MIDDLE-AGED WOMEN 40-60ish

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  • justamy
    justamy Member Posts: 532
    edited August 2014

    Talked to hubby last in night. He worried that the insurance won't pay unless the doc says I need it. He wants me healthy over everything else but he trusts the doctor. I think by the time we get to surgery in 6 months it will all be OK. I do not want to do this twice.

  • barsco1963
    barsco1963 Member Posts: 2,119
    edited August 2014

    I sure wish I had known about this site prior to my mx. I was so naïve and "obedient" doing just whatever I was told needed to be done. MX - could choose to do recon at anytime. I had no idea that there was time to stop and think about it all and to gather some info as to what options were out there.

    You gals are a wealth of information and experience - thank you so much for being here and sharing your thoughts, experiences and knowledge.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    kathe, the loss of sensation we talk about in a breast is not from a lumpectomy (I had four before my double mast), but the lack of sensation when you have your breast removed. All those wonderful sensations are gone, even though skin is still there. I actually asked my surgeon where those wonderful nerves from the nipple snapped to when they were cut. He told me to have fun looking for them...hehehehehe!

    As for nodes - thank GOD! that surgeons aren't taking as many as they used to!!! That was the harder surgery part to recover from and has blessed me (not!) with truncal LE (mild). I HATE hearing that someone had 2 out of 4 nodes positive so the surgeon went back in and took more...WHY?????????? The nodes did what they were supposed to do!! They weren't ALL positive, so why take more?? You were going to get chemo probably anyway, so what was the point??????? I really DO think they are streamlining and customizing the process to the individual, but the individual does have to gain knowledge, too. THIS is the kind of information we all need from actual PATIENTS, not someone sitting in an office somewhere typing up a website!!!

    I had a general surgeon for my masts (no recon) and my scar line is BETTER than others who had breast surgeons!!! I showed it to some bco ladies here and they were envious of my clean, flat line. They had bulges and dog ears and folds and basically a crappy line. I had told my surgeon I had NO intention of recon and he respected that. I think a breast surgeon leaves excess skin because they want to SAVE and/or rebuild a breast. It's in their nature....

    Back to my "good" breast (right one). Well, I bled all over the mammo machine from my LEFT nipple. Then they wanted me to get an MRI on my RIGHT side due to "architectural changes" (calcifications) and I was upset they were ignoring my left side - MRI did both sides thank goodness!! Then they wanted an ultrasound-guided biopsy on my RIGHT side!! The tech took me to the department and kept insisting it was the right side and I kept saying LEFT!!!! Well, she left me there and then came back 15 minutes later while I was still waiting and KNELT down in front of me and took my hands, said I was right, it was the LEFT side and GOOD LUCK.

    Gee...thanks for the warm fuzzies, sweetheart!! 

  • elimar86861
    elimar86861 Member Posts: 7,416
    edited August 2014

    Barbe, I can really see now why you went BMX.  If you went UNI, they probably would have lopped off the wrong one!!!  You missed a good opportunity to give her a kick while she was kneeling right there, too.  

  • shycat
    shycat Member Posts: 76
    edited August 2014

    I was spared the lymph node dissection because I argued that since I was Stage IIIc and those other nodes could not be removed, relying solely on chemo and radiation should be good enough for my poor blameless armpit if it was good enough for my collarbone node, etc.  I was so bummed when I left the surgeon's office where she had insisted it was standard protocol, but she had actually listened to me and consulted with her partner, my MO and RO, and the other doctors on the tumor board.  They all agreed that if my post-chemo PETscan was good, I didn't have to be subjected to "standard protocol".  My MO was happy to have an excuse to order a post-chemo PETscan, and said that the trend was towards not removing so many (or any) lymph nodes.  That second PETscan was absolutely clear and I consequently had a quick recovery from a bilateral mastectomy without ALND.  There's still a risk of lymphedema due to having radiation on that side but it must be a much lower risk than having both surgery AND radiation to the same area. 

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    Good for you for sticking up for yourself, shycat, that is EXACTLY what I was talking about that we have to be our own advocates. You done good! 

  • 3rdtimenow
    3rdtimenow Member Posts: 256
    edited August 2014

    Barbie is absolutely right, we have to ask lots of questions, do our homework and speak up for what we want, good doctors will respect that. When I had lumpectomy 3 year ago there was a second questionable spot near the first and they wanted to do a second biopsy, my husband spoke up and said if you are going in anyway why put her through another biopsy? Doctor said you are absolutely correct.

  • Tomboy
    Tomboy Member Posts: 3,945
    edited August 2014

    man, that was alot of stuff going on in there, 3rd. the lumpectomy after mastectomy is what really sucks, you would think that havin em off would just take care of the whole business, right? thats why a ladie and i that met on another thread discussed multiple lumpectomies. she has a good reason, though, she has rheumatoid arthritis, and it would be a very dangerous thing for her to have such a surgery. and she also had necrotising fascitis, and i guess that can happen to you easily when you have that, and also from the medicine they give you for that. she had told me also that her oncologist told her that anyone that has chemo has a greater possibility of NF, because of compromised immune systems.

    i knew that about mastectomies, Barbe. its just that the BS i had told me that since my tumor was close to the nipple, there was a great possibility that i would lose nipple sensation. the thing is, i dont know what i was thinking,when i chose a lumpy. they WERE a good feature of mine, even at 52, and my man was crazy about them. they were his favorite thing.and i didn't realize that there would be so much scar tissue, and also the huge hematoma i had after surgery, has turned into fat necrosis. funny thing tho, after taking tamox and an AI for over a year, i can really see on the mammos that my breast are less dense than they were two years ago, when they were all white inside,now they are not so much. the tissue "rearangement" that they did on me feels like a slightly flattened slightly bigger golf ball is in there. And like you too, barbe, there is an area with no feeling on my skin towards the axilla, and the node dissection has left me with both numb areas, and painful areas. pretty much it all sucks, having it anywhere, and having the treatments. Cancer of any kind is just....so wrong. the best thing about all of it, is i met all of you here. it seriously makes me happy to talk here with everyone, i would hate to be alone with it. thank god again for the internet, and for all of you.

  • 3rdtimenow
    3rdtimenow Member Posts: 256
    edited August 2014

    You're right Kathec, it all sucks, but grateful to have people who understand what we are going through. Hope you all have a restful and peaceful weekend. Stephanie

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    I went to a mall with my DH yesterday and kind of choked as we passed Victoria's Secret with all the beautiful new lingerie and bras/panties now..... He was (is?) very much a boob-man and I know he feels this as much as I do. I used to be able to just flash him some cleavage and that was enough.....

  • elimar86861
    elimar86861 Member Posts: 7,416
    edited August 2014

    I come to this page via the "dashboard" and usually I don't scroll down to the bottom of the dashboard but today, when I scrolled down, I had one user blocked and one topic blocked.  I didn't block them, so that was weird.  Could be I inadvertantly clicked something wrong.  But twice???  Check and see if any of you have things mysteriously blocked.

    Maybe I have multiple personality disorder and one of my other selves did this?

  • Calico59
    Calico59 Member Posts: 8
    edited August 2014

    ShyCat, I declined to have any chemo, rads, or allow them to touch my lymph nodes AT ALL.  Man, did I get a lot of flack for that!  I have been blessed to have clean margins from just DMX. Awaiting swap of TE for squishys - next month can't come soon enough. After explaining myself to Hubby & attempting to explain myself to one dr, I simply declined to explain myself any further. My treatment is my decision. Lots of stress induced by the "counseling" of well-meaning drs did not help my state of mind, but I am past that for now. Once I have the squishys installed, I'll be declining any more surgeries. Doesn't make sense to me to have nipples if I can't feel them anyway. These things are just so I don't look like a total freak with clothes on. Maybe I'll get flowers tattooed over the scars some time next year, and then what I look like with clothes off will at least be interesting. LOL

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    Calico, gotta admit I was loving your post until you said you would look like a "total freak" with clothes on (and a flat chest from DMX) and a double mast. I have had a double mast and go flat. Dead flat. No recon, no foobs. I have "won" so far over cancer and am NOT ashamed of my victory! I don't NEED fake breasts to feel normal. I am so sad that you do......forget the tattoos over your fake breasts, who cares?

    I am a large woman, many on bco have met me and I do carry my 210 pounds well, even though I am only 5'4.5". My belly is larger than my chest, yes. But it's the way I stand and project myself that counts. Because I am not ashamed of my cancer, or embarrassed, or guilty or whatever it is, I stand with pride that so far, and God willing, many more years, I have won. I didn't get chemo or rads and am not on an AI, either, but you'd better believe I didn't NEED recon surgery!!

    Devil

    Edited to add the word "recon" to the last sentence. I DID need surgery to get rid of the cancer. But I certainly didn't NEED recon. No one does. They desire it. They want it. They bitch and moan till they get it. Someone coerces them into it. Their DH's demand it. They have no self-confidence. They feel useless without tits. I have NO friggin' idea why many women get recon but after almost 6 years on this forum I've heard all the reasons, but not the truth.

  • glennie19
    glennie19 Member Posts: 6,398
    edited August 2014


    I had a uni MX, no recon, and I don't feel like a freak. I just have a scar on half my chest. Big whoop.  Recon is up to the individual. With all the potential complications, there is no way I wanted it.

  • Tomboy
    Tomboy Member Posts: 3,945
    edited August 2014

    barbe, every one is just different, the heart wants what it wants. if it comes back on me, i would want another lumpy, cause to me, there is more "room" if it comes back again after that, i would not want it on my chest wall. they can get out the melon baller, especially since i went thru all of the trouble of rads. if i had to have em both off, i dont want recon, cause i dont want my muscles messed with. at all. and both just for the sake of symmetry.

  • Momine
    Momine Member Posts: 7,859
    edited August 2014

    Calico, what stage were you DXed with? 

  • Momine
    Momine Member Posts: 7,859
    edited August 2014

    Barbe, I am not sure what "truth" you are looking for. How people feel about the tit-less thing varies a great deal, and I do not think someone is somehow "better" or more enlightened for going flat.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    My point was just that. To prove a point!! So my post was to show that it goes both ways. And just as much as some people think being totally flat is looking like a "freak", some of us think the Frankenstein-stitched breasts with cadaver skin (Alloderm) and all those scars look "freakish" to us.

    I do know that if I only had one breast removed I would wear a foob for my OWN comfort level, not anyone elses. But when I told a woman at work I wasn't going to wear foobs she was shocked and I said "Why should I wear fake breasts to make YOU feel better?"

  • HomeMom
    HomeMom Member Posts: 1,198
    edited August 2014

    To each his/her own I always say. No one should be made to feel like they are making the wrong choice, it shouldn't even be a debate. We do what will make our recovery from this easiest for us individually.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    We know "to each their own"...the point was that someone called being flat "freakish" and there are a TON of people who read but don't post and I stick up for them. I get a LOT of PMs thanking me for saying what they are too afraid to say. We have to be careful what we post as it could affect someones' entire decision!!!!

  • Momine
    Momine Member Posts: 7,859
    edited August 2014

    Barbe, fair enough, but I am still confused about the "truth" thing.

  • HomeMom
    HomeMom Member Posts: 1,198
    edited August 2014

     Her statement was a little insensitive to those who choose no recon, but it was just one sentence, but apparently it offended you which I understand.  Let me ask this though, why do you think  that if you want recon you have no self confidence? I have a ton of confidence and I don't think I would look like a "freak" if I didn't get the recon, it's just what I want. I don't have to convince anyone of anything, especially if they think I'm not telling the truth when it comes to this personal choice.  No one has forced me to make this decision or to make me feel like I have to in any way, and I certainly didn't "bitch and moan" till I got it.  So you're right, we have to be careful what we post because there are people out there in the decision mode and they shouldn't be made to feel they are making the wrong decision for themselves when their inner voice tells them otherwise. In defending your choice and others who chose no recon you also put down those who did.  JMHO

  • staynsane
    staynsane Member Posts: 213
    edited August 2014

    Barbe, I feel compelled to address one of your posts.  First I'd like to say that I generally love your candor and that you don't mince words.  But your statement "I don't NEED fake breasts to feel normal.  I am so sad that you do.  Forget the tattoos over your fake breasts, who cares?" left me stunned.  You know our decisions are all individual.  You are a strong, confident woman and I'm glad that you are happy with your decision not to do recon.  But my choice was to do recon to try to get back to the look of the pre-surgery me because I like myself and wanted to put the cancer experience behind me and look as normal as possible TO MYSELF first, and others, because self image is important to me.  And the suggestion to forget the tattoos...!  I understand you said what you did because that is how YOU feel, but to tell someone you are sad about their desire to do recon was a misstep, in my mind.

  • glennie19
    glennie19 Member Posts: 6,398
    edited August 2014


    I've seen some amazing nipple tattoos, 3D and very realistic. 

    It's an individual decision. Every woman has to do what feels right for her. And it's a hard decision to make when you are suddenly told you have CANCER, and now you have to make decisions about treatment and recon, etc.

    My surgeon and the PS I later consulted thought I was nuts that I wanted to stay flat and just tattoo over my scar. (a lovely vine of purple morning glories,, had it all picked out)  Around here, recon is HUGE and most women choose to do it, especially at "my young age" (so I was told,, I'm 55, btw)  I personally just knew that I wanted the least amount of surgery and treatments possible. That's why I chose the MX instead of LX and rads.  But that was my choice.

    Never got tattoo,, ended up with LE and now I can't get one. So I'm sad about that part.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    The tattoo comment was because the OP (original poster - you guys remember the "rules" where you aren't allowed to mention another member's name...right?) said she would get a flower tattoo rather than nipples.

    My comments were MEANT to rustle up some feathers!!! Again, that was the point. I know I hurt some of you that have followed me in my 20,000 posts over almost 6 years, and I am sorry, but felt compelled to show it from another very important side. Those of us who do NOT need recon because we DO "like ourselves"! In fact, I love myself so much I just couldn't put my body through the 8-14 hours of micro-surgery and then years of tweaks and adjustments! I love you all and am sorry I have stunned some, but I got a knee-jerk reaction to that post (obviously) and I don't edit or change my posts when they have been responded to or others can't see what the following posts are referring to. May this be a lesson to all.

    As for the truth comment, I hear a lot of "my DH made me", "counsellor told me I had to so I could get closure", "my friend said I'd always be reminded if I didn't" and on and on and on. It heartens me to hear "I did it because I WANTED TO". Full stop. We don't need to hear "wanted to so I wouldn't feel like a freak". That makes those of us who didn't get recon think that those who did see us as freaks? And, to say you got recon because you like yourself, well, that is very admirable, but see my comment above. At least that was an honest comment. 

    This is ALWAYS a hot topic among the recons and the nots. I was invited to a Facebook page by a member here called "Flat and Fabulous" (the FB page, not the member :)) and all they talked about was how to "hide" their flatness and what are the best foobs!! I'm sorry, I am truly FLAT and fabulous!!!

    I know I am very lucky I have adjusted so well and truly didn't know it would go like this. I thought I might break-down over the passing years, but further surgery for removing my thyroid after 2 biopsies, 4 more biopsies through-out my torso and a pace-maker inserted, I am truly glad I didn't chose an optional recon.

    Love you all, and thanks for the PMs...they validate me.

  • elimar86861
    elimar86861 Member Posts: 7,416
    edited August 2014

    Good Morning, Ladies!   

    When it comes to my two cents, I usually cough up a nickel...where can you find such value?

    Welcome, Calico59!  Your phrasing "total freak" certainly ignited some discussion.  When read by ladies who have chosen no recon, it could sound like anyone going flat looks freakish.  Being new here, I doubt you gave that consideration and I took your statement to mean that clothing would fit differently without boobs/foobs filling up the space clearly tailored for them.  Certainly true.  Some flat sisters have to experiment with new styles to find what they consider to be a nice fit for their new shape.  If you choose recon to retain your former figure, that's another way around it.

    Barbe, it is well known that you are militantly no-recon.  That's cool, and that view definitely needs representation on BCO.  To me, it represents a break from the breast = beauty mindset that has been perpetrated upon us culturally.  (In full disclosure, I may have come to that opinion as a result of being a late-bloomer and having been emotionally scarred by the taunting of middle school boys.)  However, we all possess a body identity.  When our bodies get changed, I think some just have a stronger desire to "put things back the way they were."  This is where individual choice prevails.  I don't think there is a strict correlation to how secure a woman feels about herself either way.  Or, shall I say that insecurity can come in flat OR double D models.  You, Barbe, are very open about your BC.  You have used your flatness as a springboard to educate the people you encounter.  Totally support that endeavor!

    Thinking about this more broadly, going flat is outing your BC to the world.  It is like chemo bald, but more permanent.  Now we all know that some people are just uncomfortable making their BC know to society at large.  I have never seen a comment chiding anyone for wearing a wig.  (I know that is a poor analogy because wig wearing involved no surgical procedure.)  My point is that not everyone wants to be identified (by strangers, even) as "the woman who has/had BC" for the rest of her life.  We are all in the same club, some just carry the "membership card" in a more discreet way.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    I get your point elimar, but I don't WANT to be identified by the woman with breast cancer! It's just not that obvious if you don't try to hide it! I wear flat T-shirts all the time as well as stretchy tops that cling to my chest. I worked with someone for six months before mentioning it and her jaw literally hit her desk!! She was absolutely stunned!!! (This is only one person of many who have been surprised - most people say "Oh, but you are such a happy person, I had no idea!" - like breasts make us happy....sigh.) Anyway, this one gal was shaken and began to apologize saying she had not noticed and hoped she hadn't said anything in the past 6 months that might have offended me....uh, no. We think people are looking us over and checking us out, but really, they are worried MORE about their own image and being checked out!! I'm sure a couple of guys have figured I'm just flat and sucks to be me, but that doesn't matter to me. On another occasion I had an old acquaintance say "OMG you lost a TON of weight!!!!!" I had to laugh as my breasts were "only" six pounds (think of 3 pounds of chicken wings on each side to get perspective) and I told her that I had just lost my shelf of breasts that entered the room before I did!

    My arthritis is better, my posture is better, I actually probably have a better self-image without my huge breasts. I was at least a 38D since grade 8, so it's been a long haul with a big chest (even had a reduction at 45 before my diagnosis at 50). I often find it's smaller breasted women that are happy to get "new bigger breasts" with recon and I feel sorry for them as they age. They have NO idea how damaging that load is to their skeletal system!!! My neck arthritis was so bad I had bone spurs poking into the back of my throat and choking me when I tried to swallow bigger pieces. I've heard of many, many ladies that have chosen to de-construct as well....be careful what you wish for.

  • 3rdtimenow
    3rdtimenow Member Posts: 256
    edited August 2014

    Barbie, I can totally see how the freakish remark would upset you, because your choice was not to reconstruct, was right for you and a comment like that from a fellow BC patient was harsh. I imagine you reacted from a place of self defense, but your comments about those of us who choose to reconstruct were hurtful as well. I choose to think you meant no harm. Now let's move on and help each other. Have a nice day.

  • barbe1958
    barbe1958 Member Posts: 19,757
    edited August 2014

    The point of my post WAS to show how HURTFUL comments like that are!!!! For the third time, now the fourth, I repeat, it was INTENTIONAL.

    I have never posted a post like that, but didn't want to hear the usual "oh, we all do what is right for us" and let a comment like that pass without those of you who GOT recon feel what it is like to read a hurtful post about your decision!!!

    Is everyone on the same page NOW?????

  • marlegal
    marlegal Member Posts: 2,264
    edited August 2014

    wow, page 944...how bout that? Man did I pick a hell of a time to come in and read back a few pages :)

    Support and celebrate. Unless you're on a retreat, you've seen the ALS ice bucket challenge the last few weeks. My sister in law died from ALS in 1991 and her daughter, my niece Karen, is living with ALS right now. Our family have all posted our videos on FB. Barbe (no i before the e!) is probably tired of seeing them...I have a big family!

    My point? All those videos are to celebrate our loved ones affected by a killer disease, and to support all efforts to find a cure. Luckily, BC is often NOT a killer, and thank God we have this forum to support each other whether we agree or not, and to celebrate our differences and individuality.

    Hugs sisters :)

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