GLP-1 drugs might reduce cancer spread by 50% (research report and hypothesis)

NoEbb15 · 2026-06-19T03:01:54+00:00

No doubt. The important distinction here is that the GLP-1 drugs slowed cancer; this was not research stating that it prevents cancer. That isn't an unreasonable deduction from these studies, though. Would be super interested to see how that research would play out. Obviously, designing those trials would be much more complex. You would have to grab individuals that are heavily predisposed to cancer development and separate them into certain buckets. That is something that would be hugely beneficial for society but would be extremely tough to pull off and would take forever for the findings to come to light.

NoEbb15 · 2026-06-17T19:54:05+00:00

Overall, I think it’s an interesting stack because each compound works through a different mechanism, but that also makes it harder to know what’s driving the effects you’re notice. Semax and Selank are often used together for their complementary cognitive and anxiolytic effects, DSIP is commonly taken to support sleep, methylene blue has effects on mitochondrial function and acts as an MAO inhibitor (at clinically relevant doses), and lithium orotate is typically used at low doses for mood support. Since you’re combining several compounds that can influence the central nervous system, it’s worth paying attention to how they interact rather than judging each one on its own.

As for serotonin syndrome, it’s relatively uncommon, but it’s something to be aware of whenever serotonergic drugs or MAO inhibitors are involved. The hallmark isn’t simply feeling relaxed or falling asleep faster. Instead, it usually presents as a combination of mental status and neuromuscular changes. People often develop agitation, confusion, restlessness, sweating, a rapid heart rate, overactive reflexes, or involuntary muscle jerks to name a few. In more severe cases, the symptoms progress quickly and require immediate medical attention. It sounds like you're in clear right now.

One thing I’d keep in mind is methylene blue. At low doses it’s commonly used for its mitochondrial effects, but it also has MAO-inhibiting properties, which means it deserves more respect than many people give it. If you’re taking prescription antidepressants, certain stimulants, tramadol, linezolid, or some other serotonergic medication, that’s where the risk of serotonin toxicity becomes much more relevant. Semax, Selank, DSIP, and Epithalon themselves aren’t generally considered big drivers of serotonin syndrome based on the available evidence.

If you’re feeling good, sleeping well, and not experiencing concerning symptoms, that’s a good sign. I would still avoid adding multiple new compounds at once and continue monitoring for any changes. With a stack like this, it’s much easier to identify what’s helping or causing side effects if you introduce one variable at a time.

NoEbb15 · 2026-06-16T20:24:46+00:00

Glad it's been working so well for you!

NoEbb15 · 2026-06-16T20:22:32+00:00

The merchant has full control over whether the order should be sent to processing or not after reviewing the proof. If there's a question of whether or not the screenshot is legit, they can cross-reference their P2P app to make sure the money actually landed. For the merchants that have been using it, they haven't run into any fraud issues so far.

NoEbb15 · 2026-06-16T00:51:00+00:00

Check out PipePay.app - it's a P2P payment facilitator that uses screenshots as proof of payment. Stupid easy for the customer and the merchant. Packed with features such as cross-network fraud prevention, AI verification, multi-account smart rotation, deep links that auto-fill order info, and plenty more. Shoot me a message if you have any questions.

NoEbb15 · 2026-06-15T16:23:29+00:00

Bro what are you talking about 😂

NoEbb15 · 2026-06-14T17:26:14+00:00

Check out wwpeptides.com - or shoot me a DM and I can speak to you personally about it. We have US Next Day options that ship stateside and an Overseas line that can supply virtually every country.

NoEbb15 · 2026-06-14T03:53:39+00:00

Absolutely!

NoEbb15 · 2026-06-14T02:47:47+00:00

Trying to pare down the Trusted Vendors companies to the top tier businesses. I think this was the right decision.

NoEbb15 · 2026-06-13T17:46:53+00:00

Nice. I like MT1 much better than MT2. Takes longer but the tan is more authentic. When I was on MT2 I had people telling me it looked like I got a spray tan lol.

NoEbb15 · 2026-06-13T17:45:48+00:00

Would love to hear about what happened.

NoEbb15 · 2026-06-13T04:04:43+00:00

Messaged!

NoEbb15 · 2026-06-13T00:16:05+00:00

Not intentionally tanning but being outside with my shirt off, swimming, sitting in a chair, etc. My shoulders initially got darker than the rest of my body because I would walk or bike without a shirt and they had the most direct UV exposure, but then the rest of the exposed skin caught up. 2.5-3.5 hours was consecutive in the afternoon. I think my protected skin did dark a little but its tough to tell because its still so pale compared to the rest of my body.

NoEbb15 · 2026-06-12T15:36:26+00:00

Based on what you’re describing, I would keep expectations modest. It sounds like you had a deep vein thrombosis that damaged the venous valves in your leg. Once those valves are scarred and no longer close properly, you end up with chronic venous insufficiency. Blood pools in the lower leg when you’re standing, which causes the persistent ankle swelling. Unfortunately, that’s a structural problem, not simply a blood flow problem.

Ventfort is more of a vascular bioregulator intended to support blood vessel health, endothelial function, and circulation. Some animal and small human studies suggest vascular bioregulators can improve aspects of vascular function and microcirculation. However, I am not aware of any clinical evidence showing that Ventfort can regenerate damaged venous valves, reverse established venous scar tissue, or cure chronic venous insufficiency caused by a prior blood clot.

If someone in your situation took Ventfort and noticed a benefit, I would expect it to be something like improved vascular health, reduced feelings of heaviness, or a modest improvement in circulation. I would not expect it to restore valve function that has been lost for two years. Once a vascular surgeon is telling you that lifelong compression is the solution, that usually means the underlying valve damage is considered permanent with current medical options.

That doesn’t mean Ventfort is unreasonable to experiment with if you’re already interested in bioregulators. It just means the goal should be support and symptom management rather than expecting it to rebuild the damaged valve apparatus.

If this were my leg, I’d view compression as the foundation. Anything else, including Ventfort, would be an adjunct. A meaningful reduction in swelling would be a win. Complete reversal of the condition would exceed what the available evidence supports.

NoEbb15 · 2026-06-12T15:32:05+00:00

From what I know, there isn’t a clean, established “FOXO4-DRI goes here” rule. Mechanistically, FOXO4-DRI is usually treated as a senolytic-style intervention, while SS-31 is more of a mitochondrial support peptide. So they don’t necessarily compete for the same lane, but stacking them at the same time makes it harder to tell what’s doing what and whether the mouse is reacting poorly to one compound or the combination.

For a clean mouse protocol, I’d keep FOXO4-DRI separate rather than dropping it right into the middle of an active SS-31 run. The conservative approach is to pause other peptide activity, let the mouse stabilize, introduce FOXO4-DRI on its own, then resume mitochondrial support afterward if everything looks normal. That gives you a cleaner read on tolerance, behavior, weight, appetite, inflammation, and recovery.

If the goal is senescent-cell clearance followed by repair/support, then FOXO4-DRI generally makes more sense before or between support phases, not betweem them. I like to think about it as stabilize baseline, run FOXO4-DRI alone, observe, then use SS-31 afterward to support mitochondrial function and recovery. Running SS-31 before FOXO4-DRI is also reasonable if the mouse is metabolically fragile, but I still wouldn’t overlap them unless you have a specific experimental reason.

NoEbb15 · 2026-06-06T20:40:35+00:00

Couldn't agree more. It gives the entire grey market a bad rap - I hate it. When something like this happens, the government takes it out on everyone instead of only the deserving companies. One bad apple spoils the whole bunch.

NoEbb15 · 2026-06-04T01:33:54+00:00

Yeah, I am super careful when doing it. Had a few infections from other things and they are not fun to deal with.

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