Peptides: where to begin?
science.org
science.org
The first is collagen: I'd love to see Lowe's take on recent peer review which says boosting oral collagen does appear to show signs of improved joint pain and skin resilience. Obviously modulated through how protein deprived you are, but for older people, eating enough protein can be an issue: it's not rapidly absorbed so you need 3 squares a day to get to the higher numbers. Collagen powders and vitamin C (oj) at breakfast might kick start this.
The second contradictory point is that this entire thread makes me want to shout GELL MAN AMNESIA because it's an exercise in otherwise intelligent people who can distinguish between anecdata, their personal experience and some cold hard facts in their core field, but not when it's self injecting unknown chemicals from China bought off-script.
> Collagen powders
In that case if you're eating collagen powder you could be eating just regular protein powder then?
https://pmc.ncbi.nlm.nih.gov/articles/PMC10180699/
It has a Mechanism section which explains that when collagen is digested, one of the products of that is Gly-Pro-Hyp, which is what has the effects. I don't think that conflicts anything in this post?
...BPC-157 itself is said to be among this class. As are certain milk tripeptides: https://en.wikipedia.org/wiki/Lactotripeptides
Interestingly enough, those two, as well as Gly-Pro-Hyp, are proline/hydroxyproline-rich, which might suggest that proline-rich small peptides are resistant to degradation in the gut.
Anyway, in general oral proteins and peptides are broken down prior to systemic absorption, but not always...
Do you know of any studies that suggest BPC-157 absorption from gut?
Among others. If you read the paper, it's actually apparent that there's little difference between i.p. and oral administration in terms of efficacy -- both were roughly equally effective in improving MCL ligament healing.
Admittedly the paper's in rats -- as are 99% of the others -- as there's no incentive for anybody to run human trials.
There are two groups, those with oral administration those with sub-q administration. There is not group without administration.
This means you can't say that oral vs injected is "equally effective" because you can't assert that BPC 157 is effective at all. You can't tease out the effect size because you don't know if any or all of the MCL ligament healing was done via normal pathways
Is that true? It seems that you can say that they were equally effective without quantifying an effect. It could be the case that both are equal in that neither has an effect, which this would validate. Then you can just point to other studies to claim effectiveness of injected.
There were control groups.
> Methods:
> [administration] as follows: (i) BPC 157 10 mg or 10 ng/kg or saline 5.0 ml/kg (controls), intraperitoneally, or (ii) BPC 157 in neutral cream (1.0 mg dissolved in distilled water/g commercial neutral cream) or commercial neutral cream (controls), as a thin layer, locally, at the site of injury, administered once daily with the first application 30 min after surgery and the final application 24 h before sacrifice; (iii) BPC 157 0.16 mg/ml or nothing (controls) in the drinking water (12 ml/day/rat) until sacrifice.
There was a big difference vs. the control groups.
> You’re not going to be taking these things orally... These mail-order peptides are injectable items.
Every single YouTube video and blog post I have read about peptites is exclusively about injectable supplements.> because unless a really substantial amount of engineering has gone into it, any given peptide is going get the same treatment from your digestive system as a chicken breast does, i.e. a complete teardown
> Every single YouTube video and blog post I have read about peptites is exclusively about injectable supplements.
Collagen peptides, ghk-cu, and many other peptide supplements are often taken orally.
And with very rare exceptions, it's as useful as watching someone workout when you want to gain muscle. Every meat we eat is awash in peptides, and to keep our body from getting hijacked by the signaling for, say a chicken, our body has to break down almost all peptides ingested orally.
There are a few exceptions, notably there's one that is produced by our own bile acid, that can be taken orally, and then SNAC, which was developed by Novo Nordisk over thirty years and has extremely limited capabilities and is fully patented and cannot be made by your fly by night distributers. SNAC achieves a whopping 1% bioavailability of the peptide, and it's ability to work depends on the size of the peptide, specifically the only commercially available use for this is Rybelsus.
Oral peptides are snake oil for the most part.
Who cares? I never made broad claims about their efficacy, the author did.
> Oral peptides are snake oil for the most part.
The author's claim is not nuanced by "for the most part", that's why I quoted it directly.
Besides, I was merely clarifying what the other poster was likely referring to.
That age group (and all others) should be eating real/whole fruit or having the juice fresh (I.e. just juiced). They would be better served getting this advice than creating more anxiety about protein intake.
> Commercial orange juice with a long shelf life is made by pasteurizing the juice and removing the oxygen from it. This removes much of the taste, necessitating the later addition of a flavor pack, generally made from orange products.
> Commercial squeezed orange juice is pasteurized and filtered before being evaporated under vacuum and heat. After removal of most of the water, this concentrate, about 65% sugar by weight, is then stored at about 10 °F (−12 °C). Essences, Vitamin C, and oils extracted during the vacuum concentration process may be added back to restore flavor and nutrition.
So essentially there are components that vaporize during processing. The make sure to condense the same components and add them back in so that the orange juice contains all the components of fresh orange juice.
Mechanistically it makes sense, as I understand the ingredients in Collagen are largely a subset of the ingredients in whey powder, albeit at different ratios.
I always wondered if there were nutrients we can’t measure though, because collagen is typically made from skin or bones whereas whey protein is dairy. Even though both have similar “nutrition facts” maybe there are some unmeasurable differences. Both are highly processed though so who knows.
FDA approval is expensive slow process. Doctors train for a long time and then work 40+ years entire careers, some without a ton of continuing education.
But then we have an entire gray market because enough legal and practical loopholes to drive a freight train through, such that people are self medicating with dubious substances of dubious origin of dubious purity sourced via dubious means.
Even if peptides work, you have no idea what side effects they have, or if the ones you are taking are even real, not contaminated/tainted in some manner, etc. Given a lot of the hype comes from social media for otherwise healthy people to take them for lifestyle / augmentation reasons.. to me the risks still outweigh the rewards.
Real solutions like regulatory reforms to find ways to bring down testing costs seem more important than reforms to make it easier to slap anything on the shelf at GNC as a completely untested “supplement”.
> some without a ton of continuing education.
Where did you get this idea? I did a simple, five second Google search and learned that on average, US doctors are required to complete about 50 hours of continuing education for each one- to two-year recert cycle. (On HN, I also hear similar complaints about public school teachers. It isn't true. Public school teachers are required to do similar continuing education.)Compare how seriously many SWEs take mandatory HR/compliance trainings vs hanging out on HN, taking online courses, arguing about code, trying new frameworks, coding in spare time, etc.
Overall I'm quite pleased with the effects and many of the properties of this treatment that people dislike are actually properties I was looking for. Essentially, for pharmacological interventions I want impermanent effects with a clear dose-response relationship and ideally minimal or no adaptation.
So the fact that people gain weight when they go off it and then lose weight again when they go on it was good. That meant it's fairly easily undoable. The fact that the more you take the more you lose also was pretty good to know though for the majority of the time I took less than any tested dose (and the effects were quite strong on those).
I did experience quite a bit of adaptation so I needed to up the dose until I was in the range tested by the end. I've been off it for a month now and been pretty much flat, but we've been traveling since I stopped and so a lot has changed (no more lifting, lots more eating, lots more walking).
Rough cost for the retatrutide is $1.25/mg.
Even with free healthcare that seems like a foolish place to save money when very widely used alternatives exist in the regulated market.
Which ones? Semiglutide costs orders of magnitude more.
> had access to free tirzepatide
I fear this kind of post will encourage gullible people to go chasing reta on the grey market, where they might as well be getting a placebo, as there's no mechanism for your typical person to verify that they're getting what they think they're getting.
And given it's an injectable, and bacterial growth, or a variety of other toxins that can remain in poorly manufactured pharmaceuticals, can do a great deal of harm.
Think what would happen if there was one.
In the spirit of selling shovels in a gold rush, the first company to commercialize a tricorder is going to make bank off all the fitness fads and off-label/DIY medicine markets.
Bench 1rm: 315
Squat: 5x10 225
Deadlift: 5x5 315
After: same height lol, 154lb
Bench 1rm: 285
Squat: 5x10 205
Deadlift: 5x5 275
Suffered some anhedonia towards the end but that went away ~1wk after stopping. Overall pretty good, not any side effects. Definitely fixed my food craving problem. I didn't have a high intake of protein during the 10 weeks, so I suspect thats why I lost muscle mass :/
I thought that this was not yet substantiated in human trials? There's a plausible mechanism and, I think a mouse trial, right?
It's also not borderline impossible to maintain the majority of your muscle mass, but it depends on how you eat and train. We don't know enough about the person above's diet, training, current body composition, etc. to say anything for certain.
How did you actually feel? Disinterested in stuff, ennui, or other?
Large caloric deficits (1000+/day) in leaner people is known to tank T levels among other things. When I was on such large deficits, I had very weird mood/arousal swings. Nothing that problematic for someone with as much executive control as me but it was very weird to be held hostage to.
> In this study, rapid weight loss was associated with the loss of kidney function in males with normal weight, and with improvement of kidney function in overweight males.
> Our study showed that BMI and BMI change were not associated with eGFR change in females.
I owe my health to early adoption of experimental peptides, I have life long ME/CFS and there is no known treatment for this nor is there any on the horizon. At least they finally have a diagnostic test and know it's not psychosomatic but I could have told them that from day 1. Most doctors are not researchers and have little understanding on statistics instead preferring to rely on discrete classifications and simple decision tress. As someone with hEDS from TNXB I am a walking bag of symptoms and yet not a single doctor could figure it out. I had to research it myself which involved post-doc level textbooks and research journals. I came across the work done by Prof. Khavinson (USSR) and it did appear to me that peptides were incredibly under-explored. Given the poor quality of life with ME/CFS I was willing to take serious risks so previous trials were helpful to give an idea on dosing and lethality, I went through most of the research peptides one by one. I actually waited on semaglutide a bit because I suspected there was a small minority who would have hyper sensitivity and I both expected that to appear in the data, which it did, and I expected to have hypersensitivity, which I did. Others who were less careful ended up with pretty bad gastroenteritis. Semaglutide has been the most effective and with it and a few others I am largely able to lead a normal life. I was getting gray market from the US but now I get it direct from China.
Most of the stuff I’ve tried that worked usually has an immediate or overnight effect. Notably Low Dose Naltrexone was overnight, Low Dose Abilify was near immediate. I believe this is due to their immunomodulator properties. So I studied psychopharmacology and focused in on finding weaker ligands than typical as a way to try and safely modulate my immune system. I landed on Modafinil in the morning and Amitryptiline at night, both off label treatments for the probably related dysautonomia.
The N of 1 with many overlapping signals and medications was of course very noisy but I treated it like a ML optimization problem. I could tell it was likely beneficial within the first week even with the small dose. I probably could have statistically determined it was working within a few months but I was distracted by work so it took a little longer to be sure.
Also I don't understand how semaglutide did help you while you're at the same time part of a minority risk group with a hypersensitivity to it. Isn't that a contradiction?
I'm giving you a thorough response because I'm detecting a cavalier anti scientism which I think is sadly becoming more common. This stuff is hard; are you sure you understand it enough to have an informed opinion?
I understand that the symptoms of ME/CFS might be similar to being obese/depressed or housebound, but the problem is that doctors often jump to that conclusion too quickly and don’t take efforts to diagnose ME/CFS leading to situations like my aunt’s. She was also obese and depressed and has been struggling with those symptoms for about 30 years and has constantly been misdiagnosed the entire time because doctors didn’t figure out that those were symptoms of ME/CFS and not two unrelated conditions coming from two different diagnoses.
Thanks to long-covid putting the symptoms of ME/CFS on the forefront lately, there’s finally been some much needed research into the disease and people like my aunt finally get the diagnosis they should have been getting many years ago.
I have followed closely the research for many years and there has been false promise of good diagnostic tests previously. What I'm arguing for is that we need a test that is specific for ME/CFS. E.g. it will test positive for a patient with ME/CFS regardless of they are obese or not, but more importantly it will not test positive for everyone who is obese. This is known as the sensitivity and specificity of the test.
What I've seen in the past is some previous ME/CFS tests show positive for groups with related symptoms but who don't have ME/CFS. This then becomes a worthless diagnostic tool. For example this would not have helped your aunt.
Hope this explains my thoughts!
Thank you for clarifying and I wholeheartedly agree.
Welcome to the powerful world of the placebo
> Peptides are a revolution and you don't need to know how they work to know that they work
Perhaps. But knowing the mechanism of how they work sure seems fundamental to ensuring that they are safe to use.But for self-use? Go right ahead.
Crack is really moreish.
I had an ME/CFS patient that had tried 100s of things and documented the effects thoroughly. She had a quite impressive list. Roughly 30% had had an effect to begin with, but the trend she observed was that it lasted for around a month at most. Placebo was her overall conclusion, but she occasionally got relief anyways so we both agreed that there was no harm in continuing. I'm sure several "peptides" is on her list by now.
There is nothing new under the sun, and fad cures for diffuse conditions have come and gone many times before. This is especially the case for conditions involving pain or tiredness, which are extremely sensitive to both placebo and nocebo.
What would be revolutionary would be 2-3 double blinded RCTs showing a lasting effect. Which would be great if someone did! But you have to actually bother to do it. And personally I would put money on the outcome being "no effect".
Amen to this. The plural of anecdote is not data.
People have been hawking snake oil for centuries, and people have been believing snail oil cured them for centuries.
For medical research, the goal is to find general practices that will broadly help, and identify risks with the intervention. Even then, with many interventions, it's understood that they will effect people differently.
For individuals, they don't care about variation in communities, or standard medical practices, they are looking for relief for their specific condition.
Of course, declaring that just because something worked for one person, it should work for others, is wrong in both camps.
I feel like a big part of the disconnect here, and a big reason why people are talking past each other, is that they actually have different goals, and aren't really aware of that difference.
Basic human thought patterns usually lead people to think that anecdotes about their personal experience is valuable for understanding the world, but this is wrong. The scientific revolution basically illustrated the flaw in this premise outside of hypothesis generation. It takes specific education to make human beings truly believe that their anecdotal experiences are mostly irrelevant beyond understanding their immediate circumstances. The proportion of humanity that truly think this way is relatively small.
Understanding the world through anecdotes still works okay-ish for a lot of areas, but ascertaining relatively subjective effects of experimental pharmaceuticals is not one of them. But to many people it's non obvious that this is the case. And as a general method of thinking about this issue, it is just the wrong way to go about things.
And that's the disconnect, in my opinion. The OP drew a conclusion from a thought pattern that comes easily to human beings, but that is just wrong in this situation. Of course, perhaps this is reinforced by underlying motivations, but that's not what makes people talk past each other. These kinds of discussion are usually driven by so called "deep disagreements" in epistemological understanding, in my experience.
I would encourage everyone interested in peptides to read about the state of medical science before the establishment of the Pure Food and Drug Act of 1906.
Isn't one of the bigger problems with ChatGPT that it's much too supportive of whatever the human is talking about?
But it does require to know the bias that LLMs have ahead of testing this.
Doctors, at least 15 years ago, were definitely bad at statistics.
They were not required to take a statistics course at all. Most programs would require Algebra and Calculus as part of their science reqs.
Some would maybe take one basic research course, and they would then become obsessed with p values of 0.05.
They did not have a basic understanding of how to interpret research unless they were an auto didactic and went out of their way to improve. It's something my director (a doctor and software engineer), and the Dean complained about relentlessly.
You reminded me about another idiosyncrasy: Doctors are addicted to double blind randomized control trials.
Which yes, those are powerful. But good evidence can come from many other study designs. Especially when mechanisms and first principles are being studied.
This is a deeply unfair statement, and also a false dichotomy. Medical science is of course empiric. What you call "fundamentalism" is that compounds need to undergo a rigorous regiment of empiric testing before they are given to potentially millions of people. And no, it's not just because of Thalidomide. Many, many compounds fail clinical trials because of severe side effects, like liver toxicity, severe immune reactions or heart problems. Then there's of course increased risk of cancer, which can take many years to manifest itself empirically. You argue that you prefer living with these uncertainties rather than ME/CFS, and that's of course entirely understandable, but disparaging the field of medical science as focused on "fundamentalism" because we do not give large patient cohorts untested compounds is polemic. I understand where you are coming from, and I'm sorry that you suffer from this terrible condition, but likewise, you should try to understand the other side.
Some examples: aspirin (willow bark used for thousands of years, drug synthesized in 1897 and mechanism explained almost 100y later), or general anesthesia used again since mid 1800s and the mechanism is quite still debated.
This is not to downplay all the long term, or developmental, risks that using something novel can result in. But we can empirically know something about the effects without having good mechanistic models.
Anyway, I don't think we really disagree, I rather misunderstood your original post. It's good to hear that these new peptides are helping with your condition, and I wish you all the best!
As a fun aside, consider the effect of the birthday paradox on empiricism, as the pool of candidates grows larger the probability of a match increases substantially as potential matching candidates increases quadratically.
Particularly when the mechanism behind most of these peptides comes down to "promotes more rapid cell growth". The intent may be to repair the skin, muscles, or ligaments, but biology is rarely that specific.
Doctors, like many professions, have institutional blind spots, I studied these in my search because I was looking for something that had not been found. Most doctors have to consider all people and all conditions, I only have to be concerned with one.
Notably they only recently adopted Bayesian statistics for medical trials despite that math being around for hundreds of years.
ME/CFS research is severely underfunded. The reasons for this are not simple, it's partly due to the complexity of the disease which, as cynical as it is, does not make it an attractive research topic for ambitious scientists. Same goes for "Big Pharma". Clinical trials for ME/CFS are extremely complicated, and hence expensive, due to the myriad of symptoms in how the condition can appear. It makes research in this area very difficult and expensive. There's very little funding for ME/CFS research, and that needs to change. Unfortunately, especially in the US, this is not going to happen for Kennedy reasons.
The Bayesian statistics thing is a bit of red herring, though. While your are correct that the math is old, the needed compute resources for doing Bayesian modeling on large trials was simply not there until recently. But it is also correct that it also took a long time until there were official rules regarding this from FDA and EMA. These regulatory things move very, very slowly.
The UK led the world with explicit psychologizing of it in large part to prevent insurance companies being liable for such an expensive and debilitating condition. A legacy that continues to this day, the main people responsible are still very influential. Fauci was instrumental in diverting research away from the autoimmune aspect and preventing a lot of important research. The $1B set aside for LongCovid appears to largely have been wasted. The official classification for hEDS was explicitly changed to reduce the number found so that it could remain a rare disease and continue to have access to specific funding for rare diseases (goal seeking). I could go on and on. It is a highly dysfunctional industry with many perverse incentives pulling it in all sorts of directions. There was the healthy at any size movement despite obesity being a massive cause for mortality, perhaps the only stronger signal would be smoking and consider how long it took them to figure out smoking.
There have been insanely impressive improvements to medical science but this seems to be largely due to tooling and access to information rather than the lumbering bureaucracy which appears to do very little of benefit.
Yes they will miss rare cases or where symptoms aren't quantifiable or where no understood biological mechanism exists. Yes you can take on research and treatment yourself with the risk associated. No a bunch of anecdotal evidence on experimental treatments do not substitute for structured research. No you won't come back here in 3 years if you develop serious side effects that would have been identified in clinical trials and tell everyone you were wrong.
So I’ve been doing this for over 4 years now, and commenting on this with this account for a bit less than that, so far no serious unwanted side effects other than the usual ones for semaglutide which went away. Of course that has a survivorship bias but in the forums people do often tell others what they’re about to try and we would notice if they stopped showing up.
There is always tension between objectives in real-world systems. There are essentially two frontiers in our healthcare system--a core of educated professionals that are conservative and move slowly with ample evidence behind decisions, and a wide range of laymen who are comfortable with personal risk (e.g. bodybuilding community). I have respect for both, and they work together. The core will always have too many false negatives and the horizon group will have too many false positives. Saying the balance right now slows things down too much needs more support as an argument, there will always be things on the roadmap for medicine and there will always be edge cases that can't get addressed perfectly
From what I've seen medical researchers are champing at the bit for new areas of treatment that they think are promising and they just need the smallest amount of convincing evidence to research. If they don't have it for something you think is valuable, collect the information in a systematic way and find someone to send it to.
Unless you have a research lab built out in your house, you have zero way of knowing what it is that you're actually getting. Whether the dosing matches the claimed dose. Whether there are bacterial growth, or other manufacturing chemical left in by bottom-of-the-barrel chinese manufacturer.
I understand your risk profile may be different than others, but when you can get the real thing officially, I'm not sure why anyone would risk this.
The article itself raises the issue of "lack of clinical data", given that these substances are relativelly new. But the lack of data may originate from a certain stiffness, or lack of accessibility and high cost of clinical trials. An alternative source of information are these people who self-experiment, but unfortunatelly this information is mostly lost instead of being captured.
How could this proposal work in practice? clearly the data would be noisy, contain some false reporting, biased, subjective etc. But statistical processing of a large number of reports (coming from hudreds of thousands or millions of self-reporting subjects) may still extract relevant scientific information; that we're dropping on the floor right now.
An example: I'm experimenting with a radical diet. I keep observations for myself, but they're not shared with anybody and don't contribute to science.
What the altervative would be: I would enroll on a web page, where I would describe the experiment I plan to do before I start it. I would be get a code for a blood/urine work for the "before" state, with the agreement that the results, anonimized, are shared with the platform. Weekly I would report on the platform observations, such as: got sick in this particular way, wheight variations, sleep eval, or any other changes.
At the end, or periodically I would get new free blood/urine work with the results shared.
Research institutes and pharma would get access to the data, to aggregate and denoise as they can to extract the latent information.
https://www.newyorker.com/magazine/2026/04/13/why-are-people...
But the way "peptide" is used by all the bro/gal-science influencers that push them online makes it blatantly obvious that they have next to no idea what they're talking about.
Also, if you plan to be on it a good long time, you can buy a bunch of kits yourself (a kit is 10 vials), run a bunch of tests, and then just have a nice stockpile that will last you years. The testing will likely cost as much or more than the product itself, but given how inexpensive the product is, you still come out way ahead financially.
It is illegal, but it doesn't stop people from doing it. In fact, if you don't have any sort of test results for your peptides people will absolutely avoid buying your wares until you have them. Purity and mg/ml are the 2 basic test results that any shop worth their stuff will have.
After nearly getting hosed in a group buy (I did get refunded, but that is far from a guarantee) because of a product mismatch, I decided to just pay for nexaph. Love him or hate him, his popularity relies on his reputation and he has been more careful than most suppliers to cultivate it with more extensive testing and quality control.
<Insert that "one of us, one of us..." GIF here>
I know a bunch of people with multi-year stockpiles. I've got ~5 years of reta and ~6 years of tirz. This is too much, of course, but I determined a while back that under no circumstances do I ever intend to find myself unable to source it. My life is immeasurably better after losing 110 pounds.
There's this company that offers free testing: https://finnrick.com/
Another popular testing company is https://janoshik.com
Some other useful resources: https://graymarket.substack.com/ and https://glp1forum.com/
There are a few subreddits as well.
FWIW, I never ended up buying any myself.
Where do you think Hims, Ro, Brello, or the rest get the APIs they sell to their customers? They get them from grey market suppliers in China. They don't go to Ely Lilly or NovoNordisk and say, "politely sir, may I skirt around your IP and sell your drugs for 10x what they cost instead of 10,000x what they cost?" Hopefully, they test them and filter them and use sterile/pharma processes for what they sell to their customers. Well, except for the Medspas, those are just wild west snake oil farms.
Today ... who knows? It might just be the same gray market stuff us plebes can get.
They did not make the peptides. They sourced them from China.
My gf is in medicine so she had a friend test it through their work.
There must be an irony that it was Trumps crackdown on peptides, I presume to prop up his prescription company, that forced me to switch to Chinese supply. By doing it all at once it created a critical mass for that market.
How so? Is there a particular characteristic of the US that makes it so, or of the channels through which this is done? I get that in general it's impossible as with recreational drugs, but when you look at cocaine then at least to traffick it to most wealthy countries it takes a large amount of resources and is at high risk of getting caught. Which is why they're increasingly starting to use narco submarines. This greatly increases the price of the product. Why can't the same happen to peptide imports?
They drop ship a box containing cold packs and the meds.
You dont need the idiocy of trumprx to get these prices, just go directly to Eli Lilly or Novo Nordisk.
Tirzepatide is $400-450 (depending on dose) per month directly from Eli Lilly.
https://www.lilly.com/lillydirect/medicines/zepbound
Novo Nordisk's drugs can be had as low as $250/month through third party (which is weird), though they'll probably honor those prices in direct sales before long.
https://www.cnbc.com/2026/03/31/novo-nordisk-wegovy-subscrip...
These are all cash pay prices, no insurance.
How did they test encapsulation? I thought the whole problem is your stomach acid breaking it down.
Even drug addicts heat up the thing they inject so theyre actually safer than you can ever be. Dont inject things from China into your blood!
Back when I started few people were doing this and it was more of a risk, I was buying from research peptide vendors who had their own testing practices, but now a huge number of people are doing it and there are markets where reputations matter and it appears to be reasonably efficient.
I would prefer not to inject peptides from gray market China but practically all of the gray/black market supply is from there. I will likely switch to pharma grade when generics become available.
The synthesis of peptides uses some NASTY chemicals. I would be worried about lax manufacturer policies leading to contamination, even if one batch passes. The costs of FDA certification are the effect of that protection.
But whatever, this is the same attitude that people have against owning insurance. It is hard to recognize the cost of risk.
At this point, broscience is considered no less valid than actual clinical trials, and the FDA should blame itself for this. Not "human nature being what it is in this fallen world" in a sort of general or abstract sense.
Another point I could raise is that telemedicine has turned the entire prescription system into nothing more than a parasitic middleman/gatekeeper.
FDA reform is very badly necessary. That ought to come before harsher enforcement, and I think that much of the populace already intuitively understands this.
I’m curious what you mean by this. I’m not sure what you mean by “prescription system” specifically.
If you can call up a teledoc and they give you a prescription based on your description why could you not just go buy the meds yourself without a prescription. You have essentially diagnosed yourself and just asked the doctor for permission to buy the drug you want.
It’s really clear that some of you are really mad about something you don’t understand.
> https://www.nytimes.com/2026/04/02/technology/ai-billion-dol...
People want GLP-1 drugs. They can't get them without a prescription. They pay $$$ to a "telemedicine" "doctor", recite a list of well-known symptoms, and buy the prescription.
The system is that you can't buy these drugs without the piece of paper, and the piece of paper is basically something that anybody can buy regardless of whether or not they actually need the drug. Wanting it is usually enough.
Also, most doctor's visits aren't any different from getting it if you want it except it's gated on the mood/attitude of the doctor, maybe your ability to sell some sob story. And then you book a different doctor until you get it. Telemedicine just makes the process easier an arbitrary system.
The prescription hurdle is absolutely necessary -- these are not drugs that anyone can safely take without guidance. It's the price that needs to be fixed.
You take a dose every two weeks. And if you accidentally double dose because you misread 1U to mean 1 dose, it just gives you some nausea.
Are we going to pretend it's hard to take this drug now too? Or that the doctor has some magical insight into your getting-on? Remember to eat. That's it. I guess a few people might need the doctor to go "you're eating, right?" but I don't believe in infantilizing everyone over that.
Additionally, getting the correct dose is not straightforward for a layperson as it is for other OTC drugs with standard doses.
I do think GLP-1s are just about right. It is appropriate to take them under personalized professional guidance.
Certainly you can abuse a GLP1 and get yourself very sick, or not abuse it and still end up with pancreatitis. But smoking and alcohol presumably cause way more cases of pancreatitis, and you don't need a script for a handle of Popov.
Indeed. In fact, I think just recently there were updated studies for at least one of the popular GLP1s that disclaimed entirely a link to pancreatitis.
Apparently we have forgotten people who died from eating disorders (previously called anorexia nervosa)?
There is a VAST difference between someone who weighs 300lbs asking for GLP-1 to combat morbidity and someone who is barely 100lbs asking for a GLP-1 to take off weight for bikini season. That's what needing to ask a doctor for a prescription is for.
Weekly, if you are following guidelines correctly. The half-life of most GLP1 peptides is 5-6 days.
I otherwise agree with your point entirely. Though anecdotally, I may have given my brother-in-law a single small vial of tirzepatide at his request so that he could experience it, and the results were ... not good. Turns out he's an idiot, thought that 'more is better', 'drinking enough water is for weenies', and 'I am not an alcoholic even though I get plowed most evenings.' All against my very specific advice on how to give it a try. Whoops.
My fault, yes, I should have realized he was too stupid to do it without adult supervision. He made himself so sick he almost went to the ER. Nothing really dangerous, of course, tirzepatide is pretty safe stuff, but overdosing on it can make you feel very shitty for a few days until the blood concentration drops.
You're totally missing the point thought. The prescription hurdle effectively does not exist. It's just a paywall.
You pay your $100, get a 3 minute call with a NP/PA/whomever, and basically the robot writes you a prescription for whatever you want. The point is you pay and you get the prescription. Patient safety has nothing to do with anything.
The advantage to a telehealth is not getting the prescription written -- it's that they'll fill it for cheap through a tiny compounding pharmacy that is making it, technically illegally, but are small enough to be off the FDAs enforcement radar for the moment.
It's slightly cheaper for me to use telehealth vs. billing through my insurance. The downside is it doesn't go towards my deductible of course.
The stuff you are describing are entire supply chains of a sort where you want a GLP-1 or perhaps a few other things like TRT. Those you are signing up for the drug itself, which happens to include the prescription part with it.
Telehealth can be used for any old medication you want. It removes the permission slip part of the process and replaces it with a payment gateway. If you have $75-150 you can just click some buttons and have a prescription for nearly anything you want at most a day later. This includes antibiotics, ADHD meds (getting harder on these), certain benzos, etc.
HIMS/HERS/etc. and their smaller ilk are super popular, but they are the tip of the iceberg.
Telehealth providers can certainly work with compounding pharmacies but not necessarily. If you are looking to get a prescription for Diazapam you are going to be getting that sent to your local Walgreens or whatnot.
How? Usually PCP visit are cheap and everyone gets one for free.
> HIMS/HERS/etc. and their smaller ilk are super popular, but they are the tip of the iceberg. > Telehealth providers can certainly work with compounding pharmacies but not necessarily.
Yeah I’m aware there are a whole host of services telehealths provide but the primary reason people use them for GLP1s is to avoid the name brand cost.
Unless that risk is egregious, informed adults should be able to accept it if they so choose.
What we might not agree with is specifically what "informed" or "egregious" might mean.
FWIW I do not think that most people agree with this.
I can tell you that the conversations I've had with people who take these drugs from telehealths or from med spas -- they generally don't understand how these drugs work, what the risk profiles, are or how dosing should be managed. There's a lot of misinformation going around about all these drugs.
"immiment" is a different word than "egregious" isn't it? Malnutrition, cancer, and death are pretty egregious as well, even if they occur maybe months or years in the future, aren't they?
Literally, enough people are fucking this stuff up that we have pop culture references to it: "ozempic face". Losing weight this rapidly is unsafe. Sure, a lot of people might consent to the idea of rapidly losing weight, but there's nothing "informed" about it.
Sure. I don't think that that implies we have the right system currently or that we can't come up with good definitions. And again, "informed" is almost definitely already an understood term in medicine since "informed consent" is already understood.
> they generally don't understand how these drugs work, what the risk profiles, are or how dosing should be managed.
That's fine. I don't think they have to understand how they work. They have to have the risks conveyed appropriately to them. They might make a call that's ultimately harmful. Adults can do that, they should be allowed to do that.
> "immiment" is a different word than "egregious" isn't it?
Well, yes. If I had defined "egregious" as the same word, that wouldn't be very helpful.
> Malnutrition, cancer, and death are pretty egregious as well, even if they occur maybe months or years in the future, aren't they?
Not really. Things that take years to happen are a lot less serious, especially as they can be monitored for. But again, this can all be explained to the patient. I'd say the bar for "egregious" should be very, very high. When in doubt, give patients the power to choose.
> Literally, enough people are fucking this stuff up that we have pop culture references to it: "ozempic face". Losing weight this rapidly is unsafe.
That isn't compelling. How many of those people are getting ozempic from a nurse practitioner at one of these compound pharmacies? If anything, I'd bet that doctors taking the time to ensure patients are informed would lead to a reduction here.
It's that your health care system the doctor is in builds a few extra hurdles. I've talked to my (non-tele) doctor about GLP-1. I've tried losing weight before, with her, there's a long history.
To get approval, between the hospital my doc is in and the insurance, I need to:
1) Have a BMI of >30. Since it's only 29.5, I get to stuff my face if I want to lose weight.
2) Have six sessions with a nutritionist. Which are massively useless, their advice is roughly equivalent to reading Cosmopolitan. I know because I had prior conversations, and they're documented. But still, gotta do it again.
3) Do six months on Weight Watchers. Which is one massive scam leading you right to disordered eating. Also, I've tried for years to lose weight via diet changes, documented and talked through with my doc.
4) Before I can get tirzepatide, I have to get semaglutide for three months to see if it works. Never mind there's study over study over study showing it's slightly less effective and has massively more side effects.
Or I can just cough up the cash directly and buy from Eli Lilly, if somebody signs that receipt.
I'm fortunate enough I could afford that, so I did. (After a second consultation with my family's doctor back home - both they and my doctor agreed it was appropriate, so it's not just a case of "wanting is enough")
And after six months, my weight was in a much better region, lipid panels were much improved, other related biomarkers looked better as well - exactly as numerous studies and my doctors said one could expect.
So, as long as I cough up enough money, sure, I can bypass all the hoops. My health didn't enter the equation, just screw the poors (whose treatment for worse outcomes because they couldn't get access will cost a whole lot more than GLP-1 would've cost).
So, fuck the "prescription hurdle" and the medical system in the US with a hot white glowing iron rod right up the ass.
As for "these are not drugs that anyone can safely take without guidance", that's not really true either.
They're neither hard to take - "inject one vial once a week into the flabby part" isn't rocket science - nor does it cause massive health risks by itself. (And the hazard ratios for diabetes 2 and cardio events are so spectacularly low that they dwarf the other risks)
Yes, talking to a doc is a good idea. No, the current gatekeeping is in no way necessary.
The diagnostic criteria is simply (BMI > 30) OR (BMI > 27 + a weight related comorbidity like high blood pressure or high cholesterol)
> They're neither hard to take - "inject one vial once a week into the flabby part" isn't rocket science
It's not that they're difficult to administer, it's that dosage needs to be managed appropriately.
In Mexico, for meds like mine, you can just buy them at the pharmacy. There's no reason for all this nonsense.
(Edit: same PCP refused to prescribe GLP-1s early, without any scientific or medical reason not to. Delayed my weightloss by months until I found a place that would.)
Due to drug advertising rules, the prescription system has been turned on its head, and the patient now goes to their doctor asking for a specific prescription.
Telemedicine took advantage of this and has effectively removed the middleman (the doctor) in many cases and you just sign-up look at a person on a camera, and get your drugs sent to you.
This is only true for a handful of drugs that are basically OTC already (or that have OTC formulations). Additionally, telemedicine didn’t take advantage of drug advertising- that’s an odd assertion.
I think this enabled telemedicine to work in the way it does not. The patient says "I want wegovy" and the telemedicine platform says "ok, here you go".
Would telehealth pill-pushers exist without this mentality?
They basically operate as a "pay for a prescription" service.
Figure out what drug you want, google the drug name and telehealth. You will be marketed in a wink wink sort of manner over how easy it is to get them, just hours away! Then if you are not a total idiot, you answer certain questions in the right manner on the intake form, the doctor (usually NP/PA or similar for most things) will quickly run through that and expect you to answer correctly - perhaps guide you a bit if you don't.
5 minutes later you have a prescription in the web portal and it's sent to your pharmacy of choice.
It really shows how the whole "permission slip" program is BS. I've used these services a couple times vs. my normal doctor just to save time and expense of an office visit. If I can click some buttons, have a call 30 minutes later, and be on my way to the pharmacy for $50 it's sometimes the path I take now vs. traditional route.
Someone used to the traditional doctor/patient relationship thing and prescriptions being "holy" would be shocked at how easy and gamed it all is.
And doctors are not dietitians.
Doctors in the US receive an average of under 20 hours of training in nutrition over four years of medical school. What little they do receive is often focused on nutrient deficiencies rather than on meal planning for health and chronic disease prevention. Less than 15% of residency programs include anything on nutrition.
To become a registered dietician requires at least a Master's degree in dietetics or nutrition or a related field, and at least 1000 hours of supervised internships.
PS: before any Europeans hold this up as an example of the poor US health care system, doctors in Europe average 24 hours of nutrition training.
In the drug division specifically, the number is about 75%.
And it shows on the research: e.g. does creatine help muscle building? No.[1] But cue some anecdote from someone where they also changed a dozen other things at the same time but are sure it was that.
[1] https://www.unsw.edu.au/newsroom/news/2025/03/sports-supplem...
[0]: https://pmc.ncbi.nlm.nih.gov/articles/PMC12665265/ - Meta analysis results; "after intervention, the Cr group exhibited significant strength gains"
[1]: https://www.mdpi.com/2072-6643/17/17/2748 - "A total of 69 studies with 1937 participants were included for analysis. Creatine plus resistance training produced small but statistically significant improvements... when compared to the placebo."
1. Most people don't believe it anyway. People want to hear they can eat hamburgers and milkshakes and be healthy. Telling them "we know that gives you heart disease and cancer" does nothing.
2. Nutrition is complicated and different for every person, because everyone has different things they can tolerate. The "perfect" diet is actually worthless because it has a 0% success rate. Really, we have to optimize for how miserable people are willing to be.
3. Most people are unhealthy enough that nutrition is the least of their concerns. That sounds crazy, I know, but if you're obese (which most people are!), then priority is being not obese. Not your nutrition. I know those sound related but they're way less related than you think.
Maybe because so much of it is wrong, or (very charitably, as much is industry-biased) outdated?
Lifestyle modification is a definite challenge and I’m not dismissing it.
Still, hamburgers and milkshakes don’t give you heart disease and cancer. Overeating, oxidative stress from low-quality ingredients, etc might.
What? “Oxidative stress”? Oh come on, at least go full “seed oil” if we’re going to talk nonsense.
Seed oils are not as bad as painted but some caution is needed given for instance the industrial processes used to bring them to market sometimes. Plus the way the oils are cooked when they create free radicals. This is not nonsense.
I don't know what else to tell you. Except maybe that if one gets this single concept, that quantities matter, it becomes immediately apparent why most of the "healthy eating" / fitness fads is just pure bullshit.
They absolutely do, particularly if you're getting most of your calories from them. If evidence-based medicine doesn't convince you, uh, hamburgers and supermarket milk tends to be processed.
Individual foods are—with some exceptions—neither bad for you nor good for you. A healthy diet can occasionally include doughnuts, and milkshakes. Your overall diet is what matters.
Messaging matters. When you tell people hamburgers and bacon and everything they love are bad, they stop listening, give up, or just eat some other junk that wasn’t prohibited. When you tell them some foods are good, they start buying into superfood marketing.
Diet is the only thing that matters. Lots of veggies are extremely useful because they add bulk without adding calories, and along with fresh fruits are great sources of fiber. Cheeseburgers can only come so often because they’re extremely calorie dense and send enormous reward signals to your brain.
Give people the tools they need to thrive, not just “don’t eat these specific bad foods, eat these specific good foods”.
Reading this chain of responses from the original is making my internal bullshit alarm (Brandolini's law) go "wee woo wee woo".
Not at all an expert, but from what I understood saturated fat isn't particularly good but it's not “no healthy level to consume” either (fortunately because you practically cannot avoid them).
I think you're confusing them with trans-insaturated fat (which I don't think are as bad as cigarettes either, but are still bad).
> Nutrition is run on fads - see whole fitness and healthy food bullshit.
You raise an interesting point. I watched a YouTube video recently of someone walking around a large US supermarket pointing out all of the processed foods that now claimed to be high protein. It is nuts!I wonder what will come after the protein boom? My guess: Fiber is back because you need to "fibermaxx" when taking GLP-1 antagonists. I can remember some of the funny adverts in the 1980s of old people taking fiber supplements to "stay regular". (See SNL comedy skit "Colon Blow" for a good laugh.)
When I brought it up with other physicians the answer was always that I probably get all the nutrients I need from regular food. Whatever that may be.
Dietary changes have helped me feel better and healthier and perform better, and a few vitamin and other supplements as well.
I’m not selling a lifestyle. I’m criticizing the foolishness of a food and drug industry based in the idea that preventing death or lifelong disability is sufficient.
As for broscience, moving into peptides was a logical next step after exhausting anabolic steroid "research". In fact, I'd say that biohackers are actually behind the bros when it comes to trying various peptides out and documenting experiences.
Agree. Unless it's addictive or in short supply, you should be able to buy it OTC.
I have it from good authority.
Ok, and? At worst you waste a couple hundred dollars and deem the alternative therapy not worth it and go back to your doctor but I know dozens of people at my gym that used BPC 157 and TB 500 that fixed their chronic tendon/joint issues within weeks of starting the therapy that physios couldn't fix for years.
They shouldn't be. If someone has chronic tendon or joint issues, that's something to discuss with a doctor and a trainer.
I am a super introvert and know at least half a dozen folks with such issues, more if you include my close friend group.
Any place that has a lot of physically active people stressing their limits a bit is going to have a lot of injured folks over a decent period of time. And of course it gets talked about quite a lot, since it limits performance and ability.
My trainer knows I have a chronic shoulder issue, and an adductor issue at the moment I'm working through that we need to avoid stressing too much. The few other folks who tend to work out around my schedule know of this, and I know of theirs.
Not very uncommon really.
I'm very on the fence over BPC-157/TB500, I really want to see some actual clinical trials ran on it. I have a feeling the effects are overstated, but I also have had a number of "insider" conversations where I know these and other compounds are very much being utilized in pro athlete injury recovery programs. Those athletes certainly are getting state of the art medical care via traditional sources, plus elite level physio therapy - so it's hard to say if the illicit injury recovery drugs are doing much or not.
I don't think I even know dozens of people, full stop, let alone well enough to talk to them about their peptide use.
According to our new AI overlords, a short synopsis of potential risks of BPC 157 based on mechanistic and animal work to date (don't know human risks because there haven't been sufficient clinical studies):
* Possible pathologic angiogenesis (abnormal blood‑vessel growth), which theoretically could support tumor growth or inflammatory and autoimmune processes. * Modulation of nitric‑oxide pathways that, at high levels, might contribute to anemia, altered drug metabolism (CYP enzyme activity), and possibly neurodegenerative processes in theory. * Concerns that its pro‑healing, pro‑growth signalling (e.g., FAK–paxillin) could encourage cancer spread if malignant cells are already present; this remains theoretical, with no proof in humans. * Possible liver and kidney toxicity suggested in some commentary and extrapolated from preclinical work, but not well characterized in people. * Immune reactions or allergic responses, including fevers, rash, hives, muscle aches, or systemic inflammatory responses
These do not appear to be results that would appear overnight. It would be "nice" if the folks injecting random shit into their bodies also disclaimed any subsequent medical intervention as a result of said shit, but that I suspect that's unlikely.
People for so upset that GLP-1 has no long term side effects.
There's still the crowd completely sure everyone will get HyperCancer in 10 years or something (they won't).
It seems to be like treating alcoholism with disulfiram: it's a miracle in clinical trials but in the real world the patients just lower the doses or discontinue treatment after 1-2 years and go back to their old habits.
This is totally false. I know a number of people who took GLP-1 to treat their obesity and then stopped and have stayed not obese.
This study found that 84.4% non-diabetic patients stop taking GLP-1 drugs within two years. https://jamanetwork.com/journals/jamanetworkopen/fullarticle...
Do you have a source for this "lack of real-world efficacy"?
> This study found that 84.4% non-diabetic patients stop taking GLP-1 drugs within two years
"With a with a median on-treatment weight change of −2.9%" [1]. Of those who discontinued and experienced "weight gain since discontinuation," they were "associated with an increased likelihood of GLP-1 RA reinitiation."
I'm genuinely struggling to see how this source shows real world inefficacy. In my friends, all of them stopped taking GLP-1 drugs within 2 years because all of them lost the weight they wanted to.
Out of curiosity, what sources lead you to believe this?
> it's like the drug disulfiram
Have clinicians made this connection?
[1] https://jamanetwork.com/journals/jamanetworkopen/fullarticle...
> In my friends, all of them stopped taking GLP-1 drugs within 2 years because all of them lost the weight they wanted to. Out of curiosity, what sources lead you to believe this?
Anecdotes like this are interesting but in medicine they are not sufficient to make factual statements about drugs. In meta-analyses there is weight regain which is steeper as more weight is lost during treatment [1].
The weight regain seems to be rather slow, it can take years until the baseline weight is reached.
What does "steeper" mean? The studies I've seen show a net weight loss, even after regain, for the median patient.
> The weight regain seems to be rather slow, it can take years until the baseline weight is reached
Maybe. Right now, however, the evidence shows solid effects outside clinical settings. Your original statement was wrong–your sources own refute the claim.
If you're arguing the effects in the real world haven't consistently been as ridiculous as they were in clinical trials, sure, you get a brownie point. But broadly speaking, these drugs are terrifically effective, both when taken for life and when taken intermittently.
This is one of the wildest claims I have ever seen on this website.
Would you claim insulin is ineffective outside of clinical trials for treating type 1 diabetes because people have to keep injecting it?
Type 1 diabetes (or majority of diseases) doesn't involve addiction.
We do not have robust clinical data for things like BPC-157 but we do have strong preclinical data and an understanding of the mechanisms in play.
I use BPC-157/TB-500/Ghk-CU/KPV - so I'm certainly OK taking the risks. But those mechanisms mentioned before? The same things we're counting on for healing and inflammation reduction are the same things that we know can cause an increase in tumor growth rate and chance of metastasizing. VEGF/VEGFR2 expression are even suppression targets for some cancer therapies.
Are there powerful and useful medications out there, available today, that we both don't have good scientific data on and are free enough of serious side effects? For sure! Is everything out there that, though? No. Some things that work will have too serious of a side effect profile to be feasible. Some things won't work at all, despite however much anecdata is out there.
As for the general idea... I agree there's no law that says a medicine with a strong positive effect must also have strong side effects. And we have plenty that don't - statins, particularly the latest generation, like pitavastatin, are effectively side effect free for the hugely overwhelming majority of people and have great lipid lowering effects. Even older ones showed extremely minimal incidents of things like muscle pain - a vanishingly small number of people relative to the total amount on the medications report muscle pain, and when investigated, quite a lot of even that ends up being unrelated to the statins. Yet the narrative persists that make it sound like anyone on statins is going to have their muscles ache 24/7
At worst you inject unknown substances into your bloodstream that could do more or less anything.
Not something I would do at any point for fun. But anecdotally, it's materially better than other alternatives offered/available.
And yet they use unhealthy amounts of avocado oil, consume unhealthy amounts of “good fats.” They discount caloric intake and solely focus on eating loads of what they consider to be good food.
1: https://www.reddit.com/r/endocrinology/comments/1jb2cce/grow...
This feels new. I thought the methylene-blue-for-cancer types continued their medicine while taking other things as extras.
Personally, I've swung over to the laissez-faire side of medicine. At the end of the day, if you're an adult, it's your body. You should be given the chance to educate yourself. But if you want to inject yourself with a prion, like, go for it. Maybe you won't fuck up your own research.
(Marketing should be tightly regulated, possibly banned.)
Chesterton’s Fence rears its ugly head again. This is the same thing as vaccine skepticism (those diseases can’t be that bad, I never hear about them killing anyone these days) applied to a different context
Arguing for modern reforms is one thing, but there’s a reason we have the FDA. Statistically, most individuals do not have the medical expertise or the desire or ability to wade through enough clinical data to make these sorts of decisions with any hope of good outcomes, particularly in the face of an entire Internet of people trying to push questionable substances on them.
There's no way you don't know that for example Steve Jobs ignored his cancer until it killed him because of absurd beliefs about "health". Surely you know about cancer patients dying because they found someone who promised them a cure rather than their doctor offering them a 60% chance through immense pain and struggle.
>Personally, I've swung over to the laissez-faire side of medicine.
We had laissez-faire medicine. It cured almost no one and killed hundreds for no reason. We HAVE laissez-faire medicine. There's almost no regulation in the "Supplements" aisle.
So why doesn't it work?
So, it is not just chemist but molecular biologist too. And the above is also not entirely correct. Yes, the author refers to size as threshold, before something is called a "protein". But the term protein has additional meanings that a peptide does not automatically have. For instance, a protein typically has a specific 3D conformation. It may be "sticky" after degradation or unfolding, but for the most part a protein is something with a 3D structure. A peptide does not necessarily imply the same. A protein may also have several polypeptide chains - insulin is a simple example for that: https://en.wikipedia.org/wiki/Insulin#Structure (A and B chain)
> So the number of different possible peptides is just ridiculously huge.
That's no surprise either - that's due to the code used. You add to the code, so of course length plays a role, as does the variety. There is a DNA->aminoacid mapping. The first has four possibilities per slot; the latter 20 (or more if you include e. g. selenocystein or pyrrolysine; and you have various post-translational modifications too, so you have more variety per slot).
> For comparison, it has been about ten trillion seconds since Homo sapiens emerged as a separate species.
The whole species concept is IMO outdated. It was created before people knew that DNA codes for the complexity in pretty much any species (excluding RNA viruses but they have reverse transcriptase, at the least some viruses, so ultimately RNA->DNA).
> The other one (by Sarah Hood) relates all this to RFJ Jr.’s advocacy. The flip side of “the government shouldn’t be able to force me to vaccinate my kids” is “I should have the right to take whatever medicines I want to without the government getting in my way”.
I don't see why that would be questionable. Would people do as Trump tells them to do? I would not. If you see Trump as a lobbyist, how many private interests may his government have? If they have a commercial interest then their statements may be biased.
> You don’t have an LC/MS or an NMR machine in your garage, so you can’t be sure what it is you’re really injecting
Right, so the whole system depends on trust. This is already a problem because you have to trust not only the government but ALL who were involved in scientific publishing. There were lies told in science too: https://en.wikipedia.org/wiki/Retraction_in_academic_publish...
Even if you almost always end up paying the bill + 20% tip, Americans like the idea that they could not pay the tip if the service was bad.
The appearance of free action is appealing and preferable to being forced to pay the extra amount, even if you almost always pay the amount willingly anyway.
Numerous restaurants in NYC tried and flipped back over the last 10 years. Restauranteurs reported illogical / innumerate behavior where sales went down when they switched to untipped higher prices.
https://www.eater.com/21398973/restaurant-no-tipping-movemen...
The only restaurants that it stuck were Japanese restaurants that cater primarily to Japanese ex-pats, because culturally its familiar to them.
Oddly enough, the fact that I was initially sold a product where a tip wasn't expected has made me continue to not tip Uber drivers. Not sure what that says about me.
To assert that people are sad and anxious while not putting the effort to understand the people involved is such an intellectually lazy position to hold.
HN, in particular, loves anything that allows them to discredit science (like the constant banging on about the replication crisis) and replace it with their own pet theory.
I've been shouting this from the roof tops for years now and it's one of the biggest problems we face today. I live in a rural area and 100% of the Joe Rogan-ified men I know are mindless reactionaries. They aren't educated, they don't read books, they don't travel, heck, they barely leave the county. They think they're so smart because they say no to everything anyone else says. They never offer solutions. They never try to fix things. They barely even vote. If you say the sky is blue they will say it's green because they're just oh so smart. It's a massive massive problem.
I’m genuinely not aware of a DIY or grey market in vaccines. Peptides, yes, but vaccines?
In the absence of this, I suspect you’re either confused or straw-manning…
To clarify, is your concern the inadequacy of the approval process FDA uses for (all) vaccines (noting that many vaccines --e.g. influenza-- are refreshed on a fairly regular basis to account for new strains of viruses) or something specific to approval of the MRNA vaccines?
Or is it that MRNA vaccines were a new approach for vaccines more generally, and so there wasn't/isn't the same long-term data that there was/is for multiple generations of vaccines based on older technologies (viral vector, toxoid, etc.)?
I disagree; "untested" is a very definitive statement. Not tested. Especially when it's in a thread discussing people using all manner of less tested or sometimes literally untested peptides. (Hence my initial thought that maybe you were aware of people taking a DIY route that I wasn't.)
Anyway, when discussing a subject so popularly controversial as vaccines, it's probably better to be precise.
> And the second, but what’s your point?
I wanted to understand your perspective.
* Not if we're actually in literate company, but that seemed to be the common consensus after I skipped the jab, having recovered from covid right before the shots became available. Nevermind that my doctor was on board and I've had all the other ones (minus the flu shot). I was still a selfish grandma killing Republican who probably voted for trump to the commentariat.
Your right to swing a fist ends where the other fella's nose begins. That doesn't mean you aren't free, it just means you recognize that the right not to suffer grievous bodily harm trumps the right to swing your fist willy-nilly.
As a fist-swinger you may not always agree, and you may even get hurt one day because you couldn't swing your fist whenever you wanted, but that's just the cost of living in a world filled with other human beings.
Dealing with doctors is kind of a pain in the ass. I was very sick a month ago and my doctor is pretty "anti antibiotics", he wanted me to go over for an in person check-in. This was after 10 days of having symptoms that I did everything reasonable to take care of. I got on a call with another doctor (at a perfectly reputable hospital) who immediately prescribed antibiotics. It took 5 days of antibiotics just to feel somewhat better - all while using saline rinses, showering, sleeping, eating properly, etc. I still have a lingering cough. I am very reluctant to take antibiotics unless it really feels necessary, this was easily the worst sinus infection of my adult life.
My friend wanted to try out a weight loss medication. Their doctor refused because they felt that my friend hadn't tried hard enough without it. So they got some from another friend who hadn't ended their prescription because they also were worried of being cut off. They've lost weight, which has motivated them to exercise more, eat better, and are generally happier and healthier.
From the article,
> Unfortunately, point two is that we barely have any of these effects worked out - at least not to the degree that you would want before you start injecting them into your leg.
This is what was said to a friend whose doctor took them off of one of those GLP medications, basically. They didn't have enough evidence to know the risks of continued use, even at lower doses.
The reality is simply that there's a big gap right now between what people want and what people have access to. The supplement industry exists to fill that gap.
Medical professionals can complain about users taking these peptides, but plenty of people are not "anti medicine" while still feeling underserved. If doctors aren't in a position to have these conversations, people will go to Youtube or wherever else to look for answers.
Personally, I have mixed feelings about a number of medications requiring a prescription. I frankly do not see why my doctor is involved in me taking a drug unless it would be negligent to allow me to or if it would have community health impacts (ie: antibiotic resistant strains etc). I'm an adult, if I've been properly informed of risks, etc, then I'm inclined to say that it should be up to me to pay full price for some medication or not.
I know plenty of people getting their GLP1 from compound pharmacies. None of them went their first, their doctors wouldn't give them the medication (sometimes they were just a pound under the BMI limit, often because they had been slowly losing weight) so they went elsewhere. These aren't anti-vaxxers who won't take their medication, they're people who want help and there's a gap that companies are taking advantage of. The medical establishment needs to find a way to address that. Right now the answer appears to be compound pharmacies and nurse practitioners.
> In my own view (and it ain’t just me) you also have regulatory agencies to force people to show that their drugs actually have some benefit before they can sell them, too. But that’s going further and further out of fashion. Can’t get ahold of the New Hotness to inject into your upper thigh if there are a bunch of stick-in-the-mud folks asking for human data, infringing on your freedom and all.
Many of us will be dead before there's a medically approved treatment for something. Hell, I got eye surgery before it was FDA approved - I'd probably be blind (or at least far worse off) if I'd waited the years it took.
How many people taking supplements are "naturopaths" who reject modern medicine as opposed to just people who want to be healthier? I really wonder that.
As a side note more dangerous than any drug is stopping a prescription drug cold turkey. Watch what happens when global trade to/from China and India are cut off for a year. Attitudes will change.
This is briefly addressed in the article, but basically it's one thing to eat a peptide and quite another thing to inject it. Your digestive system is extremely adroit at taking peptides and proteins and breaking them down into individual amino acids, which are then absorbed via "transporters" in the gut. (e.g. SLC6A14 for glutamate and cysteine.)
If you eat insulin, absolutely nothing will happen. If you inject just a little bit too much, you're dead.
So, generally: Ingested proteins/peptides aren't drug-like, whereas they can be extremely potent drugs if administered via injection.
Granted, there are exceptions. If you accidentally get a drop of botox into your mouth, you'll be okay, but if you drink a vial, you'll be poisoned. And people have been trying to make orally-active peptides and proteins for decades, with some noteworthy successes, however few and far between in the general case.
GLP's are all the rage these days. Doctors seem to be giving GLP peptides out like candy and those are injected. People are looking like zombies. That said if doctors are going to be so liberal with them I should be able to buy it in the grocery store and slap it down on the conveyor belt. Again I can buy things far more dangerous than any prescription drug. There are very dangerous supplements, some that are shilled heavily on youtube. For example, Glycine (for me specifically used without a specific process) is more dangerous than heroine and the vast majority of doctors would have no idea what I am talking about.
Can you point to the clinical trials that demonstrate this?
> Doctors seem to be giving GLP peptides out like candy and those are injected.
There have been several _thousand_ clinical trials that have shown GLP-1s to be safe and effective.
Pretty much all venoms are mixes of short (10-15 base) peptide chains.
It's the naturalistic fallacy in an utterly perverse form ( and also goes to show why a regulatory system is good: the average person has no idea that they're dealing with or even common sense about it).
Nullify the FDA, FAA and at least half of the other orgs. Give at least half of those budgets to the people. Make aircraft smart enough to evade all obstacles. Make it technically damn near impossible to collide with anything. Make aircraft coordinate themselves. All doable. Force retire all FDA and FAA and give them a balloon, a golden wrist-watch and send them away.
Give people an app to paste in all the things they take or plan to take in terms of foods, supplements, drugs, their allergies. Let the best AI figure out what will happen.
It’s also just a silly rhetorical technique. The ability to construct a grammatical sentence of that form does not constitute a valid argument.
“Restricting nuclear material is silly given that nearly all the stuff I interact with every day contains atomic nuclei.”
The reason we don't need tight regulations on bleach is because we don't have a societal issue causing people to drink it and hurt themselves... at least, not anymore: most of the locking lids on household cleaning chemicals are there by law.
I think you missed out on a long time period of 4chan. They managed to get a number of people to mix ammonia and bleach.
This is a deeply weird take. You think anyone ought to be able to buy, for instance, warfarin and freely take it without a doctor’s involvement? We should let parents self-diagnose diabetes and administer insulin without a prescription or discussion? We should just hope that patients heard their doctor say hydralazine and not hydroxyzine?
> As a side note more dangerous than any drug is stopping a prescription drug cold turkey.
Abject nonsense. It was very easy to stop my prescribed amoxicillin. It’s clear you don’t have any actual idea what “prescription drugs” are, in aggregate, and that should maybe inform your decision to have Big Opinions about them.
Yes.
I don't. But the cost of access is significant. And with pharmacies in India, China and Mexico willing to ship basically anything into America, it's a purely-cosmetic tax now.
I guess I don’t hate everyone else enough to agree with that.
No reason required. People can already buy incredibly dangerous things with a doctors permission, as if a doctor actually knows what other compounds a person is consuming to begin with. Doctors are not omniscient and patients lie. Most of them barely even know the compounds that are FDA approved to begin with. Be honest, most of them barely remember 10% of what they were taught in medical school and the schools even state that half of what they will be taught will not be relevant or will be entirely wrong by the time they graduate.
Again, I can buy apples and apricots without permission. There is nothing capable of more risk or harm that has ever been approved by the FDA than apples and apricots.
Weird examples. You can buy insulin without a prescription today in the USA.
In much of the world -- including almost all of Asia, Africa, and much of Eastern Europe -- you can buy almost any drug without a prescription. The only exceptions are potent CNS stimulants or narcotics, and in some rare cases antibiotics.
This is legitimately a better system. Takes out the middleman.
In the US you can get any drug if you pay $120 and recite the magic words to a telemedicine "doctor."
Doctors in the US get a nice $200 to $500 per doctors visit, required to extend the prescription drug. I only notice because I pay cash. This is why they will argue against anything I am saying until they are code-blue in the face. I will leave them with my code brown.
In the US you can get any drug if you pay $120 and recite the magic words to a telemedicine "doctor."
That's how a number of us in a particular circle stock up on anti-biotics. That said anti-biotics are a last resort for me whereas I find doctors are quick to prescribe them.
That’s exactly what some biological drugs are too - peptides!
And peptides are just short chains of amino acids. Almost all the other biological drugs are just longer chains of amino acids - antibodies, enzymes, antigens, some hormones, and others.
Derek is right that the safety risks are exponentially higher when you inject peptides - you basically skip a bunch of protective mechanisms like enzymes that quickly break them down if taken orally or routes.
As a former R&D scientist there is no way I’d inject any peptide that hasn’t at least gone through a phase 1 safety study in humans. Otherwise you have no idea what it could be doing to your body.
A good example was a drug that was quickly pulled from market for causing fatal anaphylactic reactions. It wasn’t even caught in the clinical trials!
At the same time, I think people have the right to take whatever substance they want. But I worry a lot of people aren’t aware of the risks.
A lot of people do not understand the trial system or the value of Phase 0/1 tests when it comes to the substances that they put into their body. And thanks to the influencer/grifter/biohacker ecosystem that exists, more people would put their trust in accidental evidence, from people who's incentive it is to make money off of them, while complaining about the pharmaceutical industry operates off of a profit motive.
That's like saying that since neither one nor zero requires regulation, neither does software. Maybe software does or doesn't, but in either case its best based on the nature of the aggregate, not the nature of its components.
I mean, why regulate anything? Everything is just different arrangements of hydrogen and time. It's so weird that certain arrangements of hydrogen and time try to claim to have things like "morals", and try to force other arrangements of hydrogen and time to not do arbitrary contrived concepts like "murder".
All is one. Just hydrogen and time. Therefore everything should be legal.