How's The Radiance of Your Magnetic X Today?

by

Dan Winter 1/15/99 , url: ../magneticx , other articles at ../sitemap.html

Originally Inspired by Dan Winter, Assembled by Ken Wyrick , for:

CalTek Distance Learning : Home Page | Mission | Curriculum | Human Resources | Presidents Message | Application Links

 

dedicated to Linda and Darcy in Florida...

should be ready 1/15 - www.magneticx.com or link via www.swordsong.com

The Dizzy DNA syndrome, is caused when genetic engineers fail to prioritize what EMBEDS long waves in DNA.

Pulling the sword from the stone, is the WORM..squirt from successfully embedded DNA..

 

 

This article is a follow up to sacred geometry bleeds in genetically engineered food...Will Genetic Engineering in Food Cost Your Children their "Soul" Force.

 

When DNA blesses itself by properly making the 'the sign of the cross', recursively...

then in a very feminine way, what is created is a radiant..

Magnetic X

New Pick up Lines:"How Many Waves at Once Can You Contain in those Designer Genes"?

"Your Curves Look EmBedable to me"..

As the seXy X Chromo said to Y, cross THEN branch EUgene..

HERE IS THE WAY A PROPERLY OVERLAID RECURSIVE BRAID AT THE X CROSS OF DNA CREATES embedding survival RADIANCE BY RECURSIVE WAVE BEAT NODE HETERODYNING:

...go girl 'phi-re away' !'

(complete 3D animation at: How the Heart Song Ignites the Earth Grid.. )

added 4/21/2000:

from: DNA Learning Center's lovely - Animated Primer on the Basics of DNA ( http://vector.cshl.org/dnaftb/ )

 

Phi - Golden Ratio Heterodyning -- Implosion in the "Wratcheting Rung"?

Phi Harmonics in the Power Series of Hydrogen's Balmer Series, (Randy Masters work)

Pics of Hydrogen As the Key to Implosion / Fusion at http://www.danwinter.com/fusion

below from book:"Biochemistry"by Mathews&VanHolde, Artwork Copyright Irving Geis.

above also note the 36 degree wratchet angle 5/10 symmetry from center column (PHI? H Bond) indicated bottom right..

As explained to me by Professor John Hubbard, PhD Univ Buffalo Medical School in Pathology and Microscopy.. that the stability of the central non- linear hydrogen bond spark gap zipper to the DNA helix, in many ways explained the quantum mechanics of aging. Namely, that the wave geometry of this bond determined the success and accuracy of base pair matching. So in effect, the determinant of replication success.. not making mistakes in coding up the next protein, was limited by the wave fit geometry in this bond center. He suggested cell deterioration associated with aging, at one level, correlated with the decay of this central bond. If the non-linear hydrogen bond tears from it's RECURSION geometry (based on PHI) THEN DNA begins to make more replication mistakes. This is because the ability of the field effect reaching out from the bond center, to attract the right protein/codon fit is limited by the geometry of the bond itself. A spark gap is q square wave, which by definition could have an infinite series of contained harmonics. Yet we know, that no harmonic series can heterodyne or beat with itself infinitely, unless the ratio of the wave lengths are Golden Mean. (The only completly non-destructive wave interference geometric). If we look at the harmonic content of this bond then as being a GOLDEN RATIO (rectangle as depicted in the center of DNA rung above), then it's harmonics become a log function of PHI / The Golden Mean Ratio. In this case then, DNA's central rung as a wave function, (zipper/linear accelerator/superluminal? access to "spirit"? see /superDNA/superDNA.html) becomes an adder and multiplier of both wave length AND WAVE VELOCITY heterodynes.. according to this chart ( a top down view:)

When the wholly gene becomes distributable as a wave, by PHIllotactic (Golden Ratio)"embedability" that wave unfolds itself...

(above pics concept extended at http://www.danwinter.cancer )

The main point is that 1.618 is also the ratio of the DNA structure and is the only ratio that allows complete information or geometry to cascade down the harmonic series without destructive interference (acheiving perfect fractal "implosive' data/wave compression) - spin path to zero point.

One 360 degree turn of DNA measures 34 angstroms in the direction of the axis. The width of the molecule is 20 angstroms, to the nearest angstrom. These lengths, 34:20, are in the ratio of the golden mean, within thelimits of the accuracy of the measurements. Each DNA strand contains periodically recurring phosphate and sugar subunits. There are 10 such phosphate-sugar groups in each full 360 degree revolution of the DNA spiral. Thus the amount of rotation of each of these subunits around the DNA cylinder is 360 degrees divided by 10, or 36 degrees. This is exactly half the pentagon rotation, showing a close relation of the DNA sub-unit to the golden mean.

resuming here the Magneticx Story:

When the Orion Queens (MAG / Dragon Queen / Oil of Messeh)

laid down their law to the arriving ANunaki ..(Ea for whom Earth was named)

the instructions were clear..

branch yes, cross NO.

This meant Annunaki Males could contribute Y, (give sperm),

but their Females -telepathic MAG X genepool- were not to receive.. sperm.

In this way there would be no dilution of their fractal egg embedded matriarchy bloodline.

In addition all crosses required approval. Their gene splicers, N/Hiburu 'priests' created sex guilt over this issue. (also see:"Inquisition" - murder all psychokinetic eggs..) The key moment was when Ninhursag put an Annunaki sperm impregnated cromagnon egg, into her womb. That was where the illegal fertile EVE was created. (Line of Cayin origin of our word King -"Genesis of the Grail Kings" /Gardner)

If once the worm in DNA got free, it might sting the cloners. (Scorpio's like this.. sting is the first topological move to recur which is to become sweet...braided!)

We the TakAdama (borgs from Orion) might evolve more psychokinesis than those tending our petri dish (Draco/Dragon breeding our Royal families for Millenia as if they were show dogs).

In todays news on Alta Vista, cloning breakthru creates Monkey, while Kentucky Fried Chicken is shown serving up genetically engineered food to kids. Reki tells us the gene splicer Annunaki came here originally specifically because of the reign of chaos that swept across the galaxy when the DNA could no longer steer, as a result of widespread cloning. (See the story of the "Golden Ones": reason the Annunaki returned here, at danwinter.com/origins bottom piece..). They traveled BACK in time across thousands of inhabited planetoids to locate the original temporal source of this disturbance. They aimed their time travel (see "Stargate" film) Niburu back at EDEN on Earth, specifically when they realized that our soon to evolve epoch of GENE splicing WAS THE SOURCE OF THIS GALACTIC CATASTROPHY!

The importance of proper gold embedding GENE harvesting to the success of star commerce was becoming evident. Whoever inhabited the BIG wormholes got to steer the BIG trading vessels. (see 'Deep Space Nine' series and Guild Navigation in "Dune"... like convincing congress in the movie "Contact" that your dodeca antennae really squirts you out there..). Getting your genes up to speed for the big squirt down the tube, was more than just status posturing, it was WHO MADE THE BIG BUCKS. (And whole artificial gene splicing planetoids .. called 'Arr' {gonaut}, like Niburu with Hiburu priest gene alphabet staffing, do not come cheap.. Gold Powder harvesting was a cover story for a deeper search for the heart of gold /recursion embedable faster than light enabled DNA!!).

Apparently the success of the MAGNETIC X squirt gun SWORD up the ladder of DNA thru lightspeed, was specifically what enabled genepools to:

1. Steer themselves in time travel without embarassing heavy metal craft.

2. Succeed in lucid dream, bardo death navigating, and shamanic star navigating "Contact"..

3. Radiate a sustainable immune system into their young thru an EKG phonon programmed, radiant thymus..

4. More subtly, whole star systems gravity centroids were destabilized when the centering force generated by inhabiting "time lord", "ophanic", "angelics", SOLURUs.. weakened.

Climbing the ladder of DNA symmetry to "ascend" to these velocities STOPPED..

ALL AS A RESULT OF DNA AS A WORM GETTING SHUT DOWN FROM FREEDOM TO CHOOSE! (steer).

 

As a result, one of the primary LIONPATH agenda, (see the Morph Orion Queen Drac to Sumerian Goddess statue, Genesis = watered down mistranslation of Sumerian... which means Dragon in Celtic) in resplicing themselves as a recursive SCION (jon)-branch-, back onto their own genetic root stock at Edin (Edenic Annunaki spaceport), WAS TO PREVENT THE GENETIC ENGINEERING WHICH ULTIMATELY BLED THE GENEPOOL OF A...

"Willed Mutation of the Species". (book by Satprem).. (This is how DNA loses "will"/intent ).

 

So now as our genetic history waltzes back around to that recurrent point of choice... will we short circuit the free will of DNA?

Sacred is the freedom in Star Trek's Prime Directive. If you do not set them -their DNA- FREE... their children will be DIZZY. If you do not set the characters in your own dream FREE, you will never learn from them. Degrees of Freedom which limit how much newness evolves in chemical reactions has the same sacred meaning in Magic, Alchemy, and GeneSplicing. The CHEM in AlCHEMy and CHEMistry means 'from the blackness'.. that is from the THROAT OF THE MAGNETIC X. (implosion steerage / survive the black hole and you steer in time..Einstein's revenge..)

Failure to EMBED DNA IS... AN ELECTRICAL GROUNDING ISSUE. Access to ground - electrical AND psychological, is access to fractality, is access to the geometry of braid embedding. This is similar to the biomagnetic shock schizophrenic alienation universal among urban dwellers ripped from exposure to the fragile long wave Earth's long wave 'schumann' magnetic blood stream. How different are those kids, after 20 minutes barefoot in mud around a spring in an old forest... I have an idea, let's measure the change in attention span!

MANY ET races look on our planet with the trepidation we look at a dangerous petri dish with a potent virus that MIGHT escape.

 

Now if you were a genetic engineer, asking practical questions about how to convince the stockholders to change corporate policy, the conversation might go something like this:

(I think Monsanto got the message when their stock crashed after Europe vomited back their multimillion dollar PR campaign for Genetic Engineered food.. now they merely need intelligent redirecting....?)

Ahh look boss, it MIGHT be that the huge bulk of this DNA chain we have been regarding as useless, non-encoding, and snip-able... MAY have some information context /embedding value (like a million years of genetic learning), which we should consider before hacking it out of next weeks Kentucky Fried Chickens.... and the bleached genetically screaming in pain WHEAT we dump into the microwave which costs children their attention span (CONTEXT ABILITY).

Commentary from Molecular Biologist, Georgia Tech Ph.D. researcher..

  With the discovery of recombinant DNA biotechnology, humanity made off with Mother Nature's scissors. Unfortunately we know less than She. Editing the code of life with incomplete knowledge of meaning is like an electrician inside a supercomputer hacking out pieces assumed to be useless in order to make a "better" machine.

Specifically, genetic engineers are currently redesigning plants, animals, and people ostensibly for herbicide resistance, and disease immunity. It is assumed that the preponderance of "junk" DNA that intervenes between coding regions is inefficient, useless and could be removed for greater stream- lining. In actuality these spans serve multiple biological functions (cancer prevention, gene induction) and should be left in place within the genome.

Eukaryotic organisms (those with a double DNA library) have small sequences of DNA able to remove themselves and reinsert elsewhere in the genome. These "jumping genes" are usually latent and immobile, but under stress, become active. If they reinsert into a coding region of the genome they can disrupt a gene's biological function causing a mutation and potentially cancer. Fortunately, the genome of eukaryotic organisms is characterized by vast stretches of non-coding "junk DNA". If a jumping gene becomes active it is more likely to reinsert somewhere without causing harm. If genetic engineers attenuate non-coding regions, they may increase the likelihood of "jumping gene"-induced cancer.

Further, intervening sequences (introns) can be necessary for effective gene induction. For DNA to be converted to RNA from a coding sequence (gene), an upstream promoter must be induced. In some instances the DNA-binding protein required to turn on the gene must bind to the DNA in two places at once separated at times by hundreds of intervening base pairs (rungs of the ladder). DNA achieves this by bending the intron to accomadate dual binding by the DNA-binding protein. In this case, removal of the required intervening sequence would destoy proper gene induction.

In addition to the molecular necessity of introns for genetic function, there is also a less immediately tangible requirement for non-coding DNA stretches for biological health. It has been hypothesized that DNA serves as an antennae for electromagnetic capacitance. If the genome has been fragmented to such a degree that it can no longer vibrate with the long wave within which other waveforms nest, those waveforms (memories) will be lost. The tingle of life transmitted through healthy, coherent DNA becomes absent. Humans feeding upon chickens and grains adulterated through genetic engineering may soon find themselves feeling devoid of the charge gleaned from organisms whose DNA was able to infuse their tissues with the electromagnetic charge known as life force. With rampant cases of chronic fatique syndrome in adults, and attention deficit disorder in children, one may infer that our cellular batteries are being insufficiently charged.

Adonia McKinzi, Ph.D.

Molecular Biologist

--

Here's a finding no one was expecting.. BOB

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Date: Sun, 28 May 2000
From: dj <djhewitt@jps.net>
Subject: GM genes can jump species, says expert

http://www.guardian.co.uk/uk_news/story/0,3604,319704,00.html

GM genes can jump species, says expert

GM food: special report

James Meikle
Monday May 29, 2000

A claim that genes used to modify crops can jump the species barrier into other
forms of wildlife was last night raising new concerns about the potential threat
to human health and the environment.

Unpublished work by Professor Hans-Hinrich Kaatz of the University of Jena,
Germany, suggests genes from GM rape seed can be transferred to bacteria and
fungi in the gut of honey bees, posing serious questions for GM supporters and
the biotech industry who believe the chances of gene transfer are very limited.

The findings, if substantiated, could further dent public confidence in
scientists and the government, whose handling of the crisis surrounding the
growing of GM-contaminated conventional crops over thousands of acres in the
last two springs has provoked anger from farmers, anti-GM campaigners and the
Tories.

Prof Kaatz has been experimenting for three years with honey bees on a field
sowed with GM rape, engineered to resist certain herbicides while surrounding
weeds were treated. He removed pollen gathered by the bees on their hind legs
when they returned to the hive and in a laboratory fed it to young honey bees
which naturally eat it as part of a high protein diet.

Then he took intestines out of the bees and spread the contents on a growth
medium to grow micro-organisms. In some bacteria and in a yeast from the gut he
found the gene that conferred resistance to the herbicide.

Prof Kaatz told the German television station ZDF that the "bees had obviously
taken up these genes. They were in the bacteria in the intestinal tract of the
bees and seemed to have come from the genes of the original plant and to have
been taken up into their own genetic make-up." He said this happened rarely,
but it "does happen".

The Ministry of Agriculture made clear that it would only study the research if
it was published in a scientific journal, after being reviewed by other
scientists. A spokesman said the work "made an interesting point we will have
to look at, and will do, once it is published. We are not going to jump to any
conclusions."

Adrian Bebb of Friends of the Earth said: "I think this is pretty alarming
research. It shows us how little we know."

CLIP

DNA Wiring: DNA as Radio Transmitter / DNA as Magnetic Superconductor disturbing DNA as a {heart modulated?} radio station might intimidate genetic engineers from further rushing in where angels fear to tread, now that more technical references are available to support this.

We thank molecular biologist Dr.McKinzie who wrote this piece for us. And also there is another fundamental issue which the academic community IS COMPLETELY BLIND ABOUT. That is the obvious fact that DNA is a RADIO STATION. Biologists determine DNA densities using UV signatures. No one to my knowledge even followed up on the early Russian work showing that there was a strong UltraViolet Light and Radio Frequency burst MEASUREABLE FROM DNA PARTICULARLY AT THE MOMENT OF MEIOSIS/MEITOSIS. Of course academics have their head in the sand about the hi frqeuncy DNA broadcast signatures (the Boson 7 story), which were used to screen who could time travel at Montauk.

a starting place for GENETIC RADIO?

dna
as spectral emitter..
in defense of the concept:
genes as antennae.. http://web.idirect.com/~showcase/althealth/morfreqs.htm

Genetic academics seem to be like Father Tom Porter the Jesuit Dean at University of Detroit, in Psychoanalysis of Literature class. He assured us pacing the front of the classroom, that RITUAL could have no other function than just than the pure satisfaction of being itself. (Phenomenolgy's ONTOLOGY of BEINGNESS language takes on some MEANING with the wave mechanics of self-reference). When in fact we know know that RITUAL does make a morphic resonant waveguide SELF SIMILAR (fractal) TO THE ENERGY FIELD IT YEARNS TO ATTRACT. In this way, the sonic motion of dance for example, or a whale song, can create a long wave sonic hologram, which specifically by PHASE DISCIPLINE ALLOWS SOUND TO ENTRAIN/TOUCH/SHARE ENERGY WITH AN OPTICAL HOLOGRAM AT A RADICALLY DIFFERENT WAVELENGTH. (This is common in surface acoustic wave non destructive holographic materials testing for example.) Sonic implosion atmosphere pressure change 'blows the doors off' the temple during the true Druid ritual.

So we KNOW that ritual is a specific wave guide approach to connecting short waves (us) to long waves (the field effect of the collective self aware DNA genepool, childishly named 'GOD' by the weak minded). CLEARLY IF SCIENCE KNEW THE LONG WAVE TO SHORT PHASE ALIGNMENT TO EMBED PRINCIPLE THAT IS RITUAL, they would know how long wave phonons/sonics (gland emotion related) choreograph the DNA alignments during the ritual dance of cell replication.

Star Trek 4 came to Earth to find if she was dead specifically when the Whale song long phonon moire switcher of the ocean thin film piezoelectric galactic antennae had stopped working. Massive coherence in a wave song, IS THE ONLY PHYSICS OF MEMBRANE MAKING AT ANY LEVEL. (book:"Structural Stability and Morphogenesis") & see wave membrane geometric origin of cancer. Shades here of "Bioacoustic Habitat Theory" and "Signature Sound Works". (use my sitemap search or altavista.com..).

There can be no doubt that all of Cleve Baxter's (web search at altavista.com: 50 hits on "secret life of your cells"..his book) work to show that living cells communicate exquisitely at a distance, MEANS SOMETHING. A little saliva cell with electrodes in it miles away from your body, CLEARLY AND UNDENIABLY KNOWS EVERY INTENSE EMOTION YOU ARE HAVING!?

THERE IS NO OTHER WAY TO EXPLAIN ANY OF THIS OTHER THAN TO AGREE THAN DNA MUST!!! BE A GREAT RADIO ANTENNA.. (Starting with phonon/uv/rf and heterodyning to the superluminal which folks like William Pensinger have already measured.. faster than light and time penetrant)

Of course NO ONE IN THE ACADEMIC COMMUNITY HAS EVEN BOTHERED TO RENDER A DETAILED ANSWER TO WHY GENETICALLY ENGINEERED CORN CAN MESS UP A MONARCH BUTTERFLY. Oh here's a little detail THEY DONT EVEN KNOW THAT OLFACTION IS MEDIATED IN THE INFRARED!!! almost certainly one of the resonant bandwidths of DNA..(See the Phil Callahan..'love bug' story..) Phee Phi Pho Phum I smell the BLOOD of an ANgelish mAN. (Celtic blood source of RHneg means the rhesus monkey part of the reptile cross nibURU.. did not stick there... highlander...) Note how genetically effective are co-ed dating studies which only offer the smell of potential mates used underwear!

Yet these academics, who choose to ignore the most basic genetic radiance into environment FACTS OF LIFE FORCE, are the decision makers congress CONSULTs before OKing a wholesale destruction of YOUR PLANETARY DNA MEMORY LIBRARY!!!!!

 

Here is molecular biology 101 graduate intro class blissfully telling YOUR POLITICAL LEADERS, that it is perfectly safe to hack up the DNA of your food...ALL THE WHILE NOT EVEN HAVING A CLUE!?!?! OF WHAT MAKES DNA ABLE TO SHARE KNOWLEDGE WITH ITS SPECIES WIDE RADIANCE FIELD. Scientists agree a tree hundreds of miles away knows when it's species is getting infected even at a distance. (We know now there is a lo frequency very broad capacitance elf 0-20hz radiance, in the same musical spectra as the ekg and eeg and schumann.. Heart entrains tree at moment of bliss / measured..Measuring the Effect of Tree Hugging!)

Sure cut out those intervening spaces in the DNA.. we earlier believed hacking out tonsils, pineals, and frontal lobotomies were JUST FINE.

And here is another detail, guess what we learned about the intervening spaces between heartbeats!? We thought we had it kool when we found that the power spectra of the ekg averaged over 5 beats could identify focus, and emotional quality (../hrv ). Guess what? (acknowledgement to Rollin McCraty at HeartMath who emphasized this). When you take the relatively flat electrical line OF THE SPACE BETWEEN HEART BEATS and crank up your sample rate to say 100,000 samples per second, GUESS WHERE THE MOST INTERESTING INFORMATION RICH MUSICAL HARMONICS FILL THE HEART!! It is in the STILL POINT BETWEEN BEATS THAT THE HEART GATHERS THE SUBTLE RADIANCE OF ITS MOST EXTENDED ELECTRICAL ENVIRONMENT! This is exquisitely important, because it tells us how relaxing into the stillness enables you to touch the distance like it was you.

Of course only later, do the grudging academics (Arthur T Winfree "When Time Breaks Down", origins of cardiac arrhythmia) admit that yes it is probably true from chaos theory that the occasion the heart breaks down electrically IS THE MOMENT IT FAILS TO BE ABLE TO RELAX BETWEEN BEATS!? They all admit the hearts rhythmia is key TO EVERY KNOWN CHRONIC DISEASE.. (../dardik ).

Yet those same academics won't give the loving GENE the privelege of relaxing between beats / nodes. They don't even acknowledge there is an electrical enviornment to phase lock to. Yet they still ignorantly read Arthur to their kids at bedtime, explaining that when Arthur and the Land became one, the weather emerged from chaos. They let Lovelock WRITE THE SOFTWARE that made DOLMEN PLACEMENT (long wave magnetic embedding) in the program SIM-EARTH speed up self aware evolution. Yet it never occurred to them that the real ""LONG WAVE MECHANIC"" MUST BE DNA. It is the MOST SELF SIMILAR (and therefore cross harmonically radiant) MOLECULAR STRUCTURE IN THE BODY. (As at the tissue level are the PHI branched Fibres of Perkinjole firing the heart, and the branching algorhythmn of the Alveoli of the LUNGS where we CATCH PHI-RE IN GENERAL!!.. Talk about a Priori of Scion..priority of the branch.. could this be the true orating transmission line of jon..short for scion..?)

DNA cannot maintain its exquisite piezoelectric radio connecting between the long wave phonons (0-20hz ekg/eeg/schumann resonance common band/bond), and the hi frequency rf and uv, IF YOUR SCIENTISTS CONTINUE TO HACK OUT THE MECHANICAL INTERVAL DISCIPLINE. ONLY HELICAL structures are piezoelectric (quartz and DNA are molecular slinkys). This gives a common place of touch dance rubric for long waves and short waves to share spin (yellow brick road kinda thing). It stands to reason then that the conformation shaping of this mechanical dance, not only programs which RNA enzymes get replication access, but the way the willful gene embeds its long wave grail magnetic back yard..'imprinting'. The way DNA does its dance INTO VERY LONG WAVES, is by doing a BRAID ON TOP OF A BRAID.. recursively. (see superDNA link /animations below). So clearly the (sacred) geometry in the self similar symmetry between these orders of braid wave mechanics... IS WHAT GIVES DNA IT'S MAGIC. The fact that academia has not even considered that this SONG OF THE DNA, in fact EXISTS AT ALL!?!?!?!?!? is the absolute tradgedy of the "human genome" project catastrophy. All the while those same lab technicians will run around like little mice, looking for the pre orgasm bliss tingle of falling in love... never even pausing to think that it was the RADIO radiance of their GENES which was tingling!!!!

 

 

My inference to all this is that a way must be found to quantify the life or soul force in DNA. This would allow us to determine which DNA splices did in fact deplete our "batteries". Clearly there is precedent for this, in the way we pioneered teaching coherence in EKG. There we took a 2nd order (septrum) frequency signature showing that the interval between contained harmonics became a multiple of Golden Ratio, during bliss. Since DNA has spectral emissions in the phonon as well as the UV, a similar procedure could be used here. In this way, the more recursive the DNA braid, the more recursive would be its contained harmonics. We would optimize our genetics to the radio signature (multiples of Phi), of SELF AWRENESS! (Just like I proposed for healing the atmosphere loss by tuning magnetic long line spectra.. the physics of exquistive geomancy). This way with a radio fingerprint, WHEN OUR GENETIC ENGINEERS DAMAGED OUR DNA, WE COULD TELL THEM.

I believe that this was referred to in multiple sources in the Montauk literature, as the Boson 7 spectral emissions in the DNA, which predicted who could steer the time chair as an empath without getting dizzy.

I made a prediction in previous articles about sound waves induced by glandular emotion, being the mechanism of braiding and programming DNA.

http:www.danwinter.com/emotion

../braidingDNA/braidingDNA.html

../superDNA

This triggered the Glen Rein, HeartMath study showing DNA braid conformation changed measureably in response to EKG coherence AND focused INTENT!

Long wave conformation or braiding in the DNA is accompanied by a long sonic or phonon wave, travelling in the liquids of the cell, induced by glandular emotions ring. This bends the DNA conformation to 'assume the position', to put the rna enzyme re-entrant sites, properly exposed in the braid... so all the cutting and pasting can happen in the right place! (DNA'S hi signal to noise ratio as an info transmitter is due to 'context richness'.. which MEANS long wave braid coherence/embedding, reference the book "Grammatical Man: Information, Entropy, Language and Life" by Jeremy Campbell.)

So what do we do now, knowing that the future of our genepool may depend on NOT trapping the field effect around our genes, in the fractionating scissors of our biolabs. It is probably true that the long wave magnetics stored in old growth seeds genes, may be the only sustainable source for bliss for our grandchildren. This would sound merely like another new age romance novel, excdept for one thing. THE MECHANISM IS HERE DESCRIBED HOW TO MEASURE the life force of DNA. (Spectral contained harmonics space themselves in non linear phi progressions, in ALL bandwidths, as life force is acheived.)

It is about time we assigned freedom and dignity to the enlivening worm, whose replication success IS us. The significance of people is that we are a container to enable DNA's way of acheiving replication. This means that we as people are therefore only sustainable as a race, to the extent WE GIVE OUR GENES THEMSELVES FREEDOM TO LEARN SELF DIRECTION!

THIS MEANS THAT IF DNA IS NOT GIVEN A MEANS TO EXPRESS WILL, IT WILL LOSE THE ABILITY TO HAVE WILL! (And then there will be only chaos instead a "Willed Mutation of the Species").

To set our DNA free, means to respect it's ability to have will. This means recognizing the physics that happens when the worm develops an eyeball (sufi heart with wings bird tribe from snake root..coatel) at the squirtgun business end: The Magnetic X.

(see the superDNA link on how a superconducting gold monofilament welding to a DNA strand yields a faster than light signal progation thru both..)

 

 

Their psychadelic artwork may prove by wormhole penetrating superluminal vision,

that the X-Generation knows that MAGnetic-X is named for them.

Poem by JOHN ALAN LEE

 

 

SPIRALING MESSENGERS

As evolution progresses
Nature's intelligence reveals
Crystalline structures
with an animate essence
unfolding in intuition
of
Beings of Pure Light
Ascending and descending
Jacob's Ladder
As messengers of meaning
Between Man and his Creator

The coiled serpents
Of Yin and Yang
Pinwheel galaxies
spinning in space-time
Rotating Vortices
Pulsating Plasma
Magnetic light
Quantum and cosmic
knowledge flowing
through our veins
into our consciousness

Hurricanes
Monsoons
Meandering streams
Flowering buds in our gardens
Shells from the sea
Pinecones in the forest
Seedlings grown on the plains
Our pineal glands
The shape of our genes
Each a reflection of
Rotational flow
A universal shape
We are beginning to know

The whirling dervish
experiences the Holy Grail
A cosmic code
transmitted through genetics
Our DNA
A double helix
Of twin salt water dragons
Entwined but not touching
Spitting fire
Emitting coherent communicative light
Vibrating strings
A fundamental foundation
In multi-dimensions
For spiraling curves
The hidden universal
Of matter and life

 

JOHN ALAN LEE©
November 26, 1999


RACHEL'S ENVIRONMENT & HEALTH WEEKLY #685 .
. ---February 3, 2000--- .
. HEADLINES: .
. TROUBLE IN THE GARDEN .

. Environmental Research Foundation .
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. E-mail message to info@rachel.org. .

TROUBLE IN THE GARDEN

Wall Street investors lost confidence in agricultural
biotechnology during 1999.[1,2,3] Agricultural biotechnology is
by no means dead, but investors drove down stock prices of ag
biotech companies during 1999 in a stunning reversal for the
industry. The WALL STREET JOURNAL said Jan. 7, 2000, "With the
controversy over genetically modified foods spreading across the
globe and taking a toll on the stocks of companies with
agricultural-biotechnology businesses, it's hard to see those
companies as a good investment, even in the long term."[2]

Hardest hit was Monsanto, the St. Louis chemical giant that had
spent 5 years and billions of dollars morphing itself into a
"life sciences" company, betting its future on biotechnology in
pharmaceutical drugs and agricultural crops. As the WALL STREET
JOURNAL wrote December 21, 1999, "Billions of dollars later, that
concept of a unified 'life sciences' company -- using technology
to improve both medicines and foods -- has become an affliction
itself for Monsanto. The crop-biotechnology half of the program
has grown so controversial that Monsanto has agreed to a deal
that is likely not only to push biotech to the back burner, but
also to cost Monsanto its independence. And investors are
reacting harshly."[3]

Monsanto agreed late in 1999 to merge with Pharmacia & Upjohn,
Inc. and the combined company will be run not from St. Louis but
from Pharmacia headquarters in Peapack, New Jersey. Monsanto's ag
biotech business will be spun off into a separate company and as
much as 19.9% of it will be sold.

Two other leaders in ag biotech, the Swiss pharmaceutical giant
Novartis AG, and the Anglo-Swiss drug firm AstroZeneca PLC,
announced during 1999 that they will combine their ag biotech
divisions into one and sell it off, "effectively washing their
hands of crop biotechnology," the WALL STREET JOURNAL said.[3]

Thus by the end of 1999, ag biotech companies found themselves in
trouble, worldwide, for the first time. Here is a short list of
reasons why:

** A lawsuit against the U.S. Food and Drug Administration (FDA)
forced the release of government documents showing that FDA
scientists had expressed grave doubts about the safety of
genetically modified foods even as the agency was publicly
declaring such foods "substantially equivalent" to traditional
crops.[4] It seems clear from these documents that the scientific
integrity of the U.S. regulatory system has been compromised for
political purposes, to provide a "fast track" for the rapid,
large-scale introduction of genetically modified foods.

** The insurance industry has consistently refused to write
policies covering liability for harm caused by genetically
modified organisms. Steven Suppan, research director at the
Institute for Agriculture and Trade Policy (IATP) in Minneapolis,
said last June, "It is worth asking what kind of regulatory
system approves for commercialization a technology whose risks
are so undetermined that the products developed from the
technology have not been insur- ed? An intuitive response is that
the U.S. rejection of liability suggests that U.S. agribusiness
and the U.S. government have less confidence than is proclaimed
publicly in the safety of the products approved and in the
integrity of the product review process," Dr. Suppan said.[5]

** A growing body of literature has begun to show that
genetically modified crops are creating new kinds of
environmental problems for farmers, and that genetically modified
crops are exacerbating already-severe economic problems on
American farms.[6]

** Europeans and others overseas have continued to insist that
the safety of genetically modified foods has not been
sufficiently documented and that import of such foods must be
prohibited, or they must be labeled. The doubts expressed by FDA
scientists, and the growing list of economic and environmental
problems are likely to stiffen European resistance to
genetically-modified seeds, crops, and foods.

** It became apparent in 1999 that the public rationale for
promoting genetically modified foods -- that such foods would
"feed the world" -- was based on wishful thinking, not economics.
It is now clear that U.S. genetically modified crops are too
expensive to "feed the world."[6]

** The rationale for refusing to label genetically modified foods
came unraveled in 1999 as biotechnology companies began to
announce new crops with special traits (rice with increased
vitamin A, for example). For years, biotech companies, the U.S.
Department of Agriculture (USDA), U.S. Environmental Protection
Agency (EPA), and FDA have argued that labeling genetically
modified foods was impossible because it would require food
companies to segregate genetically modified crops from
conventional crops and it simply couldn't be done. All the crops
were mixed together in the grain elevator, so labeling would be
impossible, they said.

This silly and disingenuous argument evaporated in 1999. As soon
as biotech firms announced specialty foods created by genetic
engineering, the labeling problem miraculously disappeared.
Labeling is suddenly easy -- indeed, required -- because
consumer's can't be expected to pay premium prices for specialty
foods if those foods aren't clearly identifiable on the grocery
shelf.

Polls have shown that more than 80% of American consumers want
genetically modified foods labeled as such. Now that labeling is
acknowledged as feasible, will the biotech industry, USDA, EPA,
and FDA bend to the public will and start labeling ALL
genetically modified foods? Not on your life. Government and
industry argue with one voice that labeling is not necessary
because genetically modified foods are "substantially equivalent"
to the conventional foods they have replaced. They even say
labeling would be "misleading" because it would imply that there
are differences between biotech foods and conventional foods.

Federal regulations governing biotech foods are founded on the
premise that there are no "material differences" between
genetically modified crops and conventional crops. This argument,
it turns out, was thoroughly discredited by FDA scientists before
the regulations were issued.

The FDA spent 1989-1992 developing regulations governing
genetically modified foods for humans and feed for animals. This
was back when President Bush and Vice-President Quayle were
advocating "regulatory relief" for industry.

FDA's rules -- which were announced by Mr. Quayle in 1992 --
allow a biotech company like Monsanto or DuPont to decide for
itself whether its food products are "generally recognized as
safe" (GRAS). If a company decides that its new genetically
modified corn or soybean or potato or wheat is "generally
recognized as safe" then no safety testing is required before the
products are introduced into the food supply. FDA said these
rules -- like all their rules -- are based on "sound science."

However, during 1999 a lawsuit filed by the Alliance for
Bio-Integrity in Fairfield, Iowa, forced the FDA to release some
44,000 pages of internal documents for the first time.[4] Among
them was a series of memos from FDA scientists commenting on the
FDA's proposed "substantially equivalent" policy for biotech
foods.

A key issue is whether "pleiotropic effects" will occur when new
genes are inserted into plants to give the plants desirable new
traits. Pleiotropy means that more than one change occurs in a
plant as a result of the new gene. For example, a gene that
allows a plant to grow better under drought conditions might also
make the entire plant grow smaller. The smaller size would be an
unexpected "pleiotropic" effect.

FDA regulations assume that pleiotropic effects will not occur
when new genes are inserted into conventional foods such as corn
or potatoes or wheat or soybeans. Therefore, FDA says,
genetically modified crops are "substantially equivalent" to
conventional crops.

Internal memos make it abundantly clear that FDA's scientific
staff believes pleiotropic effects will occur when new genes are
inserted into food crops. [In the following quotations, words
inside square brackets have been added for clarity but words
inside normal parentheses were in the original memos.--P.M.]

Commenting on the FDA's proposed biotech regulations in early
1992, Louis Pribyl, an FDA microbiologist, wrote March 6, 1992,
"It reads very pro-industry, especially in the area of unintended
effects.... This is industry's pet idea, namely that there are no
unintended effects that will raise the FDA's level of concern.
But time and time again, there is no data to backup their
contention, while the scientific literature does contain many
examples of naturally occurring pleiotropic effects. When the
introduction of genes into [a] plant's genome randomly occurs, as
is the case with the current [genetic modification] technology
(but not traditional breeding), it seems apparent that many
pleiotropic effects will occur," Dr. Pribyl wrote. "Many of these
effects might not be seen by the breeder [meaning Monsanto or
DuPont or other biotech firm] because of the more or less similar
growing conditions in the limited trials that are performed.
Until more of these experimental plants have a wider
environmental distribution, it would be premature for FDA to
summarily dismiss pleiotropy as is done here," Dr. Pribyl wrote.

On the same subject, a memo from the Division of Contaminants
Chemistry within FDA's Division of Food Chemistry and Technology
said November 1, 1991, "Pleiotropic effects occur in genetically
engineered plants... at frequencies up to 30%. Most of these
effects can be managed by the subsequent breeding and selection
procedures. Nevertheless, some undesirable effects such as
increased levels of known naturally occurring toxicants,
appearance of new, not previously identified toxicants, increased
capability of concentrating toxic substances from the environment
(e.g., pesticides or heavy metals), and undesirable alterations
in the levels of nutrients may escape breeders' attention unless
genetically engineered plants are evaluated specifically for
these changes. Such evaluations should be performed on a
case-by-case basis, i.e., every transformant should be evaluated
before it enters the marketplace."

Instead of heeding the concerns of its scientific staff, FDA
issued biotech food rules that assume no pleiotropic effects will
occur, therefore no safety testing is required. All biotech foods
are assumed to be safe. The stage was thus set for confidence in
biotech foods to plummet as soon as word leaked out that the
scientific underpinnings of the regulatory system had been
compromised.

To be continued next week.

==============

[1] I am indebted to Steven Suppan, research director at the
Institute for Agriculture and Trade Policy (IATP) in Minneapolis,
who provided me with several brief, thoughtful summaries of the
state of agricultural biotechnology. Contact: ssuppan@iatp.org.
Telephone (612) 870-3413.

[2] Christina Cheddar, "Tales of the Tape: Seed Co. May Yet Reap
What They Sow," WALL STREET JOURNAL January 7, 2000, pg. unknown.

[3] Scott Kilman and Thomas M. Burton, "Biotech Backlash is
Battering Plan Shapiro Thought Was Enlightened," WALL STREET
JOURNAL December 21, 1999, pg.A1.

[4] The FDA documents are available at
http://www.bio-integrity.org/list.html. And see Marian Burros,
"Documents Show Officials Disagreed on Altered Foods," NEW YORK
TIMES December 1, 1999, pg. A15.

[5] Steven Suppan, unpublished paper, "National Summit on the
Hazards of Genetically Engineered Foods, June 17, 1999, Capitol
Hilton Hotel, Washington, D.C. 2 pgs.

[6] Some of this literature is summarized in Charles M. Benbrook,
"World Food System Challenges and Opportunities: GMOs,
Biodiversity, and Lessons From America's Heartland," unpublished
paper presented January 27, 1999, at University of Illinois.
Available in PDF format at http://www.pmac.net/- IWFS.pdf .

Descriptor terms: biotechnology; monsanto; dupont; novartis;
pharmacia; astrozeneca; agriculture; hunger; fda; regulation;
labeling; alliance for biointegrity; pleiotropy;

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