sfearl1
Well-known member
If they include it, then they are encouraging you to reconstitute it and use it. That was the reason given for no longer carrying AA.
lol that is ridiculous!!
If they include it, then they are encouraging you to reconstitute it and use it. That was the reason given for no longer carrying AA.
lol that is ridiculous!!
If they include it, then they are encouraging you to reconstitute it and use it. That was the reason given for no longer carrying AA.
poop
There are no sources posted in this thread.
Another one of my stupid questions, I know I've seen it before on this thread but it's such a large thread I can't find it again. But can someone (anyone) explain to me IM and SQ pinning? I know what they stand for but don't know how to derive the two.
Any new news grunt?
40mcg E3D still the best protocol?
10mcg ED good?
Indespensible during post cycle therapy, agree?
Pretty sure 40mcg PWO is going to go systemic no matter what.
Did you read the entire thread or will we have to repeat things infinitely within the thread?
I think the argument bottom-line at where there is mostly an agreement that SOME will go systemic but some will also be taken up directly by the muscle before going into the bloodstream.
Did you read the entire thread or will we have to repeat things infinitely within the thread?
I think the argument bottom-line at where there is mostly an agreement that SOME will go systemic but some will also be taken up directly by the muscle before going into the bloodstream.
Don't be such a d1ck...especially to Xodus. He is one of the nicest guys on here and far from naive.
You started this thread and became a self-proclaimed expert many moons ago. There wasn't then and there isn't now indisputable proof that IGF-1 is directly responsible for muscular hyperplasia in humans. As for localized growth effects that remains wishful thinking...glycogen pumps & inflammation from the acid is all.
You aren't going to get any new muscle tissue in the site you inject in...it is the insulin-like propeties of IGF-1 that are important.
dat.... unless you have proof than your just another opinion. maybe you are the one that needs to start at the top and read the forum. grunt is just passing on his knowledge, i would be frustrated as well if lazy people repeatedly asked the same questions rather than read through the entire forum. those are the same lazy people that want the easy way out at the gym without putting the work in..... let me be the first to tell you, there is no such thing as the easy way out when it comes to getting bigger.
dat.... unless you have proof than your just another opinion. maybe you are the one that needs to start at the top and read the forum. grunt is just passing on his knowledge, i would be frustrated as well if lazy people repeatedly asked the same questions rather than read through the entire forum. those are the same lazy people that want the easy way out at the gym without putting the work in..... let me be the first to tell you, there is no such thing as the easy way out when it comes to getting bigger.
First off, I didn't ask the initial question, nor am I a lazy person and don't like the insinuation much, as I have put in countless hours of reading VARYING OPINIONS on IGF for months, but I was the one that got jumped on for whatever reason.
I suppose I could have just answered the question with 'Jesus, did you read the thread or do we have to repeat ourselves infinitely', but I did not, nor will I ever respond to the countless posts where that response could be used. ie Nolva dosing, etc.
I did NOT state that it goes systemic ONLY. I did NOT state that it is LOCAL only. Even if only SOME IGF goes systemic, it is STILL systemic. I am not disagreeing with muscles worked=receptor's primed for IGF binding, etc. But the question was regarding full body COMPOUND exercises and deciding where to pin IGF. If you shoot 40mcg bilaterally, all of it is not going to stay local, thereby it goes systemic and is viable for up to 72 hours and will hit receptors in other parts of your body that were worked.
I appreciate datBtrue for kind words, he is someone that can have a rational discussion, has a lot of experience/knowledge and I humbly respect his opinion.
First off, I didn't ask the initial question, nor am I a lazy person and don't like the insinuation much, as I have put in countless hours of reading VARYING OPINIONS on IGF for months, but I was the one that got jumped on for whatever reason.
I suppose I could have just answered the question with 'Jesus, did you read the thread or do we have to repeat ourselves infinitely', but I did not, nor will I ever respond to the countless posts where that response could be used. ie Nolva dosing, etc.
I did NOT state that it goes systemic ONLY. I did NOT state that it is LOCAL only. Even if only SOME IGF goes systemic, it is STILL systemic. I am not disagreeing with muscles worked=receptor's primed for IGF binding, etc. But the question was regarding full body COMPOUND exercises and deciding where to pin IGF. If you shoot 40mcg bilaterally, all of it is not going to stay local, thereby it goes systemic and is viable for up to 72 hours and will hit receptors in other parts of your body that were worked.
I appreciate datBtrue for kind words, he is someone that can have a rational discussion, has a lot of experience/knowledge and I humbly respect his opinion.
Thanks for the response XI did NOT state that it goes systemic ONLY. I did NOT state that it is LOCAL only. Even if only SOME IGF goes systemic, it is STILL systemic. I am not disagreeing with muscles worked=receptor's primed for IGF binding, etc. But the question was regarding full body COMPOUND exercises and deciding where to pin IGF. If you shoot 40mcg bilaterally, all of it is not going to stay local, thereby it goes systemic
Apparently it's not worthy of much discussion because it didn't get much responsehmmm the idea of full body compound exercises and systematic use of igf is definitely intriguing. i'd like to hear more thoughts about this.
If you look at the post which you quoted, it starts with "dat" which would be datbtrue. Unless you have 2 handles, the other one being datbtrue, that reply was not addressed to you.
And what's that about 72 hours? LR3 IGF-1 binds to receptors almost immediately. It clears the bloodstream VERY quickly.
tshaw024 said:grunt is just passing on his knowledge, i would be frustrated as well if lazy people repeatedly asked the same questions rather than read through the entire forum.
That's why injecting 250mcg isn't a good idea.Sorry, you are correct, half-life of IGF-1 LR3 is 6-10 hours. I'm not saying that is how long it takes to bind to receptors, but if all are 'local' receptors are filled, it is going to bounce around until it finds a free one (whether that is in your intestines or calves).
Don't be such a d1ck...especially to Xodus. He is one of the nicest guys on here and far from naive.
You started this thread and became a self-proclaimed expert many moons ago. There wasn't then and there isn't now indisputable proof that IGF-1 is directly responsible for muscular hyperplasia in humans. As for localized growth effects that remains wishful thinking...glycogen pumps & inflammation from the acid is all.
You aren't going to get any new muscle tissue in the site you inject in...it is the insulin-like propeties of IGF-1 that are important.
Sorry all, not trying to make this one of "those" postings. But I still don't understand why datbtrue is saying you won't gain any hyperplasia from localized injections??? The results are out there, how do you explain the gains in strength and size people are getting from using only igf-1???
Anecdotal evidence is just that...anecdotal. I would love to see any study that truly proved localized growth.
All I know is that my shoulder healed in few days versus months...
Using what, IGF-II?
I mean if there is risk of growing guts with IGF-1, the risks become certainty with IGF-2.
Is there any info on people useing igf1-lr3 sub q?
I know everything in this thread points twourds using it intramuscular, but I am curious to see if there has been people using it sub q and what thier results were.
Is there any info on people useing igf1-lr3 sub q?
I know everything in this thread points twourds using it intramuscular, but I am curious to see if there has been people using it sub q and what thier results were.
The question is WHY on earth would you want to do that?
Why would anyone NOT choose which tissue they prefer regenerating? And if you need to go systemic you use GH, that way your tendons, cartilage, eyes and everything else get the regenerative drive.
ok,
Im currently in the "being a pussy" stage since I never have injected into the muscle!
zimm
ok,
Im currently in the "being a pussy" stage since I never have injected into the muscle!
What if you were using igf1-lr3 for full body muscle growth. Would you just hit every group of muscles over a several week period , then start from the the first days group and go through the complete cycle again over and over?
Do you have to inject every muscle group including abs,calves and forearms or will they still get good growth over time from a small ammount of igf1 going systematic?
zimm
inject your lagging bodyparts. i personally wouldnt inject abs as so near the gut and dont want to look pregnant.
but yes inject everywhere you want growth directly after training them. I try to be exact with this and it works.
e.g i go to the gym to train calves and quads.
I train my calves then go to toilet and inject them with 12.5mcg in each calf muscle.
then back into gym and train quads, then immediately back to the toilet and inject them both with 12.5mcg.
there possibly could be a systemic effect for other muscles you dont inject but as the gut has so many receptors it prob uptakes most of what isnt used by the muscles.
get some pegMGF to take along with the igf(not at same time) if you want systemic growth of non-injected muscles.
Do you inject E3D, E0D? ED? 40mcg E3D seemed a little on the low side for me. I'm thinkin 60-80mcg ED-EOD.