Class of 2005, just saying hi

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  • MargaretB
    MargaretB Member Posts: 1,305
    edited November 2006
    I'm in the class of 05 as well. Diagnosed 12/23/04 surgery March of 05, finished chemo 6/05 and revisions were complete 8/05 - what a difference a year makes. Thank you all for your help - and Saskia, welcome back.

    Margaret
  • tflowers
    tflowers Member Posts: 442
    edited November 2006

    Saskia's back...Where have you been? Hope all is ok.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2006
    One year ago I wore a news boy cap cause I was bald. Today I wore a news boy cap cause, well - its stylish!

    Saskia its so much fun having you back.

    I say lets all help out. Let the 2005 girls throw a Christmas party for ourselves and all the other members here on the boards. Sure sounds like fun.

    Today is exactly 11 months since my last chemo. Amazing how we keep track of dates and things. I think at this time last year I had 2 more rounds of taxotere left.

    Whew, its so true, what a difference a year makes.

    Ok ladies. Time to party.

    Nicki
  • Odalys
    Odalys Member Posts: 2,103
    edited November 2006
    Saskia, I remember your virtual Christmas party. I was in the middle of chemo and feeling so scared when I ran into your posts. What an inspiration to see you all having so much fun. You all taught me it was possible to have fun again after chemo and this hidious diagnosis. I'll be forever grateful. God Bless you. So when is the next party? Count me in!
  • BRSTN
    BRSTN Member Posts: 166
    edited November 2006
    I'm a class of 2005 member, also.

    I found the lump in 2002, but had a rotten hot-shot Boston doctor who told me it was nothing but a fluid filled cyst and made me feel like I was a whiner. Stupid me, I believed him or at least wanted to believe him.

    It wasn't until we moved back to TN that I got the correct dx. That was in Feb. 2005. It was no fluid filled cyst...never was one. I still think of ways I can torture that *&^% Boston dr. But I stay more mad at myself.

    I had a mastectomy on the 25th. AC started on March 31 and ended on May 30. No radiation. I'm on Arimidex and my little happy pill (Effexor). Like a lot of you I never thought this would happen to me. I pull my prosthesis out every morning and still wonder what happened. And look in a mirror, no thank you. I can't stand the sight.

    I have a wonderful DH who has cared for, cried with and loved me through it all. He deserves better.

    I'm still mad, sad, hurting from the SE's of Arimidex, losing my hair (again) and gaining weight. I'm always waiting for the other shoe to fall. People don't understand. It's something you just don't get over even if you look normal. All of you are the ones that really get it.

    I've been on the boards sparely, but feel the need to participate more. And it's because ya'll (as we say in the south) "get it."

    Thanks,

    Betty
  • Anonymous
    Anonymous Member Posts: 1,376
    edited November 2006

    Betty, it is UNBELIEVABLE in this day and age that doctor's still don't check out the lumps. My friend's sister in law was in her mid 30's and told she was too young for cancer and that it was probably a fatty cell. She is dead. She had breast cancer and it spread, obviously. By the time she found out, she had about 6 months to live. Disgusting. I am sad for you.

  • Topaz1110
    Topaz1110 Member Posts: 7
    edited December 2006
    Havent been on this site much in a long time, and it is great to see familiar names!
    I was dx Jan 2005, Stage I, 2 cm HER@ and ER +, had lumpectomy 2/7/05, 3 courses of A/C (which ruptured my appendix so no more A/C!) a year of Herceptin.. elective bilat mast with DIEP Jan 2006, going for final stage of DIEP (tatooing) Dec 19. Am in my 2nd year of Arimidex ( I have found TURMERIC capsules really help the joint pain from aromatase inhib!) Effexor helps keep my depression in check. but I still have hot flashes on Arimidex, even tho I went thru menopause before BC.

    Two year anniversary coming up!! It's still scary sometimes... but, know what? I think of it as a mostly positive experience! It was my "sabbatical" from a crazy job and a lot of changes and stress (I am back to the crazy job.. for better or worse).. and I met so many womderful women like all of you! During Tx, had time to reflect and enjoy the simple pleasures in life... Now Im getting so busy, I fear I have lost that calm cenetered place I lived in during active treatment..
    Do you experience this too?
    Thanks to this website and to you all for the life saving support and comraderie during that crazy year of 2005.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited December 2006
    On December 2nd, 2005 I had my last chemo! What a difference a year makes. Last year at this time I was bald, puffy from the steroids, and couldnt walk 50 feet without getting short of breath.

    No I have hair, actually need to spend time styling it now before I go to work. The fatigue is gone and I was actually strong enough to shovel snow yesterday.
  • KariLynn
    KariLynn Member Posts: 1,079
    edited December 2006
    Good for you!!!

    I only had to work up the strength to write a check to the kid who shoveled ours...
  • linny
    linny Member Posts: 204
    edited December 2006
    Dec. 5, 2005 was my last chemo - I agree "what a difference a year makes"

    How did you shovel snow? I always used to shovel the steps and walkway (liked doing it) but am afraid now because of risk of lymphedema on the cancer side (axillary node dissection)

    Linda
  • rmmom
    rmmom Member Posts: 168
    edited December 2006
    Just found this thread.
    I'm class 2005. DX March 2005 on St. Pat's Day. Mast & Recon on April 18th, Weekly chemo June~Nov(or was it Dec?).
    But everything has been great since. I can't get onco to say remission yet-told me I had to wait until Feb 2007.
    But everyhting else is good-I was lucky and got the nice curly hair which came in darker with less gray!
    Linda I know what you mean about shoveling snow-I made the mistake of using the lawn mower one time this past summer-BAD IDEA! I was lucky the swelling went down without any extra problems. So I am staying away from the shovel-but then again I did fly to florida at the last minute when my father-in law died-didn't even think of the sleeve! No swelling at all. So who knows!
    Bev
  • Anonymous
    Anonymous Member Posts: 1,376
    edited December 2006
    Most of you girls know so much about all this, I'm not even sure what some of the lingo means. I don't remember exact dates of anything either. I went through it all in a fog, just now surfacing.
    I know I had a tumor that was found on my annual mammo & it was less than 1cm, but invasive. Oct.05
    Had 2 lumpect. sometime in Nov.05 along with a reduction
    started chemo in Jan 06, was hospitalized with a breast infection soon after that & had to be drained..twice. finished chemo summer 06 and finished rads I think the beginning of Oct.06.
    Last Christmas was a blur so this is better.

    Cheri M.
  • newvickie
    newvickie Member Posts: 3,939
    edited December 2006
    Wow...what a difference a year can make. Merry Christmas 05, you have cancer, Happy New Year, you get chemo, Happy Easter, you get a bilateral mast, happy Birthday you get 6 weeks of rads. Lets hear it for 2007 and moving upward and onward.
    Hugs all
    Vickie
  • purplehaze66
    purplehaze66 Member Posts: 136
    edited December 2006

    HEAR!!! HEAR!!!

  • Katief
    Katief Member Posts: 11
    edited December 2006

    Agreed! I hope 2007 is better for all of us!!!

  • kimmie11
    kimmie11 Member Posts: 30
    edited December 2006
    Hello! 2005!! Exhausted!!! Stage 1 grade 2 er per + her2-. Since then I was finally dx with hypothyroid, started taking meds and feeling a lot better now.
    2006 recouped, dealt with the fear issues.
    2007 I am ready live!
    Happy New Years to all and may there be many more!
    Kimmie

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