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by fnordpiglet
1484 days ago
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You should investigate clomiphene citrate instead of testosterone directly. Clomid mutes the brains response to estrogen, the final feedback product of the testosterone cycle. This causes the body to produce more testosterone in the testes rather than front loading the cycle. The primary impact is your testes continue to function, while testosterone over time will chemically castrate you. This has been in use for 60 or so years but isn’t an FDA approved use of clomid. The primary reason is clomid is cheap to produce and not patented. It’s extremely safe and if you shop around you’ll find a urologist that’s aware of it and will prescribe it - but most urologists get marketing benefits from the rather expensive testosterone replacement products so not all are either aware or are willing to forego the lucrative marketing funds. I switch to this about 10 years ago after starting testosterone for a few months. I wanted to have kids and I was very worried. I researched the biological processes for testosterone and stumbled on clomid as a relatively well known but unmarketed low T therapy. I went to a top urologist at NYU and he ranted about urologists that don’t use clomid. He gave me a prescription and it worked like magic. Two years later I had my first kid. I still take it at a low dose because I feel great. My testosterone levels are high normal range. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5182219/ https://en.m.wikipedia.org/wiki/Clomifene (other uses section) |
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In my opinion it would be much safer to suggest recombinant FSH and LH. The brain testes axis seems to have the least amount of atrophy over time from anecdotal experiences of those online and in a few case reports. I do not think HCG should be used long term due to the non-bio identical nature, but it is a good short term LH mimic if my memory serves me correctly. Would be a great addition to a TRT protocol.