aromatizer
Member
just had a look at vidalista, up to 80mg a tablet?!? oh..my...godI got powder from qsc and it has no taste but its not that potent as vidalista
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just had a look at vidalista, up to 80mg a tablet?!? oh..my...godI got powder from qsc and it has no taste but its not that potent as vidalista
I had horrible reaction site issues from KLOW blend. However, I can independently use each compound(kpv/ghkcu/tb500/bpc157) with no issues. I've read that ghk-cu shouldn't be mixed with anything as it can ruin other peptides bioavailability.What about things like KLOW / GLOW etc that are pre mixed?
Got my 20mg vidalista from Opti, they hit harder than the Cockbombs(tadalafil 20mg + 50 sildenafil) from WWB.just had a look at vidalista, up to 80mg a tablet?!? oh..my...god
Wdym are they already out of stock?The 36iu vials of gh dont last long. Can't seem to get my hands on them... any feedback from the smaller IU vials
Word thank youmethenolone 200
Yes m200
Coming up on 12 weeks 100mcg Ipa / 2mg Tesa 5x a weekTesa+secretagogue is uncharted territory, with all the risk that entails, in exchange for mediocre results compared to the well worn path of rHGH.
I've seen this discussed, and what baffles me is...if that is true, how does a KLOW vial make it to Janoshik, get reconstituted and tested, and the test verifies proper quantities of each of the compounds? Do they stay intact only in quantity, but some reverse alchemy still violates the bioavailability despite the intact mass?I had horrible reaction site issues from KLOW blend. However, I can independently use each compound(kpv/ghkcu/tb500/bpc157) with no issues. I've read that ghk-cu shouldn't be mixed with anything as it can ruin other peptides bioavailability.
Its been well worder that ghk-cu doesn't really mix well with almost any peptide. I guess that's why klow is starting to get a bad reputation.I've seen this discussed, and what baffles me is...if that is true, how does a KLOW vial make it to Janoshik, get reconstituted and tested, and the test verifies proper quantities of each of the compounds? Do they stay intact only in quantity, but some reverse alchemy still violates the bioavailability despite the intact mass?
Would you consider moving on to gh from the tesa ipa combo?Coming up on 12 weeks 100mcg Ipa / 2mg Tesa 5x a week
I'm also on Reta, so to the degree it contributed to this result maybe we call it 50/50 at best. But I took Tesa specifically for visceral fat reduction. Dexa scan last week shows reduction from ~1.5 lbs of VAT to .75 lbs. I'll take a 50% VAT reduction as a win. Curious based on the FDA studies if discontinuing Tesa will bring VAT mass back to baseline, or if those findings had something to do with the limited lifestyle habits of HIV patients, vs my lifestyle of daily fasted cardio & weight training 6x a week.
Either way I think the risks of combining secretagogues is dose-dependent, and it seems the fitness community is sold on overdosing Ipamorelin to a concerning degree. This is perpetuated by the retailers who combine the two peptides so the Ipa dose is orders of magnitude larger than it should be.
The Huberman episode with Craig Koniver discusses proper Ipamorelin dosing to be in the range of 100mcg daily. People taking multiple milligrams to "feel" it are not doing themselves any favors. As pointed out in the above discussion, looking to side effects as a sign that a compound is working is not a valid or healthy pursuit when administering drugs. I mean, you all can do what you like, but I don't think doses in MG are serving the purpose you hope they are.
Its been well worder that ghk-cu doesn't really mix well with almost any peptide. I guess that's why klow is starting to get a bad reputation.
That is part of the plan. Going to start TRT early next year. Want to give that some time on its own, then will add some sprinkles on top down the road, including GH, which I've already amassed a fair amount of in preparation.Would you consider moving on to gh from the tesa ipa combo?
Coming up on 12 weeks 100mcg Ipa / 2mg Tesa 5x a week
I'm also on Reta, so to the degree it contributed to this result maybe we call it 50/50 at best. But I took Tesa specifically for visceral fat reduction. Dexa scan last week shows reduction from ~1.5 lbs of VAT to .75 lbs. I'll take a 50% VAT reduction as a win. Curious based on the FDA studies if discontinuing Tesa will bring VAT mass back to baseline, or if those findings had something to do with the limited lifestyle habits of HIV patients, vs my lifestyle of daily fasted cardio & weight training 6x a week.
Either way I think the risks of combining secretagogues is dose-dependent, and it seems the fitness community is sold on overdosing Ipamorelin to a concerning degree. This is perpetuated by the retailers who combine the two peptides so the Ipa dose is orders of magnitude larger than it should be.
The Huberman episode with Craig Koniver discusses proper Ipamorelin dosing to be in the range of 100mcg daily. People taking multiple milligrams to "feel" it are not doing themselves any favors. As pointed out in the above discussion, looking to side effects as a sign that a compound is working is not a valid or healthy pursuit when administering drugs. I mean, you all can do what you like, but I don't think doses in MG are serving the purpose you hope they are.
Unfortunately the predisposition to accumulate visceral fat, “central adiposity” is mostly regulated by growth hormone.
Keeping weight off will delay any reaccumulation, but unless you stay in perpetual perfect caloric balance or a deficit, in the normal cycle of your endogenous GH pulses triggering free fatty acids release from fat cells, any that go unused, regardless of where they come from (ie subQ if you already got rid of most visceral), they’ll preferentially redeposit in visceral fat.
Hence my question. If it doesn't mix well, why do KLOW tests show the separate peptides still intact?
The reason cagri sema is a difficult one to formulate is because both are stable at different pH’s. Not because they interact with each other.Sorry, what tests show this? No simple HPLC test can detect determine peptide interactions.
There are NO multi-peptide pharma drugs. Cagri-Sema would be the first if its approved, and requires careful formulation and use of specific excipients that prevent them from interacting in solution.
I’m aware my guy.Primo is methenolone and mast is Drostanolone
Sorry, what tests show this? No simple HPLC test can detect determine peptide interactions.
There are NO multi-peptide pharma drugs. Cagri-Sema would be the first if its approved, and requires careful formulation and use of specific excipients that prevent them from interacting in solution.
They react inside your body not in the vial my man. Hence jano test shows the contents and has absolutely nothing to do whith what that/those compounds will do to an individual.My only claim is that the tests show the mass of each separate peptide. So if the mass of each is still detected, what indicates their denaturing, or the lack of bioavailability, or the lack of effectiveness?
