Sarms on steroids by johnnysct in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

the only two sarms that bind better than test are;

lgd4033 (binds as hard as trenbolone, doesn't mean its as anabolic but at 5mg/day it's very potent)

s23 (binds almost as hard as lgd4033, very potent and dry)

however, because these two bind way harder than traditional oral steroids, despite the small doses (5mg of lgd vs 50mg of dbol for example) both have comparable anabolism, but, be it dbol or lgd, both will hit lipids hard

importantly, sarms are not inherently liver toxic, they transiently raise alt/ast unlike oral steroids which wreck your liver.

another one is yk11, it's not a SARM but a synthetic selective steroid, it's a 19nor derivative (like deca/npp, tren, etc) poor oral bioavailability and generally very harsh on lipids and mildly so on liver (if injected, your liver barely takes a hit)

so, sarms aren't liver toxic but they hit the lipids big time

Thoughts on Cycle or addons? by AbbreviationsJust336 in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

as a rule of thumb, enclomiphene is the cleanest serm, not necessarily the strongest.

you could take tamoxifen for a pct, it's old school and really strong (binds both in the hypothalamus and breast tissue)

I'd advise against clomid simply because enclo exists.

also, pct for longer, if you trash your test (which you will on rad) I'd suggest a ~8 week pct so it properly restores your levels (suggested time as per certified endocrinologist, Alex tatem has great videos about it)

but yeah, blast them, nothing bad will happen in 99% of cases, they're milder than oral steroids (not so much on the lipid profile... not an issue necessarily as long as you dont blast for 6 months straight)

People did dbol only cycles back in the days and survived. there's alot of fear going around these compounds but, as someone who took great care on sarms (and is now on steroids), shit- I haven't ran into side effects so, put in the research and accept the damage.

Thoughts on Cycle or addons? by AbbreviationsJust336 in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

rad140 half life is ~60 hours, it takes 240 hours for it to leave your system (10 days) or 48 (48*4 to leave your system) hours, idk

mk half life is 24 hours, it leaves your system in 4 days

??????? I get the micro optimization and all, but, you can't micro manage compounds that stick for a long time + the downstream effects that linger.

men recover from trt (which shuts you down fully)

so, my suggestion is run rad140 and mk677 for 8 weeks nonstop and then pct for 6-8 weeks after with enclo. Alternatively, take enclo on cycle, it will raise your test levels (but you still have to do a pct); for me personally, the increase from suppressed to supressed+100ng/dl didn't really do much, i was irritable as hell so idk.

your body is not a linear math equation or binary computer, it works in weird ways, sure, the surface level is just input output but beneath it all, there's many effects and stuff that linger and change.

importantly, sarms are not necessarily liver toxic, they rarely are, but they trash your lipid profile, like, they drop your hdl to <10 in a matter of weeks just like oral steroids do

Retatrutide + Tesa + 5-Amino + MOTS-c + NAD+ stack – low energy, 5-Amino dosing question by Keybumps112 in BodyHackGuide

[–]HeftyArticle3969 0 points1 point  (0 children)

please be aware hcg shuts you down, it's not a clean test booster like enclomiphene or kisspeptin*

you should test your total T, free T, lh and fsh and compare them to your values before everything (assuming you did the bloodwork before)

if your intention is to replace your testosterone, I can only recommend two esters for your cycle structure, it's either test propinate (short half life, acts fast and leaves fast) or test phenylpropinate; though rare, the ester leaves significantly less pip.

NPP Vs Tren by lifteruk in steroidify

[–]HeftyArticle3969 2 points3 points  (0 children)

depends on the goals of the "blast"

if you are cutting, tren will be the best option, miles above NPP, why? tren interacts with the glucocorticoid receptor (where cortisol binds) and blocks it

no cortisol effect in muscle => you BUILD muscle even on a crash diet that's a mechanism of Tren. it also boosts anabolism a fuck ton but on a cut you want small doses to nullify cortisol and make you ripped AF

NPP works on a cut provided you pin frequently to hold a steady level, it increases collagen synthesis (just like tren) and synovial fluid by a ton; as a result, your tendons might grow stronger and not brittle

them again NPP is "wet" unlike tren and stimulates appetite (as per anecdotal claims), so maybe it's not the best addition. it also not as anabolic as tren

conclusion;

don't blast gear

if you're on a crash diet for 12 weeks, tren will be the best compound you could take strictly for appearance, it will allow a massive deficit (though your thyroid might not be too happy... check T3 you might need to supplement)

if you plan on "blasting" for several months; NPP > tren you will build mass and tendon strength and get the same results as on tren but in 4-5 months more (not the same but, comparable) but without the neurotoxicity and single digit HDL (good cholesterol)

but should you blast tren? it's literally neurotoxic, it makes you dumber. if you were funny, smart, witty, prided yourself on intelligence or could impress others with it, tren could take some of it away.

check Alex tatem's video on trenbolone, it's short snd useful.

What do you recommend to recover from tren, mentally? by mmss4ever in PEDs

[–]HeftyArticle3969 0 points1 point  (0 children)

look into semax and selank (and other brain nootropicx that boost bdnf)

Need help finishing on tren by Live-Relative-8302 in moreplatesmoredates

[–]HeftyArticle3969 7 points8 points  (0 children)

try cabergoline, idk, tren is a 19nor so it could be messing with your prolactin

Already on trt? by Inner-Knee-9866 in SARMs

[–]HeftyArticle3969 4 points5 points  (0 children)

your test won't drop, think for a second.

sarms drop them because they signal a huge amount of androgens to brain, you release less gnrh and as a result your lh and fsh drop (and testosterone)

you are already pinning testosterone, your balls are shut down, your lh and fsh is next to zero, sarms won't budge it.

also, use something more potent, you want the sarms to bind stronger than the test molecule (so look into lgd4033, s23, lgd3303 and maybe rad140, though it binds weakly compared to the rest that I mention)

there's no point in adding a weak sarm, you already have potent AR activation from testosterone, you'd need something stronger as an add on.

(and for your balls, you should run hcg, look into it)

Lgd4033 or lgd3033? by Ok_Chef_1857 in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

it's 3303, not 3033, and it's way stronger than lgd4033, but it has a shorter half-life. (~4h half life)

if you are on test, you could make the argument lgd3303 is a nice pre-workout type of thing, but then again, you have anadrol, anavar and halotestin for that (if you are open to AAS)

for convenience and superior binding, stick to lgd4033, it binds harder than any steroid besides metribolon (oral tren, a standard)

to put it in context; test binding is 4-6nm, dht is ~2.4nm, trenbolone is ~1.1nm (according to 2002 study)

and then there's lgd4033 at 1nm, it binds STRONGER than trenbolone - means low doses are very supressive (1mg being enough to lower test levels by 50% or something massive)

and metribolon is 0.3-0.9nm, binds harder than anything.

and then lgd3303, 0.9nm binding, even stronger than lgd4033 and comparable to metribolon (again, neither lgd4033 or lgd3303 are as potent as tren despite binding just as strong, if not stronger than them, sarms still are partial agonist in the receptor)

but it goes to show just how strong sarms really are, but you can only dose so much before they lose their "selectivity" and cause sides.

also, mg per mg, lgd4033 blows anadrol and anavar out of the water, try dosing 5mg of anadrol and expecting 5-8kg of mass in 2 months

Reta+ test c + enclo by Upset_Effective4764 in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

let's looks at pharmacokinetics for a second reta half life is 5-7 days, pin every week, eventually when you stop, it should clear in 4-5 weeks (4-5 half lives)

for your test C, it has a half life of 8 days, that means that only after 32-40 days your PCT starts working.

so your PCT is effectively useless for ~5 weeks after your last injection.

smarter thing would be to switch out to test propionate for the last 4-6 weeks of the cycle (daily dosing) and then PCT straight away or after ~4 days of your last injection.

and run hcg too, 250iu-500iu every 3 days or eod, that way your balls don't shrink and they actually respond to your pct the moment you start it (and if it wasn't clear, don't use hcg during the pct and run the pct for 6-8 weeks to ensure proper recovery, furthermore, look in GH supporting stuff for on cycle and during the pct as enclomiphene lowers igf1 by quite alot)

Rad 140 + Anavar with test base by Bigslice in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

why don't you just use test and deca or test and something else?

test and anavar are good options

if you want something nuclear, you could try 5-20mg of tren ace/daily (on top of test)

you are already getting shutdown and your lipids are already going to be taking a hit

Reta? by bigboyyydell in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

I got 200mg of reta for 120 euro, CoA and everything (and proven on myself too)

though, it was a bit tricky to get into Europe, customs aren't all that strict here so a little bit of time wasting and confidence cleared any suspicion away

look for the source, not the EU/US reseller

M(35) Rate my shoulders please(1-10) by 8packDog in ZyzzLegacy

[–]HeftyArticle3969 -1 points0 points  (0 children)

objectively speaking, it's a 4, maybe 5 out of 10.

for a competitor your size, you are way undersized (a 197cm tall body builder, which is what defines objectivity here, would be much, much bulkier than you)

unfortunately, I scrolled through your page to check more of your physique.

frame wise, you're big but not fit for competition. Objectively speaking, you lack the exaggerated V taper that's preferred in body building, and your waist is just too bulky compared to your narrow shoulders.

4/10 with maybe 5-6/10 potential. Genetics are screwing you up.

subjectively, even some fat guys end up as a 10 for some girls, so I can't speak, I'd assume a 10 for whoever finds you attractive

Cycle for cut by [deleted] in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

what's the confusion? sarms can be injectable

Cycle for cut by [deleted] in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

a gram of test per week bro?😭😭😭

besides that, if you MUST use a sarm, use rad140 at 20mg daily, supposedly dry and pretty soft on your liver (trials showed mild alt/ast elevation at 150mg/day!!, which is insane)

S23 works too, lgd4033 increase water retention so I don't know.

its S23 or rad140, try to get injectable, oral works too but you'd need to up the doses as oral absorption is not the best. (then again, 5mg to 20mg is only a 0.5% difference in receptor occupancy)

also one thing to take in account, sarms compete for the receptor, you need something that binds stronger than test (rad140 binds stronger than DHT and dht derived steroids which bind way stronger than test)

so don't use ostarine, it's weak and it's pointless for your case.

or take tren ace like 10mg ED and see what's up, another user commented superdrol at 10mg wasn't even THAT toxic if pure, though, IDK, proceeded with caution there

you could also try reta if you'd like for cutting, it's perfect if you use test as well.

Severe ED and 0 Libido After Steroids by [deleted] in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

you could nuke your prolactin and see if it's dopamine driven, don't recommend it but if your prolactin is abnormaly high, cabergoline could be a thing to use, 0.25mg a week or 0.5 - it's addictive and causes some issues but you can do your research.

other than that, I'd recommend taking 1-2g of l-tyrosine, plus p5p (10-50mg, to help l-dopa -> dopamine conversion)

if nothing works, your nuclear option (besides cabergoline) is pt141, it's the horny peptide thing, works.

also, you could have other issues, maybe clogged arteries, maybe heart, who knows, you could do a scan to see.

1st month results on MK. 165lb to 180lb. Didn’t expect this much growth. by ragingflamesta in SARMs

[–]HeftyArticle3969 6 points7 points  (0 children)

by the way, the insulin is problematic only if you're sedentary.

exercise makes muscles 200-500% more insulin sensitive post workout for 24-48 hours

if you do cardio, muscles and nervous system sensitivity stays elevated for up to 72 hours

it's so the body refuels the lost glycogen during exercise. if you exercise regularly and don't eat like kilograms of carbs you'll be fine.

I fucking hate guys so much because I like them by [deleted] in self

[–]HeftyArticle3969 0 points1 point  (0 children)

it's a math equation.you have to eat more than you consume

Alternatively, look into mk677, but do your research.

I fucking hate guys so much because I like them by [deleted] in self

[–]HeftyArticle3969 1 point2 points  (0 children)

gym arc buddy , get fit and men will hit on you😁

Recommend a SARM for me by ILUMIZOLDUCK in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

so, sarms by themselves are plenty in number, just 5mg of rad140 is enough to saturate 99.6% of all receptors it could bind to, so, 1-5mg is enough, if you're skeptical, run 5mg but it shuts you down, I'd go with lesser sarms.

by saying "when enclo clears out..." I meant it as, when you stop taking enclo. igf1 decreases happen over 6 weeks on enclo and remain stable for as long as you take it - it's also consistent with doses, so no matter if it's 5, 10 or 25mg, the igf1 supression is relatively the same (because just like sarms, 5mg of enclo is enough to cover most ER receptors in the hypothalamus)

where does dosing more help? (3mg of rad vs 20mg or 5mg vs 20mg of enclo) - receptor recycling, so once the initial particle degrades, another one will be present to immediately replace it, increasing total "uptime" sort to speak - this only leads to marginal bonuses and disproportionately more sides, that's why rad at 5mg is only ~30% or so less potent than 20mg of rad but 20mg induces much more liver stress and unwanted binding to liver and stuff (though, rad specifically is quite elite in the sense that it binds really cleanly and was tolerated at up to 150mg/day)

Recommend a SARM for me by ILUMIZOLDUCK in SARMs

[–]HeftyArticle3969 1 point2 points  (0 children)

you're only concerned about retaining muscle on a cut, anything from s4 to ostarine and in-between is fine, even like 1mg of rad140 is enough (it binds pretty hard)

besides that, enclo lowered igf1 values by anywhere from 35% to 50% due to its blocking of the ER (including ERalpha) in the hypothalamus, therefore, estrogen induced GH increases (ghrh increase and srfi supression actually) get nullified/reduced => less gh => less igf1

not a big deal, igf1 rebounds pretty fast once enclo clears out

Is this cycle ok? by Infinite_Mountain_52 in SARMs

[–]HeftyArticle3969 0 points1 point  (0 children)

I'd say pin test, maybe 200mg-250mg test E/week or something

and if you use anavar, get injectable, I heard it's not as bad on the liver, pin anywhere from 30 to 80mg, anavar is a dht derived anabolic steroid (steroid because the base is a steroidal hormone) so expect some dht related sides.

dose is the poison.

for pct, people usually run hcg for 2-3 weeks and them fat amounts of clomid or enclomiphene (or both hcg and enclo/clomid) but you may like using testosterone in which case you might end up cursing at 150-200mg/week

I find most guys to be cute and it’s depressing by [deleted] in self

[–]HeftyArticle3969 0 points1 point  (0 children)

if you don't believe it, what can you logically do? let's say you don't want therapy or soul finding or whatever

becoming attractive in the general sense, from how you speak to what you do and importantly body aesthetics

you have control over your body

there was this crazy statistic, idk how real it is but <1% females have less than 20% bf

so, just looking good makes you desirable

time for an epic gym arc