MESO "Specialized" Testing Group Fund

Some recent WWB Tren A. Lighter than Primal’s. Received a broken vial so excuse the photo.
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We are trending right. Keep going!

epic fail falling GIF by WWF_UK
 
this is or toss it.
Keeper! Definitely promoted to additional testing with Jano to see what we could find with GCMS? Maybe analyze alongside dark orange vial to see what we could detect?

Unclear to me what kinda concentration of quinone functionality is in the really dark stuff. Or probably other degradation products as well?
 
The question is whether tren has a negative rep due to tren or the shit that gets made when it is heated in oil with oxygen around?

Surely someone has figured this out?

Anyone use original parabolan by Negma? What color was it? How was it brewed? Genuinely curious.
All steroids are toxic due to Reactive Oxygen Species. Testosterone is less toxic due to aromatisation. E2 reduces some of the effects of ROS in tissues.

This is why synthetic androgens are more toxic. The stronger the androgenic/anabolic action the stronger the toxicity. Type2x covered this in his latest podcast.
 
All steroids are toxic due to Reactive Oxygen Species. Testosterone is less toxic due to aromatisation. E2 reduces some of the effects of ROS in tissues.

This is why synthetic androgens are more toxic. The stronger the androgenic/anabolic action the stronger the toxicity. Type2x covered this in his latest podcast.

 
Never had yellow tren like that. Only amber

I've seen ranges in the amber/yellow spectrum, and they all worked like a charm

Not saying I would notice if it was -10%, but I'd definitely notice if it was -90%

Moral of the story: I don't know if color has a meaningful impact on the effects of tren, but if it does it's not a very meaningful impact
 
Not at all. Let's remember that Parabolan was sold at 76.5 mg approved for human use, a dose corresponding to 50 mg of trenbolone, similar to the 50 mg of Organon's Deca Durabolin. Do you think it would have been approved if, in trials and during use, potential users (men, women, and children) had experienced the severe side effects associated with trenbolone today? The answer is obvious. On the other hand, let's remember that the production of injectables by a pharmaceutical company doesn't use the same temperature as those who produce raw materials at UGL. Pharmaceutical companies, by having a sterile environment, their production process reduces the rate of oxidation that could occur. That said, even so, since trenbolone is so susceptible to oxidation, it will usually present a variable oxidation rate, which will cause greater or lesser side effects, that is, an increased pulse rate, night sweats, a probable mitochondrial uncoupling effect, greater stimulation of the nervous system, greater neurotoxicity, and greater organ toxicity. It is true that oxidized products can promote lipolysis or energy expenditure due to this overstimulation of the nervous system (increase in strength), but not in terms of their anabolic potential.
Where did this guy come from. Good stuff.
 
Not at all. Let's remember that Parabolan was sold at 76.5 mg approved for human use, a dose corresponding to 50 mg of trenbolone, similar to the 50 mg of Organon's Deca Durabolin. Do you think it would have been approved if, in trials and during use, potential users (men, women, and children) had experienced the severe side effects associated with trenbolone today? The answer is obvious. On the other hand, let's remember that the production of injectables by a pharmaceutical company doesn't use the same temperature as those who produce raw materials at UGL. Pharmaceutical companies, by having a sterile environment, their production process reduces the rate of oxidation that could occur. That said, even so, since trenbolone is so susceptible to oxidation, it will usually present a variable oxidation rate, which will cause greater or lesser side effects, that is, an increased pulse rate, night sweats, a probable mitochondrial uncoupling effect, greater stimulation of the nervous system, greater neurotoxicity, and greater organ toxicity. It is true that oxidized products can promote lipolysis or energy expenditure due to this overstimulation of the nervous system (increase in strength), but not in terms of their anabolic potential.
This explains a lot. I ran Tracy's tren ace which was smooth as for about 7 weeks at 10-15mg a day.

It was amazing shit. No night sweats, no appetite issues, LFT were pretty good. I think I went a bit loopy on it lol

But besides the mental issues it was pretty amazing. My creatinine actually went down on my blood tests. It was a very very pale yellow. Not much darker than nandralone.

I basically felt "on" 24/7. Nothing would stop me lol

Not sure it's something you can run for long without going manick. Maybe genetic susceptibility plays a role.
 

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