We have reported for many years that low voltage EM fields will cause cancer cells to self-destruct through apoptosis. There is now a clinical trial on brain cancer patients using continuously applied external electromagetic fields of low voltage and relatively low frequencies (150-200khz). Preliminary results are quite good.

NovoCure – Pivotal (Phase III) Clincal Trial

Cancer Cells

Cancer cells divide and multiply rapidly in the brain. These cancer cells carry special types of electrically charged elements that play a role during the cell division process. Other healthy cells in the brain multiply at a much slower rate, if at all, and thus rarely include the same electric properties as the dividing cancer cells.

Tumor Treating Fields (TTFields)

The NovoTTF-100A device used in this trial delivers very low intensity, alternating electric fields to the tumor site through the scalp. These fields are known as Tumor Treating Fields or TTFields. Due to the unique shape of cancer cells when they are multiplying, TTFields cause the building blocks of these cells to pile up in such a way that the cells physically break apart. In addition, cancer cells also contain miniature building blocks that move essential parts of the cells from place to place during division. TTFields cause these building blocks to fall apart since they have a special type of electric charge. As a result of these two effects, preliminary study data indicate that cancer tumor growth is slowed and may even reverse after continuous exposure to TTFields. Preliminary data also indicate that the TTFields affect the healthy brain cells much less than cancer cells since healthy brain cells multiply at a much slower rate, if at all.

PROCEEDINGS OF THE NEW YORK ACADEMY OF SCIENCES
Published online on June 5, 2007, 10.1073/pnas.0702916104

Medical Sciences
Alternating electric fields arrest cell proliferation in animal tumor models and human brain tumors
( cancer | glioblastoma | tumor treating fields )
Eilon D. Kirson et. al.

Communicated by Joseph Schlessinger, Yale University School of Medicine, New Haven, CT, April 5, 2007 (received for review January 15, 2007)

We have recently shown that low intensity, intermediate frequency, electric fields inhibit by an anti-microtubule mechanism of action, cancerous cell growth in vitro. Using implanted electrodes, these fields were also shown to inhibit the growth of dermal tumors in mice. The present study extends these findings to additional cell lines [human breast carcinoma; MDA-MB-231, and human non-small-cell lung carcinoma (H1299)] and to animal tumor models (intradermal B16F1 melanoma and intracranial F-98 glioma) using external insulated electrodes. These findings led to the initiation of a pilot clinical trial of the effects of TTFields in 10 patients with recurrent glioblastoma (GBM). Median time to disease progression in these patients was 26.1 weeks and median overall survival was 62.2 weeks. These time to disease progression and OS values are more than double the reported medians of historical control patients. No device-related serious adverse events were seen after >70 months of cumulative treatment in all of the patients. The only device-related side effect seen was a mild to moderate contact dermatitis beneath the field delivering electrodes. We conclude that TTFields are a safe and effective new treatment modality which effectively slows down tumor growth in vitro, in vivo and, as demonstrated here, in human cancer patients.

Sound, the Trigger for Life by John Stuart Reid

Viktor Schauberger, the brilliant Austrian scientist, working in the 1940’s and 50’s, may have been the first to study micro vortexes in water. Interestingly, micro vortexes carry the same basic structure as DNA! More recently, scientists in Hong Kong have demonstrated that micro vortexes can be created in the laboratory and are used to manipulate single DNA molecules. In other words, the bore of the micro vortex approaches that of the DNA double helix. It seems like divine irony that the very mechanism that may have created DNA is now being employed to manipulate it!

To summarise, we propose that the first strands of DNA were created in the micro vortex environments of primordial hydrothermal vents. Should micro vortexes be discovered within microscopic bubbles we have a model that begins to resemble living cells: a membrane (the surface of the bubble) with strands of DNA within.

If sound was indeed the trigger for life, it follows that sound alone should be able to heal life. The sound of ocean waves is certainly calming but the sounds imbedded within them may healing at a level we can currently only guess at.

Many chronic dieseases today are caused or aggravated by bioengineered mycoplasma that now infect most of the population. The recent Lyme flu has caused long term sinus and other problems in some of those afflicted. The root of this problem appears to be mycoplasma.

Don Scott’s work on investigating the origin of these mycoplasma is provided below. Those wanting more detailed analysis of the origins of Lyme disease should read Lab 257, a thoroughly researched analysis of decades of violation of EPA regulations and common sense at Plum Island. Click here for an excellent video of blood microscopy showing the Lyme mycoplasma. They are the small spherical white dots in the video that tend to attach to red blood cells and cause energy depletion. Dr. Shyh-Ching Lo mentioned by Don Scott below has a patent on Mycoplasma fermentans extracted from AIDs patients. These are seen in the photo above and in the video.

Most research on Lyme disease focuses on eliminating the Borrellia spirochetes with antibiotics as these are the most immediately disabling. However, the spirochetes can be removed in a few hours with frequencies. The more difficult organisms are the viruses, the fungi, and the mycoplasma. The mycoplasma are often infected with nanobacteria so eliminating them will cause a nanobacteria herxheimer reaction. Thus nanobacteria needs to be dealt with as well as the primary symptom of nanobacteria infection is the need for excessive amounts of sleep. This is commonly seen in those with chronic Lyme infections.

Recent research has focused on systematically disassembling micoplasma with frequencies that target various parts of the organism and disperse the DNA. There are quite a few mycoplasma strains in the Lyme complex and it is a nontrivial task to untangle them all. Subscribers will automatically receive these frequencies.

Mycoplasma the Linking Pathogen in Neurosystemic Diseases

by Donald W. Scott, MA, MSc
Pathogenic Mycoplasma
A Common Disease Agent Weaponized

Several strains of mycoplasma have been “engineered” to become more dangerous. They are now being blamed for AIDS, cancer, CFS, MS, CJD and other neurosystemic diseases.

There are 200 species of Mycoplasma. Most are innocuous and do no harm; only four or five are pathogenic. Mycoplasma fermentans (incognitus strain) probably comes from the nucleus of the Brucella bacterium. This disease agent is not a bacterium and not a virus; it is a mutated form of the Brucella bacterium, combined with a visna virus, from which the mycoplasma is extracted.

The pathogenic Mycoplasma used to be very innocuous, but biological warfare research conducted between 1942 and the present time has resulted in the creation of more deadly and infectious forms of Mycoplasma.

Researchers extracted this mycoplasma from the Brucella bacterium and actually reduced the disease to a crystalline form. They “weaponized” it and tested it on an unsuspecting public in North America.

Dr Maurice Hilleman, chief virologist for the pharmaceutical company Merck Sharp & Dohme, stated that this disease agent is now carried by everybody in North America and possibly most people throughout the world.

Despite reporting flaws, there has clearly been an increased incidence of all the neuro/systemic degenerative diseases since World War II and especially since the 1970s with the arrival of previously unheard-of diseases like chronic fatigue syndrome and AIDS.

According to DR Shyh-Ching Lo, senior researcher at The Armed Forces Institute of Pathology and one of America’s top mycoplasma researchers, this disease agent causes many illnesses including AIDS, cancer, chronic fatigue syndrome, Crohn’s colitis, Type I diabetes, multiple sclerosis, Parkinson’s disease, Wegener’s disease and collagen-vascular diseases such as rheumatoid arthritis and Alzheimer’s.

DR Charles Engel, who is with the US National Institutes of Health, Bethesda, Maryland, stated the following at an NIH meeting on February 7, 2000: “I am now of the view that the probable cause of chronic fatigue syndrome and fibromyalgia is the mycoplasma…”

I have all the official documents to prove that mycoplasma is the disease agent in chronic fatigue syndrome/fibromyalgia as well as in AIDS, multiple sclerosis and many other illnesses.

Of these, 80% are US or Canadian official government documents, and 20% are articles from peer-reviewed journals such as the Journal of the American Medical Association, New England Journal of Medicine and the Canadian Medical Association Journal. The journal articles and government documents complement each other.

See Dr. Mercola’s web site for the remainder of this article.

If you have a newborn, before you let anyone give your baby a Hepatitis B vaccine, read Dr. Mercola’s recommendationa.

Vaccine Companies Investigated for Manslaughter

A formal investigation has been launched by French authorities against two managers from drug companies GlaxoSmithKline and Sanofi Pasteur. A second investigation for manslaughter has also been opened against Sanofi Pasteur MSD.

The investigations are in response to allegations that the companies failed to fully disclose side effects from an anti-hepatitis B drug used between 1994 and 1998.

During this time, close to two-thirds of the French population, and almost all newborn babies, received a hepatitis B vaccine. The vaccination campaign was halted after concerns rose over the shot’s side effects.

Thirty plaintiffs, including the families of five people who died after the vaccination, have launched a civil action in the case against the drug companies.

A three-dimensional model of an HIV virus. Researchers are exploring the use of lasers and sound waves to attack viruses. Credit: 3DScience.com

New Way to Kill Viruses: Shake Them to Death
By Michael Schirber, Special to LiveScience
posted: 05 February 2008 09:27 am ET

Scientists may one day be able to destroy viruses in the same way that opera singers presumably shatter wine glasses. New research mathematically determined the frequencies at which simple viruses could be shaken to death.

“The capsid of a virus is something like the shell of a turtle,” said physicist Otto Sankey of Arizona State University. “If the shell can be compromised [by mechanical vibrations], the virus can be inactivated.”

Recent experimental evidence has shown that laser pulses tuned to the right frequency can kill certain viruses. However, locating these so-called resonant frequencies is a bit of trial and error.

“Experiments must just try a wide variety of conditions and hope that conditions are found that can lead to success,” Sankey told LiveScience.

To expedite this search, Sankey and his student Eric Dykeman have developed a way to calculate the vibrational motion of every atom in a virus shell. From this, they can determine the lowest resonant frequencies.

As an example of their technique, the team modeled the satellite tobacco necrosis virus and found this small virus resonates strongly around 60 Gigahertz (where one Gigahertz is a billion cycles per second), as reported in the Jan. 14 issue of Physical Review Letters.

… Killing melanoma cells with frequencies

Here is a mainstream paper showing why low intensity electromagnetic fields destroy cance cells during mitosis. There is a strong inhibitory effect even with frequencies in the 100-300khz range. Targeting exact frequencies in the MHZ range would produce even more dramatic results.

CANCER RESEARCH 64, 3288–3295, May 1, 2004
Disruption of Cancer Cell Replication by Alternating Electric Fields
Eilon D. Kirson, Zoya Gurvich, Rosa Schneiderman, Erez Dekel, Aviran Itzhaki, Yoram Wasserman, Rachel Schatzberger, and Yoram Palti

ABSTRACT
Low-intensity, intermediate-frequency (100–300 kHz), alternating electric fields, delivered by means of insulated electrodes, were found to have a profound inhibitory effect on the growth rate of a variety of human and rodent tumor cell lines (Patricia C, U-118, U-87, H-1299, MDA231, PC3, B16F1, F-98, C-6, RG2, and CT-26) and malignant tumors in animals.

This effect, shown to be nonthermal, selectively affects dividing cells while quiescent cells are left intact. These fields act in two modes: arrest of cell
proliferation and destruction of cells while undergoing division. Both effects are demonstrated when such fields are applied for 24 h to cells undergoing mitosis that is oriented roughly along the field direction. The first mode of action is manifested by interference with the proper formation of the mitotic spindle, whereas the second results in rapid disintegration of the dividing cells. Both effects, which are frequency dependent, are consistent with the computed directional forces exerted by these specific fields on charges and dipoles within the dividing cells. In vivo treatment of tumors in C57BL/6 and BALB/c mice (B16F1 and CT-26 syngeneic tumor models, respectively), resulted in significant slowing of tumor growth and extensive destruction of tumor cells within 3–6 days. These findings demonstrate the potential applicability of the described electric fields as a novel therapeutic modality for malignant tumors.

Off Season Training with Jeff Sutherland and Dale Fawcett
8-9 January, Big Island, Hawaii
Contact [email protected] or 360 598-6585

Since so many of you have asked either Jeff or Dale about future Frequency Foundation Workshops this may assist us in getting one going for you perhaps 7 or 8 months down the road! That’s when Jeff’s schedule is opened. We had Vegas workshop scheduled for the 1st week of Dec. about 6 months ago but Jeff’s very popular Scrum workshops overflowed their banks and took that spot before we announced it.

A few of you have told us you may be in the Hawaiian Islands in January and since Jeff will as well there may be a possibility for some of you to have a cozy smaller workshop for one possibly two ½ day morning sessions this January on the Kona side of the Big Island. For those of you not in the area we do apologize for the short notice and your generous feedback as to what you’d like to see down the road would be very welcome. Let us know if you’re interested in Jeff doing a few Private sessions too.

We would be on the Big Island and meetings could be very informal working (how about outside!) on Jeff’s cutting edge Lab setup with Q & A. with possibly a surprise guest scientist with amazing new technology to enable Jeff’s Lab to reach further heights of effectiveness. You just don’t know what other guest doctors could drop in. This workshop may be one of our nicest ever and 80* maybe you’ll wish to join us this January.

So if you’re in Hawaii either living or warming up from a cold winter this January on the 8th and 9th drop us an e-mail or call soon for more details. If nothing else you may help us plan a future workshop in Vegas.

As we’ve said this will be very informal and your input will assist us in determining the content. At this time we have had requests to focus on running Jeff’s optimized Lab with his new Lyme (and other frequency sets). What else would you enjoying learning? Contact Dale Fawcett with your comments at [email protected] or call 360 598-6585.

Check out the possible locations;
www.hiltonwaikoloavillage.com/index_flash.asp more likely here.
www.outriggerkeauhoubeachhotel.com may do ½ day here.

You may choose whatever hotel/condo you wish since it’s off-season and too short notice for us to block rooms.