We have natural EMR-based communication systems in our brains, hearts, cell and
bodies. External natural and artificial EMR resonantly interacts with these communication
systems altering hormone balances and damaging organs and cells. The brain and the
heart are especially sensitive because they mediate and regulate primary biological
functions that are vital to life, thinking and heart beat, using EMR signals, the EEG and
ECG. When EMR interferes with the EEG this is communicated to the body by
neurotransmitters and neurohormones, including the serotonin/melatonin system. EMR
reduces melatonin. Melatonin is vital for the health of the Immune System, the Brain, The
Heart and every cell, because it is the most potent naturally produced antioxidant. It is a
potent free radical scavenger that plays a vital protective role to protect the DNA in every
cell. Reduced melatonin causes cancer, miscarriage, heart disease, neurological
diseases, viral and bacterial diseases, etc…
Both through reducing melatonin and through enhancing free radical activity EMR is
genotoxic, damaging the DNA and chromosomes, enhancing oncogene expression and
transforming cells to neoplastic cells and causing cancer in exposed populations.
Intense chromosome damage of fetuses in the uterus by microwaves, causes prompt
miscarriage. Less intense chromosome damage, largely but not totally repaired by the
body’s cell repair system, such as is caused by radio waves, causes fetal damage,
congenital malformation, still birth, cot death, etc..
Neurological effects, such as headache, sleep disturbance, concentration disturbance,
short-term memory loss, dizziness and nausea, are acute effects that can be experienced
over minutes, hours, days and months. However, cell damage in the brain causes
significantly accelerated cell death. Over years this means long-term memory loss, and
neurological diseases such as Epilepsy, Parkinson’s Disease, Multiple Sclerosis,
Alzheimer’s Disease, and sudden death from violent epileptic seizures.
The heart is similar with short-term problems with cardiac arrhythmia, missed heart beats,
etc, sudden death from Heart Attacks and chronic illness and death from heart disease,
especially arrhythmic diseases.
Cancer is a chronic disease problem from accumulated genetic cell damage. Latencies for
children and soft tissue cancers are as short as a few years, for most cancers they take 10
to 40 years to develop. Cancer rates rise rapidly with age over 65 years because of the
life-time of accumulated cell damage and the drastic reduction in melatonin that occurs
after puberty.
This shows how vulnerable very young children are because they have very low melatonin
levels and undeveloped immune systems. It also shows how reduced melatonin makes
older people more vulnerable and much more prone to disease and cancer….
Dr Cherry, Lincoln University: http://researcharchive.lincoln.ac.nz/handle/10182/3931