5 year survivors, post your screen name here!

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Comments

  • coltsneck
    coltsneck Member Posts: 10
    edited January 2014

    Happy to say that I am 7 years post diagnosis.  My surgeon said I am now 'officially boring' - best comment I could have received!

  • moderators
    moderators Posts: 8,739
    edited January 2014

    Jasminn and Coltsneck, congratulations on your anniversaries! 

    Coltsneck, we like your surgeon's style!  image

    • The Mods

  • maywin
    maywin Member Posts: 24
    edited January 2014

    Eleven years out!!! 

  • soriya123
    soriya123 Member Posts: 384
    edited January 2014

    congrats to all of you ladies!!!  Thank you so much for posting!  

  • moderators
    moderators Posts: 8,739
    edited January 2014

    Maywin -- 11 years!! Amazing! You are all such inspirations Smile

  • 5graces
    5graces Member Posts: 12
    edited January 2014

    8 years for me!

  • LizA17
    LizA17 Member Posts: 102
    edited January 2014

    Congrats to all of you! Love reading these posts!!

  • AndreaJ50
    AndreaJ50 Member Posts: 704
    edited January 2014

    This is the best therapy!!! Really needed this positive reinforcement today. You Go Girls!!!!

  • Sharon1942
    Sharon1942 Member Posts: 96
    edited January 2014

    Do you count from diagnosis or end of treatments or what?

  • nancyd
    nancyd Member Posts: 557
    edited January 2014

    Sharon,

    It can be from any of those. I count from my diagnosis date. Others count from when they completed active treatment (surgery, chemo, radiation). My oncologist counted from when I started Arimidex, lol. As long as you are consistent, I don't think it matters. In most cases, it's only a few months difference.

  • lago
    lago Member Posts: 11,653
    edited January 2014

    Survivor = the day you were diagnosed
    Remember there are many survivors that have mets. Also remember how horrible diagnosis was. I know that was my lowest point.

  • BanR
    BanR Member Posts: 238
    edited January 2014

    All the ladies who are 5 years out and more, could you please write something about your treatment plans and your follow up routines.

    Congratulations all of you for getting through this!!

  • PattyPeppermint
    PattyPeppermint Member Posts: 8,950
    edited January 2014

    11 years and counting. Hooray 

  • Adnerb
    Adnerb Member Posts: 727
    edited January 2014

    First diagnosed in 2005, and I am still here, so I consider myself a kind of survivor.

    Hugs to everyone,

    Brenda

  • nancyd
    nancyd Member Posts: 557
    edited January 2014

    BanR,

    I had four doses of TAC before BMX, then two more doses of TAC before six weeks of radiation.  I started anastrazole just before the radiation, and I've been on that ever since.

    (So, chemo - surgery - chemo - AI/radiation - AI)

    Follow up with onc went from every three months to twice a year at about the two year point. Just switched to once a year after my latest visit in October. 

  • moderators
    moderators Posts: 8,739
    edited January 2014

    Whenever you start to count, these are impressive milestones - congratulations!

    • The Mods

  • BanR
    BanR Member Posts: 238
    edited January 2014

    Thats great nancy! wishing you good health... 

  • ahdjdbcjdjdbkf
    ahdjdbcjdjdbkf Member Posts: 188
    edited February 2014

    I'm coming up on my 2 years and just had clear scans so I'm planning for my 5!! :-)

  • karen1956
    karen1956 Member Posts: 4,640
    edited February 2014

    don't  remember if I've posted here or not, so here goes....Karen1956...just passed 8 years!!!

  • moderators
    moderators Posts: 8,739
    edited February 2014

    mariasnow and Karen, congratulations to you both!

  • ahdjdbcjdjdbkf
    ahdjdbcjdjdbkf Member Posts: 188
    edited February 2014

    So happy to hear about Karen. 8 years is great. Adnerb, you are not kind of a survivor, you are THE kind of survivor - here and surviving. Much love to all!!

  • mo37
    mo37 Member Posts: 12
    edited February 2014

    I don't usually post but I am 10 years out from stage 4 diagnosis and still in remission.

    Mo37

  • moderators
    moderators Posts: 8,739
    edited February 2014

    Mo37, thanks for sharing your happy anniversary. 10 years deserves a celebration!

  • AndreaJ50
    AndreaJ50 Member Posts: 704
    edited February 2014

    Mo37, that is awesome!  Congratulations! And thank you for posting. What an uplifting message to read!!!

  • lago
    lago Member Posts: 11,653
    edited February 2014

    Big Congratulations mo37!!!

  • sherry67
    sherry67 Member Posts: 370
    edited February 2014

    Thanks Mo37...Big congrats

  • BanR
    BanR Member Posts: 238
    edited February 2014

    sending  a big hug to you Mo37! 10 years from stage 4- rare but wow, you did it!!!!!!!

  • goodrhue
    goodrhue Member Posts: 22
    edited February 2014

    5 years!  When I went for my checkup in January I was told I didn't have to come back for a whole year!!  My oncologist switched me from Arimidex to tamoxifen AND now I get to go to the Duke Breast Cancer Survivor Clinic instead of to her - which I love!

  • katyand4
    katyand4 Member Posts: 32
    edited February 2014

    Wow congrats to MO37 and Goorhue!  Wishing you both continued health and happiness.

  • nancyd
    nancyd Member Posts: 557
    edited February 2014

    Well, it's come around to six years for me now. Some of those years were rougher than others. But surprisingly, the "cancer year" wasn't the hardest. I put that one at second.

    It's just that sometimes, life is hard. We make the best of it and still manage to have good times despite facing losses that at times seem to overwhelm us. Hearing the news from other board members that they are still healthy is definitely encouraging. So I'm here now, to say, I'm still NED.