I dont think it will be an advantage to do so.What concentration is it at? 1mg/ml?
I wish you luck, and am really looking forward to hearing your results.
I made it at 2mg/ml, i will definitely post my results.
with the active life of this drug being around 4-6hours, what type of dosing schedule would be "best"?
i too will be on 2mg/day for ~2 weeks.
i was thinking of taking 1mg upon waking, and 1mg (1.5hr) pre workout....
thanks in advance.
It has already been discussed recently that multiple dosing of 17AA is not necessary. Not only has it been shown that receptor and ligand are recycled in the nucleus of tissues, that administration of AAS is a two-compartimental model (not capable of being monitored by half-life), the most important finding in this regard is that less thanb 10% of administered steroids (17AA or not) orally is excreted in 24h.
Good things come to those who weight.
The Big Cat is a researcher and theoreticist. His advice must never be taken in the stead of proper advice from a medical professional, it is entirely intended for research purposes.
thanks for the quick reply.....!!!!
so taking the full dose 1-2hrs. before workout would be most efficient?
It has already been discussed recently that multiple dosing of 17AA is not necessary. Not only has it been shown that receptor and ligand are recycled in the nucleus of tissues, that administration of AAS is a two-compartimental model (not capable of being monitored by half-life), the most important finding in this regard is that less thanb 10% of administered steroids (17AA or not) orally is excreted in 24h.
That is extremely interesting, where was this discovered?
That is extremely interesting, where was this discovered?
I have one specific reference, but you`ll have to w8 till I get home to post it. In the mean time, almost any GC/MS study for any steroid will confirm this.
Good things come to those who weight.
The Big Cat is a researcher and theoreticist. His advice must never be taken in the stead of proper advice from a medical professional, it is entirely intended for research purposes.
It has already been discussed recently that multiple dosing of 17AA is not necessary. Not only has it been shown that receptor and ligand are recycled in the nucleus of tissues, that administration of AAS is a two-compartimental model (not capable of being monitored by half-life), the most important finding in this regard is that less thanb 10% of administered steroids (17AA or not) orally is excreted in 24h.
How about the negatives ?
Is multiple dosing better or worse if we consider liver/organ toxicity ? Is there an increase of aromatization or 5a reduction ?
are you referring to the oral form? what about regular injectable tren/fina??
The best place for it is in the glutes.
Seabiscuit Hogg is a fictious internet character. It is not recommended that you receive medical advice from fictious internet characters.
SBH :)