18 th Dynasty Pharaoh Akhenaten and Queen Nefertiti
cuddle their 3 daughters worshipping the Most High God
Annu via the Aten Path of Spirituality circa 1370 BC.
defying the Amen-Re Cult Practice of the First born child
sacrifice to the God Moloch
20. BRCA/"OPERATION BLACKBERRY PATCH (OBP)" ISEDD/
MATERNAL AND INFANT DEATH INTERVENTION (MIDI) PROJECT, INC.
ENDORSEMENT:
THE SCIENCE OF SPIRITUALITY, INC.
FOR THE MOST COMPREHENSIVE VISION OF AND PERSONAL INSTRUCTIONS FOR THE
UNFOLDING GOLDEN AGE ON PLANET EARTH, WITH SPECIFIC STEPS AS HOW EACH OF US
CAN INDIVIDUALLY PARTICIPATE PRACTICALLY IN THE RETURN OF THE "GARDENS OF EDEN"
ALL OVER EARTH; WE BRING YOU THE SCIENCE OF SPIRITUALITY, INC. DIRECTOR SANT
RAJINDER SINGH JI's ADDRESS TO THE 1996 UNITED NATIONS GENERAL ASSEMBLY ON ITS
50 TH ANNIVERSARY CELEBRATION ENTITLED "VISION OF A NEW MILLENNIUM: GLOBAL
PEACE THROUGH MEDITATION."
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ANYTHING OF LASTING WORTHINESS ON THIS WEB SITE IS DUE TO THE DIRECT INFLUENCES
OF SURAT SHABD YOGA MASTER SANT DARSHAN SINGH JI NOW DECEASED AND HIS FATHER
SURAT SHABD YOGA MASTER SANT KIRPAL SINGH JI NOW DECEASED AND HIS SON THE LIVING MASTER SANT RAJINDER SINGH JI ON ME BEFORE AND SINCE MASTER DARSHAN INITIATED
ME ON FEBRUARY 29, 1976 INITIATED ME GEORGE W. SINGLETON INTO THE LIGHT & SOUND
YOGA.
State of the World Forum Member # 20827 photo by Franz Louis (2010)
2007 & 2009 European Union Humanitaran Grantee
www.TheUniversityofGod.org Web Master
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SEE THE BRCA//'OBP" ISEDD DETAILS BELOW
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CHRONIC POVERTY CAN BE ELIMINATED IN OUR LIFE TIMES
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THE PURPLE SEAL: BREAKING THE PLAGUE OF
CHRONIC DISEASES AND SYNDROMES
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DO NOT MISS AN OPPORTUNITY TO SEE THE URBAN GARDENING MOVEMENT CLASSIC "SWEAT EQUITY" DIRECTED AND PRODUCED BY DANIEL TRIPOLI
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THE BRCA, INC. "DRAGONFLY CIRCLE" HIGH PRIESTESS
ACCRA, GHANA RESIDENT
NANCY "NEFERTIABIT" MENSAH
INVITES YOU TO ENJOY HER FINE ART PHOTOGRAPHS AND
THE "ORIGINAL NATURE OF HUMAN SEXUALITY AND LOVE" POEM
PRESENTED ON WEB PAGE 25.
AMENSES VIRGIN "BRICKHOUSE"
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I. BRCA, Inc. "OBP" ISEDD Demonstration/Maternal and Infant Death
Intervention (MIDI) Project, Inc.
A. Statistics of the Genocidal Level of Infant and Maternal Mortality in America
1.) US Infant Mortality Rate (IMR) at 6.9% (per 1000 live births) as reported in 2008 by the US Center for Disease Control and Prevention (CDC) places America 29th in industrialized countries compared with Japan's IMR of
3.1% and 3 rd amongst industrialized nations.
The IMR amongst African Americans at 16.7% is genocida! See related 2.) below and Appendix I-1 and
Appendix I-2.
Note a: The CDC in its 2008 Annual Report on the nation's Infant Mortality Rates pointed to the lack of
progress in infant mortality prevention from 2000 to 2006__ a lack of progress in this vital health
index not seen since the 1960's. It is not a coincidence that America could once boast about its IMR; but since passage of the Civil Rights Bill has steadily lost its health status advantage internationally the last 30 years.Note b: This period from 2000 to 2006 coincides with:
i.) the proliferation of the high fat and high protein fast food restaurants in America;
ii.) the unannounced substitution of the federally subsidized production of the higher
caloric high fructose corn syrup for the lower caloric sugar cane and sugar beet
sucrose as a sweetener by America's refined food industry;
iii.) an attempt to corrupt medical science further with federal research using statistical
manipulation of death rates to give overweight and obese individuals' longer life
spans than normal and underweight individuals;
iv.) the appearance of the "Metabolic Syndrome" [the cluster of cardiovascular and
diabetic risk factors including visceral (waist) obesity, high blood pressure, insulin
resistance, elevated triglycerides and low HDL cholesterol]; and
v.) the manifestation of the Metabolic Syndrome as a major dysfunction of the people.
Note c: In a disturbing finding the infant merconum (first bowel movement after birth) as well as
neonatal newly born infant bile and infant blood contains high amounts of 22-Hydroxy Cholesterol,
C-24 mono-hydroxy bile acids called 3-beta-hydroxy cholenoic acid and Lithocholic acid which are dangerous co-mutagenic, co-carcinogenic, atherogenic and toxogenic linked to liver cholestasis (gall
stone blockage of the gall bladder) and the Oxysterols (24, 25 and 27 Hydroxycholesterols).
In particular Premature babies are associated with the at risk of high concentration of C-24 mono-hydroxy bile acids and high Dietary Cholesterol maternal diets. [F14]
Esoterically as documented below and in Appendix A-1 because the human genome is encoded as a herbivore/vegan genetically, the human liver of the pre-natal, neonatal and infant processes any Dietary Cholesterol from the
Mother's shared blood system or amniotic fluid as a "slow poison" through a "Third Bile Acid Metabolic Pathway" producing a unique mix of bile acids that persists from conception but is slowly transformed after birth by the development of intestinal flora until about 4 years of age when the adult pattern of cholesterol and bile acid
metabolism dominates.
2.) US Maternal Mortality Rate (MMR) at 13.3% (per 100,000 live births) as reported in 2006 by the UN World
Health Organization up from 7% in 1996 places America 41st in industrialized countries with Japan's MMR of
7.3% and 3 rd amongst industrialized nations.
The MMR amongst African Americans at 36.5% is genocidal! The last 10 years has seen a nearly 100% increase.
B. Addressing the Genocidal Level of Infant and Maternal Mortality in America
In March and April, 2010, Amnesty International_USA, Inc. and a United Nations sanctioned epidemiological
scholastic study identified the level of maternal and infant death rates in America as genocidal and hard to
explain given:a.) the high level of per capita health care expenditures being spent; and
b.) while the rates over the past 10 years in most of the developing countries
in the world have decreased the rates in America have increased.
Please see Appendics I-1 and Appendice I-2 for more details and documentation.
Esoterically as documented above and in Appendix A-1 the human genome was aboriginally encoded
genetically as herbivore/vegan. Thus the human liver of the fetus, neonate and infant processes all Dietary
Cholesterol from the Mother's shared blood system and amniotic fluid without exception as a "slow poison."
Using an allusive Third Bile Acid Biosynthesis Pathway (other than the "Neutral" and "Acidic" Adult
Pathways) a "unique mix of bile acids" inventoried below in TABLE VI are produced. This "unique mix of
bile acids" pattern persists from human embryonic conception through about the human infant's 4th year of
age being slowly transformed after birth by the development of a pathogenic dominated intestinal flora from
feeding upon solid animal meat food until the Omnivore diet adult pattern of cholesterol and bile acid
metabolism dominates.
It is very clear from research and development work under great public knowledge suppression that unborn
human babies in the womb are at risk from the immense co-mutagenic, co-carcinogenic, atherogenic, lithogenic
and toxogenic effects of Dietary Cholesterol and its over 25 Bile Acids and other derivatives inventoried in
TABLE III adversely affecting the fetus including its liver, heart, brain, lungs, kidneys and pancreas. Especially
pathogenic are the mono-hydroxy-bile acids; i.e. 3-beta-hydroxy 5 cholenoic acid, Lithocholic acid (LCA,
3-alpha hydroxyl 5-beta cholenoate) and its isomers Iso-LCA (3-beta hydroxyl 5-beta cholenoate) and allo-LCA
(3-alpha hydroxyl 5-alpha cholenoate).
Esoterically, the tradition of amenses women living upon the Vegan diet has been associated since ancient times
with painless and no-risk child birth. This is because the aboriginal Vegan diet produces a sanitary maternal
blood status and avoids the animal food derived mucus waste body deposits; the latter which encumber the
female pelvis preventing it as designed from disassembling and allowing a natural pain free child birth.
Consequently, the Omnivore diet by necessity has been associated with Caesarian births since ancient Rome
and constitutes approximately 20% of America's infant deliveries and encompasses the bottom line of maternal
mortality risk.
Specifically, the "great pathophysiological ramifications of dietary cholesterol and bile acid metabolism" is
highlighted no better than in the suppressed via ignoring "repercussions of Intrahepatic Cholestasis in
Pregnancy (ICP) in "fetal complications" affecting the placenta and fetal liver.
Quoting from the astute review article by Spainish scientists Jose G. Marin, et al entitled "Molecular basis of
fetal bile acids and pigments through the fetal liver-placenta-maternal liver pathway" published in the Journal of Hepatology, V. 4, No. 2, pages 70-76, 2005:
"The excretory pathway for COA's [Cholephillic Organic Anions of bile acids and biliary
blood pigments] …….. is of great importance because when it is impaired [as in
cholestasis] the repercussions on the normal development of the fetus or even on the
fate of gestation may be dramatic."
"Intrahepatic Cholestasis of Pregnancy [ICP] is a reversible form of cholestasis (stoppage
of bile flow) that may develop during late pregnancy and usually resolves soon after
delivery."
"For the Mother, this condition is usually benign since it is only associated with certain
discomfort due to pruritis [itching].
Note: That it is the Dietary Cholesterol derived Liver detox products the Bile Acids CDCA,
DCA and LCA that are the sources of this intense itching experienced by these ICP
affected pregnant women is crucial to recognize and address because the allopathic
physicians are still largely confounded by this telltale symptom."However, ICP is frequently the cause of premature delivery and increased risk of fetal
mortality during the third trimester of pregnancy in patients suffering from this disease.
"Moreover, the severity of fetal complications is proportional to the magnitude of
maternal hypercholanemia." [emphasis added]
Appendix I-3 presents Anna Glantz, et al, in the article "Intrahepatic Cholestasis of Pregnancy (ICP): Relationship between Bile Acid levels and Fetal Complication Rates," Journal of Hepatology, V. 40, No. 2, pp 467-74, 2004 the
ground breaking prospective study by Swedish scientist details her "state of the art" in vivo prospective cohort study
of ICP. In this study ICP is defined as "otherwise unexplained pruritis (itching) of pregnancy in combination with
fasting serum bile acid level greater than or equal to 10 micro-mol/liter." Her study is the first to establish the
relationship of maternal serum bile acids and ICP.
The "fetal complications" from "Intrahepatic Cholestasis of Pregnancy (ICP)" are detailed in this Swedish study as follows:
i.) spontaneous preterm deliveries,
ii.) asphyxial events; and
iii.) passage of meconium and its green staining of amniotic fluid, placenta and membranes.
Swedish scientist Anna Glantz further elucidates on ICP and its treatment from her "state of the art" in vivo
prospective cohort study conducted between 2/01/1999 and 1/31/2002 involving 45,485 pregnancies that
identified 693 ICP diagnosed women where 81% had mild ICP (10-39 micro-mol/liter of serum bile acid)
and 19% had severe ICP (serum bile acid greater or equal to 40 micro-mol/liter):a.) Simple logistic regression analysis showed that the probability of fetal
complications increased by 1 to 2% per additional micro-mol/liter of
serum bile acids.
b.) Complementary analysis showed that fetal complications did not arise
until bile acid levels were greater than or equal 40 micro-mol/liter.
c.) Gallstone disease and a family history of ICP were significantly (P< .001)
more prevalent in the group of ICP patients with higher bile acid levels.
d.) No increased fetal risk was detected in ICP patients with bile acid levels
less than 40 micro- mol/liter.
Now with the passage of Health Care Reform Legislation America can properly implement an innovative
infant and maternal mortality amelioration initiative that if it includes the following 7 elements specified below
would within 24 months show a significant lowering of the genocidal level of maternal and infant death that
exists all over America especially in its inner cities amongst Afro-Americans:
1.) Recommend that participating doctors and other health practitioners implement a no Dietary
Cholesterol regimen with no more than 5 mg/day for women who are:
a.) preparing for pregnancy;
b.) pregnant;
c.) overweight or obese at risk for maternal and/or infant mortality; and
d.) residing in America's inner cities at risk for subclinical malnutrition,
birth defects and alcohol/drug syndromes.
2.) Monitor pregnant women with serum bile acids at or greater than 10 micro-grams/liter as
potential candidates for Intrahepatic Cholestasis in Pregancy (ICP) noting that 40 micro-
mol/liter is a biomarker for ICP fetal complications.
3.) Identify Metabolic Syndrome as a maternal and infant death risk factor targeting especially
over weight and obese pregnant women.
4.) Adding the monthly 2 quart "high enema" as a pregnancy preparation and pregnancy
gestation regimen especially targeting those with ICP.
5.) following a Dietary Cholesterol detox dietary regimen daily especially including:
a.) fresh Mexican Papaya, berry (straw, black, rasp, blue) and freshly
squeezed orange juice.
b.) fresh squeezed carrot juice with spinach, celery, beet and elephant garlic.
c.) spinach and Romaine salads with "cold pressed" olive oil, avocado and garlic.
d.) raw sunflower seed and pumpkin seed drink or milk.
e.) Cell Tech, Inc. Klamath Lake, Oregon "Super Blue Green Algae."
f.) Solgar, Inc. i.) Horse Tail;
ii.) "Oceanic" and
iii.) probiotic acidophilis and bifida
g.) fresh squeezed Concord grape juice.
6.) Encourage the US Federal Executive Branch to empower the Environmental Protection Agency
to create green job grants to non-profits and governmental units targeting cleaning the urban
areas of litter __ especially zeroing in on plastic litter, as their UV light deterioration pollutes the
water table and drinking water with low levels of hydrocarbon mutagens, carcinogens and
cytotoxins showing up in Mother's milk and allows for the bile acids and other TABLE III
identified co-mutant, co-carcinogen and co-toxin derivatives to promote.
7.) Admit the truth of science that the human is a genotype vegan/herbivore and proceed to feed
Mother and baby accordingly in all federal fund receiving hospitals and health care centers
8.) America's deteriorated high Infant Mortality Rate is related to the "great ramifications of Dietary
Cholesterol and bile acid metabolism" and the proliferation of the high fat and protein fast food
diet. This is because the human is genetically programmed as a herbivore/vegan as discussed
in Appendix A-1. Ironically, under the unnatural environment of a maternal Omnivore diet the
liver and other organs of the human fetus processes Dietary Cholesterol as a "slow poison."
To survive the fetus uniquely utilizes a "Third Bile Acid Metabolic Pathway" initiated by cellular
mitochondria. The DNA of mitochondria of mother and child are identical. This herbivore/
vegan genome dictated bile acid metabolism persists from conception up to about 4 years of age.
Thus human fetuses, neonatals and infants uniquely produce highly toxic bile acids as follows:
a.) as their primary bile acid the 3-beta-Hydroxy 5 Cholenoic acid [an at risk cholestatic
(gallstone producing) C-24 monohydroxy bile acid with an at risk mutagenic and
carcinogen (cancer promoting) aromatic (unsaturated) polycyclic structure];b.) as their secondary bile acids the various isomers of Lithocholic Acid [also a
cholestasis at risk C-24 monohydroxy (saturated) bile acid produced by the liver
without as in adults the pathogenic anaerobic bacterial gut degradation]; and
c.) the tertiary bile acids the so-called normal bile acids CA and CDCA (C-24 3-alpha).
Environmental pollution of the nation's urban and rural water ways with plastic packaging,
containers cups, plates and other eating utensil generated litter leaches UV light degraded plastic mutagenic and carcinogenic compounds into the water table endangering not only human fetuses, neonatal and infants but adult human as they produce various C-24 mono- and poly- hydroxy bile
acids many with aromatic polycylic rings known to promote if not cause mutations, cancer and
organ necrosis.
TO CONTINUE ON TO WEB PAGE 22.
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