I am taking 100mg var and 50mg winny orally ed. I was thinking of 100mg var, 50mg winny and 40mg chlorodihydromethyltestostoerone in a phlojel (100mg,80mg/ml and using 1ml/day), and 150mg primo depot EOD. Want to beable to get hard do I need HCG?
HCG might help but probably not.
Also what is the thought process here with 3 methyls? If you are going ot be pinning the primo anyway why not use another injectible rather then overloading with orals?
Mr.50
Why put in phlojel? The orals you plan to compound are orally bioavailable in a much higher percentage than transdermally. BTW, too much oxandrolone IMHO.I am taking 100mg var and 50mg winny orally ed. I was thinking of 100mg var, 50mg winny and 40mg chlorodihydromethyltestostoerone in a phlojel (100mg,80mg/ml and using 1ml/day), and 150mg primo depot EOD. Want to beable to get hard do I need HCG?
What do you think the winny in phlojel will do for you that the oral winny won't, agent8?I might just do 100mg/day var, 50mg/day winny oral, 50mg/day winny phlojel for 6 weeks on, 20 days IGF-1, then back to anabolic steroids's and repeat for as long as I can stand it. I've also been taking CJC 1295, slin, T-3/T-4, and PLCAR.
What do you think the winny in phlojel will do for you that the oral winny won't, agent8?
I might just do 100mg/day var, 50mg/day winny oral, 50mg/day winny phlojel for 6 weeks on, 20 days IGF-1, then back to anabolic steroids's and repeat for as long as I can stand it. I've also been taking CJC 1295, slin, T-3/T-4, and PLCAR.
Actually, it's the opposite. Injecting winny gives you more available because it avoids first pass degradation. Meaning there's a higher blood serum level than if it had been taken orally. But still the entire dosage - whether taken orally, IM, SQ, transdermally, or however - still has to be metabolized by the liver. So you actually increase bioavailability by injecting it, but you don't reduce liver stress (although liver stress is not equivalent to liver damage and is severely over-rated).
Again, this is not a good idea. Too much var, pointless phlojel, and frankly none of it makes sense. What is the desired effect for this cycle? What are you using insulin for? And t3 as well as t4? Please research all of this more. This is a pretty risky combination of drugs you've got. Beyond that running something "as long as you can take it" has never been a good idea. In fact in all seriousness, this is one of the worst ideas for a cycle I've ever seen.
IM is slightly faster, and the IGF release is a theory only. Not to mention that little big of IGF released wouldn't be enough to matter. Drop that concept, man.I thought oral wiiny acts faster than IM and causes an IGF-1 release better than IM.
IM isn't less harsh on the liver. Did you read ANYTHING I have posted?I was thinking using with phlojel would be similar to IM and would be less harsh on liver
Half life is the same regardless of route of administration between oral vs. IM. That concept is totally flawed.and has an extended half life over dosing orally (9hr orally and 1 day IM).
IM is slightly faster, and the IGF release is a theory only. Not to mention that little big of IGF released wouldn't be enough to matter. Drop that concept, man.
IM isn't less harsh on the liver. Did you read ANYTHING I have posted?
Half life is the same regardless of route of administration between oral vs. IM. That concept is totally flawed.
Good idea, but make it bold base for greater bioavailability.
I'm pretty sure that the smaller the molecule the better when it comes to transdermals.Would the base be significantly more bioavailable than the prop. Phlojel claims it transports tests up to but not including enanthate ester. So that would be one carbon less than eneathate. Another thing is I get steroid powder so cheap I really don't care about waste unless it is primo.
I'm pretty sure that the smaller the molecule the better when it comes to transdermals.
And prop is 3 carbons long, while enanthate is 7.