Done with rads....on to oophr

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jennyboog
jennyboog Member Posts: 1,322
edited June 2014 in Stage III Breast Cancer

Finished rads yesterday, I'm so glad not to be doing that drive anymore but will miss the techs, I had a wonderful bunch of girls.  My last step is the oophr and then I'm done with tx.  Thanks girls for getting me this far.

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  • elmcity69
    elmcity69 Member Posts: 998
    edited April 2011

    Congratulations Jennifer! That is a HUGE step in treatment. I felt so good once I finished the rads.

    I did an oophorectomy October 2010. Piece of cake, compared to the MXs. Mine was laparoscopic - up and around that day. And those little estrogen bombs gone!

    Good luck. You're in my thoughts.

    xo

    Janyce

  • Karina121293
    Karina121293 Member Posts: 370
    edited April 2011

    Good luck Jenny, I had oophr and hyster at the same time with the mastectomy, recovered nice and easy from both surgeries and don't regret and happy to know it's out of the way, I am still thru my chemo tx though, then rads. Cant wait to be done as well. What a journey!!!!! Huh!!! Hugs and the best.

    Karina 

  • Bugs
    Bugs Member Posts: 1,719
    edited April 2011

    Whoot whoot!  Congrats on finishing!  My ooph was a piece of cake (also laparscopic).  Do something nice for yourself to celebrate being done with rads!

  • karen1956
    karen1956 Member Posts: 6,503
    edited April 2011

    Congrats on finishing rads....I had my ooph done laprascopic as did Cindy....recovery was fairly easy....fatigure was the biggest issue....took a week off work......no real pain...

  • Fearless_One
    Fearless_One Member Posts: 3,300
    edited April 2011

    My hyster/ooph was a cakewalk - SO much easier than my mastectomy.   Try to do it robotic/laproscopic if you can.

  • Pure
    Pure Member Posts: 1,796
    edited April 2011

    Yeah!!! So happy for you:) The oomph is the easy part - you shouldn't have a problem.

  • KiwiMum
    KiwiMum Member Posts: 704
    edited April 2011

    Hi ladies

    Just had to google what a ooph was. I now know and realize I am scheduled for this post chemo and rads. Seems a long way away - 8 months. I'm glad I've found this thread as it sounds like it's not as horrible as I'd imagined.



    Still trying to get my head around chemo and rads. I think I'll "park" thinking about ooph for now.

  • KerryMac
    KerryMac Member Posts: 3,529
    edited April 2011

    Congrats Jenny! You're nearly there!!

    I had my ooph a couple of weeks after finishing rads, had it laproscopically too, it was pretty straight forward, and I recovered pretty quickly. You should have no problems.

    And you will not miss all those dr appointments! 

  • americanpinay
    americanpinay Member Posts: 338
    edited April 2011

    Hooray!  Congrats Jenny! Good luck with ooph.  It's not part of my treatment so no advice about that. Take care.

  • AnacortesGirl
    AnacortesGirl Member Posts: 1,758
    edited April 2011

    Had my ooph last October.  The hardest part was waiting from 9:00 am till they finally called me in at 5:00 pm.  No eating all day!  They offered an overnight stay since it was late and we had a two hour drive home but I was more than happy to have hubby drive me home even if it was late!  It was easy and it was great to have it done because it marked the end of treatments. Good luck!

  • motherofpatient
    motherofpatient Member Posts: 240
    edited April 2011

    talked to my daughter's onc yesterday about this - if I may ask, how old are all of you? She is 43. Doc seems a bit old school on this issue but since he even admits that AI's are better than Tamox, I don't get his hesitation. I had no issues with menopause since I had a hysterestomy at age 29 and never knew when my periods stopped - no hot flashes, maybe because I was on Prozac. What has your experience been? Seems it is safer to get them out and stop the estrogen.

  • jennyboog
    jennyboog Member Posts: 1,322
    edited April 2011
    I just turned 35, I am doing it for the ER benefit but also I'm BRCA+ & I stand a higher chance of developing ovarian cancer so, it's a kill two birds with one stone for me.  I'm on AI's and it's my understanding they are better than tamox or at least if you switch to them after a couple years of tamox.  I think also it might be how much ER+ you are, I'm 80% so I would benefit but someone who might let's say be 10% might not benefit as much and the AI"s might do the trick for them.  Not sure exactly hope you get some real answers and a dr who might be a bit younger Laughing  Take care. 

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