DunkoroChitlu
New member
Thanks for your detailed answer. It completely makes sense what you're mentioning.When ralox binds with the ER in breast tissue, it acts as an antagonist. Meaning it bonds with but has little to no interaction with the er.
Taking this for months will in a sense, de sensitize the er.
Then when you stop the drug, that ER is now open and for your estrogen to bind with.
So you’ve went say 1,2,3 months with no interaction, the estrogen comes along and bonds with, and interacts it’s gonna be like taking that first sip of your favorite beverage after 3 long months…and begin doing what estrogen does.
And that’s not even taking into account how your hormones look at baseline.
All natty, never touching anything.
Gyno is a mix of multiple hormonal imbalances going on that start by touching anything that disrupts your hptga, from test, estrogen, to hgh, prolactin, etc.
Maybe this thread will help.
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However if you check my blood reports, my estro is relatively low (about 14 out of the 39 which is on the high side of the range). So not sure how gyno grew with such low estro in blood? Maybe it had to do with the sensitivity when removing Ralox, that every estrogen particle (even if low quantity) would bind to the tissue.
Or that or my high testosterone levels (near high end of the range) was aromatizing.
So it makes sense to run an IA at the end of the Ralox cycle and continue it after the Ralox cycle as well to avoid high test circulation.
It's a bit confusing.