New Age Order Channel
510 subscribers
28.9K photos
11K videos
184 files
22.5K links
www.newageorder.com

News, data, philosophy, art, education. Follow the evidence and the scientific method. Facts. This channel is a resource for truth, creation and liberty. Investigate. Validate. Logic. Critical thinking. You are the World.
Download Telegram
🧵 NEW EVIDENCE — and this one's simple to understand.

A professional broadcast camera (Canon XA55) was recording at UVU on September 10. Unlike every phone in the crowd, this camera records UNCOMPRESSED audio on 4 separate microphone channels at 48,000 samples per second. The Canon was roughly 46m away from the tent which provided a acoustic buffer between the onset of the events. This distance has provided clarity to the event that was missing with the other camera angles.

Think of it this way: phone recordings are like looking through a foggy window. This camera is like a clean window with the lights on.

Here's what that clean window shows:

THE SOUND ARRIVED IN ORDER — HIGH TO LOW

When a supersonic bullet passes, the crack arrives before the boom. High-pitched sounds hit first, low-pitched sounds hit last.

A bomb going off? Everything originates from the blast and arrives at the camera at the same time.

The Canon proves the high frequencies arrived FIRST — spread out over 100+ milliseconds. Followed by muzzle blast then a detonation which originates from the stage.

THREE SEPARATE BOOMS — NOT ONE

This is the big one.

Phone recordings near the stage smear everything together into one big noise. The Canon's professional audio separates THREE distinct low-frequency events:

• +114ms — Early energy (Mach cone)
• +202ms — Muzzle blast from ~120 meters away
• +321ms — DETONATION AT THE STAGE

That third event — the stage detonation — is the LOUDEST of the three. It's not an echo. It's not a reflection. It is the strongest low-frequency peak in the entire recording, and it originates approximately 46 meters from the camera.

Right at the tent. Right were Charlie was seated.

Something EXPLODED there. The Canon captured it separately from the rifle blast for the first time.

WHY THIS MATTERS

If a rifle was fired from 120 meters away, and a separate detonation occurred at the stage approximately ~185ms later — those are two different events at two different locations.

A single shooter doesn't produce a detonation under a tent 120 meters from the rifle. A device detonation doesn't produce a muzzle blast from 120 meters away.

The Canon separated what the phones couldn't: proof of events at MULTIPLE locations.

733 SUPERSONIC SIGNATURES

A supersonic bullet creates tiny pressure waves called N-waves. The Canon's shotgun microphone captured 733 of them in under 200 microseconds each.

The best phone recording? 123.

That's 6x more. The phones weren't broken — their compressed audio just can't preserve these. Uncompressed audio can. And it did.

THE SHOTGUN MIC WAS POINTED AT IT

The external microphone clipped 122,844 audio samples — it was overwhelmed because the sound source was directly in its line of fire. Meanwhile the built-in mics captured clean audio with almost zero clipping.

Zero correlation between the two signal paths. Same conclusion.

MUZZLE BLAST CONFIRMS THE DISTANCE

The +202ms blast puts the rifle at ~120 meters from the camera. The 10-camera analysis estimated 127 meters. That's within 6%.

Two completely independent methods. Same answer.

But the stage detonation at +321ms? That's only ~46 meters from the camera. That's the tent.

A rifle 120 meters away. A detonation at the tent. Two locations. Captured separately for the first time on professional uncompressed audio.

This is the 11th recording to independently confirm the same findings. Professional grade. No codec excuses. And now, for the first time, the stage detonation is isolated from the rifle blast.

Full analysis + raw audio downloads at followtheepicenter.com
🚨 This is INSANE.

CANCER has been Cured via something found in Japanese forests.

• Literally ERADICATED TUMORS IN A SINGLE DOSE
• Head to Head against chemo & immuno — worked Way Better
• No bad side effects
• Prevented Recurrence: the cancer COULD NOT be brought back

All this was possible via a single bacterium isolated from the intestines of Japanese tree frogs - Ewingella americana. 🐸

➡️ When a single dose of the E. americana was injected into the veins of mice bearing colorectal cancer, the tumors were 100% Rapidly, Completely eliminated.

➡️ No side effects (except mild necessary inflammation, gone w/in 72 hrs). No signs of long-term toxicity (multi-month observation period).

➡️ It also induced immune memory against rechallenge (prevented cancer from coming back).

➡️ And importantly: Zero colonization in normal organs + GONE from the body w/in 24 hours.

➡️ It's Highly likely these results will translate well to humans & to other (especially solid tumor) cancer types.

I pay attention to cancer studies (have for decades) and these are actually an INSANE results.

Why E. americana is the perfect CANCER KILLING MACHINE:

• E. americana thrives in the same (low oxygen, immunosuppressive) environment tumors thrive. And proteins + metabolic byproducts that cancer cells produce actually support the growth of E. americana, right there near the tumors.

• Tumor blood vessels are poorly structured, very permeable/leaky. Because of this, E. americana can easily exit the bloodstream and enter the tumor tissue.

IN OTHER WORDS: when this bacterium is injected, a perfect symphony transpires where it goes DIRECTLY to tumors & eliminates them  — while leaving normal cells & organs alone. 😯

HOW IT WORKS:

E. americana eliminates cancer via 2 mechanisms:

• Directly damages cancer cells.

• Activates immune system — E. americana attracts T cells, B cells, and neutrophils to the tumor area (which then eliminate the cancer cells).

WHY THIS IS LIKELY TO WORK IN HUMANS:

Curing cancer via bacteria has been tried before. Here's what we know.

⚫️ Efficacy results shown in mice usually DO translate to humans— ie. bacteria that accumulate in mice tumors usually do the same w/in a human body
⚫️ Toxicity results shown in mice also show up similarly in humans
⚫️ There has Never been a mice study showing results this good OR w/o toxicity (the other ones showed a lot of toxicity & even death in the mice)
⚫️ In other bacteria cancer studies: the bacteria DID accumulate in normal organs. This one does not.
⚫️ IMPORTANTLY: all other bacteria that have been tried thus far were bioengineered/GMO.
⚫️ E. americana is naturally occurring & far less likely to lead to bad side effects.

So anyway. Given these INSANENELY EFFECTIVE & safe results...they surely will FAST TRACK human trials on E. americana (perhaps on those who have nothing to lose and everything to gain) Right? ...Right?!

I doubt it. It'll probably be forever... IF they even let this get to the public.

They'll probably announce some new "miracle" genetic therapy instead, and try to pull all attention & resources toward that.

UNLESS we do something.

Be loud. Share this. Don't let this die down and be forgotten about.

This is one of the most promising "1 & done" type of cancer solutions I've ever seen.

But even if this does become mainstream, Natural Medicine & healthy living will still have it's place. This therapy does require an at least somewhat functioning immune system to work.

And know: there are ways to fix your body. 

Please see my other posts on cancer reversal via high dose IP6 (Inositol Hexaphosphate), large amounts of vegetable juicing (carrots/greens especially), high doses of specific mushrooms (Mesima, certain types of Reishi), etc. 

I've posted tons of studies & reversal reports (often stage 4).

Nature is amazing. Spread the word.