Would love to hear from some long term Stage III survivors...

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  • tina_jason
    tina_jason Member Posts: 147
    edited August 2012

    Thanks to all of the survivors that posted. I really needed to read these tonight.

  • H-Nette11
    H-Nette11 Member Posts: 5
    edited June 2013

    Hi Lanagraves,

    Just wanted to tell you that I will be 12 years out on AUG. 11, 2013- next month. I had stage111 Her2 nu + ERT+. 17 lymph nodes removed, 8 were positive and one was starting to escape lymph node but did not make it. I had a year of FEC,  a yr. of taxotere. 6 wks of radiation, a flubbed reconstuction. DR. forgot to tell me to stop Femara before diep flap surgery. Femara can cause the blood to clot and with a diep fat they use the fat and blood vessels from the stomach. I gained weight for it but came out with a tummy tuck. The nurses argued outside my rm. not to get the"flaps" because the doppler noise annoyed them. I could not wake up enough to say anything but I heard them. Long story short several surgeries later I have a lattisimus Dorsi flap and the girls are not even. I did not bother with a nipple.  To be honest I think the long surgeries are harder on the body and mind than the chemo. 

    It's all good now. I am alive and was blessed to be at my son's wedding 3 yrs. ago and getting ready to fly to see my Grandbaby in 2wks. I really don't sweat the small stuff so much anymore and my relationships are the most important thing in my life.   I wish you all the best. I hope my story gives you hope.

  • jennyboog
    jennyboog Member Posts: 1,322
    edited June 2013

    Thanks for posting, H-Nette11. 

  • joan888
    joan888 Member Posts: 810
    edited June 2013

    H-Nette11... great story!  Congrats on being such a survivor.  I am now 3 years and 3 months out.  I will say that every little ache and pain still gives me pause, but hopefully, I will get over that soon.  I have had reconstruction difficulties and LE related to radiation but all is well at the moment.  I still see my ONC every 6 months for another year, then I am on the 12 month plan.  Yeah!

  • lkc
    lkc Member Posts: 1,203
    edited June 2013

    Ok so Now I am officially over 8 years from a stage IIIC, HER2 pos  BC. I am blessed, happy as a clam and am enjoying life BIG time.

  • joan888
    joan888 Member Posts: 810
    edited June 2013

    lkc.... that is SUPER!

  • Gitane
    Gitane Member Posts: 1,885
    edited June 2013

    What a happy message you send us, Linda!  All the best to you; keep up that happy lifestyle; it must be just what you need.  Smile  Hugs, G.

  • peacestrength
    peacestrength Member Posts: 690
    edited May 2015

    This is an old thread but wanted to bump...need to hear from stage 3 survivors....please:)


  • Sarahlou50
    Sarahlou50 Member Posts: 33
    edited May 2015

    I think I can now consider myself a long-term survivor!

    Never truly sure if I am NED but like to think I am!!

  • DATO
    DATO Member Posts: 127
    edited May 2015

    It's been 9 years now since my diagnosis. I was diagnosed the day before the local Komen Race For The Cure. Every year afterwards I have participated. This year I didn't. Why? This year two of my grandsons had Little League baseball games that day and I go to all of the games and take pictures. In other words, my breast cancer is no longer the center of my universe, it is just a part of my past. I now have other important things I want to do. Next year I will try to do the race because it will be my 10 year cancerversary. Yes, my diagnosis was a major event in my life, but now I am a long term survivor. In the early days of my diagnosis I came to breastcancer.org everyday for support and information. I very rarely come here now, except on or near the anniversary of my diagnosis because I want to encourage others with a stage III diagnosis. Live long and prosper my friends.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2015

    So great to hear you're going on 10 years from diagnosis!!! And as you say BC is now just a part of your past. Live long & prosper indeed :)


  • lkc
    lkc Member Posts: 1,203
    edited May 2015

    now ten years, Livin large every day and happy as a clam!

  • sugarplum
    sugarplum Member Posts: 318
    edited May 2015

    Here I am nine years out from a horrible path report - have spent each day waiting for the other shoe but have also managed to have some fun in the meantime!

    Best to all - Julie

  • Cindi2011
    Cindi2011 Member Posts: 133
    edited May 2015

    Hey Ladies,

    Just popped in to see how everyone is doing.  So happy to hear the positive from those of you that helped me through the first two years with treatment.  It is now 4 years,1 month, 27 days, 13 hours since I heard the "C' word that changed my life.....but whose counting?

    Most days are good except for the aches and pains but I blame old age  AND  that's a good thing.

    God Bless you all and keep the STRENGTH, COURAGE, HOPE, FAITH.


     

  • JudyO
    JudyO Member Posts: 225
    edited May 2015

    I am now 7 years out stage 3A ILC, 2.2 cm, Grade 1, 7 positive nodes, ER+PR-HER-. ACT chemo, 25 rads, and 7 years of arimidex. It made me nervous to post this, so afraid of what the future may bring! but thought it may give some hope to the newer members.

  • peacestrength
    peacestrength Member Posts: 690
    edited May 2015

    I thank each of you for posting! Each of your stories give me hope in my darkest hours.

  • clariceak
    clariceak Member Posts: 752
    edited May 2015

    With my stats, I consider myself long term. I was dxed in 2009 with Stage IIIC, a mammary node that lit up and was inoperable, had vascular invasion and loads of nodes. My onc wanted to allow me extra time at my first appointment. I thought she wanted to sit down and tell me how bad my odds were. I told her I did not want to discuss my prognosis, only my treatment.

    Every year is a blessing, My kids were only 8 and 10, when I was diagnosed and I see them getting closer to graduation. My oldest is going into her junior year and my youngest just completed middle school.


  • everyminute
    everyminute Member Posts: 1,805
    edited May 2015

    On Sunday, May 31st, it will be 7 years from the scariest shower of my life. I was diagnosed within days - stage 3 bc, 5 positive nodes, er+. My oldest daughter turned 16 just a few months later and my younger daughter had just turned 13.

    My older daughter will be turning 23 soon, she got married last summer and is having a baby in October. My baby just turned 20 and is almost done with college.

    I appreciate every day, every minute (it's a struggle to appreciate the minutes stuck in traffic but I try!).


  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2015

    It is wonderful to see all of the long term survivors!  I am out about 10 1/2 years now.  When I started this so called journey I had no idea what to expect.  Looking back I realize I have been living much more in the moment than I did before diagnosis.  My kids were 20 and 23 when I was diagnosed.  They were both away at college.  Now they are both married and in successful careers.  I'm still not a grandma but I have my fingers crossed!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2015

    Jillian: I am blessed to be a grandmother of a 2 1/2 year old little "caveman". Grandkids really do keep us young -- if not forever tired !! I am going on 7 years since dx and can only keep looking ahead at this point. You will be a grandma I just know and will love it as much as I do. --Shelly

  • jenni__ca
    jenni__ca Member Posts: 461
    edited June 2015

    i'm hanging in here ... going to graduations, weddings, reunions, family get togethers ....

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