Autism and G.O.D. - Generation of Diversity Part I
Part I - Autism, Evolution of the Immune system
May 30th 2017
author: Sandra and Max Desorgher
Previously published in 'The Power of Exile. Autism, a journey to recovery', WCAP publishing 2002
http://www.saras-autism-diet.freeservers.com/Diet/Saras_Diet_I.html
Introduction
Autism and GOD (Generation of Diversity), the evolution of the immune system; immunity of the human ‘herd’ leads us to a modern day dilemma. It is the strength of the adaptability of the organism which results in it’s capacity for survival. We are at the threshold of great changes taking place in our human development. Some of these changes are a direct result of man’s creative ingenuity and the fight for survival. At the scientific level this has included vaccination. The development of the vaccine and the further development of more vaccines have contributed to evolutionary changes which can be seen in the human population and will likely be seen in the future generations in ways which we cannot yet begin to comprehend.
The evolutionary changes of modern man are seen first and are most evident in the ethno-culturally diverse populations. The areas of our chemical design are most vulnerable when two different types of people come together and this vulnerability can be additionally impacted by a dramatic change in location for which either or neither individual is biologically prepared resulting in offspring who exhibit the wide range of variation some of which is seen in modern day disease etiology. Areas of our chemical design which are most vulnerable are not exclusive to ethno-culturally diverse populations; in isolated populations where there is little change in genetic and environmental input the weakness of the population can be seen also as diseases which are prevalent in that culture. Add to this scenario the innovations of modern science which include the development of vaccines, genetic engineering of our food, the use of food additives and chemicals, crop spraying and artificial fertilizers, seasonal foods now used for year round consumption, electricity, motor transport, industry, television, computers, cell phones, chem trails.
Update 2017: M44 cyanide filled canisters to kill rodents - 100s of 1000s of these canisters have been placed in wildlife areas by the EPA (some canisters have been identified as the cause for death and injury to domestic animals & humans, rozol 'rodenticide' unleashed by the EPA in 1976 after trials in Zaire and Sudan (coincidentally taking place just before the first two outbreaks of 'ebola' virus in the same exact locations).
And, then look at the available information which indicates how we, as humans, are reacting to these changes. Interestingly, the signs and symptoms of ebola are identical to the signs and symptoms of rodenticide poisoning. The author of 'Poisoned' published 2017, Alan Bell, has stated it is estimated that 75 million Americans have chronic chemical sensitivity. That is 1 of every 4.5 people.
The molecular biologists, using some of the most advanced tools of modern man, are finding some of the patterns and changes which are taking place in our human population. Some of the most recently studied areas are the ‘hypervariable regions’ in our DNA and in particular the Human Leukocyte Antigens (HLA) histocompatibility antigens governed by genes of the HLA complex and the human major histocompatibility complex (MHC) – a region on the short arm of chromosome 6 with regions A, B, C and D - the region of our DNA which interacts with our immune system. Immunogenetic (IoGc) research is telling us that how we develop in the womb is not governed solely by our DNA and the environmental insults (impact) that the fetus is susceptible to, but is also due to the response of our own developing immune system. The immune system develops to protect the host and the impact of the immune system during fetal development includes changes which alter our genetic make-up.
Update 2017: Current research also includes that DNA carries 'trauma' memory which is passed from generation to generation.
Some of the terms used to describe these processes are so far called transduction and frameshifting. How modern day man is reacting to the environment, including everything from the womb experience to the bustling life in the city, impacts our chemical design. When we are reproducing, the chemistry of our bodies further impacts the new lives we create; even our emotional state contributes to chemical information which influences the developing fetus. At the basic level of this scenario lies the fact that, although we are different as organisms from plants and other animals, we do share much common genetic material. Genetic research is engineering ways to look at the human genome more closely as well as the genomes of more simple plants and animals. This research has led to the available techniques being used today to determine things such as paternity and is also beginning to look at the ways in which we are being altered as a result of drug use, vaccination, agricultural practice and food distribution. Food distribution is becoming more important for research because most human populations no longer have to go to the food source, nor do most of us participate in the growth and manufacture of food sources. Additionally, organizations such as the World Health Organization make decisions that affect us globally based on what they collectively think is good for the world population, but often do not account for individual practices within that population, or variables such as food intolerance within human populations or the metabolic, genetic and environmental differences that make for differences in food and nutrition needs. Research is showing us that in addition to the ethnically diverse populations such as those found in the UK and the USA the ethnically stable populations react to the same modern day influences in ways that can be measured as a response which is specific or unique for that population.
What molecular biology is finding is that the impact of modern life is resulting in and exacerbating the diseases of modern man: gout, arthritis, cancer, heart disease, immune deficiency, psychological illness and diseases relating to reproduction and ageing. What we want to know is how does this impact us individually, at the family level and at the community level? We need to understand these things because individually we might choose to take measures which could positively impact the out-come for ourselves and our families and communities. A healthy human can be more productive, a better parent and a better mate for life. A sick human takes a lot of resources, particularly in the more developed countries. A sick human is not there to care for the parents or the grandchildren, is not a good parent or a good spouse and cannot be productive in the community.
One of the modern day diseases which has made an impact on humanity is autism. Autism is said to be a lifelong disability with as yet no agreed treatment protocol. For more than 60 years autism has remained in the psychological paradigm with early work blaming the mother’s parenting for the condition. Dispelling the poor parenting theory did little towards identifying an alternative causal factor. Nearly forty years ago biochemical evidence began to emerge indicating that autism was more than a psychological illness with the publication of Dr. Bernard Rimland’s work ‘Infantile Autism; The syndrome and its implications for a Neural Theory of Behavior’ in 1964. As the field of immunology developed, additional insight into the metabolism of the autistic population was gained but still little scientific effort was applied to utilizing the new information. Therapies began to be offered: ABA (Applied Behavioral analysis, such as Lovaas); Vitamin therapy (particularly the work of Dr. Rimland at Autism Research Institute), AIT (Auditory Integration Therapy based on the work of Tomatis and Guy Berard), Transfer factor (Fudenberg), IVIG (Dr. Singh), Diet (Reichelt, Shattock, Lewis, Crook, Rapp, Braly), EPD and multidisciplinary approaches (Kotsanis), Irlen lenses, Prism lenses, Relaxation techniques such as Biofeedback, Sensory Integration, the ‘Squeeze machine’ (Grandin) and a multitude of massage therapies: Cranio-Sacral (Andrea Axt), Indian head massage, metamorphic technique, Alexander method, shiatsu as well as physiotherapy and others. In the past decade we have seen millions of dollars of research funding poured into genetics to try to find a genetic abnormality that was assumed must lye at the basis of autism.
After extensive research with more still to come it has been determined by a major autism review (Medical Research Council 2001) that the genetic involvement in autism is very variable and affects 5 to 10% of the autism population. Of this 5 to 10% approximately 2% have co-occurring Down syndrome, nearly 1% have Fragile X Syndrome and the additional 2 to 7% of the autism population present with a chromosomal or genetic defect which are markers for conditions such as tuberous sclerosis (TSC), phenylketonuria (PKU), Turner syndrome, Blindness, Deafness and hypopigmentary as well as hyperpigmentary diseases, disorders and conditions. Whereas these diseases, disorders and conditions may not appear at first glance to have much in common, a closer look reveals that the type of disease and presentation in the autism population reveals a pigment factor which supports the immunological information which has been gathered for this population. Sex chromosome disorders which co-occur with autism include Fragile X and Turner syndrome, while pigmentary or pterin disorders include PKU, TSC, Retinopathy of prematurity (ROP), blindness, deafness, Hypomelanosis of Ito and vitiligo. Autism is most easily understood as an immune system adaptation to the genetics of the individual and a response to the environment.
Changes have occurred rapidly as a result of the introduction of the vaccine in the form of a live attenuated virus placed inside a lipid filled chloroplast at the turn of the twentieth century. At the turn of the 19th century when Jenner’s smallpox vaccine was being used widely, the first descriptions of Down syndrome followed the vaccine trail as has been described by Gerhard Buchwald. Recently therapies for autism have been introduced such as the lutein-free diet (Johnson, Desorgher), Secretin (Beck), and Vitamin A from fish liver oil (Megson, Johnson, Desorgher) which address the impact of the immune system involvement on the biochemical metabolism of the autist. These therapies do not undermine or invalidate the already existing treatment options (AIT, Specialized lenses, Squeeze therapy and massage, EPD and immune therapies, restrictive diets or behavior therapy). However, the lutein free diet (nutrient balanced and provided according to ethnocultural diversity and preference requirements), vitamin therapy which is scientifically investigated (vitamin A from fish liver oil) and enzyme therapy are beginning to treat the cause. We are well past hope that science will be able to agree on a causal factor for autism. We are well past expecting that science will acknowledge a role in creating this epidemic. At this point we can only hope that science will investigate and validate the treatment options and provide medical guidance for the members of the medical profession who are under the burden of providing care for this ever increasing population.
Vaccination
As we move towards understanding the significance of this ‘syndrome’ and look at the complete picture it is evident that autism is sometimes a very severe condition, indeed especially for those who experience a vaccine reaction for whatever reason [whether it is a reaction to thimerisol and/or mercury, given when the child was suffering from an undetermined illness or when the child was experiencing a food related immune response or allergic reaction triggered by the environment, or whether some other factor was involved such as genetic predisposition, immaturity of the immune system, or an immune system that reacts atypically to the incoming pathogen(s)]. The vaccine reaction can be mild to severe and signs and symptoms can include acute symptoms - fever, diarrhea, bronchitis, pneumonia, excessive somnolence, frequent or inconsolable crying, penetrating and heart rending shrieking, fainting or shock, slowness of recall and confusion, generalized convulsions, encephalitis, meningitis, swollen limbs around the point of inoculation, whooping cough type cough, and ultimately cessation of breathing and potentially death; and chronic symptoms – recurrent colds, persistent amber or green phlegm, inflamed eyes, loss of eye contact, squinting, middle ear inflammation, chronic bronchitis, expectoration, coughing, asthma, eczema, allergies, inflamed joints, tiredness and lack of vigor, excessive thirst, diabetes, diarrhea, constipation, headache, disturbed sleep with periods of waking and crying, epilepsy, rigidity of the back, muscle cramps, light-headedness, lack of concentration, loss of memory, growth disturbance, lack of coordination, disturbed development, behavioral problems such as fidgeting, aggressiveness, irritation, moodiness, emotional imbalance, confusion, loss of will power, mental torpidity.
There is also no clear demarcation between acute and chronic complaints as the acute conditions are often the beginning of chronic suffering. These signs and symptoms are strikingly similar to those identified for nerve agent poisoning: acute symptoms - miosis (eye pupil constriction, resulting in dimmed vision), frontal headache and eye pain, runny nose, anorexia (loss of appetite), nausea, excessive sweating, tightness in the chest, heartburn, abdominal cramps, vomiting, profuse sweating, dyspnea (shortness of breath), tenesmus (painful, ineffective straining to urinate or defecate) drooling and tearing, excessive urinary frequency, involuntary urination or defecation, excessive bronchial secretion, fatigue, mild generalized weakness, twitching, jerking, and staggering, cramps, pallor (paleness), tension, anxiety, jitteriness, restlessness emotional lability, giddiness, insomnia, headache, drowsiness, slowness of recall and confusion, ataxia (lack of muscle control), slurred speech, coma, areflexia (loss of reflexes), Cheyne-Stokes respiration (alternating periods of rapid breathing/not breathing), generalized convulsions and finally, cease breathing, death.
Post-Vaccine Syndrome as a result of a vaccine reaction might increase the individuals likelihood of developing a disease, disorder or condition to which he or she had a predisposition but without the additional insult to the immune system might not have developed. Long-term, the vaccine injured child may develop a host of diseases, disorders or conditions which have been linked to vaccine reaction. These include: encephalitis (fatal in one-third of the cases), meningitis, cerebral palsy (CP) - approximately 4% of ASD’s have also CP, paralysis, Guillain-Barré syndrome (acute idiopathic polyneuritis), ADHD, allergies, multiple chemical sensitivities, aplastic anemia, autism, demyelination, Coeliac disease, Crohn's disease, dermatomyositis, epilepsy, deafness, Henoch-Schoenlein purpura, otitis media, polio, Stevens-Johnson syndrome and thrombocytopenia purpura.
Immunogenetics
Current review of the literature indicates that genetic abnormalities occur in approximately one-tenth of the autistic population. These include conditions which are predisposed to some degree of mental retardation. The genetic reviews also indicate that the genetic defect does not always result in the genetic affect for the autist i.e. albinism, rheumatoid arthritis, retinitis pigmentosa and Wilson’s disease. The literature is lacking in reports of autism with co-occurring rheumatoid arthritis, cancer and leukemia. For a population which is now reported to be at 62.5 cases in 10,000 this lack of co-occurrence may support the theory of the immune system evolution better than any other documentation. Additional reports provide information such as incidents of ‘delayed onset of visual maturation’ - children born blind who later develop visual acuity with onset of autistic symptomology. The literature also provides ample evidence for eating disorder in this population and most prominently the eating disorder involves refusal to eat green and colored fruits and vegetables.
So, investigating the autism syndrome from a new perspective, or looking at this syndrome from the same viewpoint as Dr. Gerhard Buchwald who cites Down Syndrome as a direct development of Jenner’s vaccine work, we can theorize that autism is an immunogenetic response which manifests as the signs and symptoms we use to define this syndrome. The biochemical markers for autism as well as the genetic findings confirm this theory as reasonable. Denying the relevance of this possibility is also denying the positive aspects of this same evolutionary response - a population which apparently has greater protection from cancer, rheumatoid arthritis, SLE and in a significant percentage (perhaps 39%) of the autism population the same immune system markers which have been found to result in a natural immunity to the HIV-AIDS ‘virus’.
The information relating to various populations which has been published on the HLA-DR (Human Leukocyte Antigens - D region) or hypervariable region (HVR) C4Q0 (Q0 null allele) confirms diseases such as: autism in the general population; diabetes (IDDM) generally and specifically in the Tunisian population; 62 SLE (systemic lupus erythmatosis) specifically in the Chinese, Spanish, Caucasoid and Japanese populations, CFS (chronic fatigue syndrome); spontaneous abortion in the Finnish population, liver cirrhosis, celiac disease in the Irish population, Felty’s arthritis syndrome, and IgA/IgG deficiency; and can result in a risk factor for vitiligo. We can find information in the literature that identifies a very low frequency of the C4 null allele in some populations (i.e. Greek) a very high frequency in the Swedish population and a ‘contemporary absence of the 21-OH A and C4 B genes as a constant characteristic of this extended haplotype in the Sardinian population suggesting that this and other extended haplotypes bearing C4 A or C4 B null alleles could be ancestral haplotypes which never duplicated at these loci. It has been suggested that the C4B null allele is a ‘probable negative selection factor’ as this relates to survival of the human species, based on findings in a study in Hungary of the old age population which presented a lower number of C4B null allele among the older population. However, Italy reports ‘a trend toward an increase in the older cohort’ or the C4B null allele (C4BQ0).
Message from a Star Seed Medicine Woman 2017
For nearly 200 years The People of this nation and many countries have been poisoned by vaccines just as the many great nations of this continent were intentionally poisoned by smallpox. The loss of life to the First Nation people is estimated between 60 and 100 million. A weapon had been discovered and this weapon is the first modern day biological warfare weapon. This weapon is used on The People of the so-called free world and increasingly used in as many areas of the world as possible. It has been documented that as many as 50% of infants have died when indigenous people's babies were vaccinated for the first time (Aborigine). Vaccines have been delivered to the US and European population during the First World War and it is estimated that a conservative number of deaths due to the vaccine is 50 million people.
Having been successful in this experiment the research and development produced the 1939 vaccines which were highly marketed to world travelers. The first children to be identified with autism spectrum disorder by Dr. Leo Kanner were primarily from educated parents who traveled abroad. Today headlines include that it is expected that 50% of children will have autism by 2030. The hidden agenda, government (control-mind), includes controlling the population through disease. The First Nation People who survived the 'discovery' and take over of this land are strong, the settlers who survived the move from Europe to the Americas are strong. Soon after Dr. Kanner had described autism another doctor Hans Asperger published his paper describing individuals who were unique.
These children and young people are described as often having genius IQs. Today we are learning that each generation of children has among them children with great gifts who stand out as different, new, emerging. Today we have the Star Seeds who can communicate telepathically. Some can communicate telepathically with the Ancients."
About the author
Sandra is a psychologist, teacher and autism expert who has written individualized diets for thousands of people around the world. Since 1994 she has been giving 'Sara's Diet' consultations for families affected by autism. Understanding how humanity is undergoing enormous changes in response to the environmental stresses of the modern world, she has seen how the immune system is undergoing a transformation in its function, leading to the explosion in chronic health conditions that effect us emotionally and physically.Along with her husband, Max Desorgher, she formed World Community Autism Program, and traveled the world to teach people about the relationship between diet, environment and well-being.
For more information on her autism work, visit her consultation page on the WCAP website:
http://saras-autism-diet.freeservers.com/Sandra/Consultation.html
'Little White Wolf, Medicine Woman'
Sandra is a life-long Experiencer of non-human multi-dimensional intelligent beings, that she encounters through the 'dream-state.
http://redhawk-spirit.blogspot.com/2017/04/little-white-wolf-medicine-woman.html
She has written two books on autism:
- The Power of Exile. Autism, a journey to recovery https://payhip.com/b/FGn9
- Autism, the Way Forward https://payhip.com/b/IsW9
Her most recent book has just been published as an e-book:
Meet the Ancients: Ascension Earth - Birth of a new Sun
Meet the Ancients came about as a result of my life experiences being taught in the dreamscape by the Mantid, the Guardian - my Guardian and one of the Ancients who know the history of Earth.