo we r on can cause pressure behind the eyes.Hope its not that.Momx2,it must be awful missing ur Mom and having to go through this.Hope u have nice friends like Sheila to help u through.And Sheila when i read about ur omellette i got such a craving for one,thanks for helping boost my weight up!Hugs and love to all us fighting this fight,Angela
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Hi angel,
Please let me know what your eye doctor advises. Seems like sinus pressure behind the eyes and across the forehead.
Feeling ok today after round 3. Headed in for nueulasta shot and then let the games begin. Hoping for better SE than round 2. At least I can see the finishline(at least kick the ole devil in the @#$. Love to all
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Honeybunny I think your head will get a little better after it sheds more. No great advice except I found the irritation to be improved by washing it every day rather than waiting two days.
I wondered if my dog would recognize me after the shave but he didn't even seem to notice. Maybe he can't see as much with the curly hair in his face.
Realitycheck, such a good task to get done, the photo albums. I have cleaned and re-arranged my bathroom drawers but that's as far as I got.
Hugs to everyone. Triple hugs to Momx2.
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Angela - I've had behind-the-eye pressure too and was told its the Cytoxan. It went away after the first few days - hope yours does too!!!
HVV - I'm using Pepcid for my occasional burping and reflux symptoms, but mines not too bad.
RealityCheck - glad you've found a fun task to occupy your time! I think we all need a distraction right now, to "forget" for a little while what we're dealing with. Mine's been the new job - another amazing day today, and NO Neulasta bone pain like last cycle! Of course my counts were in the pits yesterday, I'm on an antibiotic (again), and was told I'd likely have to have an infusion for my low Hbg by next cycle, but I'll just keep rolling with the punches ;-). Hate you're dealing with this as a type 1, my daughter is too, and I pray she NEVER has to deal with this!!! She has a good type 1 friend who battled non-Hodgkins her freshman year of college and the chemo wrecked havoc with her blood sugars too! Hang in there - {(hugs)}
HoneyBunny - best of luck with round #3 tomorrow!!!
Soriya - hope the fluids help with your nausea, you deserve a BIG break from SEs ;-)
JeriGrace - good luck with your "big reveal" tomorrow! I'm sure everyone will LOVE your new doo - so funny how many compliments I got on my "hair" today-
Sheila - love your fashion show. I might do that when my aunt and cousin come visit later this evening!
Momx2 - continued prayers and hugs; words can't express how horrible I feel for your loss
Love to ALL you firecrackers
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~Lynn -
Hi Everyone - I'm just doing a quick fly-by here as I'm still at work (and finally having a productive work day!).
I'm trying so hard not to think about my hair today as my scalp is tingling (not sure if it's itchy or stinging at times) and strands continue to come out. I think I can get through one more day without buzzing it to finish out the work week (fingers crossed and holding my breath). It sounds to me like most of you still have quite a bit of hair hanging around at the day 16 buzzing stage? I'm hoping there will still be enough to look okay if I have it tied up, or with a baseball cap. My ponytail has thinned to about half its former volume. I'm wondering if my BF's cats will be as perplexed by my soon-to-be bald head as it sounds like some of your dogs have been.
I had a big cry last night as I was deciding to put off the clippers at least one more night. Probably more tears scheduled for tonight and tomorrow night. I never imagined that this would hit me so hard. It has made me realize that I am a "hair girl" after all. I think it's going to be another Ativan night.
This whole process has driven me to moments of self-pity and self-absorption that I don't think are typical of my personality (I hope). It makes me feel so vain to be thinking so much about me, me, me and my hair, of all things, when some of you have gone for another infusion this week and are suffering SEs and Momx2, I am so sorry for you. How can I feel so awful for losing hair that will grow back in comparison to losing a mother?
I do wish you all an easy time this cycle. Glad to see you back, RealityCheck, but sorry about the bronchitis! That sounds miserable.
I'm also taking Prilosec for acid reflux, since that's my usual state of being. Pepcid doesn't work for me. Prilosec works, but not right away (next day relief really) if anyone runs into the same problem. I have had some breakthrough GERD with Prilosec in the first week following TC. I'm thinking of doubling my dose next round.
{{{HUGS}}} to all and I wish you a relaxing and comfortable Thursday evening.
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Thanks ref to radiation comments..even though I have made decision and read everything I can..theres always that little voice in your head..with ??...so, it makes me feel good to read your comments!
I had wierdest time after my chemo..took until day 6..then felt great..day 11 dawned and was like I was sucker punched! Felt same as I did on day 3 when chemo feeling hit. It wasnt until day 13 that I felt good again. I guess my counts dropped. I really hadn't expected that after only one treatment.
Rambo-Very happy you had felt GREAT..this makes you really grateful for the good days, huh?
Villa-I had same issue on middle of the night..kinda queazy stomach--I would get up ..half asleep and eat 3 saltines with 3 small slices of hard cheddar and it settled my stomach. I love oatmeal..steel cut..butter, salt and pepper..but have to have it with boiled egg or bacon (or both!)..but CRAVED grits the day of chemo and day after, when those horrible steroids were in me.
Im glad all of ya'll are starting to feel better! Heres to good days until the hit us again!
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Every day I look forward to getting home and turning on the computer to hear how you're all doing! It's like we're on a giant seesaw - some up, some down, then it all changes.
Rambo, I'm so glad that your new job is going well and no bone pain is a great plus.
HoneyBunny, I've had lots of positive remarks about my scarves this week too. It does make it kind of fun. I'm doing the same thing with earrings - buying the dangly ones I never wore before. The shock is when I take my scarf off and see another giant bald spot!
Mellie, I think a lot of us have been surprised at how difficult the hair loss has been. I don't think it means we're vain or self-absorbed, but it is such a low blow. Like, come on, isn't the rest of it bad enough but we have to lose our "crowning glory" too?! And some days I don't know if I can answer one more "How are you doing?" Does that sound ungrateful? I don't mean to be but I am sick of thinking about myself so much! How long until normal returns?
I am so exhausted from working so hard the last week. So much to do before the first day of school, even with friends to help. I'm getting worried that I will be going into round 2 on Monday already drained. I'm going to try to rest up this weekend. Thinking of all of you wherever you are on the chemo seesaw. -
Hello strong ladies!
I'm having a much better time on the second cycle than the first. I had 5 rough days after chemo. Tired, headache, upset stomach, Now I'm just having taste and sore mouth issues.
My doctor said I needed to exercise so I forced myself to take a walk on the 3rd day after chemo and I've been walking further each day about an hour. I really do think its helping make me stronger.
I'm thinking I might be able to go back to work in September which is great because my disability ends sept 30. I'm going to go visit my cousin who lives near the beach and enjoy a few days of the summer next week before school starts. That I am feeling well enough to do this is a huge difference from 3 weeks ago, so I really do think it was prednisone withdrawal more than chemo last cycle. -
Marsha, watch out for the sun! Chemo makes us more prone to burn quicker (at least that's what my MO told me)
Glad you are feeling better this time around.
Call for magic mouthwash if you need it.
Pat -
Hi Ladies
Day 8 -cycle 2
Neulasta jab seems to have passed fairly uneventfully -yay
Have worked about 15hrs this week and managed to get out and hit some golf balls today and did manage 18 very tired holes
Dont laugh- I ordered some CBS 'survivor' buffs and they arrived yesterday ..... Sooo comfortable ( not cheap). And got some cool comments on them today from a complete stranger today. Don't like the survivor connotation this early in the piece but bought them cos I love the show. And we can all Outwit, Outlast and Outplay this 'C' card
Also have bought a Speedo swim costume specially made for Mx with sexy zip up the front ( although DH turned and said - well that's not really the same anymore is it ???? Cheeky insensitive bogan !!
Anyone else got a bumpy, itchy scalp at nape of neck ??
And I am sure I have stubble back where I shaved my head !!!!! ??????
Stay strong ladies
NC x -
Greetings to All You Sexy, Beautiful, Wonderful, Gifts to the World!
Update from me: Had my 2nd round of chemo yesterday. 2 changes made for possible recurring side effects. Prilosec OTC for the acid reflux like some of you have received. Took some when I got home yesterday as the steroid was really causing it to flare up. It worked! I ate dinner with no acid reflux!! Yayyyy, Second change was eating ice cubes during chemo infusion for both the taxotere and the cytoxan for the mouth sore situation. I am truly hoping this works. Onc said eating the ice would cause blood vessels to constrict in mouth and chemo couldn't invade so easily to do damage. Keeping fingers crossed as that one seemed to be the worst and most painful for me. Go for my Neulasta shot at 11 a.m. I had no effects from the last one and nurse said my counts were good so that may have done the trick and my counts were excellent according to my Oncologist yesterday after my first round of chemo so hoping no side effects this time either as far as bone or hip pain.
Got another new wig and lol gotta be honest, have never been a blonde or a redhead and I'm experimenting now! I have two and one is human hair the other is synthetic. Going today to have them styled at my hair dressers. I'm still liking the headscarves, head turbans and my little ole yellow fishing hat the most. These don't make my head sweat during this heat.
It's only been a few hours since my 2nd chemo treatment but I truly have faith it won't be as my primary doctor has said and kick me to the curb this time. I just don't foresee that knowing who I am and what I can accomplish when I pray and have positive thoughts.
Hugs to all and I hope Mellie you are feeling better about losing your hair soon. Yes it's a very important part of being you but remember after chemo it will grow back and maybe better than before!
I am so very glad to see most of you are doing things, planning things, having an upside to all of this that you are going through. Just remember it won't last forever and then we truly can get on with our lives! Heal On ladies, Heal On!! xoxoxoxo
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Hi everyone - I was feeling like I needed to stop thinking about chemo so much for a few days. I just get overwhelmed with it all. Didn't really work though. When you're living with it constantly its hard to get away from. You were all on my mind anyway so I thought I may as well try to read up.
I had my 3 round of AC yesterday. Went well. Just felt a little light headed and groggy by the time I left. Doc said my WBC are good, but reds are a little low so expect to feel more fatigue. 😒 At least she didnt have to reduce the dose. I want to kick these buggers as hard as we can! Didn't sleep much at all last night. Ativan just doesn't cut it the first night after chemo.
HVV - my mo gave me a prescription for Protorix 40mg for reflux yesterday. I was only taking Pepcid when I felt I needed it because it wasn't bad all the time. My mo said I should be taking something everyday to prevent it. Since I already have the pepcid I may try taking it everyday before I fill the script. Good luck.
Angela - my mo said to wait on the eye appointment because the vision problems usually go away after chemo. She said not to spend alot on new glasses, just use cheap readers. Problem is the bluriness is not just during reading. Your eye dr may have some ideas to help tho. I'll be curios to know.
Was able to go to the beach with my docs approval last weekend. Stayed under an umbrella AND had on 50 sunscreen for the sun glare and for when we were walking around. My skin was fine. Marsha do be careful, but enjoy. It was good for my mental health.
Speaking of wigs, a nurse told me a funny story from another patient. She wore her wig to the grocery store then ripped it off as soon as she got back in the car and put on a hat. She then decided to make a quick stop at the drug store so she left the wig on the seat and went in with her hat. A woman walking by saw the wig on the seat and thought it was a dog that had passed out from the heat! No windows were cracked open and she was very worried. She stayed by the car for a few minutes and was about to call the police. Fortunatley the patient came back to the car and the woman immediately realized her mistake and started to walk away. But the woman in the hat asked her if there was a problem. The embarrassed woman owned up to her mistake and they both laughed. I rip my wig off in the car all the time, so this cracked me up. Going to start putting it in a bag so no one calls the police on my unconscious dog! My biggest fear is that it will blow off at one of my sons soccer games and scurry across the field like a rat in the grass. I have visions of everyone screaming over the huge rat AND my bald head. Guess a hat's a better idea for soccer. So nice that some of you feel pretty in your scarves. I'm not there yet. -
Lark thanks for the story I laughed so hard.
Nocompromises love the idea of being compared to survivor....Out wit, Out last, and Out play the "c" word!
Realitycheck love your faith!
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Hi All,this round 3 has hit me hard,the worst headache and nausia ever,i don't know how any of you can get up and go to work,i feel like i've been hit by a truck.I'm only 48 but feel 80 these last couple of days. Taking steroids,zophran,prilosec,claritin,ativan,aleve(if i can keep food down)I've never had so many pills to take in my life,i can't even imagine how bad i'd be without them though.I know how u feel Mellie ,feeling pretty sorry for myself today.
Angela
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Angel-I am day 3 of Round 3 and feels like round 3 of a boxing match ! Thank goodness I don't have the nausea(thanks to the drugs), but the analagy of "getting hit by a truck" pretty much sums it up.
Mellie-I think we all have days we want to quit, but we have committed to kicking Cancer in the ass. Just keep looking toward that finishline. I keep a journal, and mark each day off on the calendar. I don't care for winters here in the midwest, but can't wait for the snow to fly.
Lark-loved the story.......especially since I run an animal control agency and we may get a call like that. Will have to warn my officers, as it may be my car next. lol.
While waiting for my neulasta shot in the waiting room yesterday, I spoke with a woman who was coming in for her consultation of her breast cancer that had returned after 3 years. Long story short, she chose NOT to receive chemo the first time. Her diagnosis was alot like mine, so made me feel better about my decision. There are many of us who use every excuse we can not to receive treatment(I know I did at first-maybe it was denial), but even now as I lay here feeling lowsy, I know it was the right thing to do. There are many of us that don't get a treatment plan because the cancer has advanced. I guess my point is to be grateful we have a chance at a full long life, we just have to get through the bad times. Keep the Faith ladies......we can and will do this........
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Thanks Hannariggs,this suffering does have an end and I'm glad my family insisted on me getting chemo because the thought of this coming back,well all I can say is God bless that poor woman and everyother woman thats had it return,i can't even imagine. I'm lucky to have excellent health insurance,wonderful doctors,and a very supportive family,those are blessings alot of women don't have. Thank God for all of you on breastbook,I also count you all as blessings.Angela
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Hannariggs, thanks for sharing that story about the woman who didn't do chemo. I was feeling so upset this past weekend about chemo and was thinking well maybe I just won't do it. In the back of my mind I know that wouldn't be the right decision. My doc did the adjuvant online tool to show my rate of non-recurrence; without chemo its 55% and with chemo 77%. At first I was like that's not a major difference, but I'm going to do what I can to prevent this cancer from coming back.
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Absolutely ladies.......if this disease does rear its ugly head in the future(God Forbid), we cant at least say we did everything humanly possible to rid ourselves of it. Hard as it is, and yes, I want to quit, each and every day.......we have to keep going. I am so glad to have others to share thoughts and feelings with. God Bless all of you.......
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Hannariggs, stories like the one about that poor lady's recurrence do make us feel like maybe we did make the right decision. The chemo is hopefully like the final Spring clean before, for some of us, the new paint job of reconstruction.
It is strange, Jerigrace, Soriya123 and Mellie289, how this hair thing hits us. I was actually excited about wearing my wigs (I have two) and trying out different colors on myself. I'm getting a lot of grey, which was making the texture like straw, so it seemed like it wouldn't be a great loss to me. But when that day hits, you're right, it's like the final blow ... okay, you feel like crap and now you're going to LOOK like crap and everyone will know! I had DH give me a buzz cut this morning and wore my wig to the ps office. She walked in and seemed genuinely in awe of it, wishing her hair looked like that. I said, "Me too!" I think the thing's giving me a headache now, though.
Honeybunny9, my hair's still about an inch long, so don't know about the blackheads yet, but there are definitely zits up there I'm going to have to be careful about. Still fighting the nasty raised, red, infected acne bumps on my face from round 1. The topical antibiotic gel my mo gave me doesn't seem to do much.
Momx2, I hope you can feel your mom with you, giving you strength, because I'm sure she's there. I hope, too, that you can find a way in this difficult time to be open to the healing love and light everyone is sending to you.
RealityCheck, ugh, bronchitis is the worst! Hope you're well over that now. Peeing in your pants I can also relate to ... but that's another story!!
Ckmoss, it does sound like a lot of us are getting the stomach upset problems in various ways. Maybe I should keep some crackers by my bed, too.
Marsha1970, I do agree that exercise helps. I'm trying to get back into my Pilates routine. I have been walking, but getting bored with the same old route around my neighborhood. Walking anywhere else means getting in the car, which is too much hassle.
Nocompromises2013, what are survivor buffs?
Loved your funny story about the wig, Lark
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So, my daughter starts this new homeschool on Monday. We've been doing orientation the last couple of days and I've been so glad to feel my old self for it. Part of it is on campus, which will be good, but I'm still concerned about how much I'll be able to help her on chemo "down" days. I have to know the software, too, and I have a low frustration tolerance for computers
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My ps has put me on antibiotics for some redness on my right "breast" (if you can call it that). She doesn't think it's infected but wants to err on the side of caution considering I'm on chemo. My second round is next Thursday. It seems as soon as you start feeling better, the next one is due!
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