• All new members please introduce your self here and welcome to the board:
    http://www.professionalmuscle.com/forums/showthread.php?t=259
Buy Needles And Syringes With No Prescription
M4B Store Banner
intex
Riptropin Store banner
Generation X Bodybuilding Forum
Buy Needles And Syringes With No Prescription
Buy Needles And Syringes With No Prescription
Mysupps Store Banner
IP Gear Store Banner
PM-Ace-Labs
Ganabol Store Banner
Spend $100 and get bonus needles free at sterile syringes
Professional Muscle Store open now
sunrise2
PHARMAHGH1
kinglab
ganabol2
Professional Muscle Store open now
over 5000 supplements on sale at professional muscle store
azteca
granabolic1
napsgear-210x65
esquel
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
ashp210
UGFREAK-banner-PM
1-SWEDISH-PEPTIDE-CO
YMSApril21065
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
advertise1
tjk
advertise1
advertise1
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store
over 5000 supplements on sale at professional muscle store

How much test for best sex drive?

How much testosreone per week gives you the best overall sexual performance?


  • Total voters
    39
TRT dose + Proviron + daily Low dose cialis
What’s the least amount of proviron you’ve been able to use and still get sexual benefits? That compound at only 25 mgs per day harms my cholesterol levels. Has 12.5 mgs daily worked for you? I may try that in the near future and see how my cholesterol levels react.
 
your trt dose and u add some proviron or mast
Masteron affects me differently than proviron. Masteron rapidly causes my prostate to swell making it difficult to urinate and to maintain an erection. Masteron makes my sensitivity decrease whereas provision increases my sensitivity during sex. Explain that one!?
 
Sex drive and keeping your dick up during sex is a different thing .. libido is East to get.. lasting is what a lot of men struggle with without going limp
 
Why is that do you think , why does sexual performance go down when you up testosterone dosage

Cuz MORE isn't "better" ..... its about balance.... And Yes.. Proviron is the shizzzzzzzzzzzz
 
Cuz MORE isn't "better" ..... its about balance.... And Yes.. Proviron is the shizzzzzzzzzzzz

10mg of cyp (Gorilla) a day and I swear I'm hornier than I was taking 210. Thankfully the lady friend doesn't mind because this shit is patently fuckin ridiculous.

I'll get bloods soon, I'm trying to find my "true trt" dose, so to speak. But I still feel enhanced at this dose.
 
Do you find that doing a daily shot with a slin
10mg of cyp (Gorilla) a day and I swear I'm hornier than I was taking 210. Thankfully the lady friend doesn't mind because this shit is patently fuckin ridiculous.

I'll get bloods soon, I'm trying to find my "true trt" dose, so to speak. But I still feel enhanced at this dose.
Do you feel that doing a little bit of test c every day is better than shooting the same amount divided into 2 shots per week? If so, why?
 
Do you find that doing a daily shot with a slin
Do you feel that doing a little bit of test c every day is better than shooting the same amount divided into 2 shots per week? If so, why?
I DEFINITELY like every day shots of test C better than twice a week. First off, using a slin pin is worlds better than a regular dart IMO. Secondly, its kept my estrogen and test levels more stable on a daily basis over once or twice a week. Less peaks and valleys so to speak. Been using 30mg a day of test c and loving it.
 
Do you find that doing a daily shot with a slin
Do you feel that doing a little bit of test c every day is better than shooting the same amount divided into 2 shots per week? If so, why?

I honestly didn't run it twice a week long enough to compare, I pretty much always pin every day. Takes five seconds with a slin pin after a shower. I've not run that much, either, but 10mg every day honestly feels like a lot.
 
What’s the least amount of proviron you’ve been able to use and still get sexual benefits? That compound at only 25 mgs per day harms my cholesterol levels. Has 12.5 mgs daily worked for you? I may try that in the near future and see how my cholesterol levels react.

Yes, Mesterolone has been shown to have negative effects on lipids. Its also liver toxic and not a long term TRT combination drug IMO.
 
What’s the least amount of proviron you’ve been able to use and still get sexual benefits? That compound at only 25 mgs per day harms my cholesterol levels. Has 12.5 mgs daily worked for you? I may try that in the near future and see how my cholesterol levels react.
I wouldn't worry to much about lipids with proviron. It comes down to user sensitivity and genetic predispositions in many cases, my personal blood work doesn't speak for all but I have no issues.. Further more in many medical journals older and even newer updated ones it cites that proviron is very safe. Compare these statements to many other drugs,medications and oral hormones, it hardly translates into liver toxic.

OVERDOSAGE Acute toxicity studies using single administration showed that Proviron is to be classified as practically non-toxic. No risk of toxicity is to be expected even after inadvertent single administration of a multiple of the dose required for therapy.
This right here was from MOH - The format of this leaflet was determined by the Ministry of Health and its content was checked and approved by it in July 2012
Plus there's number studies that contradict what is toxic compared to slight lipid changes.. You'll find not only just a good amount of users but also people that it hardly effects liver functions..
Some people have seen changes in blood work, and that has to be noted for research purposes along with everything and anything that people may experience. Again that hardly translates into being liver toxic.
Compared to many other oral AAS of drugs, you won't see a LARGE amount on one side citing its not liver toxic, than an other side saying it is.. With other oral AAS why do you not see overwhelming data saying that its not toxic and than some suggesting it is toxic? Why isn't there similarity with other oral AAS on such a lopsided scale? In all fairness I'm talking truly lopsided, greatly supporting these notions..

Mind you MOH say's practically because the amount of effected users is so small, and data from other studies and testimonials has provided them with enough evidence to make this statement, confidently. This drug is old too, and has been in and out of research and studies, a lot! We should always take safe measures and use it for 6-8 weeks and discontinue, and repeat if needed..

25mg is a basic starting dose, you can expect to feel the effects relatively quick, within days.
 
I don't know why I need to do some reading on it but when I added 50mg of DHEA per day I see a noticeable difference in drive and morning wood and i'm fucking old
 
I wouldn't worry to much about lipids with proviron. It comes down to user sensitivity and genetic predispositions in many cases, my personal blood work doesn't speak for all but I have no issues.. Further more in many medical journals older and even newer updated ones it cites that proviron is very safe. Compare these statements to many other drugs,medications and oral hormones, it hardly translates into liver toxic.

OVERDOSAGE Acute toxicity studies using single administration showed that Proviron is to be classified as practically non-toxic. No risk of toxicity is to be expected even after inadvertent single administration of a multiple of the dose required for therapy.
This right here was from MOH - The format of this leaflet was determined by the Ministry of Health and its content was checked and approved by it in July 2012
Plus there's number studies that contradict what is toxic compared to slight lipid changes.. You'll find not only just a good amount of users but also people that it hardly effects liver functions..
Some people have seen changes in blood work, and that has to be noted for research purposes along with everything and anything that people may experience. Again that hardly translates into being liver toxic.
Compared to many other oral AAS of drugs, you won't see a LARGE amount on one side citing its not liver toxic, than an other side saying it is.. With other oral AAS why do you not see overwhelming data saying that its not toxic and than some suggesting it is toxic? Why isn't there similarity with other oral AAS on such a lopsided scale? In all fairness I'm talking truly lopsided, greatly supporting these notions..

Mind you MOH say's practically because the amount of effected users is so small, and data from other studies and testimonials has provided them with enough evidence to make this statement, confidently. This drug is old too, and has been in and out of research and studies, a lot! We should always take safe measures and use it for 6-8 weeks and discontinue, and repeat if needed..

25mg is a basic starting dose, you can expect to feel the effects relatively quick, within days.

Mesterolone increased LDL by 34% and decreased HDL by 31% by and increased total cholesterol 18% at 100mg per day as shown here. They're not small numbers.

Full paper: Effects of androgen substitution on lipid profile in the adult and ...eje.bioscientifica.com › downloadpdf › journals › eje
 
Yeah being on 500/w is somewhat better than 150/w but man if my estro is tanked there is zero libido. To me it seems after a certain point estrogen is more important . I like my estro slightly high. Not out of range just slightly high. That gets me going all day.
 
Mesterolone increased LDL by 34% and decreased HDL by 31% by and increased total cholesterol 18% at 100mg per day as shown here. They're not small numbers.

Full paper: Effects of androgen substitution on lipid profile in the adult and ...eje.bioscientifica.com › downloadpdf › journals › eje

Yes, but with all due respect, that is with men using 100mg of mesterolone per day as testosterone replacement, which of course would result in suppression of endogenous testosterone, and consequently suppression of endogenous estrogen that is aromatized from testosterone, with suppression of all of estrogen's beneficial effects on the lipid profile.

Whether the same would be true for men taking injectable exogenous testosterone along with the mesterolone remains to be seen. I suppose that depends on the level of estrogen suppression, just as it does for men taking an aromatase inhibitor, which typically also have a negative effect on the lipid profile.

But of course, you will probably never see a study done of men taking injectable testosterone along with mesterolone, so it falls to the individual user to watch their own bloodwork and see what happens, at what dosages.

Personally, my own lipids have been good using either Proviron or Masteron, because I was always taking them along with testosterone. Both Proviron and Masteron are good at blocking some of the negative effects of excess estrogen...yet estrogen has many beneficial effects as well.
 
Mesterolone increased LDL by 34% and decreased HDL by 31% by and increased total cholesterol 18% at 100mg per day as shown here. They're not small numbers.

Full paper: Effects of androgen substitution on lipid profile in the adult and ...eje.bioscientifica.com › downloadpdf › journals › eje
This study concludes at the end that "studies pertaining to androgen substitution are conflicting"... Stated here - androgen substitution therapy on lipids are conflicting but might be favorable..
They faintly suggest they "might" be "favorable"..

Maybe I missed it, or didn't see it mentioned, yet environmental circumstances can pose as huge factors with blood readings..Were these individuals fasted when blood was drawn, did each individual live by the same diets and life habits, was the environment controlled, did the subjects adhere to the same protocols, what about about body fat and mass index and physical activities, how about smoking,alcohol or even history of genetic predispositions? The lack of this information changes the entire dynamics, these adjustments need to be greatly considered..Lack of a controlled diet/lifestyle will dictate results, knowing the regular amount of caloric intake is vital - calories are transformed in to triglycerides and stored as fat, what is the physical characteristics of these men/body mass index? If calories are reduced they will reduce triglycerides especially under physical activities fitness/exercising will lower triglycerides and boost HDL cholesterol, this can drastically shift these numbers .. Furthermore, the data that was presented can be contradicted with the fact that these are "ageing men", how does this compare to the average age of those that use PED's who most likely are younger or middles aged "supposedly healthy-physically active men" in most cases?

In addition what is the amount of subjects that partaken in these findings? Can the headline of the study or the entire thesis "Effects of androgen substitution on lipid profile in the adult and aging hypogonadal male".. Explain the outcome and evidence in others other studies that simply contradict the one in question, where subjects weren't even using oral androgens? There's data that supports high triglyceride and HDL ratio can be associated with low test and SHGB levels in middle aged and elderly men.

There's simply to many factors that can contribute here. Pharmacology reports have cited numerous times, throughout the years that mesterolone is practically non-toxic, why would this information be regurgitated by multiple highly credible resources if it was false? In all the reports that I have personally seen, nowhere was there a controlled study focusing on proving its toxicity and lipid change, in comparison with multiple groups. Yet, we've seen lipid and TG ratio differences with testosterone deficiencies which has been associated with elevated atherogenic lipoproteins, elevated triglycerides, and decreased high-density lipoprotein cholesterol (HDL-C) in males where no exogenous hormones where initially employed - This information is available with basic research, and that's hardly peeling back the layers..
 
Okay so for me it varies. Overall best sex drive and all around ability is at between 200-300mgs Test E/wk. When i go on cycle and go up to 750-1000 my sex drive does get bat shit crazy and like the other guy above said, i start getting weird too, lol. However on doses that high the sex drive eventually plateaus and even gets to a point where it falls and performances seems to suffer as well. Ancillary drugs dont seem to correct that even when everything looks good on bloodwork. Trt dose still seems to be the best.

Nothing beats dbol for me though. That shit is like a straight up sex drug for me. Even with one or two doses.
 
This study concludes at the end that "studies pertaining to androgen substitution are conflicting"... Stated here - androgen substitution therapy on lipids are conflicting but might be favorable..
They faintly suggest they "might" be "favorable"..

Maybe I missed it, or didn't see it mentioned, yet environmental circumstances can pose as huge factors with blood readings..Were these individuals fasted when blood was drawn, did each individual live by the same diets and life habits, was the environment controlled, did the subjects adhere to the same protocols, what about about body fat and mass index and physical activities, how about smoking,alcohol or even history of genetic predispositions? The lack of this information changes the entire dynamics, these adjustments need to be greatly considered..Lack of a controlled diet/lifestyle will dictate results, knowing the regular amount of caloric intake is vital - calories are transformed in to triglycerides and stored as fat, what is the physical characteristics of these men/body mass index? If calories are reduced they will reduce triglycerides especially under physical activities fitness/exercising will lower triglycerides and boost HDL cholesterol, this can drastically shift these numbers .. Furthermore, the data that was presented can be contradicted with the fact that these are "ageing men", how does this compare to the average age of those that use PED's who most likely are younger or middles aged "supposedly healthy-physically active men" in most cases?


In addition what is the amount of subjects that partaken in these findings? Can the headline of the study or the entire thesis "Effects of androgen substitution on lipid profile in the adult and aging hypogonadal male".. Explain the outcome and evidence in others other studies that simply contradict the one in question, where subjects weren't even using oral androgens? There's data that supports high triglyceride and HDL ratio can be associated with low test and SHGB levels in middle aged and elderly men.

There's simply to many factors that can contribute here. Pharmacology reports have cited numerous times, throughout the years that mesterolone is practically non-toxic, why would this information be regurgitated by multiple highly credible resources if it was false? In all the reports that I have personally seen, nowhere was there a
controlled study focusing on proving its toxicity and lipid change, in comparison with multiple groups. Yet, we've seen lipid and TG ratio differences with testosterone deficiencies which has been associated with elevated atherogenic lipoproteins, elevated triglycerides, and decreased high-density lipoprotein cholesterol (HDL-C) in males where no exogenous hormones where initially employed - This information is available with basic research, and that's hardly peeling back the layers..

I call this the 'I can't find my own evidence, so I'll pull apart the study stated' strategy.

As you know 95% of the studies and clinical data we look at when we formulate an opinion isn't 100% relevant to the individual. Otherwise you would go claiming Tamoxifen wont work on my gynecomastia because I'm not a female with breast cancer.

How about you show me a study that confirms Mesterolone does NOT negatively impact lipids?
 
I call this the 'I can't find my own evidence, so I'll pull apart the study stated' strategy.

As you know 95% of the studies and clinical data we look at when we formulate an opinion isn't 100% relevant to the individual. Otherwise you would go claiming Tamoxifen wont work on my gynecomastia because I'm not a female with breast cancer.

How about you show me a study that confirms Mesterolone does NOT negatively impact lipids?
Answer the questions in my above post without getting sassy with an unnecessary undertone.. I'll call your response the "I'll dodge the questions with a question by making more comparisons that are irreverent to the substance just to support the I'm Swifto and I'm right narrative".. I'm a pacifist and I'm not interested in going back and forth. No matter how well it's presented and calculated you'll discombobulate the substance, no matter what is presented you will argue because your motive is to just "prove people WRONG" with your type of logic "welp, for your information", clearly as it's very transparent by your response by coming off smug. It's not of importance to prove yourself right Swifto. I could have posted studies but I gave you enough ester eggs to do your OWN leg work as well as the readers..Again, it's an easy find in just a basic search with the results that you provided vs men that are middle age or "aging" that have similar lipid changes due to conditions that impact triglyceride and HDL ratios and other changes that can be associated with the underlining condition, non drug related. The are real facts, not something to "formulate an opinion or interpretation off". These are REAL influences that are indisputable, avoiding them or failing recognizing them is equivalent to refuting there existence.

Answer the questions: Are you saying that the results could not have been impacted by the factors below and you're suggesting I'm pulling it apart by what is logical influential factors that could contribute to the findings with the final results? Let's not get ahead of ourselves, lets stay on topic.. That's what a debate is all about, don't inject other analogies or examples, because they can create distortion.

Could the results have been influenced by the following -

Post #30
This study concludes at the end that "studies pertaining to androgen substitution are conflicting"... Stated here - androgen substitution therapy on lipids are conflicting but might be favorable..
They faintly suggest they "might" be "favorable"..

Maybe I missed it, or didn't see it mentioned, yet environmental circumstances can pose as huge factors with blood readings..Were these individuals fasted when blood was drawn, did each individual live by the same diets and life habits, was the environment controlled, did the subjects adhere to the same protocols, what about about body fat and mass index and physical activities, how about smoking,alcohol or even history of genetic predispositions? The lack of this information changes the entire dynamics, these adjustments need to be greatly considered..Lack of a controlled diet/lifestyle will dictate results, knowing the regular amount of caloric intake is vital - calories are transformed in to triglycerides and stored as fat, what is the physical characteristics of these men/body mass index? If calories are reduced they will reduce triglycerides especially under physical activities fitness/exercising will lower triglycerides and boost HDL cholesterol, this can drastically shift these numbers .. Furthermore, the data that was presented can be contradicted with the fact that these are "ageing men", how does this compare to the average age of those that use PED's who most likely are younger or middles aged "supposedly healthy-physically active men" in most cases?
In addition what is the amount of subjects that partaken in these findings? Can the headline of the study or the entire thesis "Effects of androgen substitution on lipid profile in the adult and aging hypogonadal male".. Explain the outcome and evidence in others other studies that simply contradict the one in question, where subjects weren't even using oral androgens? There's data that supports high triglyceride and HDL ratio can be associated with low test and SHGB levels in middle aged and elderly men.

There's simply to many factors that can contribute here. Pharmacology reports have cited numerous times, throughout the years that mesterolone is practically non-toxic, why would this information be regurgitated by multiple highly credible resources if it was false? In all the reports that I have personally seen, nowhere was there a controlled study focusing on proving its toxicity and lipid change, in comparison with multiple groups. Yet, we've seen lipid and TG ratio differences with testosterone deficiencies which has been associated with elevated atherogenic lipoproteins, elevated triglycerides, and decreased high-density lipoprotein cholesterol (HDL-C) in males where no exogenous hormones where initially employed - This information is available with basic research, and that's hardly peeling back the layers..
 
Such an individual thing.

Test E/C, no matter the dose, does nothing for me in terms of sex drive.
The faster stuff like prop, ace and sust (my fav) gives me a better overall well being feeling AND better sex drive.
I think lower is best tho. Around 300 i feel great.
 

Forum statistics

Total page views
559,664,384
Threads
136,131
Messages
2,780,533
Members
160,448
Latest member
Jim311
NapsGear
HGH Power Store email banner
your-raws
Prowrist straps store banner
infinity
FLASHING-BOTTOM-BANNER-210x131
raws
Savage Labs Store email
Syntherol Site Enhancing Oil Synthol
aqpharma
YMSApril210131
hulabs
ezgif-com-resize-2-1
MA Research Chem store banner
MA Supps Store Banner
volartek
Keytech banner
musclechem
Godbullraw-bottom-banner
Injection Instructions for beginners
Knight Labs store email banner
3
ashp131
YMS-210x131-V02
Back
Top