10+ Survivors

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Abby20
Abby20 Member Posts: 102

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  • Abby20
    Abby20 Member Posts: 102
    edited January 2014

    Happy New year!

    I was wondering how many of us are 10 (or more) years survivors this year? 

    To those who have made it CONGRATULATIONS and wish you and others many more healthy and happy years.

  • Abby20
    Abby20 Member Posts: 102
    edited January 2014

    I can't believe there are no 10 years survivors among us!

  • Barbarella60
    Barbarella60 Member Posts: 48
    edited January 2014

    Hello, Abby20 

    I am an 18 year survivor! I'm 60 years old, diagnosed pre-menopausal. Stage 1 idc. Lumpectomy, chemo, radiation, chemo, 5 years tamoxifen.  Experiencing major side effects from aggressive radiation therapy. Glad to be alive.  And you? 

  • PaulaK62
    PaulaK62 Member Posts: 1
    edited February 2014

    Hi Abby20 

    I am new here just because I want to see what I can do to make a difference at this point in my life. I am a 13 year survivor! Yay me! :-) I was dx at the age of 39 in 2001.  I recently had a scare with my good breast but it all checked out good. Congratulations to you and Barbarella!

  • Abby20
    Abby20 Member Posts: 102
    edited February 2014

    dear barbella,

    Congratulations! And wish you a happy and healthy life. Your story is very inspiring 

    Hope the side effects from radiation are pretty much in control??

  • Abby20
    Abby20 Member Posts: 102
    edited February 2014

    Dear PaulaK62

    Wow 13 years out is a BIG milestone. Congratulations and more happy and cancer-free years for you

    Just wonder if you had to change anything in your life to keep the cancer away?

    Do you mind telling us how your pre-cancer life is different than your life after diagnosis?

  • Barbarella60
    Barbarella60 Member Posts: 48
    edited February 2014

    Abby, thank you.  I can not believe that it has been so long!  But I am truly fortunate.  I do believe that my choices in treatment may have played a role.  I chose the most aggressive treatment, especially with adriamycin instead of methotrexate.

    Maybe too aggressive in retrospect but who knows if I hadn't. Looking at it now, isn't it like a crap shoot? You can only do as best as you can with the information given to you. That was many years ago, and a lot of things have changed. It was routine then, to have all lymph nodes removed.  No longer. Now I would chose not to have radiation & go with a double mastectomy, because with the side effects I will most probably have the double in the near future. 

    Abby and you?

    Congratulations & thank you Paula, it is truly a huge milestone.  Those "scares" always bring me back to the reality of this disease.  Nothing is for sure and can change in an instant.  Were you put into menopause from treatment?  I see that you had the same treatment as I did, except for the taxol.  I had 5FU, which is associated with "chemo brain, or chemo fog".  

    Have a good day, Barb   

  • Sierra
    Sierra Member Posts: 1,638
    edited March 2014

    Hi there Abby:

    I just now saw your post here

    sure, I am at l4 years and did post in the Canadian forum

    I hear you, cant believe there are not more of us but some have left

    or dont post whatever

    best wishes to you

    keep on, and we are so blessed, arent we?

    Hugs,

    Namaste

    Sierra :)

  • Moderators
    Moderators Member Posts: 25,912
    edited March 2014

    We have initiated a new section called Acknowledging Our Members.  The first honorees are women who have been members and survivors for 10+ years.  You can visit the new section at this link:

    10+ Survivors and Members

    Their stories are truly inspiring (as are so many on the boards and on this thread).   Their stories are also highlighted in our first community newsletter -Check out our first quarterly newsletter.

    Let us know what you think!

    Best wishes

    The Mods

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