We Cured Our Son's Autism
by Karyn Seroussi
http://www.chetday.com/autismdiet.htm
When the doctors said our son would be severely disabled for life,
we set out to prove them wrong.
When the psychologist examining our 18-month-old son told me that
she thought Miles had autism, my heart began to pound. I didn't know
exactly what the word meant, but I knew it was bad. Wasn't autism
some type of mental illness -- perhaps juvenile schizophrenia? Even
worse, I vaguely remembered hearing that this disorder was caused by
emotional trauma during childhood. In an instant, every illusion of
safety in my world seemed to vanish.
Our pediatrician had referred us to the psychologist in August 1995
because Miles didn't seem to understand anything we said. He'd
developed perfectly normally until he was 15 months old, but then he
stopped saying the words he'd learned -- cow, cat, dance -- and
started disappearing into himself. We figured his chronic ear
infections were responsible for his silence, but within three
months, he was truly in his own world.
Suddenly, our happy little boy hardly seemed to recognize us or his
3-year-old sister. Miles wouldn't make eye contact or even try to
communicate by pointing or gesturing. His behavior became
increasingly strange: He'd drag his head across the floor, walk on
his toes (very common in autistic children), make odd gurgling
sounds, and spend long periods of time repeating an action, such as
opening and closing doors or filling and emptying a cup of sand in
the sandbox. He often screamed inconsolably, refusing to be held or
comforted. And he developed chronic diarrhea.
As I later learned, autism -- or autistic spectrum disorder, as
doctors now call it -- is not a mental illness. It is a
developmental disability thought to be caused by an anomaly in the
brain. The National Institutes of Health estimates that as many as 1
in 500 children are affected. But according to several recent
studies, the incidence is rapidly rising: In Florida, for example,
the number of autistic children has increased nearly 600 percent in
the last ten years. Nevertheless, even though it is more common than
Down syndrome, autism remains one of the least understood
developmental disorders.
We were told that Miles would almost definitely grow up to be
severely impaired. He would never be able to make friends, have a
meaningful conversation, learn in a regular classroom without
special help, or live independently. We could only hope that with
behavioral therapy, we might be able to teach him some of the social
skills he'd never grasp on his own.
I had always thought that the worst thing that could happen to
anyone was to lose a child. Now it was happening to me but in a
perverse, inexplicable way. Instead of condolences, I got
uncomfortable glances, inappropriately cheerful reassurances, and
the sense that some of my friends didn't want to return my calls.
After Miles' initial diagnosis, I spent hours in the library,
searching for the reason he'd changed so dramatically. Then I came
across a book that mentioned an autistic child whose mother believed
that his symptoms had been caused by a "cerebral allergy" to milk.
I'd never heard of this, but the thought lingered in my mind because
Miles drank an inordinate amount of milk -- at least half a gallon a
day.
I also remembered that a few months earlier, my mother had read that
many kids with chronic ear infections are allergic to milk and
wheat. "You should take Miles off those foods and see if his ears
clear up," she said. "Milk, cheese, pasta, and Cheerios are the only
foods he'll eat," I insisted. "If I took them away, he'd starve."
Then I realized that Miles' ear infections had begun when he was 11
months old, just after we had switched him from soy formula to cow's
milk. He'd been on soy formula because my family was prone to
allergies, and I'd read that soy might be better for him. I had
breast-fed until he was 3 months old, but he didn't tolerate breast
milk very well -- possibly because I was drinking lots of milk.
There was nothing to lose, so I decided to eliminate all the dairy
products from his diet.
What happened next was nothing short of miraculous. Miles stopped
screaming, he didn't spend as much time repeating actions, and by
the end of the first week, he pulled on my hand when he wanted to go
downstairs. For the first time in months, he let his sister hold his
hands to sing "Ring Around a Rosy."
Two weeks later, a month after we'd seen the psychologist, my
husband and I kept our appointment with a well-known developmental
pediatrician to confirm the diagnosis of autism.
Dr. Susan Hyman gave Miles a variety of tests and asked a lot of
questions. We described the changes in his behavior since he'd
stopped eating dairy products. Finally, Dr. Hyman looked at us
sadly. "I'm sorry," the specialist said. "Your son is autistic.
I
admit the milk allergy issue is interesting, but I just don't think
it could be responsible for Miles' autism or his recent
improvement."
We were terribly disheartened, but as each day passed, Miles
continued to get better. A week later, when I pulled him up to sit
on my lap, we made eye contact and he smiled. I started to cry -- at
last he seemed to know who I was. He had been oblivious to his
sister, but now he watched her play and even got angry when she took
things away from him. Miles slept more soundly, but his diarrhea
persisted. Although he wasn't even 2 yet, we put him in a special-ed
nursery school three mornings a week and started an intensive one-on-one behavioral and language program that Dr. Hyman approved of.
I'm a natural skeptic and my husband is a research scientist, so we
decided to test the hypothesis that milk affected Miles' behavior.
We gave him a couple of glasses one morning, and by the end of the
day, he was walking on his toes, dragging his forehead across the
floor, making strange sounds, and exhibiting the other bizarre
behaviors we had almost forgotten.
A few weeks later, the behaviors briefly returned, and we found out
that Miles had eaten some cheese at nursery school.
We became completely convinced that dairy products were somehow
related to his autism.
I wanted Dr. Hyman to see how well Miles was doing, so I sent her a
video of him playing with his father and sister. She called right
away. "I'm simply floored," she told me. "Miles has improved
remarkably. Karyn, if I hadn't diagnosed him myself, I wouldn't have
believed that he was the same child."
I had to find out whether other kids had had similar experiences. I
bought a modem for my computer -- not standard in 1995 -- and discovered an
autism support group on the Internet.
A bit embarrassed, I asked, "Could my child's autism be related to
milk?"
The response was overwhelming.
Where had I been? Didn't I know about Karl Reichelt in Norway?
Didn't I know about Paul Shattock in England? These researchers had
preliminary evidence to validate what parents had been reporting for
almost 20 years:
Dairy products exacerbated the symptoms of autism.
My husband, who has a Ph.D. in chemistry, got copies of the journal
articles that the parents had mentioned on-line and went through them
all carefully. As he explained it to me, it was theorized that a subtype
of children with autism break down milk protein (casein) into peptides
that affect the brain in the same way that hallucinogenic drugs do.
A handful of scientists, some of whom were parents of kids with autism,
had discovered compounds containing opiates -- a class of substances
including opium and heroin -- in the urine of autistic children. The
researchers theorized that either these children were missing an enzyme
that normally breaks down the peptides into a digestible form, or the
peptides were somehow leaking into the bloodstream before they could
be digested.
In a burst of excitement, I realized how much sense this made. It explained
why Miles developed normally for his first year, when he drank only
soy formula. It would also explain why he had later craved milk: Opiates
are highly addictive. What's more, the odd behavior of autistic children
has often been compared to that of someone hallucinating on LSD.
My husband also told me that the other type of protein being broken
down into a toxic form was gluten -- found in wheat, oats, rye, and
barley, and commonly added to thousands of packaged foods. The theory
would have sounded farfetched to my scientific husband if he hadn't
seen the dramatic changes in Miles himself and remembered how Miles
had self-limited his diet to foods containing wheat and dairy. As far
as I was concerned, there was no question that the gluten in his diet
would have to go. Busy as I was, I would learn to cook gluten-free meals.
People with celiac disease are also gluten- intolerant, and I spent
hours on-line gathering information.
Within 48 hours of being gluten-free, 22-month-old Miles had his
first solid stool, and his balance and coordination noticeably
improved. A month or two later, he started speaking -- "zawaff" for
giraffe, for example, and "ayashoo" for elephant. He still didn't
call me Mommy, but he had a special smile for me when I picked him
up from nursery school. However, Miles' local doctors -- his
pediatrician, neurologist, geneticist, and gastroenterologist --
still scoffed at the connection between autism and diet.
Even though dietary intervention was a safe, noninvasive approach to
treating autism, until large controlled studies could prove that it
worked, most of the medical community would have nothing to do with
it. So my husband and I decided to become experts ourselves. We began
attending autism conferences and phoning and e-mailing the European
researchers. I also organized a support group for other parents of autistic
children in my community. Although some parents weren't interested in
exploring dietary intervention at first, they often changed their mind
after they met Miles. Not every child with autism responded to the diet,
but eventually there were about 50 local families whose children were
gluten- and casein-free with exciting results. And judging by the number
of people on Internet support lists, there were thousands of children
around the world responding well to this diet.
Fortunately, we found a new local pediatrician who was very
supportive, and Miles was doing so well that I nearly sprang out of
bed each morning to see the changes in him. One day, when Miles was
2 1/2, he held up a toy dinosaur for me to see. "Wook, Mommy, issa
Tywannosauwus Wex!" Astonished, I held out my trembling hands. "You
called me Mommy!" I said. He smiled and gave me a long hug.
By the time Miles turned 3, all his doctors agreed that his autism
had been completely cured. He tested at eight months above his age
level in social, language, self-help, and motor skills, and he
entered a regular preschool with no special-ed supports. His teacher
told me that he was one of the most delightful, verbal,
participatory children in the class.
Today, at almost 6, Miles is among the most popular children in his
first-grade class. He's reading at a fourth-grade level, has good
friends, and recently acted out his part in the class play with
flair. He is deeply attached to his older sister, and they spend
hours engaged in the type of imaginative play that is never seen in
kids with autism.
My worst fears were never realized. We are terribly lucky.
But I imagined all the other parents who might not be fortunate
enough to learn about the diet. So in 1997, I started a newsletter
and international support organization called Autism Network for
Dietary Intervention (ANDI), along with another parent, Lisa Lewis,
author of Special Diets for Special Kids (Future Horizons, 1998).
We've gotten hundreds of letters and e-mails from parents worldwide
whose kids use the diet successfully. Although it's best to have
professional guidance when implementing the diet, sadly, most
doctors are still skeptical.
As I continue to study the emerging research, it has become
increasingly clear to me that autism is a disorder related to the
immune system. Most autistic children I know have several food
allergies in addition to milk and wheat, and nearly all the parents
in our group have or had at least one immune-related problem:
thyroid disease, Crohn's disease, celiac disease, rheumatoid
arthritis, chronic fatigue syndrome, fibromyalgia, or allergies.
Autistic children are probably genetically predisposed to immune-
system abnormalities, but what triggers the actual disease?
Many of the parents swore that their child's autistic behavior began
at 15 months, shortly after the child received the MMR (measles,
mumps, rubella) vaccine. When I examined such evidence as photos and
videotapes to see exactly when Miles started to lose his language
and social skills, I had to admit that it had coincided with his
MMR -- after which he had gone to the emergency room with a
temperature of 106°F and febrile seizures.
Recently, a small study was published by British researcher Andrew
Wakefield, M.D., linking the measles portion of the vaccine to
damage in the small intestine -- which might help explain the
mechanism by which the hallucinogenic peptides leak into the
bloodstream.
If the MMR vaccine is indeed found to play a role in triggering
autism, we must find out whether some children are at higher risk
and therefore should not be vaccinated or should be vaccinated at a
later age.
Another new development is giving us hope: Researchers at Johnson
and Johnson's Ortho Clinical Diagnostics division -- my husband
among them -- are now studying the abnormal presence of peptides in
the urine of autistic children.
My hope is that eventually a routine diagnostic test will be
developed to identify children with autism at a young age and that
when some types of autism are recognized as a metabolic disorder,
the gluten and dairy-free diet will move from the realm of
alternative medicine into the mainstream.
The word autism, which once meant so little to me, has changed my
life profoundly. It came to my house like a monstrous, uninvited
guest but eventually brought its own gifts. I've felt twice blessed -
- once by the amazing good fortune of reclaiming my child and again
by being able to help other autistic children who had been written
off by their doctors and mourned by their parents.
Adapted from the book Unraveling the Mystery of Autism and Pervasive
Developmental Disorder: A Mother's Story of Research and Recovery by
Karyn Seroussi. Published by Simon & Schuster February 2000.
For more info, contact:
The Autism Network for Dietary
Intervention (ANDI)
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