February 2015 surgery

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  • justamy
    justamy Member Posts: 532
    edited March 2015

    Dancingdiva: My TE's are as wide as a d cup and one of them is larger than the other....my PS said that during the exchange he will go in and sew a pocket that is the correct size. Specifically he said he would sew permanent stitches under my arm that would make the permanent implants stay in place. The TE's are just there to stretch skin and he says he will sculpt everything during the exchange.

  • jabec
    jabec Member Posts: 70
    edited March 2015

    dancingdiva - I also feel like my TEs are somewhat also in my armpits (they have not moved - just seem to be wide). I asked my PS about it and he said that the natural breast tissue does expand to under the arms and he thought my TEs were perfectly placed. I guess to me it's still lumpy and noticeable there. I've only had one fill so far and am hoping that as they get filled, they will push more forward and/or smooth out under my arms. Last resort is to really discuss with PS what result I want from the exchange and make sure that the pocket and implants are the right width for me.

    I have come to the realization being 5 weeks out from surgery that the pain/discomfort that I'm continuing to feel has nothing to do with the surgery itself (I feel like I'm healed), and probably won't be totally gone until I get these TEs exchanged. I'm not sure if that realization makes things better or worse, but at least maybe now i'll stop waking up every day thinking I will feel great. In general, the discomfort isn't too bad, but i feel like one of my TEs is pressing on a rib and it's just overall discomfort, not really pain. I'm hoping to start PT this week and I hope that stretching will help with some of the tightness.

  • Copperlisa
    Copperlisa Member Posts: 24
    edited March 2015

    Add me in:

    R mx, SNB 2/26

    It's been a wild ride. Nice to see y'all. I need to update my sig, and will add details there. Still stomping around a bit about the final path report.


    Lisa

  • JustAJennifer
    JustAJennifer Member Posts: 85
    edited March 2015

    welcome copperlisa

  • faithhopecourage
    faithhopecourage Member Posts: 37
    edited March 2015

    Morning All. I also have the annoying swelling under my armpits. I went to ps yesterday and he attributed the swelling to the breast surgery itself, not the expanders. I'm thinking node removal.

  • RAK1
    RAK1 Member Posts: 240
    edited March 2015

    Good Evening Sisters,

    I hope you are all well!

    I have been enjoying my daughter, my heart is do happy seeing her!

    She went with me to my first fill

    Nurse added another 100cc making it a total of 500cc now. When she told me to look down I could believe these things. She said I will probably be done filling by the end of the month. I will need to wait three months then have the exchange.

    This whole thing has gone by so fast.

    I am still having that very sensitive burning sensation. They said it will go away in time. I am still having a difficult time sleeping, from the tightness. PS said once the TEs are removed they go inside clean out all scar tissue and position permanent implants. She said they will look normal not like now. The sides of my breast seem weird but she said that is from the nerves being cut. No lifting anything more than a pound for the next several weeks. She began to do this massaging with with her hands, it hurt and felt good at the same time. She told me to do it everyday. It feels so strange when I try. I am afraid of hurting myself. Is anyone else doing the massaging, please let me know what you are doing.

    Love Robin

    P.S. Here are what they look like now.image

  • RAK1
    RAK1 Member Posts: 240
    edited March 2015

    From the side.image

  • sunseta1969
    sunseta1969 Member Posts: 33
    edited March 2015

    I really give kudos to everybody on here. Being able to read about people that are going through the same things I am going through is such a relief! I also give kudos to those that keep up with each person. I have to sit and read and make a list and then post. And since I started back to work on Monday......needless to say, I am just glad I was able to get caught up with the reading. But in general, like some have said, I had the sunburn feeling in between my TEs and under the arm that had the SNB. It has for the most part subsided. I was 5 weeks post op on Monday. I really thought I was ready to go back to work. I didn't take into account that I've not been sitting in an office chair for hours at a time. So the past 2 days have been really hard. I went back on my norco. Very low dose and that keeps it so I can stand the pain. I also had a Lupron shot a week ago Monday because they are chemically shutting down my ovaries and I will start Femara on this coming Monday. I can't tamoxifen because I got a huge blood clot when I was 39 and have to stay on blood thinners for the rest of my life. But the other thing the Dr. did was change me from coumadin to Xarelto. As a result, I am having the worst period of my life. I know that sounds kind of dramatic but I had had endometrial ablation so my periods were very light and I only had cramps on the first day. This one is so not like those. I already called the Dr to make sure I can still take the femara and she said yes but I'm calling her again today to let her know how much I'm bleeding. My fills seem to be going fine and I feel like I have little booblets now but of course they look awful and not shaped like a boob at all. My PS said he will fill to 800 CCs (I'm at 400 now) and then I wait a month and have my exchange. So it's looking like I will have the exchange at the end of April or beginning of May.

    Gentle hugs to everybody and maybe this weekend I can get caught up again and post a less generic post. I hope everybody has a really good day and please know that I do think about each of you and pray for you each day. I do feel like this is such a special group and I'm happy that you allow me to be a part.

    Amanda

  • faithhopecourage
    faithhopecourage Member Posts: 37
    edited March 2015

    Good evening sisters!! I just received my oncotype score, 21. MO says most likely no chemo just hormone therapy. I should be celebrating and yet I find myself uncertain and confused. Should I have chemo anyway?? Will it increase my odds? Does the risks of chemo outweigh the benefits??

  • farmerjo
    farmerjo Member Posts: 518
    edited March 2015

    FaithHopeCourage,

    My oncotype was 19. That has me at a 10 year recurrence of 12%. With chemo it would have been around 10%. So the risks of chemo aren't really worth it to me. We are considered low-intermediate so it's a decision you and your doctor have to make. The oncotype score is assuming you will be on hormonal therapy. Score less than 18 = no chemo.

  • alaskamommao3
    alaskamommao3 Member Posts: 2
    edited March 2015

    Hey Everyone,

    I'm new to the boards only having been diagnosed a month ago. I've come here for information and found so much encouragement in your posts to one another, so I decided to jump in. I had a my bmx two weeks ago and am healing pretty well. I returned to work this week half days. I drove about 9 days after surgery, as I was home alone and needed a diet coke. :) At this point, I don't have plans for reconstruction, but I figure once the reality of it all sets in I may change my mind....which I'm good at doing.

    The only post surgery issue I'm having is seromas on the right side, which is where the cancer was. I'm so afraid of lymphedma, so I'm trying my best to follow the protocols to avoid the possibility. I've been in once to have the fluid aspirated and go again in a few days. Anyone else experienced that? Can fluid build up under the armpit (like on my side) lead to lymphedema?

    Thanks gals!

    Sheri

  • justamy
    justamy Member Posts: 532
    edited March 2015

    ok...I'm going to have to call PS again and I'm sure he thinks I'm a hypochondriac. My TEs are both filled with only 50 right now. One looks like a half full zip lock bag. The other used to look like that but now is HUGE and so tight that I can find the TE. I feel like its going to bust out of my chest. The crazy part is that the side that's so big is the side that had no lymph nodes removed, so it can't be that. I am never even getting these TEs filled. I am just doing an exchange in 2 weeks. I don't want anything to stop that. Any ideas?

  • zjrosenthal
    zjrosenthal Member Posts: 2,026
    edited March 2015

    Hang in there dear Amy. If your docs think you're a hypochondriac that's their problem. You have been through the wringer and are close to what will hopefully be your last surgery. Love, Jean

  • RAK1
    RAK1 Member Posts: 240
    edited March 2015


    Hello Sisters,

    I was thinking about you all.

    How is everyone doing?

    I pray everyone is as well as you can be!

    Have a great day!

    Love Robin

  • DentalChick
    DentalChick Member Posts: 6
    edited March 2015

    Hi everyone!

    I hope you don't mind me joining you ladies! My name is Sherry, & I had a double mastectomy, lymph node dissection on the right side, & tissue expanders placed on 2/26. I have been following this group for a bit, but I have finally decided to jump in the deep end & post somthing! This seems like a great group of women, and I know how important it is to have people you can ask questions to that can actually relate to what you are going through. The funny thing is I kept telling my husband today that I feel like I have a sunburn on my right arm from underarm to elbow. He told me to check online to see if that was normal. I had no idea that I would find a bunch of you posting about it in this forum!

    I was diagnosed on August 15, 2014, and I started chemo first, so I am thrilled to finally feel well enough to post on here. I will be doing 6 weeks of radiation, but I don't know exactly when I will start yet. I am meeting my radiation oncologist on 3/31.

  • faithhopecourage
    faithhopecourage Member Posts: 37
    edited March 2015

    Welcome alaskamamma!!! I am 3 weeks post-op and I have serious fluid build up under both my arms. My plastic surgeon looked at it and just said it was a result of the surgery. I know, not too helpful, but at least I share your pain!!!

    Thank you jilly59!! I'm in a better place now. I haven't met with my MO yet. The information came from a conversation with my nurse navigator. She went over my case with the MO. Once I meet her next Wednesday, I should have a better understanding of the statistics.

  • farmerjo
    farmerjo Member Posts: 518
    edited March 2015

    Welcome, Dental Chick! I just joined back in January and this forum has been a Godsend. You will make life-long friends in addition to the wealth of knowledge these women have. 

    Best of luck! 

  • RAK1
    RAK1 Member Posts: 240
    edited March 2015


    Welcome Dental Chick and Alaskamomma03, I'm glad you decided to join our thread.

    The ladies here are very caring and helpful!

    It wasn't until I read what my fellow sisters were sharing when I was able to put into words what I was feeling.

    "Sunburn" such a strange sensation, nothing is soft enough against my skin.

    Joanne, I haven't gotten a number yet.

    Love Robin

     

  • NurseShark
    NurseShark Member Posts: 176
    edited March 2015

    welcome Alaska momma and Dentalchick ! Ill go back and look at your dates and add to page ;)

    My Rad onc appt is on 3/23. I was cleared by PS to start anytime.

    Finally allowed to start ROM exercises today. I am 4 weeks post Op. Still nothing over 10lbs to lift . My PS said I could go to physical therapy at 6 weeks. I am so stiff.tried exercises today barely can lift my arms.


  • dancingdiva
    dancingdiva Member Posts: 475
    edited March 2015

    I went to get rads info and found out that I need to be able to have both my arms at 90 degrees. My ROM is not that good.

    I also feel major pain between my TEs and under one side. Sometimes I feel like I'm ripping! I thought I was getting better but then he did one fill and it got worse again. But it's not the TEs that bother me. I don't know if it's muscle or nerves but one side is totally screwed up.

    Filling the TEs btw did not hurt at all. Little pinch and that's it. I was worried

  • zjrosenthal
    zjrosenthal Member Posts: 2,026
    edited March 2015

    I do so admire you gals who had MX or BMX. I had just a lumpectomy and ALND and that was so hard. Facing all the reconstruction issues, wow. You are all amazing. Love, Jean

  • JustAJennifer
    JustAJennifer Member Posts: 85
    edited March 2015

    Today is 5 weeks out from surgery, 1 week out from Tamoxifen. I'm regaining physical strength but feel like I'm losing mental strength! I've done yoga, treadmill, elliptical, bike. Had a great massage today, pedicure earlier this week and reiki last week. Diet is getting back under control. Physically, I'm feeling pretty comfortable, and heading back toward 'normal.' My mental state is not doing as well. I have a lot of thoughts along the line of "did that all really happen?" I've had a lot of reflection time this week. It's not all ok, I guess it's a work in progress.



  • AudreyB
    AudreyB Member Posts: 377
    edited March 2015

    I agree Jean. I faced both choices and went with lumpectomies, rads and hormone treatment. While I have been in pain for a month due to sx for lumpectomies and SNB, I can only admire all of you who had MX or BMX. I am fortunate I had an option. I know we don't all have options. It's the courage and strength on this and other boards that truly amazes me.

  • JustAJennifer
    JustAJennifer Member Posts: 85
    edited March 2015

    I tried for lumpectomies- had two but no clear margins. I have to say while the discomfort is totally different with MX, I remember the pain I had from lumpectomy, and it's bad enough on its own. It's been a relief to not having that pain anymore.

    It all sucks.


  • greenae
    greenae Member Posts: 540
    edited March 2015

    Hi All

    Finally getting some energy and attitude back, so wanted to say, "Hi," and thank you for all the good thoughts and prayers. And I am happy to see a lot of you are receiving good news!

    I had some trouble with post- op hemorrhage and anemia, almost had a trip back to the OR, and can I mention that my TE freakin hurts? I am still pretty pale, taking iron, resting too much and feeling so weak and frustrated. I got rid of the narcs a few days ago, just occasional valium for the spasms. I apparently am pretty funny on meds...e.g. texting and facebooking at inappropriate times, and telling too many jokes (some bad!) while at the hospital. It was a little fun that first week, but then I sorta "crAshed' AND NOW I CRY FOR NO REASON, PRETTY OFTEN. UGH. oOPS, SORRY BOUT THE CAPS. I am supposed to start chemo in 2-3 weeks. I really wanted a mini 4-5 day vacay before this next fun begins...but I feel too tired to even try to plan anything. Besides, it's near Spring Break time, so I imagine Myrtle and Fla are mob scenes and over=priced now? And can we go in ocean or pool 4 weeks post-op with TE? Oh well, anyone have any ideas? I live in SI, NY and can drive 4 hours to hang somewhere nice for a few days before my chemo begins, if its too crazy to try somewhere warm and beachy.

    Also, a bit ticked at my path report...Ca was never seen on Mammos, USs, MRIs, Biopsies ,etc, Anywhere near my skin .Was 3-4cm below surface, in medial region, 10:00. Now, after having skin and nipple sparing L MX, I am told margins are close and I will most likely need radiation after chemo, GRRRRRRR. OK,-- Attitude Time. I will get through this ,as all of you have!. It just makes me feel good to vent on here. Have I mentioned I still have my lovely Carvel Flying Saucer Hemi-vac drain? Been 16 days with this lovely apparatus.Am I the only one without JP? It's gotten so beaten up I have duct tape holding it together...lol I Am sure looking forward to kissing it good=bye...and I will never eat another Flying Saucer, again.

    I hope all are doing well. Thank u so much for your encouragement. I know I tried to post on here a few times last week (while on Percocet and valium) and it seemed I would type in "tongues" or somehow delete the msgs. So, if I 've written this before, I apologize...have missed all of you, and am trying hard to get my Normal back,

    love, Arlene

    OMG! MY Best News...Nothing in Sentinel Node! YAY!

  • faithhopecourage
    faithhopecourage Member Posts: 37
    edited March 2015

    Morning Arlene!! Great news about the snb!!! Just wanted to let you know I'm also a Staten Islander. Where did you have your surgery?? I had mine at Staten Island University. LIJ.

    Much Love,

    Joanne

  • AudreyB
    AudreyB Member Posts: 377
    edited March 2015

    Hi Arlene. Nice to hear from you again. Best wishes for continued healing.

  • NurseShark
    NurseShark Member Posts: 176
    edited March 2015

    I am 4 weeks out from bmx. The first 4 were rough but now that I can do ROM exercises I feel so much better.

    Ladies that had lumpectomy and alnd or snb, I had mine back in July and to compare I felt more pain from the lymph node dissection than this surgery.. I remember not being able to move my arm and hand awful nerve stuff all the way down to hand....bmx is definitely no picnic but both come with challenges.I just started exercises and feel like I am getting ROM back quicker than the first surgery.

    Good luck and prayers to ladies starting chemo and rads. I have finished chemo (dd AC/T) I know there are chemo support boards that are great too but many of us surgery sisters have gone through it so feel free to ask here.

    I am nervous about starting radiation soon but strangely excited to get (what I pray) is the last step over with. Meeting RO on 23rd and see my MO 27th (to plan for future) also having pelvic ultrasound and ca-123 drawn for baseline on ovaries...(brca 1 risk s)

    Happy Saturday💜


  • NurseShark
    NurseShark Member Posts: 176
    edited March 2015

    RAK they look good ! I feel like my implants look to far apart. But otherwise I am happy with them I think especially now that the nipples are healed. (I had skin/nipple sparing)

    You ladies are so brave posting pics I feel like I can't bring g myself to look at mine very long let alone snap a pic...I hope I will get there.

  • farmerjo
    farmerjo Member Posts: 518
    edited March 2015

    NurseShark -

    We had our NSBMX surgeries same day.  While I don't have issues with nipple necrosis, I have issues where they ulcer, scab over, repeat. Also, one of the incisions opened a half inch so back to the PS I went.  I am STILL on antibiotics. 

    So glad to hear you are doing well. I am having depression issues, related to the sudden d/c of hormone replacement therapy. Sigh.

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