In shock
Comments
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Traii, ask the onc when the white blood counts crash. They have a graph for each chemo of when the counts crash and when they are expected to start recovering. With one of my chemos (forget which) the crash was very quick.
The taxotere threw me for a loop, I am sorry to say. Mainly because all the oncs kept saying that it would be a breeze compared to the FEC and so I wasn't really prepared. I did not have an allergic reaction to it, but I had horrible inflammation. After one of the treatments I stayed in bed for days just aching all over, like flu pain but worse. It never occurred to me to call the oncs, and when I told them about it, they sort of yelled at me for not having said anything. Apparently simple anti-inflammatories would have helped. We also extended the post-treatment steroids a bit after that.
Then after I had finished the chemo and thought I was on my way back, I got hit with more inflammation, of the muscles. The onc said it was an after-effect of the taxotere. It has since passed, but it was a real bitch. I also had some neuropathy in my fingers, but thankfully that did eventually pass too.
My best advice is to exercise as much as you can. It helps with the fatigue and improves overall well-being. Secondly, if you feel bad, call the onc. Don't try to be a hero.
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Thanks so much for your reply Momine
I will ask my onc on many things like the WBCs, anti inflammatories and the pri biotics.
I too was told that Taxotere was going to be a walk in the park for me....considering I had high dose chemo / radiation and stem cell transplant in 1996....well i'll be telling my onc that I'm still waiting for that 'walk in the park' lol.......I don't know if it's because I blocked everything out from that far back but I don't remember waking up one day feeling normal and the next like all achey....then coming good again.....its just unpredictable!!!
I must say fatigue is whats getting me, luckily there's no nausea ... i've been trying to drink more as I'm getting headaches a lot lately, more like tension ones. but even water is tasting like crap!!
My bones though now you mention it were that bad yesterday, I'd rather have gone through child birth no drugs (like I did 3 years ago) opposed to the bone pain I had encountered yesterday, mainly on my bloody bum cheekys, knees and thighs....and I have my neck thats really, really itchy!...annoying....
I'm glad all the effects have passed for you now on this bitch of a drug

Did your nail beds hurt ? mine are a little and before treatment I was told which I did, put clear hardner on them but they feel so sensitive and I don't know if it's because of this hardner but they are growing longer like they are on steroids !!!
I don't have any inflammation thank goodness, had no reaction at all....I actually felt good day 1-6 , yesterday day 7 bad bad bone pain and today happy as larry NORMAL again, actually DID go out for a walk in the park with my son to feed the ducks ! lol
Excercise, well thats not so hard, I have a almost 3 year old so he doesn't exactly let me sit on my back side long enough to chillax.....so walking or 'running' after him is generally done 'most of the time' ..... I'm not trying to be a hero in all of this...I'm a strong person but nows the time I'm letting everyone close that wants to help help me out even something small so I can just get better

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Rain finally stopped here in Ohio and I found a gal right down the road who will let us use her indoor arena. Jax, my horse, and I had a little test of wills last night with some rearing and head shaking doing his lunging. I am almost afraid to get on him! Yikes, will do lots of lunging first!! Glad to hear everyone is doing ok.
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Traii, are you icing your nails during the Taxotere infusion? Here in British Columbia, Canada, it is standard procedure. They have iced mittens which they come and change halfway through. It helps to prevent nerve damage/neuropathy to your fingers and nails. My nails held up well. They were a little sensitive, but I only lost one toenail a few months after chemo ended. I did not ice my toes - should have done that, because I still have numb toes six months later. Some people bring big bags of frozen peas, and dig their toes into that.
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Hi gorgeous BC sisters !!
Carlads how are you, how did it go today ?
Bearcub, thanks chemo still going ok 9 days later. Had a good laugh with friends at Bingo and GD for tea was a perfect end to a pleasant day. How are you ?
Traii, you poor love ! Hope things are getting better, you have been through the mill with your chemo. You are amazing.
Sure you are right about Mum being around someone is stopping me cracking up and she would do just that.
Got my wig this morning, yay, DH came with me looked at display and says fifth one from the right is just you. He was right ! Very similar to my style, short and spikey but a much nicer richer colour with blond highlights. Tried on a few more but that was the one.
Put it on when GD came for tea, as I walked in the room her ladyship pipes up with" youve got your wig on." I was gutted, how do you know says I." You don't look like my Nan she says," :-( tells me to sit down then carefully pats and tweaks at wig. "There, she says, now you do".You could have knocked me down with a feather when I looked in the mirror I did ! Who said five year olds are children ? mine is a little old lady in a childs body.She taught me more in five minutes than the lady in the wig shop did in an hour.lol
Embarassing bodies eewww, watch that one from behind a cushion. DH hates it, I find it fascinating.
Momine. You have been through it too with chemo, the one you and Traii were given sounds awful. I know it's for a good reason but doesn't stop the awful SE's. I am a bit of a baby and will contact the experts if I don't like what is happening. Touch wood not very often at the moment. Only SE so far is bit of upset tummy meaning lots of visits to toilet, makes me dread leaving the house a bit but make sure near loo if I do.
Healing vibes to all of you. Edith
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LieFie, not standard treatmen here in Australia to ice nails
......nor have I ever heard of anything before coming to these board re icing nails/toenails throughout Taxotere. I saw after my first infusion about all this so hoping its not too late , my second coming up on the 24th Nov. I'm day 9 today from first chemo.Good to hear your nails held up well
I was thinking of just icing my fingernails but you have inspired me to do the toes too..... sorry to hear about your toe nail falling off .Carlads, how did you go ?
Edi, oh Edi, sorry I did have a chuckle about your oh so clever, oh so honest 5 year old GD, its amazing how smart and honest they are at that age....Nan will always be nan.....lol but too cute . I'm sure your wig looks gorgeous. Put it this way, just because your 5 year old GD knew it was a wig, does not mean that adults out there will know...remember kids outsmart us on the best of days....!
I'm having another great day today, even went to work for 4 hours....ahh the norm...dropped the little man off at my mums and then off to work.....they were all so nice and told me not to over do it....( I don't, trust me...I do more at home than work ... lol) I only went back to work for 3 days a week 4 hours a day back in May (only to feel part of the adult world after having bubs) dx in aug and my bosses are sooooo nice they even said that on my down days when i don't want to go in after treatment they will still pay me and not take it out of my sick leave....they have been soooo nice and they don't want me to leave as I had suggested to them when first Dx.:)
Edi, don't worry, i've been visiting the loo a bit too.....hmmm not a nice place but when you gotta go you gotta go so totally understand the part about not wanting to leave the house ...lol
Enjoy your day ladies with no SE's .....I'd better start preparing dinner chicken stirfry on the menu tonight

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Traii, you are sooo right about GD, old as the hills and the best tonic for Nana. Her other Nana is a BC survivor and had a wig so she thinks they are the norm for Nana's !
Mine is a warm honey blonde with highlights and as my own hair grey and boring at the moment due to fact gave up colouring it when BC struck she sussed pretty quick !
Her Mum came to collect her and thought it was fantastic, we then laughed til we cried as GD put it on with my clip on earrings and was Nana. Even DH had a go and looked like Rod Stewart lol.
Your employer sounds wonderful, doesn't it all make such a difference ?
I work a couple of evenings a week as a waitress in our local country pub. When BC hit they were and still are amazing. My job is there when tr eatment finished and one day my lovely boss arrived with my last weeks wages, it was six times more than I expected ! Holiday pay he said. Wouldn't take no for an answer. If I needed money for anything I was just to ask.
Luckily we are retired and comfortable but how lovely and I will never forget their kindness. Night before 1st chemo told DH to bring me around to pub. Hugs and huge bouquet from them,they ring every week if I don't get in to see them. Boss did freefall from aeroplane on Saturday to raise money for BC too.
Hope ice helps with your next chemo, mine is on 20th when's yours ?
Chicken stir fry, yum, find taste buds bit funny so craving really strong flavours had cheese and piccallili for my tea. That did the trick.
Carlads, please let us know how you are, we are all thinking of you.
Momine, hope you are having a good day.
Benny, hope you are ok too.
Happy Thursday.
Edith.
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Edi, mines next ones on the 21st Nov...yours every 3 weeks as well ?
It does make such a difference having great employers...good on your boss raising money for BC.....crazy way jumping out of a plane....lols.
Oh god bless your Darling GD she sounds like quite a character ... Rod Stewart hey for a DH..lol as long as he can sing like him hey......lol
I haven't shown my DS my wig.....as he's not at the age really to know thats mummys and only mummys and I'M NOT SHARING this ... lol (just when I'm trying to teach him to share for kindy next year)!!
I'm worried we might be out shopping and he might pull on my hair (wig) and it comes off...as much as I giggle at the thought now...I have no idea how I'd react.....( I guess I just don't want to know because it better not happen !!!)
Ok I'm curious, cheese I know and love but not sure piccallili ??
Almost Friday here ladies and I'm off to bed ..... enjoy your day

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Here we go... Got my IV, waiting for my nurse. Up at 4:30 this am I am already tired!!
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Hi Everyone,
It's official. IDC I really wasn't surprised. The hardest thing was telling the kids. Two married daughters and an adorable grand-daughter who will be 3 in December. Two son's, the youngest is 15. I didn't break down until they all cried. They know I am going to be fine, it's just hard to hear the news. I think the shock for me is the fact like most of us I go every year for my Mammogram and do self exams. As soon as I felt it a month ago I went right in. Well I can't think about that now just move forward. No stage yet until surgery but he said it was about 2cm and probably grade 2 looks very contained. Surgery will be done before December 2. I have decided on a bi-lateral Mastectomy. The right side being the Prophylactic with reconstruction. I see a plastic surgeon on Wednesday. He did say I would probably have Chemo. But said I would wait until after surgery to meet with an Oncologist. I really would like to find one now and at least have a consult.
Thank you all so much for your concern! You will be hearing from me a lot! I have all of you in my prayers!
Carla
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Dakota,
I am thinking about you!! Sending prayers and hugs!
Carla
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Dakota, thinking of you ((( Hug ))). Sure you will be great, let us all know please.
Carlands, Heart goes out to you, had exactly same start of this journey not that long ago.Telling kids worst part by far. They have been amazing.
Looking at beautiful GD's ( 4 ) still makes me want to cry, but I have every intention of being around to listen to all their secrets for a long ,long time.
Like you, did all the right things but BC still happened. We are lucky we found it when we did and all my team keep telling me its the commonest form of BC and very cureable.
No reason not to believe them but it is still a shock.Now you know what you are up against just join us all on this journey and you will find it easier with the ladies on here to support you. I definitely do.
Traii, 20th for mine, yep 3 weekly. How many you having? I have four of this one then four of a different one.
Don't blame you not telling DS about wig, at that age goodness knows what he might do.Heard of a lady who's wig blew off in our local supermarket car park. She just laughed and chased after it. Don't know if I could be that brave. lol.
Piccalilli is mustard pickle, lots of bits of veggie's, cauli,onion, gherkin in spicy mustard sauce. Yummy, craved it when pregnant.Oops now THAT would be a laugh wouldn't it?
GD would be delighted ( she would look after it ) wants a baby sister/brother but ED says no way, too expensive and at 40 she doesn't think she could go through it again.I could make a fortune as the oldest Mother ever ha ha.
Hope you have a lovely Saturday.
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Traii, it is amazing how treatment protocols differ from centre to centre. I think if you start icing with the next chemo, you will be okay. It is worthwhile to try and prevent this damage, because sometimes it can be permanent afterwards. You don't want that. Start the icing about ten minutes before the Taxotere goes in, keep it going while it is running in, and keep it as cold as you can tolerate. Good luck with that!
Dakota, it's over by now, and the ice is broken. Next time will be easier, because you will know what to expect. Hope you don't get too many SE's. Lots of water/fluid to flush the chemo drugs out quickly, take something like Senekot to prevent constipation - the chemo drugs in combination with the steroids really will effect you - and take a short walk outside for fresh air now and then, and you will be okay.
Carlads, so sorry to hear this, Yes, it does impact on our families, and as you will find out they will be your biggest support through the whole ordeal. Glad your surgery date is so soon. Onc won't be able to tell you much until he has the full pathology report after the surgery; that's why your appointment is for then. Hang in there; this is so hard, but you seem to have a 'take charge' attitude which is exactly what you need to fight the beast. Hugs and prayers to you, and keep us posted.
Edithesther, your boss sounds like a darling. How wonderful of them to support you like this! You are like a ray of sunshine on this board - best wishes to you.
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Hi girls-
Ok 1 down, 7 to go. Not to bad. I have a headache, a little dizzy. i took a compazine felt a little nausea. They told me senekot and colace?? Is that right. Orrrrr will I be pooping forever??? Hope everyone has little or no S/E. !!! -
Dakota, yes, do the Senekot and Colace. You don't want to end up in the ER with a compaction which nearly happened to me. With my first chemo I did not 'go' for over a week. It was not fun, believe me, and it is better to act preventatively than trying to control the damage afterwards. Best wishes to you!
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Thanks I did!!' Have a great night. !!!
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Dakota hope you have a SE free weekend....Happy pooping!!
Carla, so sorry you have IDC. When you have surgery and pathology you will have a better idea of size and grade. They told me mine was about 2 cm. but pathology came back 1.1 cm so things can change...you will be fine, hang on, you can do this, we will be here to help you. Watch what you read on the net, some of the stuff is too old...and thank goodness you found your cancer and on Dec. 2nd it will be out of you....Take Care..
Edithester someday I am coming to the pub where you work for a beer, sounds like a cute place...take care. -
Benny, how is the infection, are the antibiotics working? Any news when your chemo starts? Hope all is well.
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Edi, I'm having 3x Taxotere and 3x CMF
Went and had my wig cut today by my cousin whom did the foils and colour in it too...its EXACTLY like my hair now, I'm loving it....so I'm all ready now for whenever my hair decides its 'time' well I shall say..."see you soon"
I don't think I could be so brave either Edi , not for the wig to fly off.....My onc told me that a poor lady he knew walked out in the wind and her ACTUAL hair started coming out and basically was bald in minutes (guess it was time for it to go) but gee not like that....so its windy here today and I'm running in and out of the car !!
Piccalilli sounds yummy...we have pickles in a spread sauce I love but not quite piccalilli. Lol, craving it hey (wink wink)
Liefie, It is so different and crazy in a way how each cancer centre has their own protocols. Mine didn't even tell me anything about icing nails...I was calling them with tips I was getting on these threads to see if it was ok I have this or do this !!!! I've decided I'm definetely doing the ice thing on finger and toe nails next chemo and thereafter....finger nail beds aren't as sore as they have been so hoping it will pass for now and icing will do the trick !
CBEAR how did your appointment go ?
Carla, sorry to hear that you have IDC.....like Bearcub mentioned, once you have surgery & pathology reports back this will help determine actual size,grade, stage, ER & HER2 stat, etc and then you can move on with the next plan of attack with you onc. Good Luck, these ladies have been nothing but a big help to me so you have definetely come to the right place. It does get easier to accept with time...its the first month that took its toll on me , the unknowing, but you have your surgery booked in soon so at least thats all organised.
Dakota, whoo hoo, 1st treatment is always the worst ...now I've had the 1st one, bring on the next 5 for me I say....bring it on so we can all kick this C in the butt !! Oh & speaking of 'butt' I can't help much with the no pooping dept , mines been quite the 'constant flow' so to speak ( ahh love the things we talk about here
lol)Well its Friday arvo here, Day 10 - feeling on top of the world and full of energy, My DS is staying over my parents house tonight and DH and I are heading into town for dinner.
Take care everyone and hope you all have a wonderful day filled with positive vibes, energy and NO SE's (or very minimal ones)
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Hi gorgeous girls.
Liefie, thanks for that, don't feel likey ray of sunshine but you all certainly make life so much brighter for me.My lovely boss sent around DVD of his fund raising tandem sky dive last night to make me laugh. It was amazing !! He was so brave and looked frozen stiff, they went up to fourteen thousand feet in tiny cold plane. Then out he came with a smile on his face. He raised a lot of money and we are so proud of him.Talking of cold the icing sounds as if it will be a good thing for Traii. The tips on here are so helpful to us all.
Dakota, Go Girl !! Yay. Well done, I had the dizzy part and turned out it was SE of anti sickness medication. Day 10 today and feel brilliant, you just rest a bit, do a bit, rest a bit. Works for me. I am like Traii, pooping like a good un, yuk. Didn't go for three days and the pain was awful. Locked myself in the loo with radio, magazine and cup of tea.I know, yuk. After one, hour finally went. Bit more info than you needed I know, but I now have a tangerine or orange each evening and seems to have sorted me out.Like Traii gone the other way now :-( Still if that's the only SE bring it on.
Bearcub, DH on compuuter doing lottery for 29 million. If we win ,will send for you all after this journey over and we will have a lovely pub meal and champagne in our local. How are you at the moment ?
Carla,I agree with the girls, BC will be cut out and gone Dec. I called mine by a name ( Mildred ) when I had my op, txt's went out to everyone " Mildred is dead !! "You will feel so much better. Think of someone you dislike and call it after them. My girls called it Mildred too, less stressful than the BC word.Then treatment to give you the best chance of a long and healthy life with your wonderful family.Try and have a good weekend.
Benny, Please let us know where you are up to. You started this thred and we all care about you.
Traii, wig sounds great. I would appreciate that link for real hair wigs if you get a minute.Wore mine for 4 hrs yesterday, almost forgot it was there. Getting hair cut really short today. Read DH what your onco said about ladies hair blowing off in the wind, the look of horror on his face was priceless ! lol. Think I might be going out with crash helmet on to the shops next week ha ha.
Know the spread you mean, like that too. Piccallili really popular here especially with cold meat for xmas buffets.
Glad nail beds bit less painful. The icing sounds really helpful.
Cbear, Hope you are ok, keep in touch.
Fabulous Friday everone.
Edi.
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Here you go Edi......
http://www.wigsbuy.com/Custom-100-Human-Hair-4397/
They are full lace wigs...so you can even see the sculp part once we have no hair which makes it look oh so much more natural......
hell yeh I'll be icing for sure.... I'm going to google the gloves that liefie was talking about that they have in their centre so that I can see if we can get them down here, if so I'll be out shopping again tomorrow.
I got a rash on my neck today..its soooo itchy I got some steroid cream that I used on my sons eczma so I called the on call nurse at my hospital and she said thats fine to use...other than that my day 10 was smooth smooth sailing

LolI could just imagine the look on your DH's face, would have looked like mine and my DH's when the onc told us....!
My brother was gardening today and parents were there helping...I decided to go but sat on the front verandah so that my hair was not out in that weather (it was really windy outside today) ...lol
hows your hair going ?? knock on wood mines got less shedding than it normally does and i have fine hair !! I'm just thinking prob this time next week will I or won't I have hair but I'm ready with my wig though

My hair is shoulder length at the moment...I'm not going any shorter....I left it like that back when I had chemo 16years ago at that length and it was fine when it came out......I just picked it off my tops when I took them off but didn't cry and now I think I'm much much more prepared for it.
Enjoy your Friday hun.....I'm off to bed after a great evening out with the DH

Take care lovely ladies
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Hi Everyone,
My morning routine is to come here and hear how everyone is doing. Makes me feel so much better you all are wonderful and inspiring. Small meltdown this morning. I do it when nobody is around. Then I pull myself together and go about my day. As I said all the kids know and my Son who is in the Coast Guard is going to come home the end of the month to be here for my Surgery. He cried and cried it broke my heart! My husband and I both reassured him I am going to be fine!
Have a great weekend everyone!
Prayers for all,
Carla
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Carlads, my heart goes out to you. Yes, us 'strong' women cry on our own - I did the same in te beginning, but after that I did not cry anymore - was too busy fighting the beast. My youngest son, 25 years old, also cried when he heard about his mom. He was overseas visiting his fiance for Christmas last year when I was diagnosed, and she told us how he cried even in his sleep. It broke my heart when I heard this. It is so hard on our families too. So glad your son will be there for your surgery; it is good to have them close at a time like this. I had two of my children home, and they spoiled me rotten. Best wishes, and big hugs to you!
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Traii, Hi thanks for wig link, may give it a go.Icing does sound good, any luck with gloves ?Hope your rash cleared up.
The look on Dh face with that story was priceless, almost as good as when he came into the hairdressers yesterday afternoon to collect me and I had almost no hair!! My beautiful stylist took it all down to a no 4 all over. Now not so much to clear up when it comes out. Wig fits better too. All prepared for next step. Look like a really funky old lady ha ha.
One of GD's birthday party today.Going to do face really carefully, lots of eye makeup, blusher etc. Nice big earrings. If don't look too scarey wig staying in box. The thought of you sitting out of the wind brought a smile to my face :-) As you say wigs at the ready, sure you will look lot more gorgeous than me but DH and I have been together 48 years and he still thinks I look like the day we met in The Cavern Club, Liverpool all those years ago. ( will have to clean his spectacles ! )
Keep strong Traii.have a fun SE free weekend.
Liefie, your post moved me to a little weep. My son lives in another city, I told him by phone and then heard nothing for about eight weeks. Really don't know how he feels but may find out one day. My two married daughters both live nearby and have been a great support, lots of spoiling. :-)
Carla, I can't wait to log on here each morning too. BC can be a lonely journey but not with these ladies it isn't. I used to wait until alone then cry like a good un. Then as liefie says thought enough and get fighting the bxxxh ! you will find that you will get to the anger part eventually. Tell DH and kids it may happen, and to just ignore your outbursts it is all part of the grieving process that your body has seemingly betrayed you.
Just try and find a bit of joy in each day, Laugh when you can, cry if you need to but just come out fighting.
Please have some joy and laughter this weekend.
Ladies, I have just heard the most heartwarming story. My friends daughter and her two friends are having their hair shaved off to raise funds to send their friend who has cancer and her four year old to Disneyworld !! They are all working Mum's with toddlers and they reckoned it would get a quick result and bring awareness of BC too.Angels without wings springs to mind.
Joy and laughter to you all.
Edi
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appointment went alright. Nothing in right breast at all and no swollen nodes in left that they could see. I just am trying my best to figue out what to do either the lumpectomy or taking them both off. Its the surgery that scares me with taking them both off and getting expanders. Plastic surgeon says i am small and not even enough tissue to move around. So its radiation and deformity or take both off. Can i get some imput on any small breasts an what happened after lumpectomy and radiation. They said its about 1.2 cm and i have heard 1.5 so not sure. Its est/pro+ and her2 neg. I never knew at 47 that i would be dealing with this. I found ou 2 days before birthday. WOW! So many questions once i leave but when they ask i cant think of any. Scared to death. I am eating a bit more but always on my mind.
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Cbear, I was also 47 at DX, and I feel for you. I did not face the choice you face, since the tumor was so large that MX was a given on the cancer breast. I chose to get rid of the other one as well, instead of having to deal with constant mammos and biopsies. I was relatively small-breasted. My surgeon asked me to delay recon for 2 years. Now that I have gotten used to being flat, I am fairly sure that I will skip the recon.
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cbear, I am only 49, so young for this too, it came as quite a shock, no risk factors other than family history (and who doesn't have some cancer in their family somewhere these days?).... I too am very small (AA at best) and when I saw the various docs at diagnosis they all agreed that based on the size of the tumor vs the size of the breast, a mastectomy was really my only option (I guess lumpectomy would just about remove the whole breast anyway). Plus radiation is required after lumpectomy but not mastectomy, and I wanted to avoid that. (The joke was on me, pathology report afterward showed it has spread to lymph nodes, even though there was no outward indication of that ahead of time and it didn't show up on PET scan, so I have to have it anyway.)
The interesting thing, to me, is that so many women on here have opted to remove both, and that was never even presented to me as an option. The docs here have the attitude to leave the healthy one alone. They even said that my chances of getting it in the other one was only minisculely elevated from someone who had never had BC in one side. (Not sure I believe that.) I didn't find this excellent support community until after my surgery. I felt like they really rushed me into the surgery. This is what you need, there are no other options, nothing to think about. I don't even remember if my surgeon asked me ahead of time whether I would be considering reconstruction sometime down the road (I would have answered no). I have no interest in having surgery to attach a fake boob, but now that I have only one, it is a little weird at times. I'd almost rather have none, if I had been given the choice.
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Jennie, the idea to remove both came from a friend who had been through it. The first surgeon I saw completely refused to do it. The next surgeon was willing to do it, but would not have suggested it, I think.
Partly it is the "do no harm" business. If the breast is assumed to be healthy, you should not traumatize the body by removing it, and that makes sense, of course. But it turned out that I had lobular cancer (more likely to recur in other breast than IDC) and the first guy had refused before he even did a biopsy (and he was planning a MX without doing a biopsy first, which is clearly a no-no, so good thing I fired him).
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cbear, first of all please get a small notebook with pen. As you think of a question through the day write it down. Next time you see someone at the end of session go through each of your worries with them and write down their answers. I have done this twice and it is such a help. They don't mind how silly you may think your questions are. I carry my notebook at all times in my bag it is my lifeline.
So sorry this is happening to you at your age, I am 64 but still can't believe it is happening to me, just as life was becoming relaxed and fun after years of family and hard work. There is no age at which it is not a horrendous DX. I do not feel or act my age, there is no history of this in my family either. BC is a bitch.
Glad to hear you are eating more, little and often is the best.
I had lumpectomy, only small dent hardly noticeable. friends who have had it are the same.Jennie is right do not rush into anything, get advice from your professionals see if there is a group at the hospital of ladies you can discuss things with, the same as you can on here.
So glad other side is ok and nodes too.All good news.
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cbear. BC hits any age now a days...I'm 34 and BC is due to radiation I had when I was 19...
I opted for Lumpectomy first as everything was happening so quickly and I have a almost 3 year old and didn't want to go through masectomy right away, was hard enough getting my head around BC then to loose a breast it was a total night mare as you ladies can imagine.
My Surgeon said, lumpectomy, axillary disection ( I had 2 nodes positive out of the 10 they took out) so I'm having a masectomy after chemo ( no radiation as I've already been radiated on) and to be honest, chemo is 'better' out of chemo and radiation !
I had my insition under the nipple area and honestly I can't tell, a little dent like Edi mentioned but no one would notice even with my DD to E size boobies.
Good luck with your decision.....I'm big boobied so I'm having reconstruction with implants and I'm going down a few sizes .... so the way I look at this, yes I'm loosing my hair, yes I'm having chemo but I'll have perkier boobies then my friends when I'm done with all this bulls%$# !! lol......
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- 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