Cod Liver Oil to Heal Autism (Vaccinations)

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[MedicalConspiracies] Cod Liver Oil to Heal Autism (Vaccinations)

 

 

 

 

 

 

(Cod Liver Oil should be taken on an empty stomach, by doing it this

way your liver has a chance to do an oil exchange and expel the

toxins, if you take it with food it becomes food and not as effective)

 

http://www.newmediaexplorer.org/chris/2004/09/20/cod_liver_oil_to_heal_autism_va\

ccinations.htm

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Cod Liver Oil to Heal Autism (Vaccinations)

Categories

Health through Nutrition

Practical Health

Vaccinations

 

.... " When these children get the MMR vaccine, their vitamin A stores

are depleted and they cannot compensate for blocked pathways. Lack of

vitamin A, which has been called " the anti-infective agent, " leaves

them immunosuppressed. 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. " ...

 

See Also: MMR AND AUTISM: The link really has been established

 

It again boils down to nutrition - if only more people should focus on

it then one should not need the vaccines and or the toxic drugs in the

first place...Unfortunately, most remain oblivious of this as the

medical and associated governmental agencies continue to ignore it...

 

Following is another great article form the Weston Price Foundation, I

urge all to visit this site and support the excellent work that they

are doing...

 

Chris Gupta

 

Autism and Vaccinations

By Mary Megson, MD

 

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.

 

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. Yet the State Department of Education reports

that there are only 1,522 autistic students in the entire state of

Virginia.

 

MHMR (Mental Health Mental Retardation) agencies have created local

infant intervention programs, and they 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 several 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

blindness or other rarer disorders which are caused by a genetic

defect in a G protein, 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. They turn on or off

multiple metabolic pathways including those for glucose, lipid and

protein metabolism as well as cell growth and survival.

 

Close to the age of " autistic regression, " we add pertussis toxin,

which completely disrupts G alpha signals. The opposite G proteins are

turned on without inhibition leading to the following:

 

1. Glycogen breakdown or gluconeogenesis. Many of these children

have elevated blood sugars. There is a 68 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 [a cancer gene] in 60 families of these

autistic children.

 

The measles antibody cross reacts with intermediate filaments which

are the glue that hold cells together in the gut wall. 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. The genetic defect, found in 30-50 percent

of adult cancers, is a cancer gene (ras-oncogene). It is the same

defect as that for congenital stationary night blindness.

 

G-protein defects cause severe loss of rod function in most autistic

children. 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 where 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 mother's touch feels like sand-paper 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.

 

The defect for congenital stationary night blindness on the short arm

of the X chromosome affects cell membrane calcium channels which, if

not functioning, block NMDA/glutamate receptors in the hippocampus

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. The frontal lobe is the seat of attention, inhibition of

impulse, social judgment and all executive function.

 

When stimulated, these NMDA receptors through G proteins stimulate

nuclear vitamin A receptors discovered by Ron Evans and his colleagues

in December, 1998. 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.

 

Of concern is the fact that the hepatitis B virus protein sequence was

originally isolated in the gene for a similar retinoid receptor (RAR

beta), which is the critical receptor important for brain plasticity

and retinoid signaling in the hippocampus. 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 role 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 [a drug related to acetlycholene, a

substance that transmits nerve impulses] 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.

 

This improves cognition, but they are still physically ill. When these

children get the MMR vaccine, their vitamin A stores are depleted and

they cannot compensate for blocked pathways. Lack of vitamin A, which

has been called " the anti-infective agent, " leaves them

immunosuppressed. 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 rapid heart rate. These and

other symptoms of attention deficit hyperactivity disorder are part of

this constant " fight 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 nightblindness.

 

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

multi-disciplinary centers to treat these children. Insurance

companies should pay for evaluations, both medical and psychiatric,

and treatment. These children are physically ill, immunosuppressed

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 were lost to " autistic regression. " Look into

their eyes and you will hear their silence.

 

Editor's note: In addition to cod liver oil, children with

developmental disorders should be given a nutrient-dense diet that

includes plenty of calcium and other minerals. Additional vitamin D

may also be helpful. (See page 11.)

 

 

 

About the Author

 

Dr. Mary Megson is a board-certified pediatrician, trained in child

development, a member of the American Academy of Pediatrics and

assistant professor of pediatrics at the Medical College of Virginia.

This testimony was given April 6, 2000 at Senate hearings on autisim

and vaccinations. Parts of this article are technical.

 

For further information, see info

 

If you enjoyed this article, you might also be interested in reading:

 

Health Hazards of Mercury, By Eric Davis, DDS

 

Vitamin A Saga, by Sally Fallon and Mary G. Enig, PhD