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Technology to treat many hitherto incurable illnesses including cancer and HIV.
Christopher Windram
United Kingdom
1 Team Member

Therapeutic Device for Electromagnetic DNA Manipulation

In December 2010 the French Nobelist Luc Montagnier released the academic paper ‘DNA waves and water’ (link 1) building on research first published in 1992 by Russian scientists, Gariaev and Poponin (2). The experiments detailed in ‘DNA waves and water’ inspired by the discovery that pathogens M. pirum and E. coli extend an electromagnetic DNA signal into water to infect cells while remaining physically separated. The paper later reveals how to duplicate viral and bacterial DNA in the absence of any physical DNA template. DNA sequences were transmitted by electromagnetic waves into a separate container of pure water imprinting a template of the DNA sequence within the water. These water DNA templates were later reconstructed into almost identical physical DNA sequences by PCR.

These experiments since reproduced have been described as “the most significant experiments performed in the past 90 years” (link 3).  I believe these experiments herald the beginning of a revolution in medical physics and here’s why: they reveal a new way to alter specific biochemical activity within cells were drugs and genetic engineering have proven ineffective. The purpose of my intended research is to provide improvements in these techniques and apply them to the problem of virus and cancer DNA replication in living hosts. Many applications are possible include treating genetic disorders, activating stem cells, rapid genetic modification, treating cancers and a valuable treatment for a variety of incurable viral and increasingly resistant bacterial infections.

It has been estimated that more than 1 in 3 people (33%) will develop cancer at some point in their lifetime. Cancer types are numerous as there are many different types of cells in the body. Treating a genetic disease means discovering a treatment that works at the genetic level and is specific to each affected cell type. Up to now, many treatments that kill cancer cells cause collateral damage to healthy cells and will often kill the host outright. The number of cancer types and limitations of chemical accessibility to different cells in a host makes the possibility of an effective drug being developed that could eliminate all cancer cell lines without collateral damage unrealistic. There are inherent advantages to this technology one of which is its influence will penetrate the body to reach all cells.  

What Your Contribution Will Achieve

  1. You will fund a team of experts and equip the worlds most creative medical physics laboratory and develop the technology that will use electronic signals to kill cancer cells, eliminate HIV and treat genetic diseases.
  2. Following our research we will have the funding to hire patent lawyers and file patents to protect the technology and bring a substantial return to investors.
  3. You will fund the necessary medical trial into the safety and efficacy of the device prior to production. A modest medical device study typically costs around $1million (link 4).

Background to the Claims

Molecular resonance is a relatively well understood phenomenon in chemistry and shows molecular interactions to be largely electrical in nature, molecules posses specific frequencies allowing them to find their targets. As both photon and phonon modes exist for electromagnetic waves molecules are able to ‘see’ and ‘hear’ each other and  influence each other at a distance and become ineluctably drawn to each other if vibrating out of phase (in a complementary way). Irena Cosic proposed the Resonant Recognition Model (link 5) to classify the electromagnetic properties of molecular interaction and analysed over 1000 proteins from 30 functional groups. Interestingly the results shown proteins with the same biological function shared the same single frequency peak in their electromagnetic spectra.

Bio molecules at a normally active concentration do not work in a medium devoid of water they are unable to produce life. Bio molecules do not directly transmit their signal this job is done by water. There are 10,000 water molecules in the human body for every molecule of protein the properties of water just as they are fundamental to life they are fundamental to this invention. The properties of liquid water that support the claims are well understood and specific to Quantum Field Theory and are found in the publications “QED Coherence in matter” (link 6) also “Water Dynamics at the Root of Metamorphosis in Living Organisms“ (link 7). The water nanostuctures that will be later mentioned are weak quantum coherent domains induced by DNA and amplified through vortexing and agitation supporting information is found in “Water as a free electron laser” (8). For evidence of the enduring changes to the structural properties of water influenced by resistance inductance capacitance circuits see “Permanent changes in the physico-chemical properties of water following exposure to resonant circuits” (link 9). Further information on the dynamical role of bound water in bio molecules see ‘Coherent Quantum Electrodynamics in Living Matter (link 10). The contribution of Luc Montagnier’s team can be found in their paper “Electromagnetic signals are produced by aqueous nanostructures derived from bacterial DNA sequences” (link 11).

Similar research has recently been published in The British Journal of Cancer using electromagnetic fields to treat cancer demonstrating its effectiveness can be found here (link12)



An electrical device comprising:
A computer & database.
A digital signal processor.
A process for isolating signals.
A coil.
Mu-metal shielding



With reference to the included drawing the following stages necessary for treatment of cancer (as an example) using the device are given below:

First stage: water is non-signalized by having previously been heated to over 70 ° C for  a time greater than 30 minutes and allowed to cool to room temperature or frozen to -20° C or -60° C for 1 hour then brought to room temperature.  Infected or damaged DNA sequence from pathogenic cells are obtained from the host and copied to reach a concentration of 1 ng/ml to 4 ng/ml per water solution and transferred to a plastic vial. Subjected to between seven to twelve dilutions via agitation or vortexing with pure non-signalized water or other non-signalized dipole solution being diluted 10-fold each time. The vial is inserted into the magnetically shielded coil and subjected to an oscillating electromagnetic field of 7 hertz for a minimum of 18 hours. Time domain electromagnetic signals are recorded while inserted into the coil.

Second stage: the process of the first stage is repeated for DNA obtained from an identical cell line obtained from the host that is absent of the pathogenic DNA of the first stage.

Third stage: Electromagnetic DNA signals are detected and compared and differences marking the pathogenic DNA sequence are identified.

Fourth stage: The electromagnetic pathogenic DNA sequence identified is processed in such a manner to hinder its incorporation into the cells in the following stage by using any suitably altered signal of the pathogenic DNA sequence such as phase inversion.

Fifth stage: The living host is placed into the influence of the device and the processed signal from the previous stage is imparted using a proprietary method and repeated until treatment is no longer required, a small portable device attached to the host can be used. The altered DNA sequence of the previous stage is imparted to the host as water nanostructures incorporated into the cells at the time of cell division.

Stage 1, 2 and 3 are unnecessary when the  DNA sequences are already known and stored on the computer database and the signal derived from aqueous dilutions are simulated.

Note this invention is not limited to viral and cancer treatment other pathogens may be eliminated by these methods and wide ranging genetic alteration is possible.



Does this infringe existing patents?
No and the important parts of the device are not disclosed here.

Explain simply how this invention works?
DNA in resonance with the electromagnetic background emits electromagnetic waves which imprint a faint structure of the molecule onto water through quantum coherence effects.  DNA of a living cell can be influenced by an artificially created imprint. Research showing pathogens exploit this phenomena to infect cells has lead to the idea for this device. It is a logical conclusion of the research of Nobelist Luc Montagnier and others.

Is this a cure for HIV infection?
In theory it is possible to cure viral infections with this device and the proper application of these methods. Research is needed as possible side effects and complications are at this time unknown.

Is this a cure for cancer?
In theory it is possible to cure cancers with this device and the proper application of these methods. Research is needed as possible side effects and complications are at this time unknown.

I like this idea but I don’t even have a dollar to donate. How can I help?
Whether you donate or not, all campaigns on Indiegogo benefit from the power of word of mouth. We are no different. So please tell your friends, everybody you know and shout it from the rooftops! And don’t forget the Indiegogo share tools.



Gariaev, K.V. Grigor'ev, A.A. Vasil'ev, V.P. Poponin and V.A. Shcheglov. Investigation of the Fluctuation Dynamics of DNA Solutions by Laser Correlation Spectroscopy. Bulletin of the Lebedev Physics Institute, 1992

Del Giudice, E., G. Preparata and G. Vitiello. Water as a free electron laser. Phys. Rev. Lett., 1988

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