::IMVA :: Internacional Medical Veritas Association ::
Diabetes is disabling, deadly and
on the rise and in certain places has reached fifty
percent of local populations.
Rising Tide of Mercury and other
Toxic Chemicals
We cannot afford to allow another generation to face the
vaccine risks that changed our children's lives forever.
Medical and Public
Health Implications
Special Cancer Presentation
Chemical Causes of Diabetes
The development
of insulin-dependent diabetes mellitus
is thought to be dependent on the interaction of
environmental agents with the pancreatic beta cells.[i] University of Calgary
Medical
science has discovered how sensitive the insulin receptor
sites are to chemical poisoning. Metals such as cadmium,
mercury, arsenic, lead, fluoride[ii]and possibly aluminum may play a role
in the actual destruction of beta cells through
stimulating an auto-immune reaction to them after they
have bonded to these cells in the pancreas. It is because
mercury[iii]
and lead attach themselves at highly vulnerable junctures
of proteins that they find their great capacity to provoke
morphological changes in the body. Changes in pancreatic
function are among the pathogenetic mechanisms observable
during lead intoxication.[iv]
Lead exposure has
been associated with an increased risk of hypertension,
and is a well-established risk factor for kidney disease.
Whether lead affects blood pressure indirectly through
alterations in kidney function or via more direct effects
on the vasculature or neurologic blood pressure control is
unknown though. Researchers at Harvard Medical School
state, “Our findings support the hypothesis that long-term
low-level lead accumulation (estimated by tibia bone lead)
is associated with an increased risk of declining renal
function particularly among diabetics or hypertensives,
populations already at risk for impaired renal function.”[v]
Cadmium[vi]
is a widespread environmental pollutant that accumulates
in the pancreas and exerts diabetogenic effects in
animals. In a large
cross-sectional study, urinary cadmium levels are
significantly and dose-dependently associated with both
impaired fasting glucose and diabetes.
[vii]
Transsulfuration
pathways in the body are fundamental for life. When
mercury blocks thiol groups cellular proteins lose their
reactive properties, lose their ability to carry out their
routine function. Insulin has three sulfur-containing
cross-linkages and the insulin receptor has a tyrosine
kinase-containing sulfur bond, which are the preferred
targets for binding by both mercury and lead. Should
mercury attach to one of these three sulfur bonds it will
interfere with the normal biological function of the
insulin molecule. Mercury, many times more toxic than
lead, is so dangerous exactly because it is
collapsing/damaging critical sulfur-containing
cross-linkages which change the geometry of both insulin
receptor sites and insulin itself.
Commercials tell
children that junk food is good food
- the latest message from an industry that spends
$10 billion a year marketing to children.
New York
Times
Food is not
considered junk just because of high fat or sugar content,
there is a long list of poisonous chemicals used by the
food industry that are striking people down.
And there are many serious nutritional deficiencies in
today’s food that diminish the bodies capacity to deal
safely with these chemicals and heavy metals - with
magnesium and selenium deficiencies at the top of the
list.
For instance,
according to Dr. Ellen Silbergeld, a researcher from the
Johns Hopkins School of Public Health, the poultry
industry’s practice of using arsenic compounds in its feed
is something that has not been studied: “It’s an issue
everybody is trying to pretend doesn’t exist.”[viii]
Arsenic exposure is a risk factor[ix]
for diabetes mellitus.[x]
Inorganic arsenic is considered one of the prominent
environmental causes of cancer mortality in the world.
Chicken consumption may contribute significant amounts of
arsenic to total arsenic exposure of the U.S. population
according to the Journal Environmental Health
Perspectives.[xi]
“Arsenic acts as a
growth stimulant in chickens—develops the meat faster—and
since then, the poultry industry has gone wild using this
ingredient,” says Donald Herman, a Mississippi
agricultural consultant and former Environmental
Protection Agency researcher who has studied this use of
arsenic for a decade. At mean levels of chicken
consumption (60 g/person/day), people may ingest 1.38-5.24
micrograms/day of inorganic arsenic from chicken alone. At
the 99th percentile of chicken consumption (350 g
chicken/day), people may ingest 21.13-30.59 micrograms
inorganic arsenic/day and 32.50-47.07 micrograms total
arsenic/day from chicken.[xii]
Arsenic is a human carcinogen linked to liver, lung, skin,
kidney, bladder, and prostate cancers. It can also cause
neurological, cardiovascular, gastrointestinal, and immune
system abnormalities. The feeding of arsenic to chickens
in the United States releases hundreds of tons of arsenic
into the environment every year in the form of poultry
manure, which is spread on fields as fertilizer.
Researchers from
the Department of Internal Medicine, National Taiwan
University[xiii]
Hospital found, “The association between arsenic exposure
and diabetes mellitus is a relatively new finding.
Up to now, there are six epidemiologic reports linking
diabetes mellitus with arsenic exposure from environmental
and occupational sources. Two reports in Taiwan carried
out in the blackfoot disease-hyperendemic villages, one
cross-sectional and one prospective follow-up of the same
cohort, indicate that arsenic exposure from drinking
artesian well water is associated with prevalence and
incidence of diabetes mellitus in a dose-responsive
pattern.
The observation of
the relation between arsenic exposure and diabetes
mellitus is further supported by studies carried out in
Sweden and Bangladesh. In Sweden, case-control analyses of
death records of copper smelters and glass workers
revealed a trend of increasing diabetes mellitus with
increasing arsenic exposure from inhalation. In
Bangladesh, prevalence of diabetes mellitus among
arsenic-exposed subjects with keratosis was about five
times higher than unexposed subjects.”
Wistar rats were
made diabetic
with a single injection of Alloxan.[xiv]
Another example is
Alloxan. Studies show that Alloxan, the chemical that
makes white flour look "clean and beautiful" destroys the
beta cells of the pancreas.[xv]Scientists
have known of the alloxan-diabetes connection for years
yet there seems to be a conspiracy that defends the
integrity of the FDA, which allows dangerous chemicals
that can cause diabetes to be used in drugs and food. "A
growing body of research shows that pesticides and other
contaminants are more prevalent in the foods we eat, in
our bodies, and in the environment than we thought,”[xvi]
all confirming the chemical nightmare in progress.
According to
research conducted by Dr. H.J. Roberts, a diabetes
specialist, a member of the ADA, and an authority on
artificial sweeteners, aspartame:
1) Leads to the precipitation of clinical diabetes.
2) Causes poorer
diabetic control in diabetics on insulin or oral drugs.
3) Leads to the
aggravation of diabetic complications such as retinopathy,
cataracts, neuropathy and gastroparesis.
4) Causes
convulsions.
Dr. Roberts said,
"The loss of diabetic control, the intensification of
hypoglycemia, the occurrence of presumed 'insulin
reactions' (including convulsions) that proved to be
aspartame reactions, and the precipitation, aggravation or
simulation of diabetic complications (especially impaired
vision and neuropathy) while using these products.”[xvii]
The FDA's own toxicologist, Dr. Adrian Gross told Congress
that without a shadow of a doubt, aspartame can cause
brain tumors and brain cancer and violated the Delaney
Amendment which forbids putting anything in food that is
known to cause Cancer.It is a
monstrous crime to poison the food and water supplies yet
this is exactly what the FDA has been approving and
undoubtedly they are, in large part, responsible for
flaming the diabetic winds.
As the use of
MSG and aspartame grows,
the incidence of obesity appears to be growing.
MSG
causes a very large insulin response after it is ingested
since there are glutamate receptors in the pancreas.
MSG opens calcium channels,
thus constricting blood vessels – this may put diabetics
with high blood pressure at risk by negating calcium
channel blocker medication. In 1968, John W. Olney, M.D.,
a respected researcher at Washington University Medical
School, St. Louis, Missouri, and member of the National
Academy of Science, found that mice in his laboratory that
were being used to replicate a 1957 study by Lucas and
Newhouse, in which the administration of MSG had resulted
in retinal damage, had become grotesquely obese. Since
1969, many scientists have confirmed Dr. Olney's findings
of damage to the hypothalamus from MSG with resulting
obesity. There is abundant literature demonstrating that
MSG and aspartic acid cause hypothalmic lesions which, in
turn, can cause gross obesity. Although there are
a number of causes for obesity, there is no question that
one of the main causes for the obesity epidemic is the
ever increasing use of MSG and aspartame.
We know that the
hypothalamus is very immature at birth. The damage to this
structure of the brain by MSG leads to severe endocrine
problems later in life, among them decreased thyroid
hormone, increased tendency toward diabetes, and higher
cortisone levels than normal. A child consuming a soup
containing MSG plus a drink with NutraSweet will have a
blood level of excitotoxins six times the blood level that
destroys hypothalamus neurons in baby mice.
And we are just
beginning to hear that a massive mistake has been made
with genetically modified foods, which can only fan those
diabetic winds.[xviii]
Dr. Alpad Pusztai, for instance, has already shown that
genetically-manipulated foods can, when fed to animals in
reasonable amounts, cause very gradual organ and immune
system damage.[xix]
Another study, carried out by Dr Irina Ermakova at the
Institute of Higher Nervous Activity and Neurophysiology,
at the Russian Academy of Sciences, found that more than
half of the offspring of rats fed on modified soya died
in the first three weeks of life, six times as many as
those born to mothers with normal diets.[xx]
Dr. Manuela Malatesta and colleagues in the Universities
of Pavia and Urbino in Italy, showed that mice fed on GM
soya experienced a slowdown in cellular metabolism andmodifications to liver and pancreas.[xxi]Researchers
are reviving fears that GM food damages human health and
certainly would not be indicated for children or for
people with diabetes.
Diabetes may in
fact be a major side effect of
antibiotics and other common pharmaceuticals.
Dr Lisa
Landymore-Lim
Independent
scientist for Atomic Health Limited
Doctors are on
notice that many drugs have toxic effects that can
participate in destroying insulin creation and cell
receptivity to it. In her 1994 book, Poisonous
Prescriptions, Landymore-Lim's says that diabetes may
in fact be a major side effect of pharmaceutical drugs.
The book provides evidence
from studies and hospital records. Diabetes, usually
thought to be largely a genetic disorder, may actually
have increased so much in the last 50 years due in large
part to the proliferation in the use, and over-use, of
medicines.
In 2004 the American Diabetes Association, the American
Psychiatric Association, the North American Association
for the Study of Obesity, and the American Association of
Clinical Endocrinologists made a similar announcement
warning people to be careful to watch for signs they are
developing diabetes, obesity or high cholesterol if they
are taking Abilify, Clozaril, Geodon, Risperdal, Seroquel
or Zyprexa.[xxii]What medicines, food and water have
increasingly in common are the chemical poisons they
contain.
Researchers at the
University of Liverpool recently released their studies
that examined the toxic effects on nerve cells in the
laboratory of using a combination of four common food
additives - aspartame, monosodium glutamate (MSG) and the
artificial colourings brilliant blue and quinoline yellow.
The findings of their two-year study were published at the
end of 2005 in the journal Toxicological Sciences.[xxiii]
The Liverpool team reported that when mouse nerve cells
were exposed to MSG and brilliant blue or aspartame and
quinoline yellow in laboratory conditions, combined in
concentrations that theoretically reflect the compound
that enters the bloodstream after a typical children's
snack and drink, the additives stopped the nerve cells
growing and interfered with proper signaling systems.
The mixtures of the additives had a much more potent
effect on nerve cells than each additive on its own.
The study reported that the effect on cells could be up to
four times greater when brilliant blue and MSG were
combined and up to seven times greater when quinoline
yellow and aspartame were combined, than when the
additives were applied on their own. What we can begin to
conclude is that future research is going to show how all
the toxic chemicals in the food, air, water and medicines
we consume are combining to destroy our health. Any one
poison discussed here in sufficient quantity can destroy
cell physiology, the pancreas beta cells, and diminish
cell receptivity to insulin.
We are depending
more and more on processed foods, and with each year, the
FDA approves more and more chemicals for use in foods.
With each year, the food industry is using more and more
chemicals in their products. These chemicals increase
shelf life, kill bacteria, improve taste, replace fats,
replace carbohydrates, and cause chronic diseases that
eventually kill people. Junk food is really a cover up
image for something quite a bit nastier than the image
that junk congers. Junk foods are actually slow acting
poisons because they come to us loaded with highly toxic
chemicals. We can only imagine the worst when we think
about FDA approval processes for in reality the FDA is
poisoning the public. The FDA is the wellhead of most
iatrogenic diseases and death. There is no excuse for an
agency charged with protecting public health to have
allowed the massive poisoning of the public via food,
drugs and public water supplies.
The CDC says that
diabetes is disabling, deadly and on the rise. The
incidence of diabetes is skyrocketing not only in adults
but in the juvenile population as well. Healthcare experts
have called the alarming rise in diabetes and its related
complications “an epidemic” that threatens to spiral out
of control.
In 1997 15.7
millions adults in the United States were reported to have
diabetes.[xxiv]
By the year 2002, this number had already swelled to 18.0
million or 8.7% of all adults.[xxv]
Diabetes and its complications now claim hundred of
thousands of lives in the U.S. each year, incurring total
expenses of over $130 billion in direct and indirect costs
to the healthcare system.[xxvi]
Worldwide, the number of people with adult-onset diabetes
is predicted to explode in the next 10 years, doubling to
an estimated 221 million people.[xxvii]
By contrast only 43,171 people in the United States were
diagnosed with AIDS and only 18,017 died.[xxviii]
Scientists have
discovered a variant gene that leads to a sizable extra
risk of Type 2 diabetes - 38 percent of Americans who have
inherited a single copy of the gene have a 45 percent
greater risk of Type 2, the estimated 7 percent who carry
two copies are 141 percent more likely to develop the
disease. What scientists are saying is that if all the
variant genes in the population were erased, so would be
21 percent of diabetes cases.[xxix]
Another way of expressing variations in genetic makeup is
constitution. Some people are gifted with stronger
constitutions (genes) than others and are more able to
stand up to massive chemical assaults on their bodies.
Genetic causes do not in anyway explain the explosive
increases in diabetes but increasing concentrations of
environmental poisons penetrating our bodies via our air,
water, food and medicines can evoke breakdowns in genetic
function.
The human race is
facing an abyss, a massive breakdown in body chemistry.
All indications suggest that the medical industrial
complex will not squarely face the facts and the research
and will not work in earnest to reduce the chemical
exposures the masses are facing. Too much money is
involved in manufacturing hundreds of millions of tons of
chemicals each year and huge fortunes are made by the
economic elite in the sale of toxins that are dragging
large segments of the population to their sick beds and
early graves. Our civilization is poisoning itself and the
medical and dental communities participate with passion.
[i]
Yoon, JW et al. Effects of environmental factors on
the development of insulin-dependent diabetes
mellitus. Department of Microbiology and Infectious
Diseases, Julia McFarlane Diabetes Research Unit,
University of Calgary, Alberta, Canada. Clin Invest
Med. 1987 Sep;10(5):457-69.
[ii] Toxicity of Fluoride to Diabetic
Rats. C.A.Y. Banu Priya et al; International Society
for Fluoride Research; FLUORIDE 30 (1)1997, pp 51 -
58
http://www.fluoride-journal.com/97-30-1/301-51.htm
[iii]Professor I.M.
Trakhtenberg. Trakhtenberg, I.M. From Russian
translation. Chronic Effects of Mercury on Organisms.
In Place of a Conclusion Thiol poisons,
especially mercury and its compounds, reacting with SH
groups of proteins lead to the lowered activity of
various enzymes containing sulfhydryl groups. This
produces a series of disruptions in the functional
activity of many organs and tissues of the organism.
[iv]
Timoshina IV, Liubchenko PN, Khzardzhian VG. Ter Arkh.
1985;57(2):91-5. [Article in Russian] Examination of
the exocrine function of the pancreas in 52 workers
exposed to lead, including 36 with the symptoms of
intoxication (mild in 33 and marked in 3) revealed the
primarily hyposecretory response of acinar cells
stimulated with pancreozymin and secretin, while the
hyposecretory and dyspancreatic responses were
recorded less frequently. The endocrine function of
the pancreas was revealed to be also lowered, which
was confirmed by the decreased blood fasting insulin
content and low blood insulin content after glucose
intake as well. The changes in pancreatic function are
among the pathogenetic mechanisms of the abdominal
syndrome observable during lead intoxication.
[v] Shirng-Wern
Tsaih et al.
Lead, Diabetes, Hypertension, and Renal Function: The
Normative Aging Study. Harvard Medical School, Boston,
Massachusetts. Environmental
Health Perspectives Volume 112, Number 11, August 2004
[vi]
Cadmium sources: Tap water, fungicides, marijuana,
processed meat, rubber, seafood (cod, haddock, oyster,
tuna), sewage, tobacco, colas (especially from vending
machines), tools, welding material, evaporated milk,
airborne industrial contaminants, batteries, instant
coffee, incineration of tires/rubber/plastic, refined
grains, soft water, galvanized pipes, dental alloys,
candy, ceramics, electroplating fertilizers, paints,
motor oil and motor exhaust.
[vii]
Increasing rates of type 2 diabetes worldwide suggest that diabetes may be caused by
environmental toxins. Cadmium is a
widespread environmental pollutant that accumulates in the pancreas and exerts diabetogenic effects
in animals. To test the hypothesis that
exposure to cadmium is associated with
impaired fasting glucose and type 2 diabetes, we
examined the associations between urinary
cadmium and the prevalence of impaired
fasting glucose (prediabetes) and diabetes in the Third National Health and Nutrition Examination
Survey (NHANES III). In this
large cross-sectional study, urinary
cadmium levels are significantly and dose-dependently
associated with both impaired fasting
glucose and diabetes. These findings, which
require confirmation in prospective studies, suggest
that cadmium may cause prediabetes and
diabetes in humans. Urinary cadmium,
impaired fasting glucose, and diabetes in the NHANES
III Pathophysiology/Complications - National Health
and Nutrition Examination Survey Diabetes Care, Feb,
2003
[viii]Vandiver J,
"Chicken Feed," Daily Times (Salisbury, Md.), January
4, 2004.
[ix]
Tseng CH, Tseng CP, Chiou HY, Hsueh YM, Chong CK, Chen
CJ. Epidemiologic evidence of diabetogenic effect of
arsenic. Toxicol Lett. 2002 Jul 7;133(1):69-76.
[x]
Mahfuzar Rahman et al. Division of Occupational and
Environmental Medicine, Department of Health and
Environment, Faculty of Health Science Linkoping
University Sweden. Department of Occupational and
Environmental Health(DOEH), National Institute of
Preventive and
Social Medicine (NIPSOM), Mohakhali, Dhaka-1212
Bangladesh. American Journal of Epidemiology
1998; Vol. 148, No.2: 198-203 The crude
prevalence ratio for diabetes mellitus among keratotic
subjects exposed to arsenic was 4.4 (95% confidence
interval 2.5-7.7) and increased to 5.2 (95% confidence
interval 2.5-10.5) after adjustment for age, sex, and
body mass index.
[xi]
http://www.ehponline.org/docs/2003/6407/abstract.html.
[xii]Lasky T, Sun W, Kadry A,
Hoffman MK. Mean total arsenic concentrations in
chicken 1989-2000 and estimated exposures for
consumers of chicken. Office of Public Health and
Science, Food Safety and Inspection Service, U.S.
Department of Agriculture, Washington, DC, USA.
[xiii]
Tseng CH, Tseng CP, Chiou HY, Hsueh YM, Chong CK, Chen
CJ. Epidemiologic evidence of diabetogenic effect of
arsenic. Toxicol Lett. 2002 Jul 7;133(1):69-76.
[xiv]
A solution of alloxan at 2% diluted in saline at 0.9%
was administered to the animals in a single dose
corresponding to 40 mg of alloxan per kg of animal
weight injected into their penial vein. Alloxan
induces irreversible diabetes mellitus after 24
hours following its administration and the condition
proves to be chronic by laboratory tests after seven
days. Experimental Model of Induction of Diabetes
Mellitus in Rats; Acta Cir. Bras. vol.18
no.spe S o Paulo 2003 www.scielo.br/ scielo.php?pid=S0102-86502003001100009&script=sci_arttext&tlng=en
[xv]
Researchers who are studying diabetes commonly use the
chemical to induce the disorder in lab animals.
Unfortunately, most consumers are unaware of alloxan
and its potentially fatal link to diabetes because
these facts are not well publicized, are hidden by FDA
approval, and certainly doctors and the food industry
are not informing parents that they and their children
are being poisoned by white flour containing alloxan. Diabetes
and Chemical Poisoning.
http://imva.info/
[xvi]
Consumer Reports (Feb. 2006):
[xvii]
http://www.curezone.com/foods/aspartame.html
[xviii]
Genetically Engineered Food Biotech, Biotechnology,
GMO, Genetically Modified
http://www.organicconsumers.org/gelink.html
[xix]
Health Hazards of Genetically Manipulated Foods;
http://www.soyinfo.com/haz/gehaz.shtml
[xx]
Dr Irina Ermakova added flour from a GM soya bean -
produced by Monsanto to be resistant to its pesticide,
Roundup - to the food of female rats, starting two
weeks before they conceived, continuing through
pregnancy, birth and nursing. Others were given non-GM
soya and a third group was given no soya at all. She
found that 36 per cent of the young of the rats fed
the modified soya were severely underweight, compared
to 6 per cent of the offspring of the other groups.
More alarmingly, a staggering 55.6 per cent of those
born to mothers on the GM diet perished within three
weeks of birth, compared to 9 per cent of the
offspring of those fed normal soya, and 6.8 per cent
of the young of those given no soya at all.
http://www.organicconsumers.org/ge/babies010906.cfm
[xxi]Malatesta M,
Caporaloni C, Rossi L, Battistelli S, Rocchi MBL,
Tonucci F, Gazzanelli G (2002) Ultrastructural
analysis of pancreatic acinar cells from mice fed on
genetically modified soybean. Journal of Anatomy
201:409-415
[xxii]
Journal Diabetes Care. February 2004
[xxiii]
Lau K, McLean WG, Williams DP, Howard CV. Synergistic
Interactions Between Commonly Used Food Additives in a
Developmental Neurotoxicity Test. Toxicol Sci. 2005
Dec 13;
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed
http://www.ncbi.nlm.nih.gov/entrez/qu
[xxiv]
American Diabetes Association: Diabetes Facts and
Figures [factsheet online] 1997 [cited August 1999][16
screens]. Available from: URL:
http://www.diabetes.org/ada/c20f.asp
[xxv]
CDC.
http://www.cdc.gov/diabetes/pubs/pdf/ndfs_2003.pdf
[xxvi]
Brancati FL, Wang NY, Mead LA, Liang KY, Klag MJ. Body
weight patterns from 20 to 49 years of age and
subsequent risk for diabetes melli-tus. Arch Intern
Med 1999;159:957-963.
[xxvii]
Kopelman PG, Hitman GA. Exploding type II
[correspondence]. Lancet 1998;352:SIV5.
[xxviii]HIV/AIDS
Surveillance Report 2003;15.
[xxix]The finding
is being reported in the journal Nature Genetics by
researchers at Decode Genetics, a company in
Reykjavik, Iceland, that specializes in finding the
genetic roots of human diseases. January 16, 2006
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