kezmusc
8 years agoMember
Question on Tamoxifen vs Zoladex and Exemestane. Does this s**t ever end?
Hi everyone,
This is my first posting here. I have read and gained so much from the many postings, wisdom and inspiration from everyone on this forum and for that I have to say thankyou. The information contained within this network, I believe, far outways what most doctors can tell you. I guess that's because they really don't involve a lot of the emotional side of the treatments and how that effects every aspect of your life for so long.
So I am eight months into the battle after being diagnosed with stage 2 invasive carcinoma (of no particular sort aparently) + DCIS with 5 of 24 lymph nodes positive ER/PR + HER2neg.
I've had lumpectomy, re excision to gain clearer margins, 4x AC and 12 paclitaxol (manged to keep my hair thanks to cold capping YAY!) and am on number 14 of 30 sessions of radiation.
So my question is:
Saw my oncologist the other week who, up until then, had only ever mentioned doing 10 years (OMG) of Tamoxifen after everything else is finished. Then on my last visit decides that Zoladex monthly injection and exemestane tablets for 5 years is the way to go although he couldn't really tell me the success rate of one verse the other.
You should get a laugh out of this.......(my Dr is Indian and sometimes things get a little lost in translation) So with a big smile on his face claims the Zoladex will "castrate" me and would be the best option..............wow......if I hadn't nearly fallen off my chair laughing I would have burst in to tears (which I did as soon as I left his office).
Has anyone had any experience with this combination? Seriously, I am already getting 20 -30 hot flushes a day, wake up 5-10 times a night due to overheating along with all the other usual things your body does when suprisingly has all its female hormones shut down unexpectedly.
There seems no end to treatment. I would be keen to also hear if anyone knows any natural ways to lower estrogen as an alternative to years of hormone blockers?
Thanks for listnening.
This is my first posting here. I have read and gained so much from the many postings, wisdom and inspiration from everyone on this forum and for that I have to say thankyou. The information contained within this network, I believe, far outways what most doctors can tell you. I guess that's because they really don't involve a lot of the emotional side of the treatments and how that effects every aspect of your life for so long.
So I am eight months into the battle after being diagnosed with stage 2 invasive carcinoma (of no particular sort aparently) + DCIS with 5 of 24 lymph nodes positive ER/PR + HER2neg.
I've had lumpectomy, re excision to gain clearer margins, 4x AC and 12 paclitaxol (manged to keep my hair thanks to cold capping YAY!) and am on number 14 of 30 sessions of radiation.
So my question is:
Saw my oncologist the other week who, up until then, had only ever mentioned doing 10 years (OMG) of Tamoxifen after everything else is finished. Then on my last visit decides that Zoladex monthly injection and exemestane tablets for 5 years is the way to go although he couldn't really tell me the success rate of one verse the other.
You should get a laugh out of this.......(my Dr is Indian and sometimes things get a little lost in translation) So with a big smile on his face claims the Zoladex will "castrate" me and would be the best option..............wow......if I hadn't nearly fallen off my chair laughing I would have burst in to tears (which I did as soon as I left his office).
Has anyone had any experience with this combination? Seriously, I am already getting 20 -30 hot flushes a day, wake up 5-10 times a night due to overheating along with all the other usual things your body does when suprisingly has all its female hormones shut down unexpectedly.
There seems no end to treatment. I would be keen to also hear if anyone knows any natural ways to lower estrogen as an alternative to years of hormone blockers?
Thanks for listnening.