Please Scroll Down to See Forums Below My friend is doing between an 8- 10 week cycle of deca by itself. He understands that he is at risk of getting deca ****. But does not want to stak it with test, because of the sides. also he is not looking to become massive to where anyone suspects any use. he is just looking to put on 15 - 20 lbs. His main ?question concerns pct. I said nolvaldex three weeks after his last stick.but im not sure as to how much and for how long. I know you are supposed to lower the doses gradually.if someone could help us with this i would appreciate it . 160 lbs age 22 works out 6 days a week, diets like a monster. thanks
Deca post cycle........
- Thread starter devinfitz
- Start date
L
lartinos
Guest
He needs to ingest his own semen for the test boost
H
hog#head#cheese
Guest
shitty deca only thread in before the move
lol
Last edited:
*The_West*
New member
lol@ southern lord. unless "your friend" (nudge, nudge, wink wink) is 4 foot tall, at 160lbs he most certainly does not "diet like a monster"
also "your friend" doesnt want to run test with it because of "the sides" does he think that deca does not come with its fare share of side effects?
also "your friend" doesnt want to run test with it because of "the sides" does he think that deca does not come with its fare share of side effects?
That's what they all say. A 160lb 22 yr old can't put on 20 lbs of muscle w/o somebody noticing. How does a monster diet anyway? Most monsters I know don't eat much. They just rip everything in half and leave it right there.
L
lartinos
Guest
incorrect, underneath the tongue for best absorbtion.
wee_man
New member
By Jenetic (First Sticky in the PCT forum)
When to begin PCT:
On average, begin PCT approximately 5-10 days after your last injection regardless of longer acting esters. Begin PCT 1-3 days after your last injection and/or intake when using short acting esters.
Keep in mind, pituitary LH secretion automatically increases as the hormones diminish from your system. The elevated androgen levels are from an exogenous source and your endogenous production is suppressed. Therefore, waiting for the exogenous androgens to completely clear from your system, ultimately results in lower total concentrations of androgens in your system when beginning PCT. This leads to an unfavorable andgrogen:estrogen ratio and the well known “crash” effect.
*As previously mentioned, the actions of HCG take place independently and is not affected by exogenous hormones and/or preexisting HPTA suppression. There are no contradictions with respect to the effectiveness of HCG usage while exogenous hormones are present in your system.
PCT Protocol(s):
1.) 1,000 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue with 20 mgs Nolvadex ED for an additional 3 weeks.
2.) 1,000 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED and 50 mgs Clomid ED for the first 3 weeks. After, discontinue HCG and continue with 20 mgs Nolvadex ED and 50 mgs Clomid ED for an additional 3 weeks.
3.) 1,500 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue 20 mgs Nolvadex ED for an additional 3 weeks.
4.) 1,500 IUs HCG 3x/wk (mon/wed/fri) in combination with 100 mgs Clomid ED and 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue with 50 mgs Clomid ED and 20 mgs Nolvadex ED for an additional 3 weeks.
Option one can be considered as a standard PCT protocol. This should apply to all basic cycles. Option 2 is generally the same as option one except for the addition of Clomid which is added as a supporting recovery aid. Option three and four incorporate a higher HCG dosage and have a relationship similar to options one and two in the sense that Clomid is incorporated in the latter as a supporting recovery aid
When to begin PCT:
On average, begin PCT approximately 5-10 days after your last injection regardless of longer acting esters. Begin PCT 1-3 days after your last injection and/or intake when using short acting esters.
Keep in mind, pituitary LH secretion automatically increases as the hormones diminish from your system. The elevated androgen levels are from an exogenous source and your endogenous production is suppressed. Therefore, waiting for the exogenous androgens to completely clear from your system, ultimately results in lower total concentrations of androgens in your system when beginning PCT. This leads to an unfavorable andgrogen:estrogen ratio and the well known “crash” effect.
*As previously mentioned, the actions of HCG take place independently and is not affected by exogenous hormones and/or preexisting HPTA suppression. There are no contradictions with respect to the effectiveness of HCG usage while exogenous hormones are present in your system.
PCT Protocol(s):
1.) 1,000 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue with 20 mgs Nolvadex ED for an additional 3 weeks.
2.) 1,000 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED and 50 mgs Clomid ED for the first 3 weeks. After, discontinue HCG and continue with 20 mgs Nolvadex ED and 50 mgs Clomid ED for an additional 3 weeks.
3.) 1,500 IUs HCG 3x/wk (mon/wed/fri) in combination with 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue 20 mgs Nolvadex ED for an additional 3 weeks.
4.) 1,500 IUs HCG 3x/wk (mon/wed/fri) in combination with 100 mgs Clomid ED and 20 mgs Nolvadex ED for the first 3 weeks. After, discontinue HCG and continue with 50 mgs Clomid ED and 20 mgs Nolvadex ED for an additional 3 weeks.
Option one can be considered as a standard PCT protocol. This should apply to all basic cycles. Option 2 is generally the same as option one except for the addition of Clomid which is added as a supporting recovery aid. Option three and four incorporate a higher HCG dosage and have a relationship similar to options one and two in the sense that Clomid is incorporated in the latter as a supporting recovery aid
6FULLMETALTRUCKIE9
New member
i WAS ALWAYS UNDER THE IMPRESSION THAT DEPENDING ON THE GEAR USED YOUR PCT CHANGED WITH THAT COMPOUND IE NOT USING NOLVADEX FOR PCT WHEN YOU CYCLED DECA OR ANY OTHER 19-NOR DRUG OR DO I HAVE THAT RIGHT????
i just recently read that to...never before in last few years did anyone mention it...im using nolva for pct right now after a tren cycle...so far no problems or issues
*The_West*
New member
its ok if the 19-nor compound is out of your system.
basically, nolva up regulates the progesterone receptor, meaning that using nolva whilst the compound is still in your system can increase the risk and severity of any progesterone induced side effects.
some people get away with it, others grow leaky breasts.
basically, nolva up regulates the progesterone receptor, meaning that using nolva whilst the compound is still in your system can increase the risk and severity of any progesterone induced side effects.
some people get away with it, others grow leaky breasts.
wee_man
New member
Does tamoxifen change oestrogen and progesterone receptor expression in the endometrium and breast?
U Karck, F Kommoss
European Journal of Cancer
September 2000 (Vol. 36, Issue , Pages 45-46)
Abstract
We studied the expression of oestrogen and progesterone receptors (ER, PR) in postmenopausal women receiving tamoxifen for breast cancer. In addition the literature addressing the question of ER and PR expression in breast tissue during treatment with tamoxifen was reviewed. We demonstrated consistent expression of ER and PR in endometria from patients receiving tamoxifen, with a trend towards a higher proportion of receptor positive specimens during tamoxifen. In breast cancer tissue, the ER content seemed to be reduced following tamoxifen treatment. After short time exposure to tamoxifen, the PR appeared to be increased, longer treatment caused the PR to go down to pretreatment levels or below.
U Karck, F Kommoss
European Journal of Cancer
September 2000 (Vol. 36, Issue , Pages 45-46)
Abstract
We studied the expression of oestrogen and progesterone receptors (ER, PR) in postmenopausal women receiving tamoxifen for breast cancer. In addition the literature addressing the question of ER and PR expression in breast tissue during treatment with tamoxifen was reviewed. We demonstrated consistent expression of ER and PR in endometria from patients receiving tamoxifen, with a trend towards a higher proportion of receptor positive specimens during tamoxifen. In breast cancer tissue, the ER content seemed to be reduced following tamoxifen treatment. After short time exposure to tamoxifen, the PR appeared to be increased, longer treatment caused the PR to go down to pretreatment levels or below.
ViperHMS
Well-known member
What??? I've been shooting into the rim of my asshole. I thought that was the best place cause my buddy said when he shoves X up his ass it gets absorbed better.
