I miss having feeling in my boobs!!!!

Options
13»

Comments

  • lisa-e
    lisa-e Member Posts: 819
    edited January 2010
    Sunflower,  Downward Facing Dog may not be the same, but Shoulder Stands should be better.  After my BLM, I  do one without being smothered by my boobs.    Cool
  • LeeMcC
    LeeMcC Member Posts: 152
    edited January 2010

    I call mine belly boobs -- cuz I had DIEP. I'm thankful for the bowls of ice cream and the cookies I've devoured over the last 20 years. Unfortunately, I only had enough to make B-cups ... but alas, it's what I was before the surgery. At least these point out, not down to my toes!

    Lee

  • Rhondakay
    Rhondakay Member Posts: 16
    edited January 2010

     3girls4me:     I feel EXACTLY the same as you, to a tee.   "we are made strong by difficulties we face and not evade"
    Diagnosis: 11/17/2008, DCIS, 1cm, Stage 0, Grade 3, 0/2 nodes, ER-/PR-

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited January 2010

    missrwe, THANK YOU so much for your perspective. (and everyone here!) I keep reading threads that scare me into thinking I should just do it, but the whole losing-all-sensation thing... *sigh* I just don't know.

  • sweatyspice
    sweatyspice Member Posts: 922
    edited January 2010

    I am currently brow beating two surgeons (BS and PS team, who are giving me different answers) about the sensation thing.  I wish I understood breast/nipple/areola nerve anatomy. 

  • Kristinka
    Kristinka Member Posts: 520
    edited January 2010

    Julia, you are fortunate that you have a choice b/w a lumpectomy and a mx.  Just keep on talking to BC ladies about their experiences and you will figure it out.  I had to have a mx but after talking with about 10 ladies and doing my own research I decided on the bmx.  I do miss the sensation a lot, but I don't miss worrying about cancer.  I've also had lots of pain since the bmx during the reconstruction but that should end after the exchange surgery.  good luck to you (and to you sweatyspice, if you are deciding as well)

  • Baxter
    Baxter Member Posts: 234
    edited February 2018

    Hello ladies,

     I haven't written here for years. This sight was my lifeboat for many months. I owe you all so much.

    My first mastectomy was late 2008. Second cancer was found in remaining breast 2009. In other words both breasts are gone. I hope I don't discourage you by saying these things almost 9 years later. I was 51 at first mastectomy. First surgery put me right into menopause.  My breasts were a big part of our sex life. You are in a different place when you are trying to get through two diagnosis of breast cancer in one year. I have to say it has changed our lives immensely. And yet, I feel like I am being ungrateful when I complain of this when many die from this disease.

    Things have never been the same. My breast sensation was a big part of our sex life for both of us. No one tells you implants  will feel cold. Age changes things for both men and women. I'm trying to figure out how much of this would be happening anyway because of our age. Things get more difficult for men (didn't want to use the word "harder!")   I remember those nights of just rolling over in bed and  touching each other....love making was so natural and easy and wonderful. You just take it for granted.

    I didn't realize that the loss of estrogen with menopause also made your vagina tissue so thin. Estriol , a compounded cream that strengthens the vaginal tissue and doesn't effect the estrogen levels in the body does help. But between the issues men have with aging  and having to mess with this cream, it just takes away the wonderful ease and spontaneity of how things used to be. It's work now.

    I so miss how things use to be. Most of our friends have children and grandchildren so that fills up much of their lives.  We don't have that. I'm still very sad...grateful...but sad. I was always healthy. I was never told I might die. I never felt sick until I had all the surgeries.Had seven total surgeries with two separate cancers. infections and reconstruction.

    Probably no one will understand this. It's different dealing with cancer that  needs to be removed and changes your entire life than those who fight for their very survival. Once my biopsies came back, I knew I had a long road, but I wasn't told I might die.

    As BC survivors some of the things we may have in common are, hearing the word cancer and mastectomy in the same sentence. Waiting for biopsy results after painful breast amputation to know what further treatments awaited you. Roads and treatments vary and diverge from there.  

    How can I express that I am so grateful and yet feel like I have a right to be sad?  I hope someone understands what I am so poorly trying to express. God bless you all.

  • Beesie
    Beesie Member Posts: 12,240
    edited February 2018

    Baxter, you expressed your feelings perfectly. You have every right to feel sad... as your story shows, breast cancer is the gift the keeps on giving, and definitely not in a good way. I understand completely.

    Many of us don't have a choice, but for those who do get to choose between lumpectomy, UMX and BMX, this thread should be mandatory reading... not to change any minds, but to ensure that this impact of having a MX is understood and factored into the decision. Losing sensation is difficult enough to live with without it coming as a surprise after the fact.

    Sending you (((Hugs)))... but come to think of it, even after all these years, I'm often self-conscious when I hug because I wonder if the person I'm hugging can feel that one of my breasts is firmer than it should be (I had a UMX).

    🙄😣


Categories