2012 Diagnosed - How are you doing?

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I wanted to see how others who were diagnosed in 2012 are doing? How are your SE's now? What treatments are you on now? Have you lost any 2012 dx friends? It's our 3 year cancerversary, check in!

Comments

  • jlow51
    jlow51 Member Posts: 88
    edited May 2015

    Jojo, I was diagnosed in 2012. Am presently on Tamoxifen after 2 years on AI. It made me nervous coming off AI but Onc said studies show 2 yrs on one and 3 yrs on another was as effective. Am certainly praying it's true!! I would say the side effects on these drugs are about the same. ( I was experiencing some bone loss from AI.) Haven't finished reconstructive surgery yet but am on my way!! Three years makes quite a difference.....there are days I don't even think about BC!! Yay!!

  • Beatmon
    Beatmon Member Posts: 1,562
    edited May 2015

    My initial was Aug. 2012. 2014 found me suddenly a stage 4 with lung mets.

  • jojo2373
    jojo2373 Member Posts: 662
    edited May 2015

    jlow I did 2 years on tamoxifen and now arimidex. The fun never ends.

    Beatmon - sorry to hear of your progression, may I ask how you found out?

  • aussie12
    aussie12 Member Posts: 462
    edited May 2015


    Hi all

    I had left breast mastectomy and have since had reconstruction, tissue expander then implant. I am on tamoxifen . The last 3 years has gone quick.

  • Obxflygirl1
    Obxflygirl1 Member Posts: 377
    edited May 2015

    Diagnosed 8/12. It's been a roller coaster 3 years of emotions. Beatmom is a special sister to me and I think about her all the time. Cancer is still front and center in my brain. . Physically I am doing well

  • Beckers
    Beckers Member Posts: 1,883
    edited May 2015

    I was diagnosed March of 2012. Tried Tami for 10 mos but came off due to SE's. Still trying to decide if I want to try AI's.

  • KrisLiz
    KrisLiz Member Posts: 26
    edited June 2015

    Diagnosed in July of 2012 at age 32. Radiation and Tamox for adjuvant therapies. Stopped the Tamox after a year and half because of SE's (with permission). Life is good despite long term effects of surgery, etc. I'll have my first MRI since getting my implants later this year, so that kind of thing always makes me nervous. I'm three years out, but I feel like all of this just happened yesterday.

  • bcbarbie10
    bcbarbie10 Member Posts: 319
    edited June 2015

    diagnosed feb 2012. Now almost 3 years on tamoxifen. Cancer is not front and center anymore. I try to live as much as I could. Finding menopause horrible, especially the tamox side-effect of joint pains

  • Jennie93
    Jennie93 Member Posts: 1,018
    edited July 2015

    Dx 8/12 also. Made it through active treatment pretty well. Frustrated by lingering issues. Docs all say you will get "back to normal", worlds biggest lie. Made it almost 20 months on tamoxifen, couldn't live with the SEs any longer, trying anastrazole now. Feel like about 90 both physically and mentally. But thankful to be alive, yes. Have lost a few sisters along the way, it is tough.



  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited July 2015

    April 2012 for me. Doing fairly well, scare a few months ago with spine, MRI says just herniated disk, arthritis, stenosis, and degeneration. No cancer. Can live with that!

  • mrenee68
    mrenee68 Member Posts: 383
    edited July 2015

    July 2012 for me, doing well after left mastectomy, with implant reconstruction, right breast lift, and the all important nipple tattoo. No hormone treatment for me, just yearly mammogram with the hopes they don't find anything each year. I don't think about cancer as much anymore, but sometimes it creeps in with some background noise. Take care all!

  • aussie12
    aussie12 Member Posts: 462
    edited September 2015

    Hi all. Just an update. I've just had major surgery for bowel /ovarian cancer. I haven't got full pathology yet, will get that next week. Pretty sure that it's not related to breast cancer but a new one all together. It's been a bit of a shock to get another cancer so soon.

  • wintersocks
    wintersocks Member Posts: 922
    edited September 2015

    Feb 2012, for me. Doing ok, but I am being plagued by constant, unrelenting UTI's. Now waiting for urodyamics testing, I suspect Letrozole and atrophy to be at least part of the problem...

    Have had recon and now waiting for second stage.

    Aussie12, You have had a tough time. Wishing you well.

  • fd1
    fd1 Member Posts: 239
    edited September 2015

    I was diagnosed with Stage IIB in January 2012 at the age of 30. I actually had found the lump in August 2011 but waited until December for a mammogram because of my low "risk profile" and the Canadian system. Because of this, I look at every August as a bit of a milestone also. :) I'm doing very well - tamoxifen and zoladex are not too bad. I still get fatigued at times and my reconstructed (and raidated) breast and arm are tight as hell, despite being very active and doing physio. Oh well - at least I'm alive! Last thing is the hope to take a break from tamoxifen in the next year to have a baby... fingers crossed. Best wishes to all of you.

  • placid44
    placid44 Member Posts: 497
    edited September 2015

    Diagnosed August 2012 at age 44. Doing ok. Periods did not come back after chemo,and that has some side effects. Just had a bone density test today to check for osteoporosis. I have some neuropathy and fatigue. I am trying to exercise more...it helps me feel fitter, but doesn't get rid of the fatigue. I'm better than a year ago, though. Trying to think about "getting out there" as I am single. Good support from this site and a group of us who go to lunch.

  • farmerlucy
    farmerlucy Member Posts: 3,985
    edited September 2015

    Aussie - New dx sucks. So sorry.

    I was dx in Feb 2012. Started tamoxifen a year late (dumb). Did two years then had an ooph and switched to femara. Doing well- busier than ever, smack dab in the sandwich generation. Getting used to menopause and trying to lose weight so my clothes fit again . . . maybe I'll buy new clothes. Hid out from BCO for many months post dx but once I got back on I was hooked.

    Special shout out to my Okie sister Beatmon!

  • Moderators
    Moderators Member Posts: 25,912
    edited September 2015

    We are thinking of you aussie, and so sorry you are going through this. Darn!


  • Moderators
    Moderators Member Posts: 25,912
    edited September 2015

    On another note,

    We would really like to put together a slide show showing all your faces to show the amazing diversity of our community, reaching around the world. Please share with us here https://community.breastcancer.org/forum/135/topic..., or PM us. We may also present this at our annual fundraiser in October.

    Photo (best quality possible)

    Where you live

    Diagnosis

    Your Age

    Quote about how the community/BCO has helped you.

    Thanks Everybody!

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