Open letter to the World exposing the LIFE system Lies of Ryan Williams:

  Like many I was enthralled by the QXCI/ EPFX/SCIO of Dr. Nelson and I went with Ryan Williams to sell the LIFE system when they broke up. I was told that the LIFE had the same basic technology and was a competitive product. I was there when I saw Dr. Nelson give fee room and board to Ryan and his family of six for over two years. I watched Ryan run up big debt to many and owe Nelson’s company over $750,000 dollars. I has seen Ryan and his family work with Desire’ Dubounet and speak highly of Desire’s  courage to be herself despite what convention thought. I saw Ryan speak highly of Desire’ in two lectures in the Bahamas and in business for over two years. There was no problem but then greed and conflict came in came in and the song switched. I became aware of thefederal criminal inquiry of LIFE’s Google adverts and I saw more. When I really looked into what was being said I started to think.

  I followed Ryan thinking business is business and the systems being similar the LIFE was an opportunity. I watched the business of the LIFE device go up and down and recently read the articles of Laima Jonusiene, www.buksveikas.com. She did a thorough investigation into Dr. Nelson’s work and the LIFE. Then I started to think. Ryan has said the LIFE was the same as the SCIO in measuring remedies, and at a different time Ryan made a video showing they were different. I started to THINK.

  Ryan was two faced saying things to make sales. The key to the workings of the device was the fact that it shows us how a person reacts to remedies. But then Laima asked for validation and verification of how the LIFE system did this and Ryan responded “if you want validation and verification and scientific studies then the LIFE system is NOT for you.” I started to not just Think, but to look closer. No validation, No verification means it is fraud. Slick talk from Ryan don’t change this

I was shocked everything about the LIFE was lies. The only studies showed on the LIFE system showed no difference from placebo. The results we got were only placebo results. I confronted Ryan on this and he laughed and said 

“the alternative medicine community will believe 

any story I tell them”. Ryan Williams

  I started to Think. Many of us who switched from the EPFX found that the LIFE device was not as good but life is life and sales is sales, we thought the LIFE would catch up with the technology. But Now I see there were no researchers, no clinical doctors working to make LIFE better. So I did my own research. 

                                                                            EPFX/SCIO          LIFE

Products bought and tested         Yes, verified by CE record         None it was a Lie

Testing technology                 Yes, verified by CE record         None it was a Lie

TVEP + EPR in registration         Yes, verified by CE record         None it was a Lie

Scientific Research                 Yes, 30 years recorded         None it was a Lie

Approved Clinical research         Yes, 20 years 200 studies                 None it was a Lie

Legal registration to test products         Yes, verified by CE record         None it was a Lie

Independent research         Yes, 20 years worth                 None it was a Lie

Peer reviewed medical publication         Yes, 200 studies         None it was a Lie

Medical Textbooks University taught Yes, verified and validated         None it was a Lie

Legal Scientific Validation                 Yes, verified by CE record                 None it was a Lie

  When LIFE says that there device is the same it is fraud and a bold faced lie. The LIFE is just a counterfeit box made up to look like the real item the SCIO. There was No science, No verification from Life.

  I was shocked everything about the LIFE was lies.The only studies showed on the LIFE system showed no difference from placebo. The results we got were only placebo results. I confronted Ryan on this and he laughed and said “the alternative medicine community will believe any story I tell them”. 

  I now can see that the fraud this man was committing, the con game he had built all masqueraded to look like the science and technology built by Nelson. The LIFE was a fraudulent counterfeit sham all just designed to look like a scientific registered validated device built by what I now know is a great person, Dr Nelson. Now Nelson has the courage and strength of conviction to choose his identity and the malicious slander and disgusting ranting of Ryan about Desire’ are just a manipulative ploy, a sales line, a lie all designed to con you into buying his bogus phony imitation sham device. Desire’ who gave food and a home to Ryan and his family for two years and now is smeared and deceitfully maligned to cover up Ryan’s lies. Ryan owes Desire’ over $750,000 dollars she lent them to start their business. Now Ryan is laughing at all of us and telling lies to make sales. And he slanders Desire at every turn to sell more.

  The companies like Oberon, Physiospect, Sensitv Imago, Introspect, CORE and a host of other  fraudulent devices have all maliciously slandered Nelson/ Desire’. They all fear the real science and due diligence of registration, studies and the work Nelson/Desire’ have done. The FDA has a bogus charge against him to just annoy Nelson. 

  It has been a word game. Who’s lying? Ryan was lying thru his teeth. All of these people have made their businesses claiming that Nelson/Desire’ is lying. In fact I took the due diligence to check and I could find no lie from Nelson. It seems that everything he has said and I mean everything is true. But let me tell you almost everything Ryan has said is a lie. These other companies have been proven frauds. Ryan has been proven a fraud and a lying conman. Nelson has done the research, the science, the statistics, the registration, the publications and these are all facts. I participated in telling lies about Nelson to sell the LIFE product. I had no idea just how pervasive these lies were. I would like to apologize to Desire’ and I hope this confession helps the industry to see the real truth. 

  But this is not about Desire’, or Ryan, or me. It is about truth. If you use a device it is about it is about how you justify the reading of reaction. It is about scientific validation, research, clinical studies, peer reviewed publications, university curriculums, medicinal textbooks. Many people have stopped using these devices because they used the LIFE and did not see good results. The SCIO worked with AC Milan, Chinese Olympic team, Novak Djokovic, Na Li, the Hungarian Power lifting team these all point to the power of the SCIO. This was all verified. 

  The question is validation and verification of how do you test the remedies. If you see a client and they ask how does the system know this reaction What do you say in court.If you have a SCIO there will be a small truck of registrations saying EPR and TVEP and studies, and peer reviewed journals and much more. If you have a LIFE system well toilet paper might be the only paper you have. Life has no verification because it is fraudulent. 

  This article might challenge you and you might own or sell the life system. You might wonder what is really going on. Is it capable for Ryan to lie to us about what the device does?

Ask a simple question: 

How does the system know the reaction and what studies and registrations verify this?

  I found out that the SCIO team has a thirty years history of research, verification, confirmation, registration, publication, university medical instruction and certified medical textbooks that validate their claim. You can ask for these publications and they can be supplied. The SCIO people did not speak a word about the LIFE. They honorably just gave us information on their device. They gave us peer reviewed medical journals, certified medical textbooks, science, studies, legal registration to test reactivity, and over two decades of clinical research. 

  If you ask for verification from LIFE you will get stories and excuses and slander. They will spend more time slandering Nelson or misquoting Nelson than explaining how they do it. 

  As an insider who was duped, I feel the need to expose the LIFE lies. I know have checked this all out and offer you this testimonial to help expose the lies and honor the truth. Some of you people will believe any lie Ryan tells you. I will not. I have checked into it and will not be lied to again.

  I feel stupid to have been so duped by Ryan’s lies and to think I myself was drawn into slandering Nelson/Desire’ makes me feel sick. To appease my soul I thought it best I tell the world of the LIFE and Ryan lies. Ask questions of validation and get answers, ask for research, ask for scientific verification but do not listen to slurs directed to other companies. Get the answer to the question how do you measure the reaction of a patient to a remedy. And try to do some due diligence on Ryan’s lies. Ask Ryan for verification of what the device is claimed to do and why it has screens like those below if it is just biofeedback. 

Thoughts of self doubt 

Nutritional deficiencies 

Toxic stress factors:

Fungus 

Bacteria 

Virus 

Chemical agents ( pesticides, cleaners) 

Heavy metals 

Prescription drugs 

Synthetic compounds (artificial sweeteners, food color) 

Vaccines 

Parasites 

Allergens 

Geopathic stressors 

Bio field contamination, Micro Waves, EFTs 

  These claims of LIFE have no scientific explanation, no verification, no studies, no research, and no legal basis for claim. These screens are just made up on completely random numbers and they are proven to be a medical fraud. No studies have ever been done to verify the results. 

  I am sorry to admit that I worked with such a fraudulent company as LIFE to sell illegal counterfeit bogus copies of a real scientific verified and validated technology. I hope this letter can atone for some of my lost self-respect. Next time I’ll know to ask for verification before I get roped into a counterfeit fraud. I hope that you will ask questions and not listen to slander of others as well.

                                                                                                                       SINCERELY 

                                                                                                                                 S.S.

PS: I put the articles from an independent laboratory on this blog to show you. 

Medical Device Fraud

By Laima Jonusiene, www.buksveikas.com
June 21, 2011 -- Updated 0315 GMT (1515 HKT)

  People don’t like it when someone has to down grade someone else’s product to sell their, but what if the product they sell is fraudulent. If you had a fraudulent Medical device that you had no registration and no scientific studies to validate it, how could you sell it? Well you could contact Google or other search engines and place your fraudulent device next to one that has proper registration, proper research and published studies. The search engines were thought to have legal risk. A section of the 1996 Communications Decency Act protects internet service companies from being held accountable for virtually any content provider by users or advertisers, but there is an exception for federal criminal cases specifically when there are devices proven fraudulent and being marketed without proper registration.

  There have been a few false claim medical devices that claim to be able to tell you about your body parts and what remedies can help you. The PHYSIOSPECT, INTRASCAN, INTROSPECT, OBERON, SENSITIV IMAGO, AND LIFE DEVICES HAVE BEEN SHOWN TO BE FRAUDULENT AND ILLEGAL FOR SALE OR USE. They could produce NO regulatory registration that allowed them to make this claim. They could produce NO comprehendible science to explain the actions of their devices. They could produce NO clinical trials or patient studies to validate this claim. Without any registration of this claim, without any science to explain the claim, or without any proper clinical studies done to accepted legal standards How could they market such fraud. Well they use search engines to post their fraudulent claims next to devices that are registered, scientific, and with long history of clinical studies done to validate the concept.

  There is a company that has the proper ability to make such claims. The Maitreya corporation now controls such technology in the EPFX/SCIO. As we investigated the claim that a device could electrically measure your reaction to various homeopathic items, the company showed us the original science dating back to research done in the seventies. The technique was registered with the FDA in America in 1989 as Electro-Physiological Reactivity (EPR) that we confirmed with the FDA literature. The research articles were very extensive and thorough. The current terminology registered with the CE mark is Transcutaneous Voltammetric Evoked Potential (TVEP). After over three decades of clinical and scientific research the technology has now been added to certified medical textbooks accepted by European Universities. We reviewed the research, the university staff and the textbooks and found this to be scientific, extensive, and properly documented. Over three decades of science, research, clinical trials, peer reviewed journal publication, practitioner testimonials, and proper regulatory registration.

  The other companies claiming to be the same, well they had none of the above. There was NO registration at all for most of them, NO registration of the reactivity claim for any of them, NO science explanation, NO clinical trials, NO publications, and NO honest attempt to comply with the law. They just all claimed to be the same as the EPFX/SCIO.

  There have been many frauds in the business of Alternative Medicine. First there is Muscle testing for remedies. This has failed every double blind test and been proven to be under operator or therapist control.

 

Next was Electro-Dermal Testing using point probes. But here also all double blind research showed the operator was in control consciously or unconsciously changing the speed of pressure on his point probe.
 

The new laser devices with no real science or clinical data came from Russia. The CORE device has been found completely fraudulent using the computer date to shape data.

In America these devices could be sold as experimental devices such as the Papini device which killed several people in Washington.

Lethal Papinni device

  Google, Microsoft and Yahoo have been changing their policies under pressure from licensed pharmacies, major drug makers, registered medical devices and the FDA to do more to filter out ads that tout prescription medications or illegal devices. Drugs are often ostensibly from Canadian companies but manufactured in China, India and elsewhere. Fraudulent devices come mostly from Russia and Ukraine with illegal distributors all over the world. But some American companies are also using illegal comparisons of their device to other devices registered for functions there device is not registered for. The game is to compare your fraudulent device to a known medical device that is registered for a function yours is not. When the person uses his computer and mentions a legal device a cost comparison comes up to direct the person to the fraudulent device for less money. (see Google close to settling U.S. drug and fraud medical device ad probe, article June 2011)

  But if you claim equivalence to a registered scientific device then how do you market yours. Well in these cases the companies could not argue with the technology, you slander the developer. They have said that Professor Nelson now Desire’ Dubounet is lying and they are telling the truth. So we decided to independently investigate both sides of this issue

  Nelson says he worked on the Apollo navigation system and helped Apollo 13 to return. The other companies said this was a lie. We saw certificates verifying the story, we checked work records of FICA and Nelson worked as he claimed, we talked to other engineers who worked with Nelson and they verified the story. Nelson told the truth the competition told a lie.

  They said Nelson’s credentials were false. We verified all of his credentials and that he was indeed a medical licensed diagnostician and health care practitioner in the State of Ohio. Nelson’ story was true the competition told a lie.

  As we went through all of the stories we saw that Nelson / Desire’ was telling the truth about all of the things he spoke and the competition was slandering him and telling many lies. They said they had registration, studies, science and all of this was a bold faced lie. They could produce none of this. They even stooped to calling Nelson/Desire’ names for her courage to express her sexuality. 

  One company in particular the CORE system exploded with anger and hate for Nelson and they went into a tirade of what was later found out to be complete lies. The content of covetousness, jealousy and cognitive dissonance displayed became evident. The science dedication for the registration and the research was mostly directed by Nelson/Desire’. These were skills the others do not have and they decided to break the law and put their products fraudulently on the net next to the Scio. The Scio has over twenty years of legal registration, science, and published double blind clinical studies and this drives the competition crazy.  So they can fraudulently market their devices. And most sadly when these fraudulent devices do not get results with patients, and we talked to many patients that did not get results from these fraudulent devices, the whole industry and the companies doing it right suffer.

  It is very difficult to deal with the greed and easy money making a fraudulent medical device generates. The authorities can do little and when confronted these frauds just sell their wares from someplace else. Google might not change, the law does not concern this giant and it is difficult for them to see what is or is not real. But look for CE registration not of safety but medical claim. Look for the studies, evaluate the science. Ask the question how does your device know that liver is stressed. Ask questions and look for answers. We hope this article has helped you.

  Now Google is close to settling a federal criminal inquiry into its acceptance of advertisements from companies selling unlicensed pharmaceuticals and medical devices, according to a person involved in the case. The leading search engine disclosed this week that it had reserved $500m to resolve an unspecified US justice department probe into its advertising practices, with speculation quickly turning toward counterfeit and unapproved medical devices and drugs.
The Wall Street Journal reported recently that the pending deal would resolve an investigation of drug medical device ads by the US justice department, with participation of the Food and Drug Administration and the federal prosecutor in Rhode Island. A person familiar with the matter confirmed the talks to the Financial Times.

The justice department, FDA and Google all declined to comment.

LIFE System Lies and Device Fraud

By Laima Jonusiene, www.buksveikas.com
June 27, 2011 -- Updated 0518 GMT (1718 HKT)




(BUK SVE) Here is an example of the claims made by the LIFE system, and a discussion of the Major health care medical device Fraud they are perpetrating. 

Excerpt from Life advertising:

The LIFE System is conceptually based upon Bioenergy (i.e.:chi) Acpuncture and traditional meridians which represent the paths of flow of this energy. Factors which may inhibit peak performance and general vitality: 

Thoughts of self doubt
Nutritional deficiencies
Toxic stress factors:
Fungus
Bacteria
Virus
Chemical agents ( pesticides, cleaners)
Heavy metals
Prescription drugs
Synthetic compounds (artificial sweeteners, food color)
Vaccines
Parasites
Allergens
Geopathic stressors
Bio field contamination, Micro Waves, EFTs

The LIFE System is a 5 point, 12-channel, harness system similar to ElectroDermalScreening (EDS) technology and a software system which has in excess of 7000 different and unique frequencies programmed within. In mainstream medical terms this device may be called a versatile Bio Feedback device. 

They Claim to be able to tell you about your organs, spine, vertebrae, nerves, heart, allergens, toxicities and a wide range of diagnostic criteria. Due Diligence will find if this is true.

Pictures like this tell us incredible things about the body, But is this true or an incredible lie?

We sought to research with due diligence and present the findings of our report to the public. We first heard of this device in an article we did on Google search engine allowing fraudulent devices to be advertised next to real accredited devices. (see Google close to settling U.S. drug and fraud medical device ad probe, article)
In this research we stumbled on a story that we thought the public should know about. The primary way of selling this fraudulent medical device called the LIFE system was to place Google ads next to another device called the SCIO. So our first due diligent process was to investigate the SCIO and ask serious questions about its operation.
The SCIO device started registration in 1989 as the EPFX. This was controversial but in the 1989 registration we see the following.
FDA 510 (k) registration for the EPFX was obtained on October 13, 1989. The following is an excerpt from the original office 510(k) application:

“The EPFX measures the Electro-Physiologic Reactivity intensity of the patient to many QQC trivector voltammetry patterns. These are patterns of reactions to Sarcodes, Nosodes, Allersodes, Isodes, Nutritional, Herbals, Imponderable and Classic Homeopathics. The reaction patterns or profiles can relate disturbances of the patient. Therapies can then be arranged to develop harmonic reactions,
desensitizations, biological resonance or rectification processes. All of these are applied and managed through biofeedback application. Biofeedback is the operation that allows for the cybernetic loop to of systemic feedback. The only indicated use of this device and all claims related to this device are under biofeedback. The loop of measured reaction and bio-varied resonance response allow for a true feedback for self corrective Electro-Physiological therapy. Hence it is called the Electro Physiological Feedback Xrroid.”

 

The CE mark Class 2 registration includes
The following excerpt is from the medical claims part of the SCIO CE Mark:

“The SCIO is indicated for use as a Universal Electrophysiological Biofeedback System. The Universal Electrophysiological Biofeedback System is made up of the following Eight Universal Items which are functions of the SCIO:
1. Stress Reduction and Lifestyle Stressors Questionnaire;
2. Simple EEG [electroencephalography] biofeedback brain wave stress reduction;
3. Three-pole ECG [electrocardiography] simple heart awareness and biofeedback stress reduction;
4. EMG [electromyography] biofeedback for simple reeducation of muscles;
5. GSR [galvanic skin response] biofeedback and TVEP [transcutaneous voltammetric evoked potential] biofeedback (electrophysiological reactivity);

Since GSR biofeedback requires a microcurrent voltammetric stimulation to measure GSR, then the microcurrent has the following secondary Therapeutic functions which function as performed through the biofeedback loop:

6. Microcurrent Transcutaneous electro nerval stimulation (MENS) for pain reduction in the cybernetic biofeedback loop, Cranial Electro Stimulation (CES) for anxiety and addiction;
7. Trauma or wound healing in the biofeedback loop;
8. Global Voltammetric Charge Stability in the biofeedback loop”

 

Here clearly is registration for the ability to measure Electro-Physiological Reactivity (EPR) and or Transcutaneous Voltammetric Evoked Potential (TVEP). Reactions of nosodes, isodes, sarcodes, allersodes, nutritional products herbals etc are outlined and validated in the FDA and CE registration. No such claim is validated for the LIFE system which is registered only as a simple biofeedback system. There is no permission for the LIFE system to make the claims made by the SCIO. This is why they need to put their advertisements next to the SCIO.

So what was the science behind this technique of remedy reaction? Well we were told of a QQC trademarked device that measures the voltammetric signature of items. Voltammetry is a science of Electrochemistry where items have a distinct electro-magnetic static field that can be detected with electrodes. We were shown several patents for a device known as the QQC which was trademarked in America in the 1990’s and now internationally trademarked. This multi patented device can measure the Three Dimensional field of a substance and convert it into an electro matrix. We confirmed trademarks and patents as part of our due diligence. The science was outlined in several studies published in peer reviewed medical journals, books and medical textbooks. Every item appearing in the SCIO matrix was first purchased or procured, prepared, tested and results recorded in a professional record in a CE registered voltammetric device. All was done to CE quality standards for the SCIO. Over twenty independent medical doctors validated the QQC. All of this was critically confirmed as true with our due diligent investigation.

The LIFE system had none of this. Our investigation found that they falsely claim equivalence to the SCIO and NONE of the voltammetric testing was ever done. There was no purchase of product, no scientific testing, no record keeping; Life system was doing a complete fraud.

This led us to the question of how LIFE started. Well a salesman of the SCIO system Chris Keser was dissatisfied and he criminally counterfeited 35 checks made out to the SCIO people. A warrant for his arrest was made in Hungary. He purchased an old obsolete 1992 software of the SCIO made before the QQC voltammetric signatures and before the subspace system. He made it to look like the SCIO in every way. But it looked similar but did not do the functions. When Ryan Williams worked for the SCIO people he ran up a bill of over $750,000 dollars and could not pay. He took money fraudulently and the police were called in. His family bailed him out and he started working with the LIFE people. Now the lies ensued and accelerated. Ryan Williams told people the LIFE system was the same but our investigation has shown his lies are pervasive. He was slick and evasive but our investigation got to the heart of the LIFE fraud.
Ryan said that the SCIO system used a random number generator to determine reactions, but we told him we saw extensive evidence for the Voltammetry, a CE marked system, complete records of product purchase and testing, research, patents, for over 20 years. We found out that Ryan was just trying to spread a rumor. We found out that this false rumor of a random number generator was being spread by the competition who were afraid of SCIO’s true technology.

If people knew the truth and could see the technology SCIO has and the lies the competition tell then they would be quite angry at LIFE and the other companies telling these lies.

The SCIO people started collecting and measuring the items in the matrix in 1985. They showed us receipts for over a million dollars spent on collecting enzymes, vitamins, hormones, sarcodes (Organic healthy tissue), nosodes (unhealthy and diseased tissue), microorganisms, and over 11,000 items. Each item tested with a CE registered voltammetric device that is made to operate like your tongue in analyzing the electric signature shape of the substance. An incredible technology fully researched, double blind tested, scientifically validated and CE registered. After over twenty years of research this technology is now in a European Medical University curriculum. We were shown over 200 professional medical doctor studies most using double blind techniques, all published in International approved peer reviewed medical journals. We were shown over 75 medical textbooks. Our due diligence found these medical textbooks to have proper library numbers, medical university clearance, faculty approval and to fit all professional criteria. Many of these books are over 1000 pages of quality science. Here are some of the University faculty certified medical textbooks that apply to the body electric and Reactivity:

 

The first of these books was published in 1982 by Prof Nelson. The QQC technique was revealed in 1992 at the Royal Society of Medicine in London England. The science is extremely extensive. The cost of doing these studies and publications are at a value of hundreds of millions of dollars. One series of studies were done by over 2,000 medically supervised therapists on over 97,000 patients, for over 300,000 patient visits on over 220 different diseases. A very costly and comprehensive study that validated the clinical results.

 The SCIO technology is so extremely meticulous and scientific that it is no wonder Prof Nelson has been nominated for the Noble Prize in Medicine for the last 15 years, a fact we confirmed with the nominating party. In fact our investigation of Prof Nelson showed that the slander about him was prompted by people selling fraudulent devices. LIFE systems writes disgusting lies with rumors and innuendos about Nelson that petty children would hesitate to write. They do this to divert attention from their fraud.

The LIFE system has no credentialed studies, no double blind testing, no peer reviewed journal articles, none of the professional science of the SCIO. The LIFE system Fraud is to place its adverts next to the SCIO, make a counterfeit system that looks just like the SCIO only has no real technology just aberrant signals coming out of it, tell every lie you can and offer a reduced price which is easy if you never invested a penny in science, or validation or publication. In other words complete fraud.

The bottom line today in our litigious society where you can sue anybody, is a key Question:

HOW DOES YOUR DEVICE KNOW I HAVE AN ORGAN PROBLEM?

Whatever organ you are told is involved or a remedy for it. In other words if your LIFE device says you have a problem in an organ say liver or you react to a remedy how does it know that. What would you say in court if that question was asked?

The SCIO Company gave us a detailed massive history of science, studies, double blinds, research, peer reviewed publications, medical textbooks, CE and USA registrations clearly and definitively saying it was legal and scientific. The SCIO people made no reference to any other company whatsoever.
The LIFE system people went into fear. Ryan Williams went into a mumble mouth spurt of nonsensical pseudo science that would make any two faced politician proud. It became clear he did not really understand any of the science of which he was misquoting. We advised him that his comments would be reviewed by the federal criminal inquiry into Google false advertising.

He got to a point where he started to bad mouth Prof Nelson, and we had to say this is just a due diligent investigation to discover how the LIFE device validates what it says and not a personal attack. The LIFE system spoke more about SCIO than their own system. We told him it is better to answer these with us than in court where he could go to jail for perpetrating the fraud on LIFE buyers.

Our due diligent investigation then revealed: The most if not all of the items in the LIFE matrix were never purchased, never tested, never validated, and never recorded. No system of product testing could be presented or described. No records of this could be found. It was Fraud. There was no scientific evidence, no double blind studies, no properly done studies of effectiveness, and not even an attempt at professionalism could be found. The registration of the device was just as a simple biofeedback which when operating it had no look of biofeedback. Ryan said there was science and testing and we later found out this was all a lie as he admitted to having falsified his first response. This was just a bogus hoax all set up to look like the SCIO and capitalize on the work done by SCIO people.

We had discovered LIFE’s complete Fraud, Chicanery, Deception and a Con-man Hoax of the worst nature. If you have a LIFE system and someone asks you in court to explain how it knows things, just reach for the checkbook and pay before you look like a fool.
People say the LIFE system works. The LIFE system knows that 50% or so get effect from placebo. A little more if you charge for therapy. So the results from the LIFE system are merely placebo. Research done at independent laboratories has shown the LIFE system to even not be as accurate as placebo. In fact many people we spoke to did not get any results with the LIFE system and thus bad mouthed energetic medicine.
As our due diligent investigation has led us to see that there is an extensive registered science of reaction testing in the SCIO that has been patented, legally registered, properly validated, published in peer reviewed medical journals and appears in Medical University certified Textbooks. This technique is developed and used by the SCIO personnel.

The LIFE system does not have any clue even as to how it works. It became apparent they did not have any scientists who could even read the medical textbooks. They had no real Medical staff to even understand the operations. We found complete Fraud in the LIFE claims. Complicative was not just the fraud but the purposeful counterfeit copying the SCIO and then slandering of the developers of the technology.
For many of the readers who were victims of the LIFE hoax this article might not sit well. To reconfirm for yourself please ask a simple question: How do you test a remedy?
What is the scientific process of determining how a remedy is good for a patient? Ask any company to answer for themselves. Do not let a company speculate on how another company does it. But ask each company how they do it themselves. What is the science, the registration permission, the studies, the books, the history and the skill to measure a patient’s reaction to an item? When they give you anecdotal stories please be advised that is not evidence. Evidence today comes from professional properly supervised legal double blind research. It is a simple question of science and research to validate your claims with double blind evidence not stories.

Our due diligent thorough investigation of the SCIO was impressive and convincing in every fashion. The SCIO people showed us research, registrations, validations of the claim.  Our investigation of the LIFE system proved the LIFE to be a complete sham ill intent fraud. We have turned over all of our research to the federal criminal inquiry of Google’s advert acceptance from Fraudulent medical companies.

Ryan’s lies were quite slick and extensive but lies and frauds just the same. If anyone would want to sue him for these lies and get their money back we would be happy to be professional witnesses and testify to his fraud.

OBAMA SIGNED CODEX ALIMENTARIUS

·          

Executive Summary – During the oil spill distraction the Kenyan Muslim with a Hawaiian birth certificate signed Codex Alimentarius. The date signed was June 10, 2010. It is executive order #13544.

What This Means – It is the death of alternative health care remedies, supplements, etc. This precedes Obama Care with their death counseling for those that are very sick that require costly treatment to prolong their life. Here comes population reduction big time. A double whammy. Oh we the people have guns and ammo but are being killed off by poisons the GMO food, the water, harmful drugs, vaccines etc. While everyone is waiting for something to happen they are steadily moving towards decimating the population. The toxic food, water, drugs etc also goes a long way towards dumbing down the population. Go eat in a fast food restaurant and see if you get tired and sleepy a little while later.

Let's Look at the Codex Alimentarius – Any mode of treatment or remedy for ailments that does not have scientific backing will be illegal. It costs many millions of dollars to convince the FDA that say olive leaf extract actually fights viruses, bacteria effectively. No one is going to spend tends of hundreds of millions on this because it is not an item one can place a patent on. Same for colloidal silver, ozone therapy, hydrogen peroxide, frequency medicine etc. Thus all the good modes and supplements that heal will be illegal to protect the consumer. After all they do not have FDA approval. Then comes Obama care and you can now get poisoned with vaccines, toxic therapies etc.

See some portions of this:

(f) contains specific plans to ensure that all Federal health-care programs are fully coordinated with science-based prevention recommendations by the Director of the Centers for Disease Control and Prevention; and

(g) contains specific plans to ensure that all prevention programs outside the Department of Health and Human Services are based on the science- based guidelines developed by the Centers for Disease Control and Prevention under subsection (d) of this section

(c) This order is not intended to, and does not, create any right or benefit, substantive or procedural, enforceable at law or in equity by any party against the United States, its departments, agencies, or entities, its officers, employees, or agents, or any other person.

The entire text of this Obamination is below:

Executive Order 13544 of June 10, 2010

Establishing the National Prevention, Health Promotion, and Public Health Council

By the authority vested in me as President by the Constitution and the laws of the United States of America, including section 4001 of the Patient Protection and Affordable Care Act (Public Law 111–148), it is hereby ordered as follows:

Section 1. Establishment. There is established within the Department of Health and Human Services, the National Prevention, Health Promotion, and Public Health Council (Council).

Sec. 2. Membership. (a) The Surgeon General shall serve as the Chair of the Council, which

shall be composed of: (1) the Secretary of Agriculture;

(2) the Secretary of Labor;

(3) the Secretary of Health and Human Services;

(4) the Secretary of Transportation;

(5) the Secretary of Education;

(6) the Secretary of Homeland Security;

(7) the Administrator of the Environmental Protection Agency;

(8) the Chair of the Federal Trade Commission;

(9) the Director of National Drug Control Policy;

(10) the Assistant to the President and Director of the Domestic Policy Council;

(11) the Assistant Secretary of the Interior for Indian Affairs;

(12) the Chairman of the Corporation for National and Community Service; and

(13) the head of any other executive department or agency that the Chairman, from time to time, determine is appropriate. (b) The Council shall meet at the call of the Chair.

Sec. 3. Purposes and Duties. The Council shall: (a) provide coordination and leadership at the Federal level, and among

all executive departments and agencies, with respect to prevention, wellness, and health promotion practices, the public health system, and integrative health care in the United States;

(b) develop, after obtaining input from relevant stakeholders, a national prevention, health promotion, public health, and integrative health-care strategy that incorporates the most effective and achievable means of improving the health status of Americans and reducing the incidence of preventable illness and disability in the United States, as further described in section 5 of this order;

(c) provide recommendations to the President and the Congress concerning the most pressing health issues confronting the United States and changes in Federal policy to achieve national wellness, health promotion, and public health goals, including the reduction of tobacco use, sedentary behavior, and poor nutrition;

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(d) consider and propose evidence-based models, policies, and innovative approaches for the promotion of transformative models of prevention, integrative health, and public health on individual and community levels across the United States;

(e) establish processes for continual public input, including input from State, regional, and local leadership communities and other relevant stake- holders, including Indian tribes and tribal organizations;

(f) submit the reports required by section 6 of this order; and

(g) carry out such other activities as are determined appropriate by the President. Sec. 4. Advisory Group.

(a) There is established within the Department of Health and Human Services an Advisory Group on Prevention, Health Promotion, and Integrative and Public Health (Advisory Group), which shall report to the Chair of the Council.

(b) The Advisory Group shall be composed of not more than 25 members or representatives from outside the Federal Government appointed by the President and shall include a diverse group of licensed health professionals, including integrative health practitioners who are representative of or have expertise in:

(1) worksite health promotion; (2) community services, including community health centers; (3) preventive medicine; (4) health coaching; (5) public health education; (6) geriatrics; and

(7) rehabilitation medicine.

(c) The Advisory Group shall develop policy and program recommendations and advise the Council on lifestyle-based chronic disease prevention and management, integrative health care practices, and health promotion. Sec. 5. National Prevention and Health Promotion Strategy. Not later than March 23, 2011, the Chair, in consultation with the Council, shall develop and make public a national prevention, health promotion, and public health strategy (national strategy), and shall review and revise it periodically. The national strategy shall:

(a) set specific goals and objectives for improving the health of the United States through federally supported prevention, health promotion, and public health programs, consistent with ongoing goal setting efforts conducted by specific agencies;

(b) establish specific and measurable actions and timelines to carry out the strategy, and determine accountability for meeting those timelines, within and across Federal departments and agencies; and

(c) make recommendations to improve Federal efforts relating to prevention, health promotion, public health, and integrative health-care practices to ensure that Federal efforts are consistent with available standards and evidence.

Sec. 6. Reports. Not later than July 1, 2010, and annually thereafter until January 1, 2015, the Council shall submit to the President and the relevant committees of the Congress, a report that:

(a) describes the activities and efforts on prevention, health promotion, and public health and activities to develop the national strategy conducted by the Council during the period for which the report is prepared;

(b) describes the national progress in meeting specific prevention, health promotion, and public health goals defined in the national strategy and further describes corrective actions recommended by the Council and actions taken by relevant agencies and organizations to meet these goals;

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(c) contains a list of national priorities on health promotion and disease prevention to address lifestyle behavior modification (including smoking cessation, proper nutrition, appropriate exercise, mental health, behavioral health, substance-use disorder, and domestic violence screenings) and the prevention measures for the five leading disease killers in the United States;

(d) contains specific science-based initiatives to achieve the measurable goals of the Healthy People 2020 program of the Department of Health and Human Services regarding nutrition, exercise, and smoking cessation, and targeting the five leading disease killers in the United States;

(e) contains specific plans for consolidating Federal health programs and centers that exist to promote healthy behavior and reduce disease risk (including eliminating programs and offices determined to be ineffective in meeting the priority goals of the Healthy People 2020 program of the Department of Health and Human Services);

(f) contains specific plans to ensure that all Federal health-care programs are fully coordinated with science-based prevention recommendations by the Director of the Centers for Disease Control and Prevention; and

(g) contains specific plans to ensure that all prevention programs outside the Department of Health and Human Services are based on the science- based guidelines developed by the Centers for Disease Control and Prevention under subsection (d) of this section. Sec. 7. Administration.

(a) The Department of Health and Human Services shall provide funding and administrative support for the Council and the Advisory Group to the extent permitted by law and within existing appropriations.

(b) All executive departments and agencies shall provide information and assistance to the Council as the Chair may request for purposes of carrying out the Council’s functions, to the extent permitted by law.

(c) Members of the Advisory Group shall serve without compensation, but shall be allowed travel expenses, including per diem in lieu of subsistence, as authorized by law for persons serving intermittently in Government service (5 U.S.C. 5701–5707), consistent with the availability of funds. Sec. 8. General Provisions.

(a) Insofar as the Federal Advisory Committee Act, as amended (5 U.S.C App.) may apply to the Advisory Group, any functions of the President under that Act, except that of reporting to the Congress, shall be performed by the Secretary of Health and Human Services in accordance with the guidelines that have been issued by the Administrator of General Services.

(b) Nothing in this order shall be construed to impair or otherwise affect:

(1) authority granted by law to an executive department, agency, or the head thereof; or

(2) functions of the Director of the Office of Management and Budget relating to budgetary, administrative, or legislative proposals.

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(c) This order is not intended to, and does not, create any right or benefit, substantive or procedural, enforceable at law or in equity by any party against the United States, its departments, agencies, or entities, its officers, employees, or agents, or any other person