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Dr Caldicott MD On Mutagenesis Teratogenesis, Entropy; Dangers Of Cumulative Dose Man Made Ionizing Radiation, Heavy Metal Poison Exposure Of Babies, Fetus, Infants, Children, Teens, Leads Human Extinction Via Gene (DNA) Damage, Accelerating Mass Die Offs From Disease, Cancers, LLRC

THE TWO WAYS IONIZING RADIATION FROM MAN MADE HEAVY METAL POISON RADIOACTIVE HEAVY METAL POISONS ALSO DAMAGES DNA


What are the two ways that man made or 'natural' radioactive elements damage DNA? The 1 minute video explains very simply how it happens, first directly, and then indirectly. 

ANY EXPOSURE TO MAN MADE IONIZING RADIATION CAN LEAD TO GENE DAMAGE WHICH THEN INITIATES BIG C


“Any exposure to radiation may cause cell damage that could lead to cancer, according to a June 2005 report from the National Research Council. …”
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1310955/

WHAT IS MUTAGENISIS?


Wikipedia; "Mutagenesis ( /mjuːtəˈɛnɪsɪs/) is a process by which the genetic information of an organism is changed, resulting in a mutation. It may occur spontaneously in nature, or as a result of exposure to mutagens (such as manmade synthetic radioactive contaminants; strontium, plutonium, uranium, thorium, Xenon, Krypton, Iodine, and approximately 900 hundred more like these.) 

Children's Cancer Rate Is Increasing Every Year; WHY?; via A Green Road

Mutagenesis can lead to cancer and various inheritable diseases, but it is also the driving force of evolution (over millions of years, with only small amounts of natural background radiation). Mutagenesis as a science was developed based on work done by Hermann Muller, Charlotte Auerbach and J. M. Robson in the first half of the 20th century.[1] 

(Man made radiation coming from artificial heavy metal radioactive poison elements, isotopes and actinides are exponentially increasing the speed and negative consequences of mutagenesis)

THE VICTIMS OF NEUTRON AND GAMMA RADIATION EXPOSURE SUFFERED FROM CHROMOSOMES THAT HAD SHATTERED LIKE BROKEN GLASS, AND THEY COULD NOT BE IDENTIFIED

WARNING: GRAPHIC CONTENT, ADULTS ONLY

Tokai-Mura: The Forgotten Criticality

"A Slow Death - 83 Days of Radiation Sickness" by NHK-TV "Tokaimura Criticality Accident" Crew (2008), published by Vertical.

At 2:30 in, the effects of radiation on DNA/chromosomes are described, as tearing apart the DNA in a process much like throwing a rock through a window, resulting in shattered glass. 


The two radiation victims received 10 and 17 Sieverts, and both of these are fatal doses of radiation. Radiation does not kill quickly, but it does kill slowly and gradually, from the inside out. There is no known way to reverse the damage, and the fatal results of poisonous neutron and gamma radiation are guaranteed, with much suffering and pain all the way to the end. 


NUCLEAR POWER IS A REALLY, REALLY DUMB WAY TO BOIL POWER AND CREATE STEAM, WHEN THE SUN CAN DO IT FOR FREE, AND WITH NO RISK OF HEAVY METAL POISONS BEING EMITTED INTO THE AIR, GROUND, WATER, MILK, ETC



THE END OF NUCLEAR POWER - A Dumb Way to Boil Water


Press TV commentary on implications of the Japanese nuclear accident - immediate, short-term, long-term and very-long- term by Kevin Sanders, War&Peace Foundation

DNA IS HARMED BY EVEN LOW DOSES OF RADIATION, SUCH AS FROM XRAYS


DNA may be modified, either naturally or artificially, by a number of physical, chemical and biological agents, resulting in mutations. In 1927, Hermann Muller first demonstrated mutation with observable changes in the chromosomes can be caused by irradiating fruit flies with X-ray,[2] and lent support to the idea of mutation as the cause of cancer.[3] His contemporary Lewis Stadler also showed the mutational effect of X-ray on barley in 1928,[4] and ultraviolet(UV) radiation on maize in 1936.[5] In 1940s, Charlotte Auerbach and J. M. Robson, found that mustard gas can also cause mutations in fruit flies.[6]

While changes to the chromosome caused by X-ray and mustard gas were readily observable to the early researchers, other changes to the DNA induced by other mutagens were not so easily observable, and the mechanism may be complex and takes longer to unravel. For example, soot was suggested to be a cause of cancer as early as 1775,[7] and coal tar was demonstrated to cause cancer in 1915.[8] The chemicals involved in both were later shown to be polycyclic aromatic hydrocarbons (PAH).[9]

DNA may sustain more than 50,000 damages per cell per day,[13] and some estimates put the number of oxidative adducts per cell generated through reactive oxidative species at 150,000.[14] If left uncorrected, these adducts can give rise to mutation. In nature, the mutations that arise may be beneficial or deleterious - it is the driving force of evolution, an organism may acquire new traits through genetic mutation, but mutation may also result in impaired function of the genes, and in severe cases, causing the death of the organism.

In the laboratory, however, mutagenesis is a useful technique for generating mutations that allows the functions of genes and gene products to be examined in detail, producing proteins with improved characteristics or novel function, as well as mutant strains with useful properties. Initially the ability of radiation and chemical mutagens to cause mutation was exploited to generate random mutations, later techniques were developed to introduce specific mutations. (The danger of this theory however is allowing uncontrolled mutagenesis out in the world due to higher radiation levels, resulting in cascading negative chromosome changes that get worse and worse with each succeeding generation, which eventually will result in the extinction of all human life on the planet.)

HOW DNA IS BROKEN


Mutagenesis may occur endogenously, for example through spontaneous hydrolysis, or through normal cellular processes that can generate reactive oxygen species and DNA adducts, or through error in replication and repair.[15] Mutagenesis may also arise as a result of the presence of environmental mutagens that induces changes to the DNA. The mechanism by which mutation arises varies according to the causative agent, the mutagen, involved. Most mutagens act either directly, or indirectly via mutagenic metabolites, on the DNA producing lesions. Some however may affect the replication or chromosomal partition mechanism, and other cellular processes.

Cancer - The Forbidden Cures; via A Green Road

Many chemical mutagens require biological activation to become mutagenic. An important group of enzymes involved in the generation of mutagenic metabolites is cytochrome P450.[16] Other enzymes that may also produce mutagenic metabolites include glutathione S-transferase and microsomal epoxide hydrolase. Mutagens that are not mutagenic by themselves but require biological activation are called promutagens.

MUTATIONS ARISE CAUSED BY DNA LESIONS DURING REPLICATION


Many mutations arise as a result of problems caused by the DNA lesions during replication, resulting in errors in replication. In bacteria, extensive damage to the DNA due to mutagens results in single-stranded DNA gaps during replication. This induces the SOS response, an emergency repair process that is also error-prone, thereby generating mutations. In mammalian cells, stalling of replication at a damaged sites induces a number of rescue mechanisms that help bypass DNA lesions, but which also may result in errors.

Spontaneous hydrolysis


DNA is not entirely stable in aqueous solution. Under physiological conditions the glycosidic bond may be hydrolyzed spontaneously and 10,000 purine sites in DNA are estimated to be depurinated each day in a cell.[15] Numerous DNA repair pathway exist for the DNA, however, if the apurinic site failed to be repaired, misincorporation of nucleotide may occur during replication. Adenine is preferentially incorporated by DNA polymerases in an apurinic site.

Cytidine may also become deaminated to uridine at one five-hundredth of the rate of depurination and can result in G to A transition. Eukaryotic cells also contains 5-methylcytosine, thought to be involved in the control of gene transcription, which can become deaminated into thymine.

Modification of bases


Bases may be modified endogenously by normal cellular molecules. For example DNA may be methylated by S-adenosylmethionine, and glycosylated by reducing sugars

Many compounds, such as PAHs, aromatic amines, aflatoxin and pyrrolizidine alkaloids, may form reactive oxygen species catalyzed by cytochrome P450. These metabolites form adducts with the DNA, which can cause errors in replication, and the bulky aromatic adducts may form stable intercalation between bases and block replication. The adducts may also induce conformational changes in the DNA. Some adducts may also result in the depurination of the DNA,[17] it is however uncertain how significant such depurination as caused by the adducts is in generating mutation.[18]

Ionizing radiations and reactive oxygen species often oxidize guanine to produce 8-oxoguanine.

Crosslinking 


Some alkylating agents may produce crosslinking of DNA. Some natural occurring chemicals may also promotes crosslinking, such as psoralens after activation by UV radiation, and nitrous acid. Interstrand cross-linking is more damaging as it blocks replication and transcription and can cause chromosomal breakages and rearrangements. Some crosslinkers such as cyclophosphamide, mitomycin C and cisplatin are used as anticancer chemotherapeutic because their high degree of toxicity to proliferating cells.

Dimerization


UV radiation promotes the formation of a cyclobutyl ring between adjacent thymines, resulting in the formation of pyrimidine dimers.[21] . DNA polymerase η may help bypass these lesions in an error-free manner;[22] however, individuals with defective DNA repair function, such as sufferers of Xeroderma pigmentosum, are sensitive to sunlight.




Ethidium intercalated between two adenine-thymine base pairs.

Intercalation between bases


The planar structure of chemicals such as ethidium bromide and proflavine allows them to insert between bases in DNA. This insert causes the DNA's backbone to stretch and makes slippage in DNA during replication more likely to occur since the bonding between the strands is made less stable by the stretching. Forward slippage will result in deletion mutation, while reverse slippage will result in an insertion mutation. Also, the intercalation into DNA of anthracyclines such as daunorubicin and doxorubicin interferes with the functioning of the enzyme topoisomerase II, by tightening the DNA's strands by the stretching, making replication as well as causing mitotic homologous recombination.


Small blue arrows in picture above indicates chromosomal breakages due to DNA damage (this is what radiation does to genes, whether that radiation comes from X rays, cancer radiation or nuclear power plant radiation via low dose exposure of ingested Tritium, cesium, iodine, or one of the other 1,200 toxic radioactive substances coming out of a leaking, melted down, melted through reactor or a nuclear bomb explosion.)

DNA DAMAGE IS CAUSED BY MAN MADE RADIOACTIVE ELEMENTS


Ionizing radiations may produce highly reactive free radicals that can break the bonds in the DNA. Double-stranded breakages are especially damaging and hard to repair, producing translocation and deletion of part of a chromosomes.

(Once the chromosomes are broken, they replicate this way, FOREVER, into infinite future generations. This means that any radiation causing damage to ANY generation is then passed on to infinite future generations. This is the danger with nuclear radiation and power plant emissions happening worldwide, day after day.. the genetic damage keeps accumulating as more radiation damage accumulates due to more and more radiation exposure. This genetic damage via dominant or recessive genes is then passed on in a negative downward life extinguishing spiral, forever.)

Alkylating agents like mustard gas may also cause breakages in the DNA backbone. Oxidative stress may also generate highly reactive oxygen species that can damage the DNA. Incorrect repair of other damages induced by the highly reactive species can also lead to mutations." https://en.wikipedia.org/wiki/Mutagenesis

All man made radioactive elements cause free radicals to form inside the body, and create highly reactive oxygen species. Chemical agents that cause cancer and breakages in genes include the various chemotherapy agents that are used in medical settings.

GENERATION AFTER GENERATION, THE DAMAGE TO DNA GETS WORSE AND WORSE, AND IT IS PERMANENT


Low-Level Radiation 
The Effects on Human and Non-Human Life
Dr. Alice Stewart, Great Britain. Medical doctor, Professor for Social Medicine, expert on low-level radiation, Alternative Nobel Prize
And I must come back to the second stream of thought that if it's germ cell-damage, it's going to skip a generation before you see anything, and it's not only going to skip one generation, it's going to skip one, two and three generations, because it's got to meet up with a pair before it shows that the damage has been done. So, the time scale of the thing you're looking for is astronomically large imposing all sorts of difficulty for the investigator.

And what will be the effect of the germ cell-damage? And this I want you to bear in mind: If there's any proof that a cancer is there, there's going to be an implication, a certain implication, a certainty, that there will be a genetic damage that may not express itself for several generations, but when it does it will lead to the deterioration of the unique human development, namely the brain. You're going to feed into the genetic pool of human genes damage which will deteriorate the one thing for which we are famous, namely that we have the capacity to think for ourselves.

Many nuclear apologists and other supposed experts still believe and announce to anyone that will listen to them, that genetic damage and chromosome changes somehow are not carried forward into future generations. They further claim that low dose radiation cannot cause harm, and that only high exposure to intense radiation that will kill someone in minutes or hours is harmful. Every other kind of radiation, according to them, is beneficial, and can be compared to eating bananas or flying in an airplane. 

The genetic effects on humans of low dose radiation has been studied for three generations around Chernobyl, since many hundreds of thousands of people are still living in low dose radiation contaminated areas around Chernobyl and these people were never evacuated.. Studies performed on populations living in Kyshtym and Semiplatinsk in the old USSR have confirmed genetic studies in other areas. See links below. As more nuclear accidents happen, these same study results show harm and negative genetic effects, over and over again. 

These studies, like others, show that the first generation has damage done to sperm, and eggs or the developing fetus. This genetic damage then gets passed on to the next generation either in the form of birth defects, one of 2,500 genetic diseases, or genetic damage that is carried on into future generations, with no end to it. In other words, unless you are a geneticist and you study this specifically by examining the genetic structure inside that person with a special high power microscope, you would not be aware of the damage. This is probably why most of the nuclear industry seems immune to this basic genetic knowledge.

DAMAGE DONE TO THE FIRST GENERATION IS MADE WORSE BY RADIATION EXPOSURE ENDURED BY THE SECOND GENERATION, AND SO ON UNTIL EVERYONE IS EITHER STERILE, COMPLETELY DEFORMED AND DISEASED OR DEAD


The second generation is also damaged, just like the first generation, from the same radiation. However, things get worse for the second generation because the damage is compounded by the damage passed through from the FIRST generation with the added damage done to the genes in the second generation, because they are still living in the same radiation contaminated area, so the two types of damage are added together and multiply. The second generation has worse health outcomes and more diseases, worse death rates and more infertility than the first generation in EVERY study done on this subject. 

The third generation has to add the genetic/chromosome damage from the first two generations and then endure or suffer from the damages caused directly from the radiation exposure suffered by the third generation. The accumulated damage adds up to a heavy burden on health in all ways; physical, mental, emotional and spiritual.

PEOPLE LIVING IN RADIATION CONTAMINATED AREAS SUCH AS BELARUS EXPERIENCE ENTROPY, AS EACH GENERATION GETS SICKER AND SICKER, FEWER CHILDREN ARE BORN EACH GENERATION, THIS WILL BE TRUE FOR PEOPLE IN JAPAN AS WELL


In areas around the radiation contaminated Belarus, the percentage of infants born healthy has been steadily going DOWN, and is now in the single digits. However, medical doctors and the nuclear industry 'experts' more often than not blame the mothers for 'infections' and lack of humor, or 'mental stress' for those problems. The 90% plus negatively affected infants at birth in Belarus is almost never found to be the fault of radiation. 

Somehow, the 'mothers' of these 90% sick or deformed children are at fault for not smiling enough, despite being exposed to human created artificial low dose radiation contamination 24 hours a day, 365 days a year. Bottom line, the body does not have a defense against this man created assault on the genetic blueprint. 

GENOMIC INSTABILITY IS INCREASING GENERATION AFTER GENERATION, DUE TO IMPACT OF LOW LEVEL RADIATION, CHEMICALS AND OTHER TOXINS



ChasAhaOctober 9, 2015 July 20, 1999 By Dick Ahlstrom, Science Editor
"The children of a person who is exposed to radiation could be susceptible to cancer as a result, according to research carried out in Britain. Even low levels of radiation could cause mutations that cross the generational divide and could be detected in offspring."

"We did not expect these results," said Dr Yuri Dubrova"

"The radiation causes a phenomenon known as "genomic instability"…"

obewanspeaksOctober 9, 2015Oh My! What have we let these evil doers do to our only world? 

Epigenetics and Inheritance
http://learn.genetics.utah.edu/content/epigenetics/inheritance/

NEGATIVE GENETIC EFFECTS TO EACH GENERATIONS OFFSPRINGS ACCUMULATES



GENETIC EFFECTS OF IONIZING RADIATION
http://www.atomicvetkin.com/genetics.html

Each exposed to radiation generation offspring will be weaker.. "

Transgenerational accumulation of radiation damage in small mammals chronically exposed to Chernobyl fallout
http://www.springerlink.com/content/d332767242p82201/

GENOMIC INSTABILITY INCREASES WITH EACH GENERATION AS DNA DAMAGE INCREASES AND THERE IS NO WAY TO REPAIR DAMAGE DONE


Genomic instability and radiation

The body tries and fails to repair all of the DNA damage caused by internally absorbed radiation from multiple man made radiation sources in food, water, and air. The sources are contaminated by 1,200 poisons which are impossible to prevent coming into the body and affecting the genes in a number of different ways. This basic and very simple to understand mechanism is WHY the children around us are getting sicker at younger ages and why more and more of them are born unhealthy at birth. This negative process is not the mother's fault any more than the moon can be blamed for the sun shining. The true blame can be laid directly at the feet of the nuclear industry. 

So where are all of these studies proving that low dose radiation causes genetic damage? Here are just a few....

SCIENTIFIC AND MEDICAL STUDIES ON RADIATION AND GENETIC DAMAGE


THE EFFECT OF RADIATION ON SMALL COMPETING POPULATIONS OF DROSOPHZLA MELANOGASTER I. THE ACCUMULATION OF GENETIC DAMAGE; K. F. DYER
Medical Research Council, Radiobiological Research Unit, Harwell, Didcot, Berks, England; Received March 25, 1968

"The genetic effects of ionizing radiations have now been studied extensively in a wide variety of systems. The study of their cumulative effects in populations has also been given increasing attention in recent years although, because of experimental difficulties, on a more restricted number of organisms. The effect of radiation on a population will be to alter its genetic constitution and, therefore, presumably, to affect the biological fitness. …”

Genetic Effects of Radiation on Mammalian Populations

"The greatest threat of radioactivity to life as we know it is damage to the gene pool, the genetic make-up of all living species. Genetic damage from radiation exposure is cumulative over lifetimes and generations. Even low-dose exposures are carcinogenic after extended exposure. The current generation, the one in utero, and all that follow may suffer cancers, immune system damage, leukemias, miscarriages, stillbirths, deformities, and fertility problems. While many of these health problems are on the rise, individuals cannot prove either increase in "background" radiation or specific exposure as the cause. Only epidemiological evidence is scientifically acceptable to impute cause. Perhaps the most extreme outcome over time would be simply the wholesale cessation of the ability to reproduce. Radiation is a known cause of sterility…."

Chernobyl Publications, Department of Biological Sciences, Texas Tech University

Over the course of human history, mutation has happened, slowly and over a period of many millions of years of evolution. The natural selection process made sure that the mutations that survived adapted all life to living better on the Earth with all of it's changes, from Ice Ages to the opposite. All life is genetically programmed for this slow cycling back and forth from Ice Ages, to the warm cycles where some of this ice melts. Humans are also genetically adapted to resist the damage caused by the 'natural' radiation present on Earth, whether that is from bananas or soil. 

Thus the human genome is fairly stable over the tens of thousands of years to the millions of years that we have been around in one way or another. Most mutations in this historical context did so little damage that it has no detectable effect in the archeology of human genetic history. 

TERATOGENESIS IS ALSO COMMON WITH HEAVY METAL RADIOACTIVE POISONS


"Dr Wertelecki’s team focused on teratogenesis – changes caused by environmental interference to a developing foetus, a foetus with with normal genes. This must be distinguished from gene mutations, inherited from parents and the two processes have different effects. The genetic, inherited defects are most likely to cause mental disability. But with the teratogenic abnormalities, the baby, if it survives, most often is of normal intelligence.

This process can begin very early, before the ovum has been implanted in the wall of the womb – before the woman knows that she is pregnant. That very early “line” of the embryo can split. In this case – the result is – twins. This split can be incomplete – resulting in conjoined twins, (“Siamese twins”). A fetiform teratoma is a sort of failed Siamese twin, a monster like mass, containing a mixture of tissues."

GENETIC ENTROPY


Now that humans have spread 1,200 different human created radioactive poisons all over the globe and exposed everyone and all life forms to these radioactive poisons, the genetic damage is greatly accelerating, especially intensely in those areas which we will call highly contaminated zones that make up about 15,000 to 150,000 square km around each major nuclear accident. Other accelerated 'death zones' are located around each nuclear research, depleted uranium, power generation or recycling facility. Researchers have found that the death and genetic damage rate grows the close one lives to these facilities. But the negative effect on genes of man made artificial radiation is not just local, it is GLOBAL. 

By current estimates from geneticists, there are globally about 300 more negative mutations happening now in each generation, compared to the last. These negative mutations bring all humanity closer and closer to extinction in a wide variety of ways. 

The radioactive emissions that come from normally operating nuclear plants, such as radioactive hydrogen (plus many others allowed legally by law), all cause genetic damage. These negative and entropic changes accumulate over time, and do not 'go away'. 

Bottom line, the human genome is decaying, just like a plant withering. What is 30 years of creating hot water worth, when it is balanced against this negative genetic 'side effect', which will affect infinite future generations, and accumulate in a negative way over time? What price tag can we place on hot water and electricity that causes extinction in the long term, literally, even without any nuclear accidents happening?



WHY RADIATION DAMAGE TO MITOCHONDRIAL DNA IS PERMANENT


via Socrates January 24, 2014 - "Mitochondrial DNA is inherited much more directly than "normal" or nuclear DNA – and damage is more likely to be permanent. Unlike nuclear DNA, Mitochondrial DNA is NOT recreated every generation from DNA strands of two different people, with the opportunity that gives for repair. Mitochondrial dial DNA is inherited directly from the mother, and then replicated trillions of times, and then one cell's mitochondrial DNA is passed on to the next generation… Mitochondrial DNA is not as protected within the individual cell as is nuclear DNA…. Mitochondrial DNA is the 'workhorse DNA of the cell, while nuclear DNA is mainly for reproduction. Mitochondrial DNA is responsible for much of the activities of the cell…."

Reactive oxygen species are "super" free-radicals caused by low levels of ionizing radiation, especially if given continuously or in "priming doses." These effects and others are published in the National Cancer Database. Fukushima is a prime example of a (gene) Code Killer. The administration of time – release of ionizing radiation is called a "dirty bomb." This is what we were told the "terrorists" would use against us. Well, they did. An expose' of the nuclear industry unfolds right across the Pacific."

DR. CALDICOTT MD ON GENETIC ENTROPY

The medical implications of Fukushima
VIDEO: http://youtu.be/8hTuqy6RpFQ 58 min.

JAPAN'S LOW DOSE RADIATION DISASTER

Japan has officially decided that massive doses of radiation are good for health and kids are not excluded from this. Now they are embarking on a huge experiment that involves the DNA being broken multiple times, with no end in sight, over many generations. As the DNA gets more and more corrupted, so does health. Mutations and 5,000 genetic diseases will increase over the coming future generations, as there is no way to repair all of that massive damage caused to millions of people who are constantly exposed to radiation both internally and externally.

PTJuly 29, 2015Radiation: Any Dose Is Too High
Sarah Todd Davidson
“Any exposure to radiation may cause cell damage that could lead to cancer, according to a June 2005 report from the National Research Council. …”
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1310955/

No Safe Dose – Japan's Low-Dose Radiation Disaster
By Richard Wilcox
http://rense.com/general95/no-safe-dose.htm

Japan, the US and any other country using radiation as a 'therapy' or as a hormesis health increasing modality will suffer increasing entropy on a genetic level.

DR. SANFORD ON GENETIC ENTROPY

A few genetic experts have written about this genetic 'decay' in much more specific and scientific terms, for those who want to dive into this subject much more deeply. One link is provided below...and a short summary of Dr. John Sanford's book and his debate with a nuclear apologist is provided at this link http://creation.com/genetic-entropy

Dr. John C Sanford's book is available on Amazon.

'Genetic Entropy'

Who is this guy? "Dr John Sanford, A Cornell University Professor for more than 25 years, John has been semi-retired since 1998. His Ph.D. was in plant breeding and plant genetics. While a professor at Cornell, John has trained graduate students and conducted genetic research at the New York State Agricultural Experiment Station in Geneva, NY. During this time, John bred new crop varieties using conventional breeding and then became heavily involved in the newly-emerging field of plant genetic engineering. John has published over 80 scientific publications and has been granted over 30 patents. His most significant scientific contributions involve three inventions, the biolistic (“gene gun”) process, pathogen-derived resistance, and genetic immunization."

Another entropy researcher tried to warn the world back in 1955, but he was sidelined and shut up by the AEC, forerunner to the NRC of today.

HERMAN MUELLER ON GENETIC ENTROPY


via Time Is Short April 4, 2014 "Herman J Mueller discovered in 1927 the following: ARTIFICIAL TRANSMUTATION OF THE GENE by radiation (Nobel Prize in Physiology or Medicine in 1946) There was the Geneva Summit 1955, about the "peaceful" use of nuclear energy. Mueller wanted to present his report in which he had calculated that people in 200 to 300 years – by the current radiation – will have genetic damage as the most affected survivors of Hiroshima. These people, in 10 generations, would have to work only for one thing: To obtain the means to take care of their suffering. This is what Mueller wanted to tell, BUT the AEC (Predecessor of the NRC) gave him no permission to speak."
http://www.sunypress.edu/p-513-mans-future-birthright.aspx

GOFMAN AND ZIMMERMAN - MAN MADE RADIATION CAUSES DNA BREAKS, WHICH ARE NOT REPAIRED


PTJuly 29, 2015 This quote is from Zimmerman's book.
"…Evidence exists that the immune system makes mistakes when repairing DNA lesions.

In chapter 18 of his book “Radiation-Induced Cancer from Low-Dose Exposure”, Gofman presents a powerful argument for why irreversible genetic damage, and thus cancer induction, can occur at even the lowest levels of exposure. His argument is based on the fact that the cellular mechanisms for repairing carcinogenic injuries do not operate flawlessly. Thus,‘repair’ is at the heart of the threshold issue:

“’The radiation-induced cancers arising from the unrepaired lesions at low doses do not wear a little flag identifying them as any different from cancers induced by higher doses of radiation, or induced by causes entirely unrelated to radiation. Therefore, threshold proponents cannot argue that the cancers arising from the lowest conceivable doses of radiation will somehow be eliminated by the immune system or any other bodily defenses against cancer. Such an argument would require the elimination of cancer in general by such defenses. Instead, we observe that cancer is a major killer (roughly 15-20% of many populations). So the proposition would lead to a non-credible consequence, and must be rejected. This means that repair is the key.’

“Gofman’s analysis proceeds by first reviewing nine reputable low-dose studies: the Nova Scotia Fluoroscopy Study, the Israeli Scalp-Irradiation Study, the Massachusetts Fluoroscopy study, the Canadian Fluoroscopy Study, the Stewart In-Utero Series, the MacMahon In-Utero Series, the British Luminizer Study, the Harvey Twins In-Utero Series, and the Israeli Breast-Cancer in Scalp-Irradiation Study. These studies involved a range of exposures from 9.0 rads down to 0.1 rad which Gofman translates into 12 tracks per nucleus per exposure down to 0.29 tracks per nucleus. His argument is that if flawless repair exists at some threshold dose, every carcinogenic lesion will be successfully undone below that dose and no excess cancers will be induced. However, in every study an excess of cancers was in evidence. Gofman summarizes the conclusion of this line of reasoning
as follows:

“4. Human epidemiological evidence shows that the repair system for
radiation-induced carcinogenic lesions has a failure rate even under
minimal strain.

“5. Observation and logic show that the post-repair defense systems
(for instance, the immune system) cannot possibly be perfect with
respect to providing a safe dose or dose-rate of ionizing radiation.

It follows that there is no safe dose or dose-rate of ionizing radiation,with respect to induction of human cancer. The risk is related to dose, right down to zero dose…” (p. 238-240)

This pdf contains the whole chapter of Zimmerman's book that shows how the nuclear industry lies and manipulates data to keep secret from the public the dangers of low dose radiation.

It is a very long chapter, but well worth reading. I read it from his book which is easier than trying to read it on a computer.

SOME SCIENTISTS AND PRO NUCLEAR APOLOGISTS CLAIM THAT MAN MADE HEAVY METAL POISONS THAT ARE ALSO RADIOACTIVE ARE GOOD FOR HEALTH 


Dr. Alex Rosen: "Claims by scientists affiliated with the nuclear industry that no health effects are to be expected are unscientific and immoral."
http://www.ippnw.de/commonFiles/pdfs/Atomenergie/Effects_Fukushima_rosen.pdf


WHAT HAPPENS TO GENES OF ALL LIVING THINGS AS THE NUMBER OF NUCLEAR ACCIDENTS INCREASES DUE TO INCREASING NUMBERS OF NUCLEAR REACTORS?

There have been over 70 nuclear plant melt downs so far. Add in DU weapons dust, 2,400 open air nuclear bombs, medical radiation, and all of that heavy metal poison and gene damaging ionizing radiation has a negative impact long term, on the gene pool of all living things. 

LARGE STUDY SHOWS THAT EVEN SMALL DOSES OF RADIATION INCREASE RISK OF LEUKEMIA IN RADIATION WORKERS


PTJuly 29, 2015 Researchers pin down risks of low-dose radiation
Large study of nuclear workers shows that even tiny doses slightly boost risk of leukaemia.
08 July 2015
“…it scuppers the popular idea that there might be a threshold dose below which radiation is harmless — and provides scientists with some hard numbers to quantify the risks of everyday exposures….

The data also challenge an ICRP assumption that accumulated low-dose exposure gives a lower risk of leukaemia than does a single exposure to the same total dose (based on the idea that the body has time to recover if the assault comes in tiny, spread-out doses)….”
http://www.nature.com/news/researchers-pin-down-risks-of-low-dose-radiation-1.17876

DNA IS NEGATIVELY AFFECTED BY MANY TYPES OF LOW DOSE RADIATION; ALL OF THEM INTERACT AND HAVE A SYNERGISTIC ENTROPY EFFECT



It is not just low dose heavy metal radioactive poisons that affect DNA in a negative manner, it is also things like cell phone radiation

DNA-Destroying Chip Being Embedded Into Mobile Phones
http://www.redicecreations.com/article.php?id=19687

What happens when hundreds to thousands of different heavy metal radioactive poisons coming out of nuclear reactors interact their frequencies and electromagnetic radiation with cellphones, WIFI, radio waves, microwaves, and chemicals? What happens at the atomic and molecular level when all of these poisons and radiations intersect? 

Combine together the effects of neutron, gamma, beta, alpha radiations, together with heavy metal poisons, chemicals and other forms of radiation and one gets a toxic stew of poisons. There is no set radiation risk analysis that can be done, due to the synergy of all of these factors. All of these tens of thousands if not hundreds of thousands of poisons must be lumped in together, because they are all present in the environment that all life lives in.

SUMMARY


We better pay attention to researchers and scientists are telling us that humanity is traveling down the road to extinction even if no nuclear war happens, and even if no further nuclear accidents happen. By not paying attention and going ahead with nuclear power and nuclear weapons, no matter what, we risk going extinct. Is this the legacy we want to leave seven future generations?

PTJuly 30, 2015 "…the Cult of Nuclearists has hatched a brilliant new public relations strategy within the last decade to convince the world that exposure to low levels of radiation is without risk. The public needs to be versed in this latest tactic so as to spot representatives of the Cult of Nuclearists and understand the reason for the current push not only to refute all evidence of detrimental low-level effects but to completely dismantle a century of study in radiotoxicology and radiation protection. What follows is a summary of the various arguments that are appearing with increasing frequency in the media and the scientific journals, implanted there to reassure the public that exposure to low doses of radiation should no longer be a concern…."

LLRC AND ECRR 2010 – European Committee on Radiation Risk

ECRR. 2010 Recommendations of the European Committee on Radiation Risk. The Health Effects of Exposure to Low. Doses of Ionizing Radiation.
http://www.euradcom.org/2011/ecrr2010.pdf

Low Level Radiation Campaign (LLRC)
http://www.llrc.org/

WHAT YOU CAN DO; RESEARCH THE DARK SIDE OF THE NUCLEAR MONOPOLY

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Zero Nuclear Weapons Peace And Justice Project; First Strike Policy, Ban Nuclear Bombs, DU, Down Winders, Acute Radiation Sickness, Nuclear War, Dirty Bombs, Bomb Shelters

Zero Rads In Children And Adults Eco Justice Project - Negative Effects Of Chronic, Cumulative Man Made Radiation Exposure

Zero Rads Extraction Eco Justice Project; Uranium Mining, Enrichment, Nuclear Fuel Chain, Open Air Testing, Fracking

Zero Internal Rads Eco Justice Project; Negative Effects Of Internal Radiation Exposure, Risk Models, Hormesis, Radiophobia, Radiation Monitoring Networks

Making Invisible Heavy Metal Radioactive Poison Visible Eco Justice Project; Ionizing Heavy Metal Poisonous Radiation In Food/Water/Products, Geiger Counters, Dosimeters, Radiation Readings, Test Labs, Conversions, Global Detector Network

Zero Harm To Animals, Insects, Birds And Plants Eco Justice Project; Negative Effects Of Chronic, Cumulative Man Made Heavy Metal Radioactive Poisons In Animals, Insects, Birds And Plants

Zero Nuclear Power Plant Threat Eco Justice Project; Accidents, Recycling Nuclear Fuel, Movie Reviews, Next Generation Nuclear Plants, Terrorists

Radiation Research, Education, Database Eco Justice Project; Individual Radioactive Elements/Isotopes, USA Radiation, Radiation Exposure Prevention, Reversal, Chelation

Eco Justice Art - Artists As Activists; Art, Aging, Poetry, Lyrics And Lawsuits Project; Lawsuits, Aging Nuclear Reactors, Recertification, Music, Lyrics, Poetry

Zero Rad Waste Eco Justice Project; Long Term Storage Of Nuclear Waste, Decommissioning, Ocean Dumping, Incineration, Decontamination, Water Contamination, Dry Cask Storage

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Index, Table Of Contents

End

Dr Caldicott MD On Mutagenesis Teratogenesis, Entropy; Dangers Of Cumulative Dose Man Made Ionizing Radiation, Heavy Metal Poison Exposure Of Babies, Fetus, Infants, Children, Teens, Leads Human Extinction Via Gene (DNA) Damage, Accelerating Mass Die Offs From Disease, Cancers, LLRC
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