";s:4:"text";s:11183:"Don’t taper up for the sake of tapering up though, if you only need 300 mg to reach your goals, use that. In any case, the judgment of the specialist and the reference internist is essential.I turned 40 a few years ago, I sometimes have some small erectile problems. Are there any legal OTC things you can buy to help?The entire premise of my protocol design is avoiding using AI’s and SERMs.Great article as always Derek. Other thought – faster clearing would be good for improving markers prior to check-in bloodwork with TRT doc. I have stopped fapping, weightlift four times per week, and am otherwise mentally well. can you recommend doses? Interval between drug intake should not be less than 24 hours.Even if the medicine has not given effect or has not fully met your expectations, it is not recommended to exceed the daily dose. Only once you’ve reached that upper limit would I look to stacking DHT derivatives. I wouldn’t use Trestolone as a base over Testosterone personally but yes you could make that work.What would the framework be for someone who is concerned about hair loss ?Will have posts on this in the future (have already covered them to some extent in the past).What’s so bad about an AI like Exemestane?
I am a 83 year old man, in 2004 my prostate was removed, but some degree of erectile dysfunction always manifested itself even when I had it still. Well, I’m using Test-C so I guess that’s mostly a wash for muscle development one way or the other…But I prefer the idea of tiny subq injections daily over larger IM injections – and if it also produces less aromatization then that’s a no brainer.Love your information and approach to using minimum effective doses. You say E.G with 300mg test/week your blood test level will go far above the supraphysiological limit, for estrogen as well…without AI. BTW, I have seen this point about 90% effectiveness with the .5 mg dose with greatly reduced sides mentioned on other boards before. Re-read the article brother.But Trestolone does aromatize, the sarm is just more for upping the anabolic effect So that i could use a lower dose of trestolone.Ah I see what you’re asking. Can I take Kamagra Oral Jelly, despite having no prostate?Dear User, prostatectomy is not an obstacle to the intake of Kamagra Oral Jelly, as well as other phosphatase 5 inhibitors. You personally how much would bring your E2 with 300mg test? Been taking it for 9 years when needed. Some people advised me to take Viagra, I tried and the results were very satisfactory but it was too expensive. with Winstrol).Taking this all into consideration, if muscle growth with a minimization of negative health impact is the goal, this is what I would suggest.Well, that depends on your genetic propensity to aromatization among numerous factors, but in general, I would say that the most intelligent approach to creating a steroid cycle should be increasing Testosterone as much as you can get away with until the need for an aromatase inhibitor presents itself.Obviously I'm not suggesting you do this on a first cycle, or perhaps even a second or third cycle, but I'm trying to lay out a framework to determine when/if it is justified for you to start stacking on top of your base.As long as Testosterone dosages are slowly tapered upwards as you gain muscle mass, side effects can be kept to a minimum with greater ease than most other compounds.The exception to this are androgenic side effects, but for the sake of this article being focused on bodybuilding outcomes and health, I will be disregarding hair loss/androgenic side effects when I lay out this framework.Testosterone wins over all other compounds when you factor in everything with exception of androgenic side effects, but there comes a point for the majority of individuals where more Testosterone is just not feasible without forcing the user to introduce an AI.For those who can blast Test into the sky with no side effects, frankly, they'd probably be better off using a slowly titrating Testosterone will produce dose-dependent increases in muscle mass.However, once you hit a certain dose (individual dependent), you will be forced to introduce adjunct drugs just to mitigate side effects, which will also impair other important biomarkers and hinder muscle growth.This dosage is typically around the 300-400 mg Testosterone per week mark for many individuals.If you don't need an AI though and your body is extremely efficient at balancing androgens relative to estrogens, then by all means, push the Testosterone higher instead without stacking if your biomarkers indicate that it is the healthier choice for you.Testosterone has proven time and time again to be the most forgiving steroid on health markers and it is more than sufficient to grow a physique to Pharmaceutical grade Testosterone is also relatively easy to find for a fair price, whereas pharmaceutical grade Primobolan, Anavar, Nandrolone and Anadrol are commonly faked, or very expensive.Once you get to a point where you're forced to use an AI just to use a higher dose of Testosterone, was it a wise choice to use that much Testosterone in the first place?Personally, I believe that is where introducing a DHT derivative would then be justified rather than increasing your Testosterone dosage even higher.Only once you've plateaued from a cycle comprised of a Test base and a DHT derivative do I believe you should even consider introducing a 19-Nor, as they are the least forgiving on health markers, despite their superior anabolic/androgenic tissue selectivity.In addition, your tolerance to androgenic activity needs to be factored in, as managing While you can get to 260+ pounds lean on a bunch of Testosterone (if you have great genetics), could you have not accomplished the same thing with a much lower androgen load, or without needing to pop AI's like candy to tolerate the dosage of Testosterone needed to support that much lean muscle growth?This is what I wish I learned about sooner, because it wasn't until after I finished trying to chase bodybuilding goals that I feel I really started to understand more optimal practices.Certain compounds that are very effective get completely overlooked because of their relative lack of potency, and oftentimes even their relative lack of side effects.“Wet” compounds like Dbol will give the user an inflated look as a result of its conversion to 17α-methylestradiol.If something bloats you up 10 pounds nearly overnight, does that mean it is a more effective muscle builder than something dry but less dramatic due to its relative lack of side effects?Compounds like Primobolan will get overlooked because of this, and they are seen as “girl steroids”.If you're in this for the long haul, long term muscle growth is our goal with the least impact on our health possible.There are very few compounds that edge out Primobolan in this regard, despite yielding what may be perceived to be better increases in size in the short term.The reality is, there are several commonly overlooked compounds with better outcomes than commonly reached for steroids not only in a clinical setting, but in a bodybuilding context as well in the long-term.Comparing someone waterlogged on a Test, Nandrolone and Dbol cycle to someone on a Test, Primobolan and Nandrolone cycle, the guy on Dbol might appear to be making significantly more progress at a much faster rate, but are those outcomes just inflated by the guy being waterlogged?Or are they actually yielding more nitrogen retention and lean muscle accrual with their inclusion of Dbol?The side effect profile of the second cycle would be far more tolerable and still yield nearly identical gains in muscle mass all things considered.Keep this in mind when you're designing your cycles.If somebody outlined these concepts to me when I was younger I could have significantly reduced my dosages and avoided so much unnecessary My dosages were excessive for my goals was the main issue, which I outline further in my article detailing my If I were to design subsequent blast phases for myself now (and hair loss wasn't a concern), it would follow the framework I outlined earlier in the article.I would use a base of 300 mg Testosterone per week split into everyday administrations.My Testosterone dosage would titrate up to as high as my body can tolerate without needing an AI or substantial detriment to my health markers.I would introduce Proviron alongside a Test base if needed in my next cycle.Not everyone will benefit from Proviron, and your use of it should be based on your blood work.For example, if you have clinically low SHBG already, smashing it with Proviron will do more harm than good.My Proviron dosage would titrate up as needed to free up Testosterone bound to SHBG and antagonize Estrogen.In the subsequent cycle I would introduce a DHT derivative like Primobolan.The dosage would titrate up as needed based on SHBG and Free Testosterone levels (Primo doesn't bind well to SHBG, but the dosage would still be based on what my limits are with Testosterone titration), Estrogenic activity in the body, biomarkers, and my tolerability of 19-Nor's.Nandrolone is my choice of 19-Nor that would be introduced several cycles later once my body had plateaued from all of the previous blast phases where I had already peaked my Test base dosage, tried a subsequent cycle of Test + Proviron (conditional based on blood work), as well as tried a subsequent cycle of a Test base with Primobolan (and Proviron if deemed beneficial).The foundation of each blast phase after I deem my body had reached an “advanced” stage of AAS use again would likely include Testosterone as my base, Proviron (if necessary), Primobolan and Nandrolone.If I was fully cycling on and off (not cruising on TRT), then Proviron would be evaluated more seriously as an adjunct during blast phases.If I cruised on TRT between blasts, Proviron would likely not be useful, as SHBG levels are typically not going to be too high for individuals who never fully clean out.Usually the issue is the opposite, and their SHBG is chronically low, in which case Proviron would be useless in this context.While certain compounds could be considered interchangeable, I see no need to The primary growth promoters of that stack are Testosterone and Nandrolone, but the dosages of each would be highly dependent on individual gene expression and health markers (as well as basic things like blood pressure).I've been on therapeutic TRT for years so I would milk this compound progression again if I wanted to and experience significant progress without needing to jump straight into an advanced stack.It should take you at least a couple years of cycling before you work your body up to a point where a protocol designed using advanced cycle framework is even necessary to deploy to break muscle building plateaus.After dedicating over 8 years to extreme self-improvement, I have created "More Plates More Dates" as a one stop shop for helping you to get yourself on the right path to the "best you" possible too.Couldn’t testosterone base be replaced by 600-1000 IU of hcg weekly? 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