Hooray ! and a note on Arimidex......

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WOW.....thanks to the administrators for seeing this need and giving us what all of us need and have found such happiness in . Thank you thank you thank you !!!!!

I mentioned the studies I am eligible for a few days ago and I am 99% sure Im going to the one next week that is specifically on post radiation and AI inhibitors specifically Arimidex and Femara etc.....also they are supposed to discuss the new drugs and treatments that are on the horizon....if I get to go, I will have notebook in hand and I will take notes so I can share the important stuff with all my *seasoned and wonderful friends*

Thanks again for *THIS*

Comments

  • Deb-from-Ohio
    Deb-from-Ohio Member Posts: 1,140
    edited March 2009

    WOW Thanks to the Admins!!!!!!!!!!!!  and I will be waiting on the Arimidex info too as I go on that after radiation in 2022............well it seems like it anyways!

    Deb

  • ritajean
    ritajean Member Posts: 4,223
    edited March 2009

    Jan,  I think we all are interested in the Arimidex info.  Thanks for offering to share!

    Rtia

  • swimangel72
    swimangel72 Member Posts: 1,989
    edited March 2009
    Wow - this is great! Thanks administrators! And Jan I look foward to any information you share with us!Smile
  • Maire67
    Maire67 Member Posts: 768
    edited July 2010
  • Mamie2
    Mamie2 Member Posts: 108
    edited March 2009

    Me too. I'm interested in s/e's of Arimidex. I see my mom who is 88 on it, and she swears she has no side effects except some thinning hair, but i was talking to one of my "real" life friends tonite and she said when she was on it and tried to have "sex" it was very painful. The Arimidex made her very, very dry, so now she has a diaphragm like thingie that actually replaces some lost estrogen. I wonder if that is safe!! There is so MUCH to learn... 

  • Mandy1313
    Mandy1313 Member Posts: 1,692
    edited March 2009

    This is just a thought and I do not have hard studies on it.  Mamie2 said her 88 year old mom does not have Arimidex se.  Part of what Arimidex does is to deplete estrogen so we are like an 80 year old. Perhaps Mamie2's mom already is mostly there so she is not having all of the negative side effects of a younger person. It is just a thought, not scientific.

  • donsuzbee
    donsuzbee Member Posts: 129
    edited March 2009

    Yes, yes!! Hooray!!!!!

    I, too, suppose ladies in their 80's are more used to less estrogen? possible???? But I know a lady in her 80's that is having side affects from Femara. Mainly the depression.

    I was on Femara and then Arimidex for 7 years. Went off July 2007. Had just had a kidney removed due to renal clear cell carcinoma - not a metatasis. I thought the adrenal had been taken with the kidney - that is what the surgical notes said. But a later PET showed them still intact. So I assumed I then only had 1 set of adrenals. I still did not go back on as by the time I found out I still had the 2 adrenals I was 7 months off ht. I had realized by then I was doing better with the depression and aching in my legs. At age 68, if ht has not done it's thing, I figure it's not going to. I have a lot of pain from lymphedema and radiation scarring, etc. Enough is enough!

    I keep thinking we are the pioneers: first to actually live any length of time following breast cancer, first to go on the hormone therapy, even first to be living longer. In some ways it is exciting to be a part of "medical research."

    God bless!!!!!

    Susan B.

  • Pegk
    Pegk Member Posts: 389
    edited March 2009

    I will be 57 next month and I've been on Arimidex for 3 years. My SE have not been too terrible, just a bit sluggish when I get up in the morning. Do I remember how I felt before BC?  After the trauma  of surgery, chemo and radiation, I guess I'm happy to be alive.

  • nelia48
    nelia48 Member Posts: 539
    edited March 2009

    After all the trauma of chemo, surgery and radiation, I'm not sure if how I feel is because of the Arimidex or if I just need to some time to get back on my feet.  I do have to say that I never had High BP before, and it has really been out of control since starting on the Arimidex!  Cora

  • hmm
    hmm Member Posts: 2,183
    edited April 2009

    I thought "samedaynurseJan" was going to share the results of the Arimidex meeting with us???? Or is it posted somewhere else?

  • samedaynurseJan
    samedaynurseJan Member Posts: 192
    edited April 2009

    the Arimidex meeting was rescheduled for a night that I couldnt get off of work it was my late night and I did post that on the main *older* board, Im sorry, I didnt realize anyone was waiting for it......there will be another entire series in May and I have already told the people at Loyola that I am going to clear my schedule and do the entire thing, of which I will share everything I can with anyone who wants the information.

    As for myself thus far, I am only on Arimidex 3 months and realize this isnt a fair assessment but so far no problems at all (save for some mmmmm digestive problems which I am pretty sure I have solved) so Im hoping to be able to say the same thing several years from now.

    Again Im sorry....but I will have the information later this spring.

    Jan

  • hmm
    hmm Member Posts: 2,183
    edited April 2009

    Jan,

    Thank you for responding. Will look for your "report" in May................ I also started Arimidex the middle of December and so far am doing fine with it....hope also that this continues to be the case. Again thanks for posting.

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