Qingdao Sigma Chemical Co., Ltd (International, US, EU, Canada and Australia domestic

damn thats crazy with the variation of location
yeah def is. not saying there arent other states that its super dangerous. i was just naming off a couple. but as long as this is the only stuff u are dealing with. u will never have to worry about going there. Thankfully the law isnt too strict with PEDs. Unless you are moving tons and tons of this stuff, which most of us arent
 
when it comes to prison it all depends who you are, what you're in for, and where you're at. Mass, New Hampshire, and Maine are a joke. if you're in cali or florida however, theres a chance of dying every single day

damn thats crazy with the variation of location
I can only speak.to where I was which is a deep south state.. southern states are from what I understand jumping a little harder.. but each state has several units sime rougher and tougher than others, it all depends on where the staff pool.is coming from.. where i did my first 3 years the nickname of the place was "gladiator school" unlike anything or any movie you could fucking imagine.. I'm not gonna go.into.detail., but like dude said carry yourself well, fight if you got to and so won't have to all.the time.. mind your bussness...
Peace
D
 
Just got my first kits of Tesamorelin. If anyone has any particular tips or anecdotal data, would love to hear their experiences.

Been using it daily for 8 months. 2mg/d in the morning.

I reconstitute with 3ml Hospira.

Switched from filtering the entire vial to per dose filtration, which reduced the site reactions 90%.

I keep the contents of the whole reconstituted vial in a 3ml syringe with filter and needle attached. Still backfilling insulin pins from that setup. Realizing the entire barrel of the insulin syringe is exposed to air even with the plunger in makes me even less concerned about the 5 seconds the plunger is removed to backfill.

No sides whatsoever.

IGF saw a ~100 point boost.

Significant stomach flattening as will as all the other expected GH benefits to hair, nails etc, but took a few months to notice.

Tesa is a marathon, not a sprint. Max benefits usually take 6-12 months to develop. It's intended for lifetime use.
 

Warning!

"This should be even more of a priority when a source is missing in action where warnings to customers of source status can prevent future harm, and reports of (unfulfilled) outstanding orders can document past/ongoing harm."
But does this source need a warning since they’re not taking any correspondence, order or payments?
 
Been using it daily for 8 months. 2mg/d in the morning.

I reconstitute with 3ml Hospira.

Switched from filtering the entire vial to per dose filtration, which reduced the site reactions 90%.

I keep the contents of the whole reconstituted vial in a 3ml syringe with filter and needle attached. Still backfilling insulin pins from that setup. Realizing the entire barrel of the insulin syringe is exposed to air even with the plunger in makes me even less concerned about the 5 seconds the plunger is removed to backfill.

No sides whatsoever.

IGF saw a ~100 point boost.

Significant stomach flattening as will as all the other expected GH benefits to hair, nails etc, but took a few months to notice.

Tesa is a marathon, not a sprint. Max benefits usually take 6-12 months to develop. It's intended for lifetime use.
This is great info. I had a reaction about a year and a half ago when I tried Tesa and have wanted to give it a go, again. I’ll google the process you’re referencing and see if I can get a better grasp on backfilling. I need to lean out and lose about 10 lbs before I start a cycle of it.
Thanks for your insight.

Also, thanks @readalot for linking that video re: filtering. I’ve just been going at it unfiltered and you guys have me a bit more educated.

Appreciate it. :)
 
This is great info. I had a reaction about a year and a half ago when I tried Tesa and have wanted to give it a go, again. I’ll google the process you’re referencing and see if I can get a better grasp on backfilling. I need to lean out and lose about 10 lbs before I start a cycle of it.
Thanks for your insight.

Also, thanks @readalot for linking that video re: filtering. I’ve just been going at it unfiltered and you guys have me a bit more educated.

Appreciate it. :)

Here's a peptide filtering vid just posted in another thread,

I was having this exact thought earlier today, and I came across this video on YouTube:


View: https://youtu.be/o7EUN3FGzPs?si=TZQqiZquolleKD03


Can anyone comment on the quality of this filtering process? Is this a safe tutorial to reference?


To back fill instead of filling a vial, pull the plunger out of an insulin syringe, put the rubber plunger tip into the plunger cap just removed from the syringe, and lay that down to keep the tip from touching non sterile surfaces, fill the insulin syringe with the filtered syringe needle at an angle inside the insulin syringe barrel. cap the filtered needle, put the plunger into the insulin syringe just barely. Flip needle side up, tap until the air bubble rises to the top, and push the plunger in enough to expel the air, Ince you have it down should take less than 10 seconds. Practice with water first.

IMG_0436.webp
 
Last edited:
Here's a peptide filtering vid just posted in another thread,



To back fill instead of filling a vial, pull the plunger out of an insulin syringe, put the rubber plunger tip into the plunger cap just removed from the syringe, and lay that down to keep the tip from touching non sterile surfaces, fill the insulin syringe with the filtered syringe needle at an angle inside the insulin syringe barrel. cap the filtered needle, put the plunger into the insulin syringe just barely. Flip needle side up, tap until the air bubble rises to the top, and push the plunger in enough to expel the air, Ince you have it down should take less than 10 seconds. Practice with water first.

View attachment 317272View attachment 317273
Thank you!!!
 
Here's a peptide filtering vid just posted in another thread,



To back fill instead of filling a vial, pull the plunger out of an insulin syringe, put the rubber plunger tip into the plunger cap just removed from the syringe, and lay that down to keep the tip from touching non sterile surfaces, fill the insulin syringe with the filtered syringe needle at an angle inside the insulin syringe barrel. cap the filtered needle, put the plunger into the insulin syringe just barely. Flip needle side up, tap until the air bubble rises to the top, and push the plunger in enough to expel the air, Ince you have it down should take less than 10 seconds. Practice with water first.

View attachment 317272

Oh, wow, excellent. Thank you.

Out of curiosity, what would be the practical application of doing this method of a syringe back-fill instead of just filtering into a vial?
 
Oh, wow, excellent. Thank you.

Out of curiosity, what would be the practical application of doing this method of a syringe back-fill instead of just filtering into a vial?

Aggregates form when the peptide is in liquid form during manufacturing or after reconstitution.

After filtration, the peptide solution will be free of large aggregates. However, depending on the specific peptide, PH of the solution, concentration, and other factors, aggregates can reform. (ie 1 point of PH difference can speed up aggregate formation 10x in HGH).

So filtering as close to administration is ideal, since there's no "incubation" time for new aggregates to form.

Tesa is compound known to induce site reactions even in pharma formulations. After filtering into a new vial there was no site reaction during the first dose vs the painful unfiltered Tesa.

However, by the 3rd, 4th, and 5th daily doses pain gradually intensified, suggesting aggregates reformed.

By filtering each dose just before use, those injection site reactions are virtually eliminated, which suggests a lower level of immunogenicity, to maintain maximum efficacy.

Not every peptide is as prone to rapid aggregation so filtering into a vial may be fine. But we usually don't even know whether the PH of a peptide solution is correct. I just per dose filter them all now. I could do it blindfolded.

That said, I'm not wagging my finger at anyone saying you must do this. I've decided this is a low effort process I'm willing to use because of what my research into aggregation has shown me the benefits likely are.

Here's a little about "incubation" in a wonky paper about GLP aggregation I was reading earlier today.

IMG_0599.webpIMG_0598.webp

 
I just got out of prison.. .. the deffo dont hand you an ipad as you walk throught he door.. not where I was anyway. They hand you a pair of boots and you had better put those mother fuckers on. .... you can tell a person comfort level in prison by what they sleep in... fully clothed boots on=new or scared.. sleep in your boxers= get me if want I don't give a fuck....
Ahh the iPads and tablets. For what it's worth, all that stems from the FCC putting limits on what Detainees could be charged for phone calls. This is one of the few "big government" interventions I agree with. It's gross what they were doing due to having literally a captive audience.

Once that happened, suddenly the GTL's, Talton, Keefe, etc...all talked their customers into deploying tablets since the FCC isn't controlling Video Chat, music, movies, email...etc.
 
Anyone ever purchased a peptide mix for sleep that has the below? I am trying to figure out dosage for tonight.

Midnight Blend 261.25mg (20ml)​

Product Contains: Histidine 75mg, GABA 75mg, Taurine 75mg, Theonine 35mg, Melatonin 1.25mg
 
Aggregates form when the peptide is in liquid form during manufacturing or after reconstitution.

After filtration, the peptide solution will be free of large aggregates. However, depending on the specific peptide, PH of the solution, concentration, and other factors, aggregates can reform. (ie 1 point of PH difference can speed up aggregate formation 10x in HGH).

So filtering as close to administration is ideal, since there's no "incubation" time for new aggregates to form.

Tesa is compound known to induce site reactions even in pharma formulations. After filtering into a new vial there was no site reaction during the first dose vs the painful unfiltered Tesa.

However, by the 3rd, 4th, and 5th daily doses pain gradually intensified, suggesting aggregates reformed.

By filtering each dose just before use, those injection site reactions are virtually eliminated, which suggests a lower level of immunogenicity, to maintain maximum efficacy.

Not every peptide is as prone to rapid aggregation so filtering into a vial may be fine. But we usually don't even know whether the PH of a peptide solution is correct. I just per dose filter them all now. I could do it blindfolded.

That said, I'm not wagging my finger at anyone saying you must do this. I've decided this is a low effort process I'm willing to use because of what my research into aggregation has shown me the benefits likely are.

Here's a little about "incubation" in a wonky paper about GLP aggregation I was reading earlier today.

View attachment 317276View attachment 317277

Interesting. I'm finally going to commit to filtering my Tirzepatide, and I'm planning on starting GH in the next 2-3 months (after I'm more confident in my knowledge base on GH). I want to maximize efficacy from the beginning with the GH, so this information is invaluable and greatly appreciated.
 
Back
Top