Still Uncomfortable with Implants

Options
1111214161736

Comments

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2012

    I just heard from another member on here that Dr. Joel Aronowitz (Suzanne Somer's PS) will swap out your implants, put the new ones over the pec muscles and then do fat grafting over the top.  He will also take out implants and do just fat grafting but for women who don't have enough fat to do all the rounds necessary this is an exciting option!  I think at least half of us who have pain after exchange have it because of the pecs being stretched.  It's great to see that doctors are addressing this issue.  

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited January 2012

    Sheila - feel guilty for what?  You are just sharing what you have learned by the hard knocks of bc and trying to help prevent others from unnecessary suffering.  

    Kate - that is great news about dr. Aronowitz!   

  • sas-schatzi
    sas-schatzi Member Posts: 19,603
    edited January 2012

    Kate and dancetrancer------ The foobs are too big. But it's now 2 1/2 years after exchange----i think I have gotten to a no pain level. The foobs for my size are not what as requested. Whats odd is Kate referred to them as dddd. I don't think they are, but I haven't had anyone do measurements. Each month they are becoming more comfortable. Not normal., but the pain of the last 2 3/4 years is gone -----to a certain point. I don't have pain now just discomfort. How is that different. Well. Lots. Now b/c the damn things are so big , I' m ware they are there. Finally the pain is gone. BUT I have to wear a bra mostly. that has an under-wire. But if the under-wire is to high I get LE increase in the left breast. I have bought by chance a bra that doesn't have the problem of causing Left breast edema.  There is a thread that has allot of bra recommendations.

    My BS----like 2 weeks ago at exam------" they look the best since I've seen you"------could have riped his throat out. But had he asked me why I would have shown him the bra an explained that it kept them central versus armpits.and that the under-wire didn't go high enough to cause and increase in the LE. Whereas, I had 2 other brs bought earlier that caused LE breast problems,

    The scars are outreagrous--------I may be repeating my self----------

    I have on each side on the scar lines nodules that I have found-------he dismissed the first-------my PCP didn't ordered a pet and it was ok---------second I found on the right -------forgot to tell him-----it's on the surgical line and is the same as the other-------a surgical scar around a stitch.  The problem being his breast exam never identified either. So, what was the value of his exam--------paying the rent?-----------May be I'm a bitch......... I just hope my PCP doesn't retire

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2012

    SAS- My doctor's are always saying how good I look.  I say it's not about how they look- it's about how they feel and how the pecs feel.  I don't think they get it, though.

    If you are anywhere near a Nordstrom's I would recommend a professional bra fitting.  Their fitters are amazing!  They recommend you make an appointment because not all their fitters are trained to work with those that have had MX.  I think it's really important for us, especially with LE, to have a perfectly fitted bra.  I had never considered them before, thinking their bras would be too expensive, but actually the ones I liked that fit the best were only about $30.  My fitter was so professional but kind, too.  I felt very comfortable and their customer service was incredible.  Some insurance companies will cover the cost of the bras and they will even submit the paperwork for you for certain ones.  

  • sas-schatzi
    sas-schatzi Member Posts: 19,603
    edited January 2012

    Kate thanks re: Nordstrom. It would be a whole day trip, but might be worth it. (H))'s sheila

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    LADIES, I have been on and off this thread quite a few times. Dr. says I have little options left. I cannot stand my implant. Nothing changes. He suggested that I go back to gym and do upper body workouts to help break the scar tissue which could be surrounding my implant. I am now working with 30 lbs and am able to do so. Question:  Have those who removed implants and used their own tissue (via tram, diap,etc.) does it still feel like something is there?  I am asking a crazy question, but I don't know what to do. I always feel like I am carrying a third person even though PS put in a lighter implant. I don't want to remove the implant and use a prosthesis.

    Has anyone had this crazyiness in their head that something is always there. Maybe the fact that I am constantly flexing my muscle has something to do with it.  Please and thank you.

    Hugs,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    ronqt- If it's craziness then color me crazy, too!  I hate these things.  I had a revision last spring and the PS put in much smaller implants with extensive fat grafting over the top.  While I love (love, love) what the fat grafting has done, and at first everything felt great, now I feel like I did before my revision.  My pecs feel constantly tight and it feels like I'm wearing a bra that is 2 sizes too small.  Yet, when I don't wear a bra at all it's even worse.  Is this what you're going through?  As far as taking out the implant all together and doing tram, diep or something I'm not sure.  You might want to post the question on one of those threads and see if someone has done that.  I know someone who has taken hers out and done just fat grafting.  I should check with her and see what that feels like.  I also know someone who took them out all together and still has tightness.  Curious about your upper body workouts- have you had nodes removed?  If so, are there any precautions you need to take as far as LE is concerned?  I've been hesitant to do much upper body stuff because I have mild LE in one arm.

  • bdavis
    bdavis Member Posts: 6,201
    edited February 2012

    Ronna.. For the record, I had DIEP and feel 100% normal... As if I have my same old breasts... I can't speak for DIEP after implants and if once the pecs have been expanded then they always feel tight .. Maybe someone else will chime in on that

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    Kate and Bdavis, THANK YOU.

    Yes, Kate, I feel constantly tight and something pushing in. I had two nodes taken out and I have no problem working with free weights and or machines. Kate, when I am lying down and/or on the side I feel nothing. Dr. said it is most likely scar tissue. Exactly also, even after removal of first implant with lighter one with no bra I feel the same, just not so heavy as when I was carrying my "football".

    Kate, what is "fat grafting", b/c I am taking a whole of notes this time with me, instead of telling me how great they look. I am completely sick of the whole thing. I have tried to stay off the site, because I wanted to move on, but realized no one else can answer my questions. None of my friends have joined our club, so I can't discuss it with them.

    Thank you again, Hugs to all.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    Ronna- Fat grafting is relatively new (though some PS's have been doing it for about 10 years).  They remove the fat through liposuction and then inject it into the breast.  Some inject it directly and there's a retention rate of about 50%.  Other PS's, like mine, believe you first have to create a space for the fat to go.  Mine swapped my implants for smaller and then injected the fat into the extra space.  With that technique the retention rate is about 85%.  Even though I dropped from a 375 implant to a 225 I remained about the same size.  The great thing about the fat grafting is it looks and feels just like breast tissue.  It covered up some rippling I was having, filled in the cleavage area and the edges of the implants I could feel under the skin.  There's a thread on here called "Has anyone had micro fat grafting?" that has more information.  But even though the FG fixed a lot of aesthetic issues I think my discomfort is coming from the pecs.  I get what you mean about them telling you how good they look.  Every PS I consulted with I kept stressing to them I wasn't there because of how they looked.  I was there because of how they felt.  

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    Thank you. Now will wait until 3/7 to see PS. Hopefully he and I can make a decision on what to do next.

    Hugs,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    Ronna- Good luck with your appointment.  Hope he has some answers for you!

  • mlp730
    mlp730 Member Posts: 89
    edited February 2012

    This is exactly how I feel too....like I'm wearing a bra that is two sizes too small! The pain is unrelenting!! I am going to Philadelphia to see a PS who has been recommended by several people. Apparently, he is known for doing "repair" work and has done fat grafting for some time. I had my implants removed in July and feel worse than I did before. I now have a caved in chest (from the expanders) as well. Not only do I feel lousy but hate the way I look. It is beating me up emotionally. I am so hoping that this doctor can help! I certainly wouldn't wish this discomfort on anyone but it makes me feel like I'm truly not crazy when I read the posts of others here. Thanks for sharing! I am praying that we all find some answers and can move on with life!!

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    MLP 730, I wish you much healing and health, you have also provided me with another answer. You stated that you had your implants removed and feel worse than before. My dr. said I would not be happy with the look of no "breasts".. I thank you for answering that for me. Plus, you also said that you are still in pain. Like you say, just want to move on. Please feel better. I  really understand.

    Kate, I said I would be checking in every day, can't get away. we are the only ones who understand....

    Hugs,

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    mlp- I think it's hard when we're not the majority.  I think most women are very happy with their recon and they don't have any problems at all.  Not sure why we do but I wish doctors wouldn't look at us like we're crazy.  The pain is very real.  If there are more women out there I hope they speak up.  Maybe then doctors would realize this is a real issue and they would start to find solutions.

    Ronna- I think that is why I continue to post on different threads, too.  This is the only place where, whatever my BC issue is at the time, I can find someone who not only gets it but isn't tired of talking about it.  I sometimes feel like those in my "real" life just want me to move on already!  They don't get that having a foreign object stuck in your chest that is causing you pain and discomfort prevents you from doing so.

  • janhart
    janhart Member Posts: 331
    edited February 2012

    I have so been avoiding posting here in hopes that I would soon feel better. But guess what? Not so. I also feel the tightness I felt with the TEs. I feel pain and pressure with every movement. My exchange surgery was five weeks ago...so I will continue to hope it gets better. On top of this I don't even like the way they look, but that has become secondary to the way they feel. The advice continue to get from my husband is that I need to exercise and stretch more. I'm just so disappointed with this whole ordeal. But then again I have to remember to be thankful that the cancer was caught early and also that I did not require chemo or radiation. Thanks for listening.

    Jan

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    It's hard for me sometimes to feel grateful I'm cured when I never felt sick.  Mine was caught early, too, and I didn't have chemo or rads, either.  So it's hard to accept you even had cancer.  It was as though they took my perfectly healthy body, wrenched it open, emptied it out, shoved a TE in there and then implants and then I'm supposed to feel lucky.  I can feel it intellectually but not emotionally.  Guess I just miss the old me today and being comfortable in my own skin.

  • janhart
    janhart Member Posts: 331
    edited February 2012

    Kate33, yes, I agree, I never felt sick either. And I get angry when I think that I had DCIS, stage zero, but yet had to have a BMX. I think, WTH? So yes sometimes I feel like you. I so miss my old self, my old body and especially the feeling in the breasts that I no longer have.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    I just read a study from the University of California, back in 1996, titled "Pain after Breast Surgery".  Their research recorded the incidence of pain one year after surgery for MX, MX with recon, cosmetic augmentation and reduction.  Reduction was 22%, MX was 31%, augmentation was 38% and MX with recon averaged 49%.  For women with implants the rate was 53% and other methods averaged much less.  Here's a link if you want to read it-

    http://www.ncbi.nlm.nih.gov/pubmed/8880841 

  • mlp730
    mlp730 Member Posts: 89
    edited February 2012

    I also had DCIS stage 0 and 12 yrs ago had LCIS followed by lumpectomy and tomoxifen for 5 yrs. When I was diagnosed in 2009 with DCIS, I chose BMX because I didn't want cancer chasing me the rest of my life. I totally understand where you are coming from finding it hard to be grateful. Millions of women have this surgery and I find it hard to believe that this is the way I feel. I've said this many times before that my PS and BS act like I'm nuts and that they've never had a patient experience this yet when I look at the stats mentioned in this article Kate, I find it so hard to believe that they've never had a patient fall into these statistics!!

    This pain and discomfort is like no other - when you have a headache/migraine, you know that you'll eventually feel better. This waking up and feeling no better than the day before is so discouraging! I so hope I can get some answers next week. I see the head of plastics at Univ of Penn next Wed.

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    Kate, you said it perfectly. No one could have said it better. I never felt sick either. Also was fortunate enough to not have to undergo chemo or rads.  Could not tolerate Arimidex now on Femara.

     I went to PT this morning for some other issues, so I decided to ask about the pectorial muscles. They showed me how to stretch to make them larger. It was almsot the same thing as "climbing the walls" after mast, but you don't move the arms up. You said against corner of a wall for 15 seconds, hands on both sides flat and stretch. I will try that now.

    MLP, yes, I stopped talking about bc to my friends, they just don't get it. Good luck with drs at Univ of Penn.

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    Janhart, I tried to stop the posting to move on, but everyone listens here. Have a feel good day.

    Yeah, I miss my old body to

    Hugs,

  • 1openheart
    1openheart Member Posts: 765
    edited February 2012

    Good morning Ladies,

    Wow, you guys so get it!  I know that my sweet husband is ready to move on and have me quit talking and thinking about my breast all of the time.  I don't have the "iron bra" feeling that some of you describe.  Mine hurts where my original stereo-tactic bx was....upper outer quadrant.  It hurts whenever I move my arm or flex my pecs or even just run my hand over that area.  And the thing that really stinks is I thought we had figured it all out.  I had a revision when we did my nipple construction.  He removed the implant and did some pocket work and low and behold...it did not hurt anymore....until Super Bowl Sunday morning.  Interesting thing is that the period of time between the surgery and the onset on pain was almost the same as when I had my UMX....about 2 months.  PS says that he broke up some adheasions when he did the revision.  I have been dilagent about doing massage several times daily and have had myofascial release PT for months before and after my surgery. It is just so frustrating.

    I am like many of you. So grateful that it was found before it had become invasive and that the treatment was only surgery and tamoxifen.  But it is alot to get your head around when you are moving through your life happy and well,  you go in for your yearly mammogram, and BOOM - you are thrown into cancer land and your life changes forever.  The almost constant pain and discomfort makes it hard to move on.  It is great to have a community of women who "get it" and are there to support each other whenever support is needed, 24/7.   

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    I have to wonder if a lot of these PS's are telling us, "I've never had a patient complain about pain before", because the majority of their patients are augmentation.  In that report I posted 38% of patients who had augmentation reported pain.  I wonder how many admit it in "real life" that they now have pain after voluntarily doing this to their bodies for the sake of vanity?  It would be a hard thing to admit to.   

  • gentianviolet
    gentianviolet Member Posts: 316
    edited February 2012

    Kate - I had augmentation about 40 years ago at Cleveland Clinic.  I have not suffered any pain from that surgery, although I used to be a stomach sleeper and did switch to side/back sleeper; not from pain but they are (and were within about a year encapsulated).  I have always been very physically active and perhaps that helped.  Some 35 to 40 years later my tumor appeared in the right breast about 10 o'clock position and I had a lumpectomy with 1 out of 14 nodes involved.  I also had no problem with arm/shoulder pain on that side although I do have a very mild case of lymphedema in my right arm.  But I also did all the stretching exercises that were prescribed both with the initial augmentation as well as the lumpectomy.  I was one of the lucky ones with no pain from either procedure.  I feel for all the ladies that suffer from unrelenting pain/discomfort, I did not realize until reading this thread just how bad it could have been.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited February 2012

    gentianviolet- I do believe the majority of women who have most breast surgeries don't have long term issues and I'm so glad you are one of them.  But I think the rate of ones who do is much higher than anyone would have imagined.  I can't believe that none of us are or were ever counseled on this possibility.  It may not have changed our minds (though I have to wonder if women choosing augmentation might give it a second thought) but at least we would have known we were warned.  Consider yourself very lucky, indeed!  

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    Hi,  here reading. Not leaving this post anymore. Yea!! I am not crazy My PS also said that I am one of the few that has complained about "pain and discomfort" and yes, most of his patients are there fo augmentation. I have been to a pain management, accupuncture, again, only at night when I am lying on side or flat down is there no pain.

    So wish I was warned ahead. Again, was shown a video of all "happy ladies" who had their t/e and then breast implants. All I think of should I have done a lumpectomy???? Well I can't go back. I don't know how the gals feel who have augmented due to vanity and not cancer. I have absolutely no pain in my "reduced" breast, due to the fact that the original tissue is still there. It is the new boob that gives me the problem.


    .

  • kriserts
    kriserts Member Posts: 224
    edited February 2012

    I had my second consult today with a doc about fat grafting, asked her what she thinks the pain is from. She says the implant, and the radiation. I remember my first PS sort of paused when he heard I was going to get radiation. This new doc says she thinks the implants are on their way out, people will choose microsurgery or fat grafting. I asked if the pain would end when the implant comes out. She said probably, but with a few people it doesn't, depends on how much radiation damage there is, like if it's gone down to the ribs. But it was interesting that she uniquivocally would put her finger on why I'm in pain.

  • gentianviolet
    gentianviolet Member Posts: 316
    edited February 2012

    Kate - You are correct, no one ever told me that I might experience long term pain with augmentation.  It was pure vanity (I had three kids and what little breast tissue there was, was sagging).  I so wanted perky and bigger breasts.  At that time they were put on top of the muscle so perhaps that was one reason why there was no lasting pain.  If they had warned me that I might have pain, I doubt that it would have made me change my mind; I was young enough that I felt in control of everything and indestructible. 

  • ronqt1
    ronqt1 Member Posts: 811
    edited February 2012

    At times my dr will say "I believe you" when I am complaining as if I making this all up. Yes in articles i have been reading, people are beginning to choose microsurgery or fat grafting. Again, upset that when I saw video at PS' initial visit, everyone on video was in happy land. However, on my augmented side where it was reduced and an implant put in because of sagginess, no problem. On that side, I am dealing with a keloid scar, but that is not the issue here. I did not have radiation so the guessing game is still on with me about uncomfortableness and pain.

Categories