stage IIB,grade 2, no mets, 1 node

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Sunflower64
Sunflower64 Member Posts: 166

hello,

does anyone have my same diagnosis?

i would like to chat with them.

thanks,

diane

Comments

  • valeriekd
    valeriekd Member Posts: 287
    edited October 2009

    Hi Diane, I am pretty close ( u can see dx down there). I'll chat anytime you'd like! Valerie

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited October 2009

    Me!  And I'm five years out.

  • Warrior517
    Warrior517 Member Posts: 355
    edited October 2009

    I am close, too....Tumor was 1.9cm, just a hair shy of 2cm , which would of made me Stage IIB!! I was also Her 2 AND Estrongen Positive so I cover both basis..lol

    Member of the Club...yeah for you!!  xoxo

  • TennesseeMichele
    TennesseeMichele Member Posts: 136
    edited October 2009

    I'm here too, pretty close to you.

    Miehele

  • joanneasiata
    joanneasiata Member Posts: 719
    edited October 2009
    hi im nearly the same as well just waiting to start chemo in the next week ive had to undergo 2 opp as the first wasnt a clear margine ill also be doing hormone treat and radiation im so scared of the chemo ill be doing about four rounds im in australia so i think we do things a bit differant then oversease same same but differant lol ::  im 45 yrs old and very lucky to have fantastic support actually  getting very spoilt at the moment but im really lapping it up im amazed at the wonderful people i have in my life well any way thats me
  • htrobison
    htrobison Member Posts: 12
    edited October 2009

    I am about the same...dx'd in July. Going thru chemo now. I would love to chat with women with a similar diagnosis.

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited October 2009

    I'm similar although grade 3. I'm on ECOG 5103 and am getting 4AC-->12T + Avastin/Placebo. What chemo are you getting?

  • NatsFan
    NatsFan Member Posts: 3,745
    edited October 2009

    Hi Diane - Me too, except I also was Grade 3.  I'm now almost 2 years out and going strong.  Did the bmx with t/e placement (with full Level I/II AND), 6*TAC chemo, and a delayed DIEP flap recon.  Now in my second year of Femara, I have a full head of hair again, and my last PET/CT scan showed No Evidence of Disease. If you're newly diagnosed, I won't kid you - the next year or so is not going to be a walk in the park, but you'll surprise yourself at how much strength you have.  You can do it.  Please let me know if you have any questions or just need to vent - I'm here.

  • Member_of_the_Club
    Member_of_the_Club Member Posts: 3,646
    edited October 2009

    I'm also a Nats fan!

  • NatsFan
    NatsFan Member Posts: 3,745
    edited October 2009

    MOTC - next year has GOT to be better for the Nats!  But they sure ended the year in style, didn't they??

    I was the MLB Breast Cancer Honorary Bat Girl for the Nats this year for MLB's Breast Cancer Awareness Day in May.  They gave me a Nats jersey with a big pink ribbon on the back with "Bat Girl" on it, pink wristbands like the players wear that day, and I even got one of the pink Louisville Slugger Bats they use with my name engraved on it.  They also gave me Lexus level seats right behind home plate that the game, plus I got to go out on the field and was recognized in a pre-game ceremony.  I was up on that big scoreboard!!  I also got to meet and chat with a bunch of players, including John Lannan.  It was right after that when he started pitching so well, so I decided I must be the lucky charm!    Of course the other two players I got a chance to talk to were Jesus Flores and Austin Kearns, so maybe my lucky charm theory is lacking something.  Surprised

    I have to say that the Nats really treated me right - I felt like a queen for a day.  Then, to top it off, they even did a 2-page spread on me in the last program of the season.  It was a lot of fun.  

  • valeriekd
    valeriekd Member Posts: 287
    edited October 2009

    Hey dmp, have not seen u since u started this thread? How r u doing? I hope you don't keep it all inside - I think its much scarier in there than when u come out here. There are lots of people who would love to hear from u! Peace- Valerie

  • htrobison
    htrobison Member Posts: 12
    edited October 2009

    Onty,

    I am getting adriamycin and cyclophosphamide every two weeks(I have two more sessions). Next I will get paclitaxel every week for 12 weeks.

  • SoCalLisa
    SoCalLisa Member Posts: 13,961
    edited October 2009

    I am near that DX too

    I did CMF for six months

    Tamoxifen for a year

    Armidex for four years

    Fosamax for three years

    I was DXed nine years ago in Nov..

  • sharkey
    sharkey Member Posts: 18
    edited October 2009

    Hi Ladies,

    Me too.  Thanks for starting the thread.  I am almost finished chemo and trying to decide about radiation treatments.  Do any of you have any thoughts about radiation risks vs. benefits?

    Sharkey 

  • Sunflower64
    Sunflower64 Member Posts: 166
    edited October 2009

    hi holly,

    thanks for responding.  question for you.  are you going to have your ovaries removed?  i'm trying to get different opinions.  how are you feeling?  i have my last one next week. if you need to talk, i'm here.

    thanks,

    diane

  • LizM
    LizM Member Posts: 963
    edited October 2009

    I have a very similar diagnosis.  Diagnosed with Stage IIb, 2 cm, grade 1 and one node - that was 4 years ago.  I had surgery, chemo, radiation, ovaries removed, then Arimidex and now Femara.  So far so good. 

  • valeriekd
    valeriekd Member Posts: 287
    edited October 2009

    Thanks Liz _ That is encouragement we can all use!

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