Stage III - HER2 - 2+ Years Out - Check In!

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  • TonLee
    TonLee Member Posts: 2,626
    edited September 2012

    Jenin!  That is awesome!  Really wonderful :)

  • evergreen9
    evergreen9 Member Posts: 131
    edited January 2013

    I posted last summer, and thought I would again. I am almost 26 months since my surgery, and 9 months since finishing my herceptin. My onc says if you recur before the 1st anniversary of finishing herceptin, that means you have a nasty version of the cancer. And that when you're at or beyond the three year anniversary from finishing herceptin, that's a very positive thing.

    Can't wait till April, my first year anniversary!

  • slousha
    slousha Member Posts: 312
    edited January 2013

    Hi,

    I finished my Herceptin on November 2010,  September 09 I was given the pathological report. I’m very glad to pass all check-ups September 12, when my MO said” You don't have cancer any more”  (for now!). I’m browsing BCO posts every day. I would like cancer not to have in my mind so often, but I couldn’t to prevent me from.

    Best wishes  to StageIII, Her2+ sisters!

    Usha

  • maryannecb
    maryannecb Member Posts: 1,453
    edited January 2013

    Hello Fellow Her2 survivors!

    I have been down your road and am quite far away from my original diagnosis in 2005. I remain happily NED thanks to wonderful care and good fortune to date.

    My oncologist refuses to call me cured but is hopeful for the future for me...and so am I.

    My children were 12,13 and 15 at diagnosis...so in 6th-10th grade. They have all graduated from high school and my eldest has started medical training. I got to my 50th birthday and celebrated big time. 

    I haven not had a cancer free day( a day where it didnt cross my mind)yet...but i bet it will come soon.

    I do feel super-fortunate to have had these last seven years...as I know others who have not been so lucky. I have tried to cherish my friends and relatives and treat others with respect.

  • PlantLover
    PlantLover Member Posts: 622
    edited October 2013


    Dear Sisters …


    1st - Thank you to others that have posted to this thread.


    I don’t come to these forums much these days. Often, it’s because the job I have requires me to stare at a computer for 9 to 10 hours a day and by the time I come home the last thing I feel up for is opening my laptop. I’m fortunate to have a job and don’t mean for that to sound like a complaint. It is just hard on my old eyes most days. Anyway, the few times I have returned to the forums for a quick look around, I’ve been devastated to read about the loss of a member and ended up in tears and not able to post.


    Last year when I logged in sometime around October I learned of the loss of a very cool lady, Marybe. She and I had chatted via PM a number of times and I followed her posts with such a sense of wonder.She had faced so much but her humor and good nature continued to be clearly present.Although I never met her, I just know she was an incredible lady and it really broke my heart to read that she was gone.


    I tried to log back in in November to post but when I did I read of the loss of Lowrider. She was one of the first members that made an impression on me when I joined these forums in 2009. I know there have been many others … each one special and a terrible loss to those who loved them.


    Today, when I logged in I guess I shouldn’t have started looking around because now I know that we’ve lost Athena. She reached out to support me when my son was having problems. I always loved to read her posts - they were always so well thought out.


    I know there have been many others … too many others!


    I HATE cancer!


    So, with a very large degree of survivor’s guilt and through tears, I’m going to go ahead and post on this thread.


    You see, I started this thread when I was so afraid I wouldn’t make it to see a third anniversary. Selfishly, I was hoping people would post and it would ease my fears and, perhaps in the future, ease the fears of others.


    Although I really mark my "years" from the date I had my first chemo, November 23rd, 2009, I just didn't want to wait any longer to post. Since I was diagnosed the last week of October, 2009, I guess this will do.



    I am four years out from my diagnosis - IDC, Stage IIIb ER/PR+, Her2+.


    Although there is so much sadness in the loss of others & so much fear when you are diagnosed, I just want to tell those that are fighting now … hold on to hope. As the mosaic I made when I was first diagnosed states …


    image

  • annika12
    annika12 Member Posts: 433
    edited November 2013


    tank you for starting the thread and for posting !! Holding on to hope is important ;) I just did #11 out of12 taxols , herceptin ,lymohnode removal and radiation (I think) still a head !! I so want to be posting here many many times in the future with good news and hope for others !!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2013


    Nine (9) years for me -- triple positive and still NED!!!!

  • LindaKR
    LindaKR Member Posts: 1,577
    edited November 2013


    3 1/2 years since surgery - triple positive! Have an appointment for a bone scan tomorrow though :-( hope it's just from a fall I took in September.


    Edited-looks like degenerative changes, not mets. :-)

  • AliceS
    AliceS Member Posts: 98
    edited July 2015

    So glad to see the bone scan was not a mets, Linda. Guess this is old news now, but just noticed your edit. Hope you're continuing to do well.

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

    now over 10 years from a stage 3C , her 2 positive bc, livin large, grateful every dayand dancin every opportunity ,

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