JoeKool’s story: Long term HCG

@Joekool my questions would be:

  1. How could this work if someone has detectable LH since LH should accomplish the same thing (my LH came back mid-range)?

  2. Why does high hCG not replenish these neurosteroids? Time? Shouldn’t any 6-month sustainable hCG protocol do the same?

My opinions are

  1. Though HCG is an LH mimetic, it’s not LH. There appears to be extra benefits to hcg over LH. That’s an important distinction that even I’ve been known to use interchangeably.
  2. I think high dose actually overwhelms neurosteroid receptors as well as over does it on the sex hormones. Even at this low dose, some ppl are experiencing high estrogen levels.
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Hey Joe, What do you think of this Estradiol and LH level before starting HcG?

TESTOSTERONE 21.7 nmol/L
PROLACTIN 11.0 ug/L
ESTRADIOL 42.0 pmol/L
FOLATE 6.8 nmol/L
CRP 0.5 mg/L
TSH 2.39 mIU/L
T4 FREE 13.0 pmol/L
LH 5.1 IU/L
FSH 7.0 IU/L
SHBG 46.0 nmol/L

it won’t tell anything imho, blood levels don’t matter. But brain is a different story. Brain enzymes and brain hormones whats important

So are you telling me that the fact that my plasma 3b-diol is low and my urine allopregnenolone is high is not important?

Before assuming you are right consider this:

3b-diol is a potent estrogen receptor beta agonist. I get worse when I inhibit estrogen. I get better when I increase estrogen. Even though you are correct that my plasma 3b-diol levels are probably not going to match up with my 3b-diol CNS levels. But that does not mean my plasma 3b-diol levels are not important. Low plasma 3b-diol levels tells me that my 3b-HSD enzyme is converting low amounts of DHT into 3b-diol. Otherwise I would have higher amounts of 3b-diol in my blood if my 3b-HSD enzyme was converting higher amounts of DHT into 3b-diol. So low plasma 3b-diol levels is giving me a clue as to the status of my 3b-HSD activity.

Here is another example:

I don’t know my CNS allopregnenolone levels. But I do know that melcangi’s PFS study found low allopregnenolone in the CNS of the PFS group. I also know that my urine allopregnenolone is high. So based on this information I can make an educated guess that maybe allopregnenolone is low in my CNS as well because I’m getting rid of high amounts of Allopregnenolone in my urine which is excretory.

Maybe my body is excreting high amounts of allopregnenolone because it needs to get rid of it for a reason possibly pointing to an issue with the GABAa receptors in the brain. Because allopregnenolone in the CNS is a positive allosteric modulator of the GABAa receptor. So If there is too much action on the GABAa receptors body may be peeing out as much Allopregnenolone as possible so that the allopregnenolone does not make it to the GABAa receptors. Additionally my plasma
3a-diol is low and my urine 3a-diol is high. My DHT is not even converting to 3a-diol in high amounts in spite of my body peeing out high amounts of 3a-diol. This tells me that my body also wants to get rid of high amounts of 3a-diol which is also a potent GABAa receptor positive
allosteric modulator.

My point is that you are thinking one dimensionally and can’t make the same educated guesses I can because you don’t know your urine allopregnenolone levels or your blood 3a-diol or 3b-diol levels. I understand that you read somewhere else on this forum “that only CNS levels are relevant” but someone else posted that who also thinks one dimensionally. I’m working on that 4th dimensional level thinking. Humans will likely never see the 4th dimension but I’m certainly not going backwards…

Anyway back to Joe’s protocol :smirk:

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Hej @NewYorker how are you doing my man?

seems like HCG can downregulate AR, but thats in female mice.

To gain an insight into potential roles of AR in this tissue, we demonstrated that eCG treatment increased AR expression in a time-dependent manner and subsequent treatment with hCG decreased AR expression in mouse fallopian tubes

Hello, and sorry for the delay in responding. I should be finishing the hCG injections in a couple of weeks. Overall, improvements are in the same areas I listed before, but still no real feelings of desire. I have a series of labs I’ll be organizing and posting, with the main improvement being testosterone numbers increasing substantially. I did feel the improvement for a few weeks, but I either got used to it, or it wore off. This pfs rollercoaster ride seems never ending.

I am under the guidance of an endocrinologist, and am meeting with him again March 6th. I’ll have another lab before meeting, and will include that and more detail soon.

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Thanks for you report Bro.

Have you improve skin quality and oil?

Recovery may come after you finish the cycle, who knows, fingers crossed, keep your hopes up. Thanks for sharing.

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How certain is that this guy actually had PFS indeed?
Sounds too beautiful to be true…,or is HCG The thing to try?

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@NewYorker Any updates? How is your hcg protocol going?

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Hi bro, what are you doing?

Are you cured?

I had an injury due to weak penile tissue at the week of my crash in Oct of 2016 and that’s filled out too.

What kind of injury?

He unfortunately failed HCG and is currently trialing Xyosted - subq injectable testosterone ethanate

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He reported improvement with hCG so it is welcome. I would paid money for his improvements

Can anyone PM me a reputable site to purchase hCG?
Going with a script is a useless effort…

Facts!! Neurological damage, same way the penile and prostate tissue is damage giving men ED vascular issue and a low amount of semen with weak pressure.