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April 6, 2000

Mr. Chairman, Honorable Dan Burton and members of the committee;

My name is Mary Norfleet Megson. I am a board-certified pediatrician,
Fellowship trained in Child Development, a member of the American Academy
of Pediatrics and Assistant Professor of Pediatrics at Medical College of
Virginia. I have practiced pediatrics for twenty-two years, the last
fifteen years seeing only children with Developmental Disabilities, which
include learning disabilities, attention deficit hyperactivity disorder,
cerebral palsy, mental retardation and autism.

In 1978, I learned as a resident at Boston Floating Hospital that the
incidence of autism was one in 10,000 children. Over the last ten years I
have watched the incidence of autism skyrocket to 1/300-1/600 children.1
Over the last nine months, I have treated over 1,200 children in my office.
Ninety percent of these children are autistic and from the Richmond area
alone. The State Department of Education reports that there are only 1522
autistic students in the state of Virginia.

MHMR agencies have created local infant intervention programs, and have had
a hard time keeping up with the numbers of delayed infants and toddlers. I
have served as advisor to the City of Richmond and the surrounding counties
as they have established entire programs for autistic children that fill
multiple classes in several schools in each district. The segment of
children with "regressive autism," the form where children develop normally
for a period of time then lose skills and sink into autism most commonly at
18-24 months of age, is increasing at a phenomenal rate. I am seeing
multiple children in the same family affected, including in the last week
four cases of "autistic regression" developing in four-year-old children
after their MMR and DPT vaccination. In the past, this was unheard of.

In the vast majority of these cases, one parent reports night blindness2 or
other rarer disorders which are caused by a genetic defect in a G protein,3
where they join cell membrane receptors, which are activated by retinoids,
neurotransmitters, hormones, secretin and other protein messengers. G
proteins are cellular proteins that upgrade or downgrade signals in sensory
organs that regulate touch, taste, smell, hearing and vision. They are
found all over the body, in high concentration in the gut and the brain:4
and turn on or off multiple metabolic pathways including those for glucose,
lipid, protein metabolism5 and cell growth and survival.6 Close to the age
of "autistic regression," we add pertussis toxin, which completely disrupts
G Alpha signals.7 The opposite G proteins are on without inhibition leading
to:8

       1. Glycogen breakdown or gluconeogenesis. Many of these children
          have elevated blood sugars. There is sixty-eight percent
          incidence of diabetes in parents and grandparents of these
          children.
       2. Lipid breakdown which increases blood fats that lead to
          hyperlipidemia. One-third of families has either a parent or
          grandparent who died from myocardial infarction at less than 55
          years of age and was diagnosed with hyperlipidemia.
       3. Cell growth differentiation and survival which leads to
          uncontrolled cell growth. There are 62 cases of malignancies
          associated with ras-oncogene in 60 families of these autistic
          children.9 The measles antibody cross reacts with intermediate
          filaments which are the glue that hold cells together in the gut
          wall.10 The loss of cell to cell connection interrupts aproptosis
          or the ability of neighboring cells to kill off abnormal cells.
          The MMR vaccine at 15 months precedes the DPT at 18 months, which
          turns on uncontrolled cell growth differentiation and survival.

Most families report cancer in the parents or grandparents, the most common
being colon cancer.10The genetic defect, found in 30-50% of adult cancers,
is a cancer gene (ras-oncogene). It is the same defect as that for
congenital stationary night blindness.11

G protein defects cause severe loss of rod function in most autistic
children.12 They lose night vision, and light to dark shading on objects in
the daylight. They sink into a "magic eye puzzle," seeing only color and
shape in all of their visual field, except for a "box" in the middle, the
only place they get the impression of the three dimensional nature of
objects. Only when they look at television or a computer do they
predictably hear the right language for what they see. They try to make
sense of the world around them by lining up toys, sorting by color. They
have to "see" objects by adding boxes together, thus "thinking in
pictures." Their avoidance of eye contact is an attempt to get light to
land off center in the retina where they have some rod function. Suddenly
mothers touch feels like sandpaper on their skin. Common sounds become like
nails scraped on a blackboard. We think they cannot abstract, but we are
sinking these children into an abstract painting at 18 months of age and
they are left trying to figure out if the language they are hearing is
connected to what they are looking at, at the same time.

The defect for congenital stationary night blindness on the short arm of
the X chromosome affects cell membrane calcium channels13 which, if not
functioning, block NMDA/glutamate receptors in the hippocampus,14 where
pathways connect the left and right brain with the frontal lobe. Margaret
Bauman has described a lack of cell growth and differentiation in the
hippocampus seen on autopsy in autistic children.15 The frontal lobe is the
seat of attention, inhibition of impulse, social judgement and all
executive function.

When stimulated, these NMDA receptors, through G proteins stimulate nuclear
Vitamin A receptors discovered by Ron Evans, et al Dec 1998.16 When
blocked, in the animal model, mice are unable to learn and remember changes
in their environment. They act as if they have significant visual
perceptual problems and have spatial learning deficits.17

Of concern the Hepatitis B virus protein sequence was originally isolated
in the gene for a similar retinoid receptor (RAR beta),18 which is the
critical receptor important for brain plasticity and retinoid signaling in
the hippocampus.19 After the mercury is removed, I understand we will
restart Hepatitis B vaccine at day one of life. Studies need to be done to
determine if this plays an additive roll in the marked increase in autism.

I am using natural lipid soluble concentrated cis form of Vitamin A in cod
liver oil to bypass blocked G protein pathways and turn on these central
retinoid receptors. In a few days, most of these children regain eye
contact and some say their "box" of clear vision grows. After two months on
Vitamin A treatment some of these children, when given a single dose of
bethanechol to stimulate pathways in the parasympathetic system in the gut,
focus, laugh, concentrate, show a sense of humor, and talk after 30 minutes
as if reconnected.20

This improves cognition, but they are still physically ill. When these
children get the MMR vaccine, their Vitamin A stores are depleted; they can
not compensate for blocked pathways. Lack of Vitamin A which has been
called "the anti-infective agent," leaves them immuno-suppressed. They lack
cell-mediated immunity. T cell activation, important for long term immune
memory, requires 14-hydroxy retro-retinol. On cod liver oil, the only
natural source of this natural substance, the children get well. The
parasympathetic nervous system is blocked by the second G protein defect.
These children are unable to relax, focus and digest their food. Instead,
they are in sympathetic overdrive with a constant outpouring of adrenaline
and stress hormones. They are anxious, pace, have dilated pupils, high
blood pressure and heart rate. These and other symptoms of attention
deficit hyperactivity disorder are part of this constant "fright or flight"
response. These symptoms improve on bethanechol.

I live in a small middle class neighborhood with twenty-three houses. I
recently counted thirty children who live in this community who are on
medication for ADHD. One week ago, my oldest son who is gifted but dyslexic
had twelve neighborhood friends over for dinner. As I looked around the
table, all of these children, but one had dilated pupils. After two and one
half months of taking vitamin A and D in cod liver oil, my son announced,
"I can read now. The letters don't jump around on the page anymore." He is
able to focus and his handwriting has improved dramatically. In his high
school for college bound dyslexic students, 68 of 70 teenagers report
seeing headlights with starbursts, a symptom of congenital stationary night
blindness.

I think we are staring a disaster in the face that has affected thousands
of Americans. The children with autism or dyslexia/ADHD are lucky. There
are many other children not identified, just disconnected.

We must direct all of our resources and efforts to establish
multidisciplinary centers to treat these children. Insurance companies
should pay for evaluations, both medical and psychiatric, and treatment.
These children are physically ill, immuno-suppressed with a chronic
autoimmune disorder affecting multiple organ systems. Funding to look at
etiology of autism, to identify children at risk prior to "autistic
regression," and to prevent this disorder is imperative. Implementing
vaccine policies that are safe for all children should become our first
priority.

Mothers from all over the country have brought pictures of their autistic
children to Washington this weekend. Most of these children were born
normal and lost to "autistic regression." Look into their eyes and you will
hear their silence.

Thank you

                                                         Mary N. Megson, MD