Understanding autism by Max and Sandra Desorgher World Community Autism Program, directed by
Max
and Sandra Desorgher, was founded in 2002, but our work towards
understanding
a biological basis of autism started in 1994 when Sandra’s adopted
daughter,
Sara, made a remarkable recovery. Her early evaluations identified
severe
delay disorder at age twenty months. At twenty two months Sara suffered
additional
insults when she stopped breathing, turned blue and developed
uncontrollable
seizures the day after she received her DPT and MMR vaccinations. At
age
two she entered special education which was followed-up with
evaluations
at age five that revealed autism, severe hyperactivity, self injurious
behavior,
no verbal language use and severe delay disorder. Sara was functioning
in
the severely delayed range. Sara was placed into Sandra’s care at age
five
through Professional Parenting therapeutic foster care and cleared for
adoption
at age eleven. Adoption Plus formalized the adoption of Sara at age
eleven
and Sara was then placed on a diet which eliminated lutein (a natural
food
pigment). Sara developed verbal speech within weeks. Sara went on to be
mainstreamed
to regular education and she achieved academic excellence and she was
accepted
into National Junior Beta Honor Society. Sara was declassified from her
diagnosis
of autism by The Marcus Center in Atlanta Georgia at age fifteen.
A long time before Sandra published Sara’s
response
to dietary intervention on the internet, discoveries were made that
pointed
to a biological basis of autism. These included the work of Dr. Bernard
Rimland
of Autism Research Institute, whose work and reviews of published
studies
on vitamins showed that there was something unusual in the way these
children
utilized nutrients. Three immunologists, Dr. Reed Warren, Dr. Vijendra
Singh
and Dr. Hugh Fudenberg reported on immune system findings. In the mid
90’s
researchers in Europe (University of Sunderland) made profound
discoveries:
the urine samples of autistic children showed elevations in certain
chemicals
and the origin of these chemicals are thought to be the dietary
proteins
casein and gluten/gliadin found in dairy and some grain foods. This
furthered
the interest in diet as it relates to autism which had been gaining
attention
through the concerted effort of Dr. Kalle Reichelt. Dr. Rosemary Waring
identified
Phenolsulphotransferase-P enzyme deficiency. Another breakthrough was
the
discovery by Dr. William Shaw of unusual yeast metabolites in urine
samples. Other findings have included brain differences (Bauman, Hashimoto), the discovery of
gastrointestinal lesions by Dr. Andrew Wakefield and those of Dr. William Walsh
reporting on more phosphotransferase deficiency discoveries, the metallothionine
enzyme dysfunction.
When Sandra Johnson (Desorgher) revealed the
story
of Sara’s recovery on the internet, there was already a growing band of
people
who were taking the biological approach seriously and applying dietary
changes,
using supplements, enzymes and anti-yeast treatments. Doctors, parents and researchers were
finding
ways to treat autism and sometimes the treatments resulted in
improvements
and even reported recoveries. In 1994 Dr. Rimland again published
information
that included his opinion that autism was a condition from which some
people
could improve or recover and maybe there would remain some signs or
symptoms
but for some the devastating impact of this syndrome could be reduced
to
quirky or odd behaviors and children or people with autism who were
provided
with ample and timely intervention could have a far better outcome than
in
the past when no treatment options were identified. Dr. Rimland
recently
released his opinion paper that autism is likely caused by vaccination.
This
forward move by one of the most well respected leaders of the autism
community
comes at a time when the human population is being forced to take a
stand
on vaccination issues. Congressional hearings are taking place in the
USA
surrounding SV40 vaccine contamination, autism, SIDS deaths, Shaken
Baby
Syndrome and the lack of scientific evidence towards supporting that
vaccines
are safe and effective. Indeed much evidence to the contrary has been
brought
to the public view. This controversy has led to speculation that the
best
prevention may lie in NOT vaccinating. If nothing else it reveals
science
and medicine have failed to produce adequate methods of identifying the
‘at
risk’ infants for whom vaccination should be delayed or suspended. No
one
can argue reasonably that giving Hepatitis B vaccines to neonates is
the
best scientific or medical course of action for a population which is
NOT
at risk for developing Hepatitis and for whom a vaccine reaction can
result
in a lifetime of serious disabilities or cause the death of the infant.
Complicating the vaccine controversy issue is the
reported similarity of vaccine related deaths, SIDS deaths and
Shaken
Baby Syndrome deaths. Add this information to the known similarities
between
children who are identified and reported to have suffered from vaccine
reactions
and their presentation. Vaccine injured individuals generally
have
similar and in some instances identical presentation to many who are
diagnosed
with autism of unknown origin. Findings which are being reported
disclosing
measles virus known to be of vaccine origin in the guts and brains of
children
with autism, immune phenomena identical to immune phenomena which is a
reported
outcome of immunogenetic changes as a result of mass vaccination,
increased
frequency of autism in families where first and second degree relatives
present
with the condition and the correlation of autoimmune disease to vaccine
research
and molecular biology research identifying susceptible populations to
disease
presentation attributed to mass vaccination.
Treatments have been developed and the
results
are sometimes making headlines. IVIG (Singh), transfer factor
(Fudenberg),
and therapies developed based on the long term classification of autism
as
a behavioral disorder which have come to be known as ABA (applied
behavioral
analysis) introduced by Dr. Ivar Lovaas. Immunology and the
relationship
of the immune system response to pathogens such as bacteria, viruses
and
food substances lead to more theories and more treatment options
including
those offered by doctors Michael Goldberg and C. A. Kotsanis. Signs and
symptoms
are being recognized as treatable and new therapies have been made
available
such as Auditory Integration Training (Berard and Tomatis) and Irlen
lenses
for Scotopic Sensitivity Syndrome.
Some doctors began to accept, include and
recommend
the most cost effective and least invasive therapies including use of
restricted
diets. Some parents and doctors followed Sandra’s advice and removed
lutein
from their child’s or patient’s diets who had autism. Some followed the
GFCF
diet approach. Allergy Induced Autism and the Feingold association
linked
by the salicylate/phenol connection began also to find ways of sharing
information.
New diets have been introduced from yeast free to removal of
carbohydrates
and more will likely come along.
Parents once faced with no treatment options
are
now fighting for a multitude of therapies and services for their
children.
Often they are overwhelmed by the massive amount of information on diet
and
at the same time they find themselves parenting children who are often
very
picky eaters, called children with ‘faddy’ diets by some. Product
manufacturers
wanting to cash in on the diet frenzy promote products but rarely is
there
research provided to support the claims being made. When the research
is
done often it is ignored. Parents and most doctors have no real
knowledge
of diet and nutrition. Medical doctors are asking for and demanding
training
now so that they can identify and collaborate on the treatment of their
patients.
Experts in the field of autism, being relied
upon
by the government and elite health organizations, are very often people
from
the field of psychology. Many achieved their rank among the experts
when
it was generally accepted that no known treatment options were
available
and autism was still a rare condition. Research has been and continues
towards
identifying a genetic cause which has been assumed by some must be the
basis
for the signs and symptoms of autism. The Medical Research Council, UK
review
of autism reported their findings that perhaps five percent and not
more
than ten percent of people with autism have an identifiable genetic
contributing
or causal factor. Interesting also is that each of the conditions
identified
in the genetic studies had already been identified as a known
co-occurring
condition including but not exclusive to Fragile X, Turner Syndrome,
Tuberose
Sclerosis and Phenylketonuria before the massive amount of genetic
research
was undertaken.
Currently autism has been accepted to have a
bio-medical
basis (Frith). Behaviors, once called sterotypies, are now called
‘coping
skills’. Some of the activities described as behaviors for some people
with
autism include finger flicking (fingers moved rapidly in front of the
eyes),
tapping and repetitive tapping, echolalia and listening to audio
material
over and over and making certain sounds repeatedly. Interesting also is
the
research on Eye Movement Desensitization and Reprocessing (EMDR). EMDR
called
also ‘Finger-flash’ therapy is said to be a treatment for some
people
who have experienced trauma or who have stress disorders such as Post
Traumatic
Stress Disorder (PTSD). Is autism a stress disorder? Have some people
with
autism been providing their own version of ‘Finger-flash’ therapy?
Still it has taken science a long time to
begin
to recognize the relationship of signs, symptoms and characteristics to
the
biochemical and immunological factors contributing to presentation. In
the
recent past, 1940’s, conditions such as Pellagra were identified with
neurological
and psychiatric presentation and were found to be caused by nutrient
deficiencies.
Pellagra resulted in signs and symptoms which are not unlike those
reported
for some people with an autism spectrum diagnosis. Research,
manufacture
and production of pharmaceuticals and the substantial profit potential
for
new drugs pushed use of diet related therapies into a class called
‘fringe
medicine’ by some. Medical doctors have not been provided training in
nutrition
studies.
Still there is no consensus as to whether
autism
is neurological, genetic, immune, bio-medical or a combination such as
immuno-genetic
(IoGc), neuro-gastro-immune. It is recognized that there are many
consistent
laboratory findings which have been identified and these consistencies
could
or should result in a test or tests which could be used to confirm,
substantiate
or lend credence to a diagnosis which is currently based solely on
behavioral
criteria. Substantial information has been gathered, reported,
published
and still the experts seek funding for more genetic research. Many
parents
of autistic children and vaccine injured children believe the rational
for
this genetic research is to find regions which can be identified
through
chorionic villous sampling or amniocentesis so that an ‘at risk’ fetus
could
be recommended for termination. Indeed autism has been associated to
Aarskogg
syndrome and genetic counselors have been given the research which
suggests
termination for specific findings which seem to be growing rapidly. The
rate
of increase in identified susceptible regions which result in
recommendation
for pregnancy termination is not disclosed to the general population.
In the recent past C4B null allele was
associated
to people who might develop immune system diseases at some time in
their
lives and NOT a justification to recommend termination. Increasing
prevalence
of conditions which can be more severe and affect humans in infancy and
early
childhood such as Congenital Adrenal Hyperplasia and autism are now
linked
to this region. This can result in increased pressure on genetic
counselors
to recommend pregnancy termination. Some genetic differences result in
very
variable outcomes. Chromosome region 15q11-13 has been associated to
Angelman’s
syndrome, Prader-Willi syndrome, autism and also genius. It is accepted
that
people present with any and all of these syndromes for whom the 15q
error
cannot be found and also people who present with the error and for whom
no
signs or symptoms can be found. Research is moving into areas called
epi-genetics
where microDNA are being identified, named and associated to diseases
and
syndromes. The evidence is mounting which suggests that genetic errors
are
only part of the causal factors and environment, sex, age and
additional
insults or injuries can alter the outcome for any individual. We are
each
unique. How many pregnancies are being terminated and are the
recommendations
always justified?
Until there is a medical test or tests which
can
be used to substantiate an autism diagnosis the participants in studies
may
or may not have autism. Many people with certain and sometimes
unidentified
inborn errors or genetic conditions can present with the signs and
symptoms
currently used to diagnose autism. The inborn error of metabolism or
genetic
condition may or may not be identified. Individuals with blindness,
deafness
or a combination of injuries, insults or illnesses often will meet the
criteria
for an autism spectrum diagnosis. Is there one form of autism or many?
Is
there a causal factor or many? We can argue for and against theories
but
currently no one has all the answers. Important also is that when
infants
die from vaccine injury and sudden infant death syndrome there is
currently
no way to know how many of these infants would have developed the signs
and
symptoms of autism. It is also currently impossible to determine how
many
spontaneously aborted fetuses would have been at risk for developing
the
signs and symptoms of autism. Even though autism has been included in
Aarskogg
syndrome and is now identified as a risk for Chromosome 6-pter deletion
no
one really knows what percentage of infants with this deletion will
present
with Turner syndrome, deafness, autism or no recognizable signs and
symptoms.
Much of the research funding comes from the
pharmaceutical
industry, government and big business. Nearly every dollar spent on
research
goes right back into the pockets of people working in these sectors.
The
pharmaceutical companies are under no obligation to publish their
research
findings, they own the information. Research which is undertaken by the
government,
such as that which is contracted to or originates in the military
sector,
is often classified. We are now living in an age when information is at
our
fingertips. People who have previously worked in these sectors know
where
to look for information and many are no longer bound by the constraints
of
their former jobs. Some of these people, including doctors, are
speaking
out. Quickly those with vested interests in pharmaceuticals, research
and
profits move to answer the charges of these individuals and in doing so
they
tend to label these individuals as ‘loose cannons’, ‘pseudo scientists’
and
fanatics.
Autism researchers from fields
as
diverse as gastroenterology, virology, immunology, genetics,
endocrinology,
allopathic medicine and alternative or natural medicine are coming
together
with parents of children with disabilities and finding evidence for
common
causal factors. The theories thus far which are the most publicized
include
vaccine injury, birth trauma, inborn errors of metabolism, genetic and
genetic
predisposition. The theories are moving closer and closer together as
parents,
philanthropists and researchers take on the task of elucidating the
cause
or causes of autism based on their determination to learn the truth
about
the new epidemics and pandemics facing all of humanity.
Current opinion on the use of early
childhood
behavioral intervention for treating autism reveals ‘there is still no
one
approach that meets accepted criteria for an empirically validated
treatment.’
(Baker, Feinfield ) This can be said for any or all of the
treatments
and therapies currently being used for treating autism. However, there
is
no shortage of interest in developing new pharmaceuticals for treating
autism
or finding new uses for some that already exist. Experts continue to
argue
as to whether or not increased numbers of persons diagnosed with autism
over
the past decade, now reaching 1 in 150 individuals in the USA and
with
the reported rise equalling to an estimated 700 plus increase, is real
or
imagined. The pharmaceutical giants don’t seem to be hesitant about
accepting
the figure and planning towards a ‘target market’ (Physiol Behav,
August
1, 2003; J Gerlai and R Gerlai). From this article we can surmise that
Eli
Lily is going to be a frontrunner in more human drug research directed
at
finding pharmaceuticals which can be used to treat people with an
autism
spectrum diagnosis. Will the drugs treat the cause or just the symptoms?
Treatment options such as dietary
intervention
are all recommending removal of non-food stuffs from the diet, non-food
stuffs
which have been approved by the FDA and allowed to adulterate our
food
supply for a century. However, the natural food substances reported to
result
in problems for some, many or most people with autism are being found
to
have more and more in common as pigments such as xanthophylls are found
to
be bound to some grains and dairy protein (carotenoproteins) are often
the
pigments in what some refer to as 'yeasty fruits' and avoided by many
autists
who simply refuse to eat colored fruits and vegetables. The red
pigments
found in shell fish which is often the cause of allergic reaction is
also
one of the carotenoid pigments identified by us as central to an
understanding
of the biological basis of autism.
Of the first 1000 individuals who received
the
‘Sara’s Diet Protocol’, about 100 reports of full recovery came back,
and
hundreds that made remarkable gains. By recovery, we mean that, after
implementing
the diet for as little as 14 days and up to 6 months all signs of
autism
were gone. The individuals are NOT cured, in order to remain symptom
free,
they must remain on a controlled diet. No other diet program has
demonstrated
this level of success.
After being unable to get grant funding for
a
diet protocol study requested from NIH we began to travel to other
countries,
such as India, Dubai, and Scotland, where we found more openness to our
discovery,
and we continued to see the same pattern of recovery and improvement.
We
then wrote ‘The Power of Exile. Autism, a journey to recovery.’ In 2002
we
were invited to Malaysia by the leading autism support group in that
country
after the daughter of one of the doctors on their team made significant
gains.
Our first conference in Malaysia was attended by 500 parents, doctors
and
specialists eager to learn about the lutein-free diet. We gave
individualized
dietary consultations for more than 100 families in Malaysia between
June
2002 and May 2003, and again we saw a 10% recovery rate and almost all
children
showed some measure of improvement. Many of these were already using
GFCF,
'yeast-free' diets, behavioral therapy, enzymes, supplements etc. After
returning
from Malaysia the second time, we wrote our second book ‘Autism,
the
way forward’, which includes full details of our dietary approach, as
well
as new perspectives on complex behavior, sensory problems and social
issues.
The book is available as an e-book through our website
http://www.saras-autism-diet.freeservers.com/
There are many theories which have been put
forward
to link together the biological evidence, including the ‘opioid excess
theory’.
In this theory, undigested protein fragments cross the gut lining which
has
been damaged by vaccination, food intolerance, food allergy or disease
and
then enter the brain as 'opioids', causing havoc with nerve signals and
hormones.
Some parents report that the child is developing perfectly normally
until
an adverse reaction to a vaccine causes damage to the brain and the
gut.
Research findings of measles virus in the brain and the gut, as well as
parent
reports that their child regressed soon after a vaccine suggests
strongly
that something has gone wrong during routine vaccination. Others point
to
toxic substances that come in with the vaccines, such as mercury
(thimerisol).
Some researchers believe that autism is an auto-immune disease, that
brain
cells are being attacked by the body’s own immune system. Some are
convinced
it is genetic as findings reveal multiple instances in some families.
What about allergies? Are these immune,
genetic
or immunogenetic? Multiple incidents of allergy also occur in families.
There
is the potential for offspring to be allergic to substances to which a
parent
or grandparent is allergic, such as pollen, penicillin or bee sting.
But,
we can be allergic to these even if our parents and grandparents are
not
allergic, and just because a parent or grandparent has an allergy this
doesn’t
mean the offspring will also have the allergy. The immune system is
always
adapting to changing environmental pressures. The areas of our genetics
where
these changes take place are called hypervariable regions. These areas
demonstrate
the relationship between diet, environment, toxins, genetics, pigments
and
the immune system. These are the areas that are found to be altered in
populations
affected with the so-called 'diseases of civilization', including
diabetes,
arthritis and autism.
We believe that in conditions such as
autism,
the immune system is altered in the womb, as information from both
parents
come together and the fetus makes a choice as to what substances are
‘non-self’
and how to evolve to meet the challenges it expects to meet in the
stress-filled
environment outside the womb. The immune system is reported as
continuing
to develop and mature through age three, leaving plenty of opportunity
for
new choices as it encounters the many dangers and challenges of the
real
world. Information obtained from families with offspring on the autism
spectrum
might include that one or both parents suffer from diseases such as
diabetes,
celiac disease, cancer and arthritis – diseases which involve
alterations
in the way the immune system works. It might include that the parents
come
from very different ancestral backgrounds, and that their genetics come
together
in ways that make for an unusual relationship to pigmentation and food
as
well as susceptibility to diseases, disorders or conditions common to
the
ancestry of either or both parents. We see this in conditions such as
vitiligo
and hypomelanosis of Ito which co-occur with autism. It might also
include
information about how the parent’s immune system reacted or changed in
response
to vaccination, insults and injuries received prior to conceiving
offspring.
Alterations in the immune system is seen in the high frequency of
auto-immune
disease in parents of autistic children. It is also seen in alterations
in
genes that control the immune system. One of these is known as the
C4B-null
allele and is found not only in autists but in families with
auto-immune
diseases and families with a high rate of miscarriage.
The adaptability of the immune system is
essential
to survival of the species. As environmental pressures increase, it is
only
natural that the immune system will adapt and find new ways to respond
to
those pressures. We believe that one of those ways is the selection of
lutein
by the immune system. Xanthophyllic pigment such as lutein is contained
inside
structures called chloroplasts or plastids. These structures are found
in
agarose gel and egg yolk. Both substances have been used as the primary
culture
mediums for vaccines since about 1929. Viruses are known to incorporate
DNA
and alter their structure. The DNA associated with xanthophyll would be
the
plastid and chloroplast DNA that would be present in vaccines cultured
in
agorose gel and egg yolk. This alteration of the virus is called
mutation.
As mass vaccination became more and more prevalent, the human immune
system
was faced with pathogens coming into the body together with other
substances
contained in the vaccines, viral pathogens along with the structures
which
had only previously been associated with plant food energy.
Preservatives,
dyes, phenols and many other known poisons are used in the manufacture
of
vaccines. Like a Trojan horse the vaccines have delivered enemies
that
altered our human immune system. As the selection occurs of non-self
substance
in the womb it leads to changes in our genetics, pigmentation, eyes,
the
brain, hormones and endocrine system. Molecular biologists are
revealing
findings that changes in the human genome can be identified and
measured
and that some of the changes can be directly associated to diseases
which
include diabetes, cancer, arthritis, spontaneous abortion and immune
phenomena.
Research into the manufacture and development of new vaccines reveal
findings
which associate autoimmune phenomena and disease to vaccine chaperones
used
as vaccine carriers called heat shock proteins (Max Planck). The
warnings
have come after a century where this type of vaccine chaperone has been
included
in the process of vaccine manufacturing before the ‘risk’ was known.
We believe that the changes may be more
severe
in girls because of the role of lutein in the ovulation cycle, and that
female
fetuses are more likely not to survive, leading to or contributing to
the
unusual male-female ratio. The changes are not always obvious in the
newborn
but manifest as lutein builds up in the diet during infancy and early
childhood.
The altered immune system is more likely to have an exaggerated or
unusual
response to vaccine and early childhood illnesses. This may be
exacerbated
by diet and other environmental factors. If it is possible to recover
it
is also possible that some people have this immune-genetic condition
and
do not present with typical signs or symptoms. Some may avoid having
symptoms
as they recognize foods that cause symptoms in infancy and early
childhood
and grow up just to be people who are picky eaters. Some may be spared
developing
signs and symptoms as they remain unvaccinated and do not suffer from
additional
insults or injuries such as birth trauma, illness or have predisposing
genetic
factors.
After working with more than 2500 families
around
the world it appears that those who have no family history of
autoimmune
disease and who are not of diverse ancestry often have the mildest
presentation
and also best chance of recovery. Those diagnosed with autism who have
a
family history which includes many autoimmune diseases and who are also
from
diverse ancestry appear to have the most severe presentation.
The immune response to lutein is unusual in
that
it doesn’t show up on an allergy test. This is because it is a chemical
structure,
little more than a vibration, and not a protein. The response is
similar
to a reaction to a poison such as cobra venom. Immune system
macrophages
engulf the pigment and remove it from the body. At the same time, it
sets
off a chain reaction including shutting down normal digestive processes
as
the immune system takes control. The reactions can alter the way
enzymes
work and result in unusual chemicals and compounds building up inside
the
body. It switches the hormonal balance towards ‘fight-or-flight’ and
away
from the ‘molecules of emotion’. Chemical reactions which should make
us
feel relaxed, satiated and ready to be sociable are inhibited as
chemicals
which make us feel anxious, afraid and vulnerable are elevated. If this
was
a one-off reaction, we would soon recover, but one reaction to lutein
may
last several days, and lutein is entering the diet on a daily basis in
most
households, so the reaction is continual, the immune system never turns
off,
and the emotional system cannot turn on. This is reflected in a
structure
in the brain called the amygdala, which is part of the limbic system -
the
mammalian center of emotional, learning and language development. The
Amygdala
responds to the adrenal reaction, and puts a hold on social
interaction,
language and emotional development until the immune response is turned
off.
When we remove lutein from the diet, as well
as
providing all essential nutrients based on individual needs, we often
see
the first signs of change after 12 days. We usually have to wait up to
four
months to see the emotional awakening that we are looking for. This is
followed
by increased socialization, language, improved behavior as well as a
reduction
in yeast related symptoms, bowel problems and skin eruptions,
improvement
in appetite, a willingness to experiment more, and above all a happier
disposition.
The individual nature of autism is reflected
in
individual needs. Some require a removal of gluten and/or casein, and
many
benefit from this approach even if it is not required. We usually take
out
wheat (some wheat also contains lutein such as spelt and semolina
varieties),
and dairy that is high in casein and carotenoproteins, but do not
believe
that it is always necessary to remove oats, whey, butter (pure), cream
cheese
and cereals such as barley or foods containing barley malt. Many do
need
to have soy protein removed, and we always recommend removal of non
food
stuff especially food dyes and aspartame. This is a diverse population,
as
diverse as the human race itself. There is a higher rate of celiac
disease
and often a strict gluten free diet is needed. For others ensuring the
dietary
precursors for producing enzymes that break down substances such as
gluten
and casein is all that is needed. And, for others support with
digestive
enzymes appears to be the best course of action.
Understanding the biological basis of autism
is
moving forward, and we believe that, as this information filters
through
to the medical community, family doctors will take over from
psychologists
as the first port of call for parents with a child diagnosed as
autistic.
If parents are going to trust the medical community then the medical
community
must hold itself accountable to reveal the truth about the dangers of
drugs,
vaccines and medical treatments. Often people will make a choice to
accept
a medical treatment even if the treatment only has a slight chance of
producing
a positive outcome. People are accustomed to taking risks but it is
only
fair that we be given the facts so that we can make an informed choice.
We
also expect our medical professionals to be educated and also given the
facts
so that they too can make informed decisions which are not based on
profits
for the pharmaceutical industry or which involve hidden agendas of
research,
government and military organizations.
Understanding autism is still a goal and not
a
reality. Until we challenge the medical community and research
organizations
to produce the unpublished material which remains hidden from peer
review
because it doesn't support their agendas, the established medical
community
and research organizations will continue to pursue their own agendas
and
ride the pharmaceutical gravy train. We cannot continue to expect that
taxpayers
will allow their elected representatives to spend our money on endless
research
and receive nothing in return but more and more drugs. We cannot expect
consumers
to continue to purchase products which have been pushed onto the market
with
inadequate research, unscrupulous research or which are promoted using
ghost
writers, advertising companies and solicitors with bogus credentials.
The world, the educated, the disabled, the
parents
of damaged and dead babies, those incarcerated unjustly, convicted for
crimes
which are now being recognized as medical negligence are demanding
accountability.
With great sacrifices we are capable of great discoveries. We are
capable
of identifying the causes and treatments for autism and renaming this
condition
as it relates to the causal factors and providing treatments which
result
in improvements. Those who only need diet and environmental
accommodation,
those who need antiviral therapy and blood cleansing treatments, those
who
need immune therapies and more expensive and invasive treatments, those
who
need a combination of therapies. If we can help one percent to reach
recovery
then the sacrifice is worth the revelation. Ten percent a joyous
result.
Fifty percent recovery in the autism population and the diagnosis in
utero
would result in many choosing not to abort, a joyous triumph for those
who
believe that life is worth preserving.
From those who improve and recover we can
learn
more about the needs of those who do not recover, who have experienced
too
many insults and have too many contributing factors. We can learn how
better
to accommodate them, how to meet their needs, how and when to provide
services
and when also to leave them alone and just love them, accept them and
care
for them.
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