Five New Abstracts * The Autism Pandemic and the MMR VaccineConnection
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Munoz Yunta JA, Palau Baduell M, Salvado Salvado B, Amo C, Fernandez Lucas A,
Maestu F, Ortiz T. Hospital Universitario del Mar, Barcelona, Espana.
Introduction. Autistic spectrum disorders (ASD) is a term that is not
included in DSM IV or in ICD 10, which are the diagnostic tools most commonly
used by clinical professionals but can offer problems in research when it comes
to finding homogenous groups. Development.
From a neuropaediatric point of view, there is a need for a classification of
the generalised disorders affecting development and for this purpose we used
Wing's triad, which defines the continuum of the autistic spectrum, and the
information provided by magnetoencephalography
(MEG) as grouping elements. Specific generalised developmental disorders were
taken as being those syndromes that partially expressed some autistic trait, but
with their own personality so that they could be considered to be a specific
disorder.
ASD were classified as being primary, cryptogenic or secondary. The primary
disorders, in turn, express a continuum that ranges from Savant syndrome to
Asperger's syndrome and the different degrees of early infantile autism. MEG is
a functional neuroimaging technique that has enabled us to back up this
classification.
PMID: 15011151 [PubMed - in process]
* * *
Comparison of High-Functioning Atypical Autism And Childhood Autism By
Childhood Autism Rating Scale-Tokyo Version.
Kanai C, Koyama T, Kato S, Miyamoto Y, Osada H, Kurita H. Departments of
Mental Health and Psychiatric Nursing, Graduate School of Medicine, University
of Tokyo and Faculty of Law, Senshu University, Tokyo, Japan.
To assess autistic symptom differences between high-functioning atypical
autism (atypical symptomatology) (HAA; IQ >/= 70) and childhood autism (HCA), 53
HAA children (mean: 6.0 +/- 0.5 years) were compared with 21 HCA children (mean:
8.2 +/- 1.1 years) on the Childhood Autism Rating Scale-Tokyo version (CARS-TV).
Because IQ on the Japanese version of the Stanford-Binet and CARS-TV total
scores differed significantly between HAA and HCA, analysis of covariance was
conducted with IQ and CARS-TV total scores controlled for.
In two items of CARS-TV (relationship with people and general
impressions) the HAA children were significantly less abnormal than the HCA
children.
Affect tended to be significantly milder in HAA than HCA. Anxiety reaction
was significantly more abnormal in HAA than HCA. These findings may be useful to
distinguish between HAA and HCA.
PMID: 15009830 [PubMed - as supplied by publisher]
* * *
Single-Strand Conformation Polymorphism Analysis Of The Fmr1 Gene In Autistic
And Mentally Retarded Children In Japan.
Department of Pediatrics, The University of Tokushima School of Medicine,
Tokushima, Japan.
Fragile X syndrome is one of the most common causes of mental retardation in
males, and patients with fragile X syndrome occasionally develop autism.
It is usually caused by an expansion of the trinucleotide repeat in the
5'-untranslated region of the FMR1 gene, but in a small number of patients
deletions and point mutations have been identified.
We screened all 17 exons of the FMR1 gene for mutations in 90 autistic or
mentally retarded children using polymerase chain reaction (PCR)-single strand
conformation polymorphism (SSCP) analysis.
No mutations were found in 76 male patients.
However, one female patient was heterozygous for a normal allele and a mutant
allele with an A to C substitution at nucleotide 879 in exon 9.
This mutation was not found in 50 controls.
Reverse transcription-PCR revealed that a large proportion of the mutant
transcripts were spliced aberrantly, causing premature termination of the
protein synthesis.
Although uncommon, point mutations in the FMR1 gene may be a cause of autism
and mental retardation in Japanese patients.
PMID: 15000256 [PubMed - in process]
* * *
Characterization of the Various Forms Of The Reelin Protein In The
Cerebrospinal Fluid Of Normal Subjects And In Neurological Diseases.
Developmental Genetics Unit, University of Louvain Medical School, B1200
Brussels, Belgium.
Reelin is a large extracellular glycoprotein that is defective in reeler
mutant mice and plays a well-established role during brain development in human
as well as rodents.
In the adult brain, Reelin is expressed in a subset of GABAergic interneurons.
Its role in disease states is not clearly defined, although it is implicated
in autism and psychoses such as schizophrenia.
In this report, we show that Reelin immunoreactive proteins can be detected
in the human cerebrospinal fluid (CSF) with monoclonal antibodies directed
against the N- and C-terminal regions of the protein.
In CSF, Reelin is present as different products due to processing at two main
sites; preservation at -20 degrees C increases processing further.
CSF Reelin originates from the brain tissue and not from plasma.
The protein was detected in comparable concentrations in children and adults,
and the signal varied largely from subject to subject with no obvious
correlation with age or neurological disease state.
PMID: 15006702 [PubMed - in process]
* * *
Monozygotic Twins With Tuberous Sclerosis Discordant For The Severity Of
Developmental Deficits.
Developmental Psychiatry Section (Drs. Humphrey and Bolton) and Department of
Medical Genetics (Dr. Yates), University of Cambridge, and Department of
Neuroradiology (Dr. Higgins), Addenbrooke's Hospital, Cambridge, and Department
of Child Psychiatry and MRC Centre for Social, Genetic, and Developmental
Psychiatry (Dr. Bolton), Institute of Psychiatry, London, UK.
A pair of monozygotic male twins with tuberous sclerosis (TS) were followed
between 18 months and 3 years of age.
Twin A with 25 large cortical tubers and hence extensive brain involvement
was moderately mentally retarded and met criteria for autism.
The other twin had more (n = 31) but smaller tubers.
He was not mentally retarded and did not meet criteria for autism.
This study provides evidence that nongenetic factors such as extent of brain
abnormality and not just number of cortical tubers are important in determining
phenotypic variability in TS.
The findings also raise questions about the mechanisms giving rise to autism
in TS.
PMID: 15007135 [PubMed - as supplied by publisher]
* * *
Understanding Co-Morbidities Affecting Children With Epilepsy.
Virginia Commonwealth University/Medical College of Virginia, Richmond, VA.
Co-morbid conditions frequently occur in childhood epilepsy and may
significantly affect epilepsy and its treatment.
Similarly, epilepsy and antiepileptic drugs (AEDs) may affect these
associated conditions.
Co-morbidities that have a significant association with childhood epilepsy
include attention-deficit/hyperactivity disorder, autism, developmental
disabilities, accidental injury, migraine, and depression/anxiety.
Understanding the interrelationships among co-morbidities, epilepsy, and
their treatments is essential to optimal management of pediatric patients.
Treatment should be individualized with consideration for specific
co-morbidities and concomitant medications.
Key treatment goals are to achieve seizure control and optimal physical and
cognitive function using the simplest possible AED regimen.
The clinician should consider whether an antiepileptic treatment can be
chosen that also ameliorates the co-morbid condition.
Newer AEDs, such as lamotrigine, topiramate, gabapentin, oxcarbazepine, and
tiagabine, may benefit children with epilepsy and some co-morbid disorders.
PMID: 15007160 [PubMed - in process]
-- > DO SOMETHING ABOUT AUTISM NOW < --
SUBSCRIBE. . . !
. . .Read, then Forward the Schafer Autism Report.
Univer. of Calif. Irvine Study Identifies How New Neurons Grow In Adult Brain
Findings have potential implications for the use of stem cells to treat
neurological diseases
A UC Irvine study on cell growth in the adult brain may provide important
clues to the potential use of stem cells in the treatment of memory-related
diseases such as Alzheimer's.
The study shows for the first time how newborn neurons in the adult brain
grow and integrate into the area involved with learning and memory. The findings
may prove significant because these new neurons begin in a primitive state
similar to stem cells, and understanding how they mature may help stem cell
research into neurological diseases.
Study results will appear in the March 12 issue (volume 1000, issues
1-2) of the journal Brain Research, a special commemorative issue in
observance of its 1,000th published volume.
While examining how new neural cells mature in the hippocampus, the area of
the brain associated with learning and memory, Charles E. Ribak, professor of
anatomy and neurobiology, found that new neurons in the adult brain grow neural
signaling appendages in a similar way to those found in developing brains. "The
process begins with undifferentiated cells, which are cells that have no
appendages, such as dendrites and axons," Ribak said. "Because stem cells also
are undifferentiated, they may have the potential to grow and mature into new
neurons in a similar manner."
Ribak's study was done on rats. He and his colleagues studied newborn neurons
to determine when synapses form, which is the point when they become a
functional part of the brain's neural circuitry. Matthew J. Korn and Zhiyin Shan
of UCI and Andre Obenaus of Loma Linda University assisted in the study, which
was supported by the National Institutes of Health.
* * *
Artists are From Venus, Scientists from Mars? Great Minds Don't Think Alike
Working with artists and scientists has demonstrated that great art
constitutes an open investigation into the human condition - into experience,
memory and love.
These subjects are also common to scientific study. Yet despite these
universal interests, Im convinced that artists are cast from a different mould
to scientists and our recent study looking into "brain types" suggests that this
is indeed the case.
This year, two Scottish art galleries have been shortlisted for the
Gulbenkian Prize for the Museum of the Year, which awards originality and
innovation in galleries and exhibition spaces across the UK. This is proof, if
any was needed, of a thriving Scottish arts scene that is well prepared to take
on its southern neighbour.
But beyond any geographical divisions, the award highlights for me, as a
scientist, a deeper cultural divide - only one science exhibition out of 13 has
been nominated for the prize.
Science consistently fails to engage the public imagination on the same scale
as the arts. Although progress is certainly being made, largely thanks to the
enthusiasm and ardour of a few scientists committed to its public communication,
this failure may have a deeper cause.
It has become increasingly evident to me that there is a limited number of
scientists who can genuinely engage with the public imagination. This certainly
reflects a lack of support given to scientists by funding bodies, universities
and heads of departments who believe that communicating science diminishes ones
scientific merit.
Yet even if the right channels were available, is the lack of good
communicators also due to the relative inability of scientists to engage with
other minds and imaginations per se? And if so, why is that the case? If I were
to take you to the faculty of engineering at the University of Strathclyde, then
to the Mackintosh building, home of Glasgow School of Art, I wouldnt have to
tell you whether you where in an arts or science institution. Scientists dress
differently to artists. Sartorial innovation and even, sometimes, awareness is a
rare thing in our science departments. But not only that - the feel of these
places is different, the way people talk, they way they walk, the sensual temper
of the place.
I have worked with artists and scientists for ten years and there is no doubt
in my mind they are different species - and thankfully, you might think.
If, as I believe as a neuroscientist, all our thoughts, emotions and
imagination are constructs of our brains, then it would appear that the mind of
the artist must work very differently to that of the scientist.
Of course, some of my colleagues would say this is all cultural and no more -
but Im not too sure. Maybe we were born to be artists or scientists.
Part of an ongoing study into science and art, which will be discussed at a
talk at the Glasgow Science Centre next week, suggests that when taken as a
group, scientists are systemisers while artists are empathisers.
Perhaps this is not surprising. The nature of the scientific endeavour calls
for an unwavering objectivity and focus on the systematic classification of
knowledge through repeatable measurement, without the presence of the
subjectivity of the researcher.
By contrast, artists work requires a constant awareness of the existence of
other subjectivities, of their own and others personal, social and historical
context.
In other words, they must have a strong degree of empathy, a trait which
scientists, at least as most science is practised today, do not need in
abundance.
The survey, using a questionnaire devised by Professor Simon Baron-Cohen, of
Cambridge University, investigated levels of systemising and empathising in
1,500 scientists and artists. Scientists scored 22 per cent higher than artists
on systemising, and artist scored 8 per cent higher than scientists on
empathising.
So if the ability to imagine the minds of others really is somewhat lesser
for scientists, then maybe that helps to explain why there are fewer scientists
able to reach out and grab the publics attention. In my mind, it s certainly
not because science is any less interesting.
Now, systemising and empathising may seem like so much psychobabble, but
these concepts have been placed on a firm scientific footing by Prof
Baron-Cohen, who argues forcefully that these two "brain types" actually reflect
heritable biological differences.
Moreover, one cause of these differences may be down to levels of sex
hormones, particularly testosterone. This is central to Prof Baron-Cohens
argument, since he claims that the "essential difference" between men and women
is that men are systemisers and women empathisers. Of course, he is talking
about population averages here, and for individuals things are not so black and
white.
The results of our study may then go some way towards explaining the
perceived sex differences in the arts and the sciences.
Finally, perhaps most tantalisingly, Prof Baron-Cohen has used a similar test
to demonstrate that people who suffer from Aspergers syndrome (a
high-functioning form of autism) score very high on systemising and very low on
empathising. And Asperger individuals - usually men - are far more likely to be
found in the sciences, particularly the "hard" sciences like maths and
engineering.
The Glasgow Science Centre lecture will look more closely at just how
scientists and artists brains might differ, and whether these differences are
environmentally or culturally mediated, or innate.
On the way, I will look at the recent discovery of a brain area that is
thought to be the basis for mathematical ability, and what happens when it goes
wrong.
Ill also look at artistic creativity, through the remarkable story of a
56-year-old builder who developed a profound sense of creativity following a
stroke, and how we might all tap into our creativity.
Dr Mark Lythgoe is a neurophysiologist at University College, London. His
lecture is at the Glasgow Science Centre at 7pm next Thursday. He was assisted
in data analysis by Tom Pollak, a visiting research psychologist.
* * *
The Autism Pandemic and the MMR Vaccine Connection.
[Paul Watson, Past President of the Autism Society of Collin County Texas.]
This is published research showing a strong correlation to the MMR vaccine
programs in the United States and England and the Pandemic increase in Autism
from 1 in 10,000 births to 1 in 150 births in the last 20 some years. The
response by the "Conventional Wisdom" of the medical community and government
agencies has been to attack the reputation of the researchers and the parents of
the Autism children rather than investigate the potential causes of this
pandemic. The majority of the sponsored research as a reaction to the
controversy has been to analyze population records that only record vaccine
reactions typically reported in the first weeks after a vaccine, ignoring the
fact that a majority of Autism cases are not identified until children enter
early childhood and school programs at age 3 to 7 years old long after any
connection to a vaccine reaction can be identified much less reported back to
the vaccine tracking systems.
These first published responses were what scientist would term as bad science
"hit pieces" whose sole purpose was to placate the public about the safety of
the system rather than to identify any new causes for the Autism increases. They
would say we analyzed the records of thousands of reported reactions and can not
find any connection, simply ignoring the huge increase in the rates of Autism or
the thousands of clinical cases and reports of parents. It reminds me of a scene
in the movie "The Wizard of OZ" when Dorothy was talking to the great OZ asking
for help and her dog Toto pulled back the curtain exposing the little old man
talking on a microphone who then said "Ignore the man behind the curtain, the
Great OZ has spoken" Vaccines are safe and their is no MMR connection! The first
published research on the Vaccine-Autism link was in 1998 yet it was not until
2004 that any real studies of Autism were funded by these same government and
medical establishments.
http://www.usatoday.com/news/health/2004-02-24-autism-usat_x.htm
A major U.S.-financed study designed to unearth the roots of autism will track
100,000 babies in Norway to identify biological and environmental factors that
could combine to cause autism and other developmental disorders.
There has been a plethora of emotional attacks by the medical and government
establishment against the researchers and the Autism community for being
anti-vaccine and quacks. The establishment keeps saying it can not be the
vaccines because we all know they are safe and the good of the herd is more
vital than the damage to individuals.
All the stunned parents are able to do is request direct research funding
into the clinical analysis of individuals with Autism and double blind studies
and long term follow up of vaccine programs. This emotional response by the
authorities seems to be the same as the Tobacco Industrys denial of the lung
cancer connection to cigarettes, the Catholic Churchs reaction to the Pedophile
priest crisis in the USA, and the English governments response to the outbreak
of Mad Cow Disease.
A "Reasonable Person" would expect the authorities to respond to the initial
reports by Wakefield by saying thats significant and important findings, and we
need to do immediate clinical research to replicate and further explore the
Vaccine connections with hands on science to find the sources and causes of
this. Instead they just re-publishing old data from statically flawed data bases
to prove the current Conventional Wisdom that there are no vaccine connections.
With no real reasons to go on all we can do is speculate that this emotional
and irrational response by the authorities is just the typical reaction of all
old bureaucratic institutions when they are first confronted with facts showing
they might have made a mistake. First it is denial, then attack the confronters,
next cover-up and hide the truth, and finally after overwhelming public
condemnation, begrudgingly give in to investigation and eventual reform.
We now know how Galileo felt when he attempted to educate the Vatican that
the Earth was no longer the center of the solar system
official: The Earth revolves around the sun, even for the Vatican. The Roman
Catholic Church has admitted erring these past 359 years in formally condemning
Galileo Galilei for entertaining scientific truths it long denounced as
anti-scriptural heresy. Unable to comprehend a non-literal reading of Scripture,
according to the commission, the judges feared that if Galileo's ideas were
taught, they would undermine Catholic tradition at a time when it was under
attack by Protestant reformers such as Martin Luther and John Calvin. The case
was important to him, John Paul said Saturday, because over the centuries it had
become "the symbol of the church's supposed rejection of scientific progress, or
of 'dogmatic' obscurantism opposed to the free search for truth."
I think today Andrew J. Wakefield is for Autism and MMR vaccines what Galileo
was to the Catholic Church.
The established safety of the childhood Vaccine program is the dogma of the
Medical Establishment of today.
God help you if you dare go against the established order of the universe.
Instead of funding more research with Wakefield he eventually was fired and
banished to the USA from England for daring to question the establishment.
A foot note to the controversy, Professor Paul Shattock MRPharmS O.B.E at the
England Autism Research Unit, University of Sunderland
http://osiris.sunderland.ac.uk/autism/ did some
un-published research looking back to when vaccines were individual shots given
more towards the 5 year old age instead of newborn to 2 years old and found that
the majority of Autism rates disappeared. His conclusion: all we have to do is
delay the shots until the kids have a more mature and robust immune system,
separate the combination shots into single shots and make sure they have no
signs of sickness or viral infections at the time of the injections or family
history of immune disorders. The English Government responded by outlawing the
individual Measles shots making it mandatory that only the MMR combination shot
can be given.
Why the Obsessive Compulsive disorder "OCD" need to inject all kids from day
1 to 18 months a "Reasonable Person" might ask? Simply that way the medical
establishment can insure all the kids are covered with vaccines and the human
herd is protected. That way its done, no follow up calls, hounding of parents
to come in for later follow up appointments or chasing poor people and illegal
immigrants who have poor well baby care follow up habits.
These are the facts: There has been a pandemic increase in the amount of
Autism cases in every state in the USA, England, Norway, and Ireland from about
1 in 10,000 to 1 in 150 births.
The huge increase in reported cases can not be due to better diagnosis or
reporting per California where all cases have been referred for clinical review
the same way with the same methods years before the recorded increases.
PCV 6 months: DTaP, Hib, PCV 6-18 months: Hep B, IPV 12-15 months: Hib, MMR6,
PCV 12-18 months: Var7 15-18 months: DTaP 4-6 years: DTaP, MMR, IPV 11-12 years:
Td** > 6 months:(annually) Influenza*** 1Hepatitis B vaccine. May be given at
any age for those not previously immunized.
2Diphtheria, tetanus, and acellular pertussis vaccine 3Haemophilus influenzae
type b vaccine 4Inactivated poliovirus vaccine 5Pneumococcal conjugate vaccine
6Measles, mumps, and rubella vaccine 7Varicella vaccine. May be given at any
visit after first birthday.
* Second dose should be administered at least 1 month after the first dose.
** Tetanus booster. Delay if less than 5 years since last tetanus vaccine
injection.
*** Influenza vaccine is recommended every year for high-risk children older
than 6 months. High-risk groups include but are not limited to children with
asthma, heart problems, sickle cell anemia, diabetes, and human immunodeficiency
virus (HIV). The American Academy of Pediatrics encourages the parents of all
infants 6 to 23 months old to immunize their children against the influenza
virus. Annual vaccination is available for other children if desired.
Types of Vaccines Four different types of vaccines are currently
available: Attenuated (weakened) live viruses are used in some vaccines such
as in the measles, mumps, and rubella (MMR) vaccine.
Killed (inactivated) viruses or bacteria are used in some vaccines, such as
in IPV.
Toxoid vaccines contain a toxin produced by the bacterium. For example, the
diphtheria and tetanus vaccines are actually toxoid vaccines.
Biosynthetic vaccines contain synthetic substances. The Hib vaccine is a
biosynthetic vaccine containing two antigens combined to form a conjugate
molecule that triggers the immune system to produce antibodies effective against
the naturally occurring bacterium.
Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive
developmental disorder in children A J Wakefield, S H Murch, A Anthony, J
Linnell, D M Casson, M Malik, M Berelowitz, A P Dhillon, M A Thomson, P Harvey,
A Valentine, S E Davies, J A Walker-Smith
Background We investigated a consecutive series of children with chronic
enterocolitis and regressive developmental disorder.
Methods 12 children (mean age 6 years [range 3-10], 11 boys) were referred to
a paediatric gastroenterology unit with a history of normal development followed
by loss of acquired skills, including language, together with diarrhoea and
abdominal pain. Children underwent gastroenterological, neurological, and
developmental assessment and review of developmental records. Ileocolonoscopy
and biopsy sampling, magnetic-resonance imaging (MRI), electroencephalography
(EEG), and lumbar puncture were done under sedation. Barium follow-through
radiography was done where possible. Biochemical, haematological, and
immunological profiles were examined.
Findings Onset of behavioural symptoms was associated, by the parents, with
measles, mumps, and rubella vaccination in eight of the 12 children, with
measles infection in one child, and otitis media in another. All 12 children had
intestinal abnormalities, ranging from lymphoid nodular hyperplasia to aphthoid
ulceration. Histology showed patchy chronic inflammation in the colon in 11
children and reactive ileal lymphoid hyperplasia in seven, but no granulomas.
Behavioural disorders included autism (nine), disintegrative psychosis (one),
and possible postviral or vaccinal encephalitis (two). There were no focal
neurological abnormalities and MRI and EEG tests were normal. Abnormal
laboratory results were significantly raised urinary methylmalonic acid compared
with age-matched controls (p=0·003), low haemoglobin in four children, and a low
serum IgA in four children.
Interpretation We identified associated gastrointestinal disease and
developmental regression in a group of previously normal children, which was
generally associated in time with possible environmental triggers.
The Yukon government plans to spend more than (Canadian) $9.5 million on
health programs in the Territory.
Health minister Peter Jenkins has announced that he'll give an additional
$3.1 million to Whitehorse General Hospital. He says some of that money will be
spent on a cardiac testing program.
More money will also be spent to support children and families with fetal
alcohol spectrum disorder and autism.
Close to $2-million will go to drug programs for seniors, like Pharmacare and
the Extended Benefits Program, as well as Chronic Disease and the Children's
Drug and Optical programs.
* * *
Childhood Autism 'Growing At An Epidemic Rate' in Hawaii
Honolulu - Childhood autism in Hawaii is growing at an epidemic rate,
according to Autism Society of Hawaii officials.
The state Department of Education has categorised more than 720 kids with
autism out of about 23,000 in special education in 2002, or about 3.1 per cent,
compared with 1 per cent nationally, said Naomi Grossman, the Autism Society of
Hawaii president.
"It's no longer just an alarming rate; it's an epidemic pace, and we're
really concerned because it could be due to a lot of things, like the Brick
Township in New Jersey," Grossman said.
In Brick Township, the federal Centers for Disease Control and Prevention
(CDC), found in 1998 that 6.7 out of every 1,000 children aged three to ten had
autism disorders. The rate - three times greater than in previous years -
suggested a possible geographic cluster. An investigation indicated the number
of cases could be affected by environmental factors as well as genetic
influences.
Usually diagnosed before the age of six, autism is a spectrum of
neuropsychiatric disorders affecting a person's ability to interact socially and
communicate, causing unusual and repetitive behaviour.
The number of Hawaii residents aged six to 22 diagnosed with autism rose to
528 in 2002 from 64 in 1993, according to Fighting Autism, a research and
advocacy organisation.
* * *
EDUCATION
The Special Education Muckraker
Newsletter, v. 2, no. 2, is now available on line at:
The headline is: USDOE - See No Rape, Hear No Rape, And Never, Never Speak Of
Rape.
No Child Left Behind mandated a study of "school sexual abuse." USDOE didn't
like the mandate, and sure doesn't like the report it commissioned and received
on March 1st. In fact, a USDOE spokesperson has already stated that USDOE will
not follow the recommendation from its own expert scholar to conduct a serious
nationwide study of school sexual abuse by educators. The feds previously
insisted that the name of the report be changed to remove any mention of the
recommended national study!
We are outraged. You should be, too. Unless you're a sexual molester working
in a public school, that is.
- Dee Alpert, Publisher, The Special Education Muckraker
COPYRIGHT NOTICE: The above items are copyright protected. They are for our
readers' personal education or research purposes only and provided at their
request. Articles may not be further reprinted or used commercially without
consent from the copyright holders. To find the copyright holders, follow the
referenced website link provided at the beginning of each item.
_________________________________________________________________
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DISCLAIMER: All
information, data, and material contained, presented, or provided here is for
general information purposes only and is not to be construed as reflecting the
knowledge or opinions of the publisher, and is not to be construed or intended
as providing medical or legal advice. The decision whether or not to vaccinate
is an important and complex issue and should be made by you, and you alone, in
consultation with your health care provider.
"A foolish faith in authority is the worst enemy of truth."
-- Albert Einstein, letter to a friend, 1901
"I know of no safe depository of the ultimate powers of the society but the people themselves, and if we think them not enlightened enough to exercise control with a wholesome discretion, the remedy is not to take it from them, but to inform their discretion by education."
-- Thomas Jefferson, letter to William C. Jarvis, September 28, 1820
"What's the point of vaccination if it doesn't protect you from the unvaccinated?"
-- Sandy Gottstein
"Who gets to decide what the greater good is and how many will be sacrificed to it?"