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This is because both androgens and estrogens suppress GnRH production at the hypothalamus. A SERM stops the negative feedback only from the estrogens. In contrast, at the pituitary the negative feedback on gonadotropin production is mainly from estrogens, and a SERM is effective. Therefore, if GnRH is delivered directly then the pituitary can be coaxed to make LH and FSH, even concurrent with TRT, as described here.I wonder if your side effects from Clomid were mainly due to zuclomiphene? It's a travesty that the FDA did not approve enclomiphene, which would have led to more widespread availability. Having only one legitimate source makes its use a tenuous proposition. Other SERMs may work, but each could have issues. For example, the liver toxicity of tamoxifen.
This is because both androgens and estrogens suppress GnRH production at the hypothalamus. A SERM stops the negative feedback only from the estrogens. In contrast, at the pituitary the negative feedback on gonadotropin production is mainly from estrogens, and a SERM is effective. Therefore, if GnRH is delivered directly then the pituitary can be coaxed to make LH and FSH, even concurrent with TRT, as described here.
I wonder if your side effects from Clomid were mainly due to zuclomiphene? It's a travesty that the FDA did not approve enclomiphene, which would have led to more widespread availability. Having only one legitimate source makes its use a tenuous proposition. Other SERMs may work, but each could have issues. For example, the liver toxicity of tamoxifen.
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