Starting Chemo, November 2013 Group
Comments
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hi.....while im reading....where is everyones port located? mine is an inch below my clavical bone under my bra strap. some of yall say your arm. i would think that would be worse. my PICC was 9mo in my arm....hated that. ended up getting pigtail pulled twice and needed new one. of course PICC and port are different. my port doesnt even hurt anymore.placed day one of chemo. I have access line all the time for meds and fluids.change weekly. just curious. ellen glad youre home! what a pain....at least ur port staid! gayle in my prayers.
imma reading! took my PROVIGIL....A MIRACLE energy pill avail by rx!!!!!!!! starting to kick in! now i can do some reading!!!!!
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ii still think its funny that yall are in energy up mode when im down! mqakes me feel like a chatterbox in catchup mode. i finally figured it is cause our cycales are diff. too baad we cant be all the same!!! it gets lonely on the off week! but i do understand! i tried....and got half thru a master list....maybe i can finish it so we all have a reference!!!! please e/cuse the miniposts till i get to reg computer and can pop back and forth while reading. forgive if they are old topics but yall really can talk during my zombie days!!!
again i say FLUIDS AND SLOW infusion makes All the difference. the third was sooooooooo much better....of course none would b better but slowing down amd getting IV fluids and toradol....big diff!!!!
back to yall! reading away!
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Hello Everyone!
I'm sitting here counting all the blessings that I have been able to behold over the past year! Yes...this has been another difficult year of facing another physical hurdle but all it all...it could be MUCH WORSE! It is because I AM STILL HERE! If it would have been our time...we would not even be given the opportunity to overcome this present challenge!
At times it feels as if we are the ONLY person on the face of the earth that is enduring whatever difficulty that we are facing. BC sucks....but there are so many other things which at times have no treatment or support. I am so thankful we have the ability in this day to connect through the internet and see how far from reality our thought processes can take us! All it takes is a few swipes on the computer and somehow...miraculously we are connected with people all around the world! This is such a marvoulous development to give us all hope and strength!
EVERY ONE in the world goes through various trials and tribulations of life. There is NO ONE unscathed. Sometimes we look at what we THINK is going on in side anothers house and assume they have achieved perfection. This is so far from the truth. Some people have developed a shell where they are afraid to reveal themselves. I am thankful that we can be honest with each other...the GOOD, the BAD and the downright UGLY stuff. Some of the things we share we cannot even speak to those closest to us.
We must remember just because we don't reveal our true selves to others does not make us lacking. If anything we are more true to who we are! What we learn during this journey will help us achieve even greater heights during future difficulties! Do not hold on to the lie that somehow we must have faltered and done something wrong to bring this hardship upon ourselves. This is so far from the reality of life! Life gives us times and situations to bring change and strengthen us THROUGH the difficulties! Then in return we can help bring a light of hope to others!
Each of us has our own trial and difficulties. We can follow a certain chain of events yet sometimes we find ourselves trapped inside our minds with as I shared the "what if's, shoulda, coulda, woulda, what ifs and whys." If we allow this mindset to overpower us...it only brings depression, dejection, degradation and death!
During this holiday time....more than ever we MUST try to keep our mind focused upon the positives of life! We are ALIVE! We are alive during a time when they can treat and heal us of this nasty disease process! Even ten years ago...they DID NOT have the ability to treat the condition AND additionally treat the side effects as they do today! When my grandmother died of BC....she had less than I did! The treatment was horrid and still perished. Now...with proper treatment we all can look forward to many more years with our friends and families!!!
Remember that our minds can be our WORST enemy! Don't allow the negative thoughts to overpower any moment of the miracle of your life! For those with families...they desire to have you around for a LONG TIME! Our friends really mean the best for us and DO NOT JUDGE us for being "naked headed"!
I can honestly saw...I have found a whole new person under the "chrome dome"!!! I am amazed at who I see beyond my hair! There is such a freedom in being able to jump in the shower, washing and yes sometimes shaving my scragglies off! Then when I get out it is a BREEZE to get ready to go! I put my makeup bag in the car and GOOOOO!!!!! I have found I can do some pretty FUN things with my makeup and WHO REALLY CARES!!!!!
I'm gonna put some temp tattoos on my head and have even more fun! I LOVE all the GLITTERY and SHINEY lotions, creams and sprays we have available this time of year at BATH and BODY WORKS! They even have them on clearance now! I have gained a confidence I have never had before! I was the one who grew up soooooooooooo shy that I could not even ask for catsup or the bathroom without running for the corner!
Look in the mirror and see the BEAUTIFUL PERSON who is INSIDE YOU! KNOW that you have a future and the person you are TODAY is only a glimmer of the SHINNING person that can come out in a short time to come! You are a BUTTERFLY!!!!! This is only a cocoon!!! In the past many of our Dx would have been a death sentence. Now...we can look forward to a full and productive life! ALL BREAKING OUT INTO THE MOST MAGNIFICENT COLORS of a NEW BUTTERFLY!
Many of us have children where we spent at a minimum 9 months going through all manner of difficulties preparing to birth them. Then came they years and years of raising these WONDERFUL creatures! For some there are now grandbabies and great-grandbabies who are looking forward to our future! Look in the mirror and see the BEAUTY of YOUR FUTURE!!!! It is hopeful all manner of glitter and grace!
These SE are ONLY for a short time and just like enduring the SE of pregnancies and other difficulties of life...are only for a season! When we break through in the spring we will sprout like beautiful flowers with all kinds of wisdom to share with others as we overcome all the present difficulties!
It seems the snow and rains of this winter are a hallmark. Showing us that in the spring life will be so much different! Stay in the NOW! Don't focus on the negative and dream of the FLOWERS and BLOOMS to come!
Love
T're!!!
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I'm still reading!!! Yall have been SOOOOO busy...but I just needed to vent some heart thoughts! Happy Holidays! Despite all the rain (which I have been drizzling in FL...and Snow for my northern sisters!) I sure WISH I had a WHITE HOLIDAY! Somehow....rain....green tropical plants and falling leaves doesnt say Holidays! lol....guess that is my growing up Buffalo girl in me! Sure miss the Icicles!
Huggs and Love!
T're!
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Pray my 15 year old lap top holds out for hubby and I till we get a new one! We lost our motherboard last week on our new one....(3-4 years old) This dinosaur is HANGING in there! Otherwise I have to revert to my wackazoid phone and tablet....argggghhh!!!!!
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Great thoughts and positive thinking Paulette! I am weak and tired today, barely off couch, haven't showered even...hoping tomorrow will be better.
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Ok....here goes...reading back more!
SMRLVR...number 4...yahoo...one more down! You will be in my prayers tomorrow! Im MO said the third is one of the worst. Your counts will drop more than the prior ones so dont be too concerned. Make sure they SLOW IT DOWN! And FLUIDS...are the key!
This past one for me...number 3 was much better than number 2. The NN gave the second dose in less than 2 hours...including premeds! I was sick as a DOG for the second infusion. This third one...was GREAT! I was surprised how long it took for any SE to hit! I had my INF on Monday Dec 23rd. Expected by neulasta on the 24 to floor me. I was able to make it to our family christmas get together with NO PROBLEMS! No Headaches or pain to speak of! We did an ULTRA hydrate IV on the 23 and 24 then took the IV toradol on the 25/26/27....The only SE I had was on the 27 I began the tummy pains from the gastroperesis (unable to poop...sorry)
I'm glad I saved my last toradol till the the night of of 27th because I would have been in the ER. Tummy pain sooooo bad....because couldnt go. OUCH! I was a little puddle on the floor crying for my hubby to administer it at 2am. I couldnt move. Yesterday I was down for the count as was most of today.
Now I am up and having minimal SE except for my NAILS....they HURT! actually a combo between hurting and numbness! REALLY ODD....think Im gonna loose my nails though....
BigT....this is actually little T.....Dont get grustrated...do what you can!!!!!
Wrenn....Sorry for ur pms....
I think for the most part the weight is fluids and steroids. The steroids make you RADICALLY HUNGRY for a short time! FAMISHED! Most of those effects will go when we are off the meds!
The Hot/cold....menopause stuff....yes is also due to the autoregulation of our systems. I have had that for years from the autoimmune pbms.With me like since my 20's....so does my daughter....autoimmune...autonomic regulation....it happened for me WAY before menopause. It causes our systems to have a problem regulating temperature. Hence my VERY LOW 96 -97 norm. When I get to 99 I AM SICK! My doc said to really watch it if your normal is low....100 is too high! I have consistantly been a bit high weeek two...which I am now. Nadir starts tomorrow....boohiss!!!
She actually wants me to go in at 99 but I choose to wait and see ...if it goes 99.5 plus and stays...THEN I will go in! Last two cycles it dropped after a week....99.7 is the most I went to. And was really sick then....
Like the past two days I have been sleeping ALOT! Took my provigil today and am trying to at least catch up with yall! I did WAY too much the past few days prior!
Audra...you are right behind me....just drink....drink....and try to walk some! Helps the tummy and pains.
Yall dont know this about me but I have walked with crutches for the past 7 years....but because of the BC surg and PORT...I have had to try to walk W/O assistance. To painful. ...If I can do it YALL CANB!!! I just go....REAL SLOW!!!!!
Pat...I still love your picture! Keep it up.....up and down...up and down!!!!! That is the only way!
Big T love Mushu!!!!!!!! cutie!
I will send this in parts as I read so not to overwhelm yall! Still reading!!
T're!
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I am back after a few days of not being able to post due to a busy home life. My 8 year old autistic son keeps us both very busy during this Christmas break(?). The word break does not quite fit what we are going through right now.
I have quite a bit of catching up to do with all the posts... I think I'll work on them backwards. I enjoyed the new pics of all the pets. Keep posting them!
I got a call from my MO's office last Friday saying that my doc wants to see me this coming Tuesday (Dec. 31st) and have chemo the same day. I called the office back saying that my inscision is about 95% healed, but not heaed completely.
I got a bit nervous with her moving up my chemo date from Jan. 7th one week earlier. I don't want her to rush the chemo, especially if I'm not physically ready and possibly risking another infection like last time. The office called back that my MO will assess me first and then decide if I am ready or not. That makes sense.
My hubby who is BTW of Scottish background got slightly put off with the new chemo date. Of all possible days she had to schedue my chemo for New Years Eve! This should be time to party or at least have a glass of wine, not being knocked out with some chemical cocktail!
I keep praying that she'll make the right decision whether my body has healed enough to handle the treatment on that date. My BS thought that Jan 7th was more of a realistic date for CT.
Today I feel quite a bit of discomfort on my chest wall around my mastectomy scar. Is it the weather? Is it healing? Is it not? I feel it every time I want to take a deep breath or stretch a little. I have not been able to really exercise since my hospitalization, and perhaps the tissue there got tighter than before, so now I hurt more if I want to get moving again.
Regarding the hot flashes: I don't think I experienced the true hot flashes, when you feel like peeling your skin off, but I have been lately waking up several times a night being totally drenched in sweat. Am I fighting a cold or is this IT?
My scalp feels rather leathery like a round volleyball. I think I might start calling it Wilson just like in the movie Cast Away. Hubby has also jokingly referred to it as a skinhead and called my wig a 'dead rat'.
Lisa: I think that people may look at us with curiosity, wondering about what we are going through, but in many ways we are for them like front runners showing the way that unfortunately many will take one day themselves or like canaries who are the first one to feel the changes in our environments.
Gayle: I am happy you are out of the hospital. I have been thinking of you intensely. I am glad that you had the best possible care. Sending more healing vibes your way!
We shall overcome some day!
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Amazon -- I actually love the fact that my chemo is on Tuesday 12/31, ringing out the old year with my last chemo! I know I will be sick into the new year, and have radiation yet to go -- but getting chemo on Tuesday seems to me more like it closes a chapter and I can simply erase 2013 from the books.
I don't want to tempt the fates into proving me wrong, but it seems like 2014 just has to be better than this year.
There seems to be a lot of us getting chemo Monday or Tuesday, and several making transitions, whether from chemo to radiation, or from AC to Taxol. Wishing us all the best on those transitions.
Ellen
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Amazon....trust yourself for the final decision!
Hot flashes....ya...they are a bit diff...but not TOO much! Ive gone thru both! lol.....apparently just before dx I went from perimenopause to post meno! In flash...but still have my same old....night sweats...dripping then freezing. But not so much diff that autonomic shift.....We SHALL OVERCOME!Keep up with the lotion on the soccer ball!WILLLLSOOOONN! Lets all draw some cool pics or do temp tats an show em!
Might as well have fun with it!!!!!!
Like I said...I LOVE all the glitter sprays and lotions now! I SLATHER my head!!!
T
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Ok....here goes...reading back more!
SMRLVR...number 4...yahoo...one more down! You will be in my prayers tomorrow! Im MO said the third is one of the worst. Your counts will drop more than the prior ones so dont be too concerned. Make sure they SLOW IT DOWN! And FLUIDS...are the key!
This past one for me...number 3 was much better than number 2. The NN gave the second dose in less than 2 hours...including premeds! I was sick as a DOG for the second infusion. This third one...was GREAT! I was surprised how long it took for any SE to hit! I had my INF on Monday Dec 23rd. Expected by neulasta on the 24 to floor me. I was able to make it to our family christmas get together with NO PROBLEMS! No Headaches or pain to speak of! We did an ULTRA hydrate IV on the 23 and 24 then took the IV toradol on the 25/26/27....The only SE I had was on the 27 I began the tummy pains from the gastroperesis (unable to poop...sorry)
I'm glad I saved my last toradol till the the night of of 27th because I would have been in the ER. Tummy pain sooooo bad....because couldnt go. OUCH! I was a little puddle on the floor crying for my hubby to administer it at 2am. I couldnt move. Yesterday I was down for the count as was most of today.
Now I am up and having minimal SE except for my NAILS....they HURT! actually a combo between hurting and numbness! REALLY ODD....think Im gonna loose my nails though....
BigT....this is actually little T.....Dont get grustrated...do what you can!!!!!
Wrenn....Sorry for ur pms....
I think for the most part the weight is fluids and steroids. The steroids make you RADICALLY HUNGRY for a short time! FAMISHED! Most of those effects will go when we are off the meds!
The Hold cold....menopause stuff....yes is also due to the autoregulation of our systems. I have had that for years from the autoimmune pbms. WAY before menopause. It causes our systems to have a problem regulating temperature. Hence my VERY LOW 96 -97 norm. When I get to 99 I AM SICK! My doc said to really watch it if your normal is low....100 is too high! I have consistantly been a bit high weeek two...which I am now. Nadir starts tomorrow....boohiss!!!
She actually wants me to go in at 99 but I choose to wait and see ...if it goes 99.5 plus and stays...THEN I will go in! Last two cycles it dropped after a week....99.7 is the most I went to. And was really sick then....
Like the past two days I have been sleeping ALOT! Took my provigil today and am trying to at least catch up with yall! I did WAY too much the past few days prior!
Audra...you are right behind me....just drink....drink....and try to walk some! Helps the tummy and pains.
Yall dont know this about me but I have walked with crutches for the past 7 years....but because of the BC surg and PORT...I have had to try to walk W/O assistance. To painful. ...If I can do it YALL CANB!!! I just go....REAL SLOW!!!!!
Pat...I still love your picture! Keep it up.....up and down...up and down!!!!! That is the only way!
Big T love Mushu!!!!!!!! cutie!
I will send this in parts as I read so not to overwhelm yall! Still reading!!
T're!
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Big T....Sorry about Mushu....she is such a cutie! I have two old kitties who about gone....not sure how much longer they will be around. Pluse I have this new cat dog my son left me! I wanted one like yours!
Quirkey...how are your hand/fee today? I know how bad that can feel....with Raynauds...plus the chem pbms....that is why I think Im loosing my nails next. Bummer!!
Pheobe...I go from freezing to frying!!!! My poor hubby! I am off and on with the covers. I put a hat on for a few minutes they begin sweating!...back to freezing. Im not sure if summer would make this whole thing worse...but almost bet it would! LOVE YOUR KITTIES!!!
Stonesmomma...LOVE your kittie! My OLLLLLLDDDDDD one is the same color! She is such a grumppy now. I wish she would cuddle me now!
Jab...adorable! What kind of pup is it?
As for the bone pain and muscle pain....FLUIDS...I cannot understate it! And walk....even if your like me and can only limp a bit at a time!!
Still reading! Gotta cool off my dino computer!
Huggs!
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funny how I get to make yall laugh when u r inthe dead zone!!!! feel like im talking to myself! except I KNOW where u r! w/o a jolt from provincial I'd be still down.rounding a bit of energy just to catch up w yall......so many thoughts about family and YOU LOOK SOOOO GOOD!!! HISS.....HOPE EVERYONE IS HOME FROM HOSP.....trying to avoid like the plague if I can! nadir starts now......boo......?pbmpbmpbpbp nailnailnainainanan elseelseelselselele anyoneanyoneanyonanyonanyoanyoanyanantana
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hiss phone....anyone else nail symptoms? gotta shower.....I STINK!!!!!
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hiss phone....anyone else nail symptoms? gotta shower.....I STINK!!!!! check out bath body works glitter spray 1/2 off!!!!
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if you have not gotten your free scarfs from good wishes.....dont miss it!!! they are NICE!!!
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btw...this was from Burlington......my Cleo look! but generally I go CHROME with glitter and shine!!!! what a freedom!!!also hurry for Marie calendar......my hubby eats anything! ESPECIALLY when all he can do is Micro himself a dinner......yay for good frozen foods!!!
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paulette: I love your new avatar! You look like Cleopatra! Lol
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For the first time in many years I had a headache today that got bad enough to make me throw up. I used to get a lot of migraines, so I don't know if it was that or a delayed SE, but whatever it was it can just stay away.
Paulette, my port is about 2 inches below my clavicle, and roughly 4 inches from my armpit. Maybe the location is why we aren't having as much pain as some of our ladies. There's jut a minor prick when they access it, even the day after they had to fix the flip it wasn't painful to access.
Amazon, I would call that hot flashed. They aren't all 'rip your clothes off and run out in to the cold' bad. Sometimes they are just a very quick, hot flush that leaves as quick as it comes. Your scar probably just tightened up from inactivity. Some light exercise when you can should get you back to where you were.
Ellen, yeah on your last treatment and good wishes for 2014. However, I have learned that the fates will quickly knock us back down if we tempt them too much. Every time I think that things can't get worse, they do, so let's just sincerely HOPE that 2014 is a great year.
Smrlver, Sorry you are having that pain in your ribs. Do you wonder if we'll ever get back to a time when an ache or pain doesn't automatically make us think of the worse possible scenario?
Oh, I go to my LGFB class tomorrow. Do they actually help you put on makeup? Should I go without any is my question?
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wall...lol.....that was my theme for the day.....draggggggggging but....figured my soldiers could fight for me "Cleo 'T're" hubby on way home for a WONDERFUL frozen dinner tonite. I think I maxed my energy writing yall!! not hungry here...but should eat..i)tsitsitIififI eveneveneveeveve.....everyoneeveryoneeveryoneveryoneveryoeveryoeveryevereveeveve isisI howhowhoh...offoffofo soundsoundsounsounsousos
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crazy phone.....even if its a iiiiikkkkkkkkkkkllll!!!!!!. im gonna shower before hubby comes close! hoping my tree makes it thru new years......only lights and no decks!!!!.....I guess less to put away!!!! its actually funny! at least it blinks!!!!!
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The top picture is our beagle/daschund mix Jazz. If you can say a dog is happy, he always is,
The next one is my beagle mix TI. That's short for Temporary Insanity (his legal name) because I though I was when I got him.
The bottom is all my babies in the matching shirts I got them for Christmas. The one in he middle is my oldest and the little ones mom and the one on the right is my younger one.
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wally: I love the pics!
Here is my new look. You gotta have fun anyway you can!
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Wally -- I guess I tempt the fates because I cannot imagine what -- war? pestilence? natural disasters? -- could be worse than the 3 months I spent watching my husband die this year. I've had the love of my life, can't imagine that happening again -- so nothing that valuable can be taken from me again. There is a certain liberation in already having faced the worst.
Compared to losing my husband, a treatable breast cancer is just a blip of inconvenience, and a time limited one at that. I chuckle when folks on this board call me easy going or positive (in person I am a rabid Type A). In part, I am just too worn out to get as upset as some others are with cancer, in part it is just a matter of perspective. Breast cancer is the lesser event of this year for me.
2014 is going to be better!
Ellen
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Wally: I love the pics!
Ellen: I hope too that 2014 will be a better one! You have gone through a lot! Perhaps after treatments and with the warmer weather we will all feel much better.
This is my new look.. Got to have fun!
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Ellen-
What a nice perspective. I would feel the same if my husband had left me...I guess we need to feel blessed to have had such a great love in our lives...some never do, right? Amazing to think the breast cancer not biggest thing this year and it helped me to read that...
Paulette-
You are too funny
Wally- Let's be positive and 2014 will be better! YEA~
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"Crash day" for me to today; that third day after chemo when the steroids have run out but the chemo is kicking. My head's in a fog, and my body thinks that getting up to do the smallest thing is Too Much Like Work. So mostly I've slept. I'm so very glad that this is the 3rd of my 4 AC treatments; I'm soooo ready to be done with all this. My husband said a little while ago that it's kind of like a prison sentence, and he's right, I guess, I just didn't commit a crime, lol.
I'll be glad when we are ALL done with this!
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Ellen, as my mother was dying of BC, I said things couldn't get worse, then my hubby totaled his car, got moderately injured, then fell on his way to physical therapy and blew out his knee. Then next year I said that it had to be a better year and a hail storm tore up our house, two friends lost their mothers, and one of my nephews had a heart attack. This year I again said it HAD to get better because it couldn't be worse than the last two years. Then we had not one, but two burglaries, my husband had to have surgery to keep his eyesight, I had to have 4 ventral hernias repaired, then the Big Ugly reared it's nasty head. And one of my sisters had a mild heart attack. While none of that compares in any way to losing your husband, the pain of which I don't even want to contemplate, for me it's enough to not even think things couldn't get worse. I don't think I'll ever tempt fate by saying that kind of thing again. But here's hoping that 2014 WILL be better for all of us.
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tired of the stubble so I got my hair buzzed as close as they could get. Enjoyed a fun day out with my DD before my trip to the BGC tomorrow. Including trying on scarves at Target. I like my wig but don't seem to want to wear it. Preferring bald but needed another head covering option since its cold outside. Had a great opportunity to talk with the hairdresser and tell her that chemo isn't the horror story it was years ago. I'm so grateful to be doing this in 2013 instead of 20-30 years ago. Go luck to my chair buddies this week and all of you splendid women. May your good days be many and SE minimal!
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Hi everyone! I haven't been on for awhile enjoying the holidays with my family. I am impossibly behind on the posts but have scrolled through and enjoy the pictures.
Audra: we were on the same chemo schedule up until this last round which I had moved to the 27th because of traveling back from the holidays. My last TC is scheduled for 1/16/14 are you still finished then too?
Saw some of the posts about being more dependent on your husband and I am right there with you but with a little different perspective. I have always been very independent and self sufficient not needing support. When this hit I made a real effort to allow myself to be cared for by my family, friends and especially my husband. Part of that is a way of giving back. Nothing makes a person feel better than to have an extended hand be taken. That's how I feel so I've tried to accept as many offers as I can. With my husband it started out as a way to help him cope with this. Letting him dictate some terms and going along with his plans without arguing to help alleviate his stress by giving him some control. The letting go and accepting help and care has added a dimension to my relationships that have surprised and helped me. My husband and I are closer now and seem more balanced than before. I see it as a strengthening of our relationship and not weakness on my part. People are stronger together.
Sorry! Sometimes I get carried away.
Well, I'm planning on a pretty good run this time with a few more weapons to keep the SE at bay. Juice with water, Colace and Senecot S, less use of straws to get more fluids, my husband's electric razor which I've used a couple of items to keep the stubble down and seeing the light at the end of the tunnel.
Take care everyone!
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- 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
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- 591 Pain
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- 109 Welcome to Breastcancer.org
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