Ateam2023
Member
1 vial of @TheLobster orange top hgh from the july promo,, 

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Thanks, very interesting. So theoretically young people can get the most anabolism out of very high igf-1 levels mit minimal risks for acromegaly?There's no basis to think IGF receptors decline evenly in every part of the body any more than androgen or any other receptors. This isn't a theory, it's clear from animal and human tissue analysis.
“The extracellular part of the IGF system is complex with various receptors, ligand effectors, high-affinity IGF-binding proteins, proteinases, and endogenous inhibitors that all, along with their biological context, must be considered”.
"Biological context" is referring to the IGF signaling system functioning differently depending on the specific tissue.
Receptor quantity can change in specific tissues because of other factors as well. Higher free testosterone levels increase the amount of IGF receptors in muscle:
“Testosterone concentrations were positively correlated with IGF‑I receptor mRNA levels in skeletal muscle..."
I'm 40 and using any sort of GH shoots my RHR like 10-15 points. I can have a low BP on deca and tren but injecting GH is like injecting pure liquid meth.Since nobody else has answered, if 2 iu gave me 372 IGF-1, I would probably stay at 2 iu. That is a really good number.
Did I read correctly that your natty number was 299?
There's no basis to think IGF receptors decline evenly in every part of the body any more than androgen or any other receptors. This isn't a theory, it's clear from animal and human tissue analysis.
“The extracellular part of the IGF system is complex with various receptors, ligand effectors, high-affinity IGF-binding proteins, proteinases, and endogenous inhibitors that all, along with their biological context, must be considered”.
"Biological context" is referring to the IGF signaling system functioning differently depending on the specific tissue.
Receptor quantity can change in specific tissues because of other factors as well. Higher free testosterone levels increase the amount of IGF receptors in muscle:
“Testosterone concentrations were positively correlated with IGF‑I receptor mRNA levels in skeletal muscle..."
Ok so we have normation problem meaning the samplesize isnt big enough to get an actual represtation of the populatiom and therefore the standarddeviation (SD) or to be more accurate the absolute numbers are very large.The problem here is a statistical one. The relationship you seek to normalize/standardize lacks a proper population distribution to validate said assumptions.. It's one thing to know how a pathway works in isolation. It's another thing to determine how the same pathway works or whether the same outcome always occurs when it's located in a 'system soup'. It's why some of these arguments will continue till someone gets permission to do wider testing.
You can even see that in one of the articles Ghoul shared:
I don't know about minimal risk, but youth is better for anabolism generally. How that relates to exogenous HGH use is also another kettle of fish. Young people with great IGF levels may do well avoiding HGH, not because of acromegaly, but other comorbid conditions that may arise with GH excess.Thanks, very interesting. So theoretically young people can get the most anabolism out of very high igf-1 levels mit minimal risks for acromegaly?
Yes, smaller sample sizes tend to widen confidence intervals for the true values of population measurements/parameters.Ok so we have normation problem meaning the samplesize isnt big enough to get an actual represtation of the populatiom and therefore the standarddeviation (SD) or to be more accurate the absolute numbers are very large.
Normal range should typically be +/- 1 SD which would include 68% of the population or 2 SD meaning 95% assuming its a normal distribution.
If the sample is to small the absoolute numbers and therefore the absolute range will be a lot larger.
Thanks, very interesting. So theoretically young people can get the most anabolism out of very high igf-1 levels mit minimal risks for acromegaly?
In your opinion. probably a bad idea to use large doses over 40? Is 1-2 iu safe?
But if hogh amounts of igf-1 receptors mean that in young people the same amount of igf-1 wont result in acromegaly like in older people not only does this mean that igf-1 is more anabolic for them but also parallel the risks of acromegaly are lowerI don't know about minimal risk, but youth is better for anabolism generally. How that relates to exogenous HGH use is also another kettle of fish. Young people with great IGF levels may do well avoiding HGH, not because of acromegaly, but other comorbid conditions that may arise with GH excess.
I will actually do some bloddwork this summer and see what my igf-1 level on 3x daily CJC no dac and GHRP-2 is as i have the feeling it will be higher than on 4 IU of GH.Yes, smaller sample sizes tend to widen confidence intervals for the true values of population measurements/parameters.
However, biology is funny. The wide range itself might be a true natural phenomenon...
If it was narrower though we might have seen more incidences of acromegaly presenting for treatment even if the patient denies hgh use. (speculation on my part). (The problem of acromegaly is not just the bony changes. There are a lot of systemic and multi organ disorders that will force a hospital visit)
So leaving all the other things aside, my take home is that:
1) people with acromegaly tend to have higher levels of IGF-1,
2) researchers based on available data have guidelines on IGF levels to medicate those on therapy with a goal of avoiding acromegaly or other unwanted effects.
3) We can use these guidelines to stay safe. Some can also skirt it and escape the consequences, come here and post about it, and it may be a true reflection based on where they fall in the (unknown) true distribution, despite how such posts may infuriate people. Arguing with them by throwing what is currently known therefore, will be at odds with their experience..
Some of us for example had better IGF on (dodgy QSC) Tesamorelin and CJC/IPA and lower IGF on 3IU QSC HGH. It may be bunk GH, it may be individual respose to IGF, it maybe blood vs muscle IGF level disparity, it may even be other issues like lack of rest, how GH is being dosed in relation to eating habits, or it may be age.. e.t.c
For example? ( Im not questioning it im just truly curious as everybody is talking about GH-head but besides examples like Stallon i rarly see any pictures. And with stallon, well aging is a confunding variable)Well, we have all seen young professional bodybuilders look drastically different in the face while still at a young age . . .
I was just trying to point out that there are other possibilities to worry about. There are more rapidly proliferating cells in youth that should be allowed to die out in apoptosis.. GH can prolong the life span of these cells or make them multiply more rapidly.. causing a host of issues, from developing larger organs, to stimulating tumors and cancers, to even messing up other hormones. These things are just as common as acromegaly..But if hogh amounts of igf-1 receptors mean that in young people the same amount of igf-1 wont result in acromegaly like in older people not only does this mean that igf-1 is more anabolic for them but also parallel the risks of acromegaly are lower
This is dreaming.3x daily CJC no dac and GHRP-2 is as i have the feeling it will be higher than on 4 IU of GH.
This is dreaming.
jfc man, that is really high, how much ius are you doing? Probably a "good responder" i take it,,Recent results
I dunno man..This is dreaming.
Currently 6 units and yes great responder. I've always seen good results with IGF1 I need to do GH serum next time thoughjfc man, that is really high, how much ius are you doing? Probably a "good responder" i take it,,![]()
Currently 6 units and yes great responder. I've always seen good results with IGF1 I need to do GH serum next time though
