Son-Rise program expanded main bar

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Son-Rise program expanded main bar
Alternate Title:
Breaking barriers + building bridges to the future...
Townsend-Rogers, Jason
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College of Journalism and Communications, University of Florida
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Autistic disorder ( jstor )
Behavioral analysis ( jstor )
Child psychology ( jstor )
Eye contact ( jstor )
Funding ( jstor )
Parents ( jstor )
Sons ( jstor )
Start up firms ( jstor )
Treatment programs ( jstor )
Volunteerism ( jstor )


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Son-Rise Program Expanded Main Bar Jason Townsend-Rogers

Arriving in a room full of observers dressed as Cookie Monster from "Sesame Street" is
not something many people would attempt. Yet it proved the best way for Susan Nelson to
communicate with her son Jake, and it gave her the reassurance she needed to address her

"If I can go into a playroom dressed up as Cookie Monster, sing, dance and act like a
crazy person with an observation room full of people watching me, then I can stand up here and
express to people that I love how grateful I am for the experiences of the last 18 months," she

Nelson delivered this speech at the Autism Treatment Center in Sheffield, Mass. The
center is the home of the Son-Rise program, a method of treatment for people with autism, a
disorder that affects the brain's development of social and communicative skills.

Autism is also a spectrum disorder, meaning that it affects different people in different
ways. Individuals with autism diagnoses can display repetitive behaviors and possess obsessive
interest in specific subjects or topics. One autistic person can turn his fixated interest in bone
structure into a Ph.D, while another can have problems speaking from birth, thus having
difficulty developing mentally.

The varying presentations of autism have made settling on a definitive means of
treatment difficult. Research into the nature of autism has yielded both official and unofficial
therapies for handling this disorder, with each of these treatments its own specific stories of both
success and failure.

Autism's unpredictability in terms of its diagnosis and its treatments leaves parents at a
loss as to the choice of the most effective method of therapy. Susan Nelson faced this situation
with her 3-year-old son Jake, and recounted her earliest experiences with his diagnosis, when she
received her certification as a Son-Rise Program Child Facilitator.

"He didn't speak or look at us," she said. "He rolled his little toy cars around, and he
stared at the wheels."

After doctors told her that Jake would never be able to function normally, Susan began
searching for ways to help her son. When she found the Autism Treatment Center of America,
she knew she had made the right choice.

"I thank God every day that this place exists and that you people are here," she said, "and
now I thank God that I am a part of it."

Many of the parents interviewed for this story echo Susan's sentiments about the impact
of the Son-Rise program on their children and endorse the program's methods and principles.

These parents have also looked to the program when other methods of treatment, such as ABA
(Applied Behavioral Analysis) Therapy, proved unsuccessful.

The Son-Rise program, originated by Barry and Samahira Kaufman, centers on complete
respect and acceptance of a child, regardless of his or her disability. It also encourages parents,
whom the program describes as the child's best advocates, to look at autism as a disorder that
inhibits social interactions rather than a disorder that results in unusual behaviors.

According to the Son-Rise program, children on the autistic spectrum the range of
syndromes related to autism benefit best in a distraction-free environment that counters the
excessive stimuli present in the outside world. The main advantage of these environments is
increased interaction, which helps children on the autism spectrum, the Kaufmans say.

Son-Rise's approach of emphasizing the role of children and parents in autism treatment
contrasts with applied behavioral analysis, the more scientifically familiar and endorsed method
of autism treatment.

Where ABA mentions the role of therapists in treatment and highlights the skills that
these therapists teach to their children, Son-Rise encourages parents to have an active role in
their child's treatments and encourages them to set the pace during their time together.

This child-centered approach would appear to fit parents who distrust the influences of
therapists and specialists' views on autism treatment. However, these perceived advantages of
the Son-Rise program also have caveats. Steven Wertz, who has served as a Son-Rise teacher for
13 years and is now the founder of the Growing Minds Program in Jupiter, Fla., believes that
Son-Rise is a valuable method for helping children with autism spectrum disorders, but views the
program as merely a facilitator that addresses some problems, but not others.

"The Son-Rise program is strong in strengthening the quality of relationships which the
child with autism shares with people. It can also help children develop better eye contact,
attention, affection and communication," said Wertz.

"However, Son-Rise is weak on effectively assessing developmental skills, cognitive and
core language and motor difficulties, along with visual anomalies. It is also weak in designing
core therapeutic programs and core curriculum that would effectively address the problems that
are left over after a child is enjoying greater intimacy with their adult teachers and caregivers."

The significant improvement in relations between children and their parents are cited as a
key benefit of the Son-Rise program, one that scholarly articles are quick to point out in their

K.R. Williams and J.G. Wishart analyzed the effect that the Son-Rise program has on
families in a research study titled "The Son-Rise Program Intervention for Autism: An
Investigation Into Family Experiences." Their method of study involved them giving three

questionnaires during a single year to parents who attended a Son-Rise start-up course. They
found that most parents felt that much closer to their children, with one respondent noting that as
they got to know their child, it helped in them becoming closer as well.

However, other parents who participated in the study pointed out that as much time as
they spend with their autistic child, it can come at the expense of their other children. One such
group of parents noted that their daughter felt jealous that no one came to spend time with her.

This last response highlights one of the key challenges of the program: the fact that it
requires a significant investment in time, money and human resources.

"In addition to taking care of Narottam and running his Son-Rise program, I also have to
tend to the needs of his younger brother, Chaitanya," said Marie Trempe."

"This is in addition to focusing on fund-raising for Son-Rise. It is too much for me to
handle at one time, as we can't afford to pay out-of-pocket."

This difficulty is why Son-Rise parents seek out helpers and volunteers to spend time
with their children when they are unable to do so. Understandably, Son-Rise parents hold these
individuals in high regard.

"I look at my volunteers as props. Each one that you bring has different qualities, and
thus able to deliver the Son-Rise program to my daughter in different ways," Barbara Fernandez

However, much like time and money, volunteers are also a finite resource, since many of
them have other commitments that sometimes conflict with their Son-Rise duties. Managing
these resources is a challenge that every Son-Rise parent faces.

The risks that are present in Son-Rise mirror the inherent challenges present in
implementing any autism treatment program. There is never complete certainty that the child will
respond to any treatment method offered. Parents may want to quit because of the tremendous
commitment of time and money that are required in the treatment of autistic children.

In fact, these inherent challenges in implementing an autism treatment program often lead
parents to experiment, adding their own unique traits to established norms. This is a point that
K.R. Williams makes clear in "The Son-Rise Program Intervention for Autism: Prerequisites For

The goal of Williams' study was to profile parents who adopted the program and gain a
better understanding of how they apply it. A parent named "Mrs. B" noted that in her application
of Son-Rise, she included her daughter or the children of volunteers, which contrasted from Son-
Rise's typical one-on-one approach. Another pair of parents, code-named "Mrs. E" and "Mrs. F"
emphasized academic progress in addition to Son-Rise's main goals of socialization.

The Autism Treatment Center's web site encourages parents to combine the principles of
the Son-Rise program with other complementary therapies, such as adopting alternative diets,
sensory integration and biomedical intervention. Most Son-Rise parents adopt at least one of
these therapies.

For instance, the Rogenys employ a GAPS protocol diet for their 8-year-old son, Zane,
alongside their Son-Rise program. This approach, originated by Dr. Natasha Campbell McBride,
emphasizes diet, detoxification and supplementation.

In applying this approach, McBride first states that all dairy products be eliminated from
the diet of an autistic child because she has seen that their removal has resulted in children that
have better eye contact and communication, as well as corrections in eczema and asthma.

In addition, other parts of the GAPS protocol include implementing supplements such as
Vitamin A & D in the form of fermented cod liver oil, which can help in building strong bones in
children and in the development of the brain and nervous system, and eliminating all sources of
exposure to toxic chemicals. This can include actions such as avoiding swimming pools with
chlorine in them and only purchasing items made out of cast iron or stainless steel, rather than

Implementing these alternative means speaks to the flexibility of these families, who are
willing to do what it takes to reach their children, all while maintaining the core Son-Rise
program concepts of unconditional love and acceptance.

Adhering to these mainstay views proved especially important for the Kaufmans when
they received a diagnosis of autism for their then 2-year-old son, Raun. Even though Raun
displayed no interest in the world around him and refused to interact with others, Barry and
Samahria said they saw a child full of spirit aching to be set free, but lacking the means to do so.

Ignoring the advice of medical experts who insisted that Raun's condition would forever
limit him, the Kaufman family worked with Raun at home for 212 years. By the time Raun was 4,
he would show no signs of his autistic condition.

Raun is now a Harvard graduate and the CEO of the Option Institute and his parents have
parlayed their success with Raun into movies and books that describe their story. Their efforts
also have been praised by parents and recognized by publications such as Parenting Magazine
and Self Magazine.

The Autism Treatment Center's website states that since the program's inception in 1983,
it has helped more than 22,000 parents and professionals around the world for the past 25 years.
Parents who participate often pay $2,000 for the Start-up program, $18,400 for the Intensive
Training class, $2,000 for the Maximum Impact course, $2,000 for the New Frontier course and
an additional $550 for phone consultation.

Given that high cost, parents need to be sure that the program is right for them. To help
them, Susan's husband, Brian, who works at the Autism Treatment Center as a family counselor,
consults with parents who wish to incorporate the Son-Rise program into their lives.

"What I do is offer free consultations to parents that are interested in the Son-Rise
program," Brian Nelson said. "These consultations are designed to make sure that what we are
offering is, one, what they are expecting and, two, really going to be relevant and helpful for
their child."

That there are many parents interested in an autism treatment program is borne out by
statistics. For example, the Centers for Disease Control and Prevention note that 1 out of 110
children in the United States have an autism spectrum disorder. Reports of such statistics have
raised awareness of autism around the world and have increased the importance of autism
treatment programs like Son-Rise.

However, though these reports paint a bleak picture of the autistic condition, Brian
Nelson believes autism is a temporary condition. "The symptoms present in children, while
different, all stem from one thing: These children have trouble relating and connecting with
people. As we create an environment with less distraction, situations where interaction is fun and
interesting, and prioritize building a connection, that impacts a change," he said. "When you
have a child's attention, when they choose to play with you, they will learn more than if they are
forced or acquiesced into doing so."

Jennifer Marks Borshiansky, who is adopting the Son-Rise program as a means to treat
her 6-year-old son Eidan, believes that the program's emphasis on distraction-free settings will
greatly benefit autistic children.

"Children with autism have very sensitive sensory systems and are frequently
overwhelmed by unpredictable and over-stimulating environments," Borshiansky said. "Hence, a
distraction-free space like the Son-Rise Program's playroom is incredibly beneficial for children
like these. Son-Rise playrooms create an environment where special children have space to learn,
grow, love, connect, and eventually find their way to our world."

The actions these parents are taking in adopting the Son-Rise program to help their
children recover from autism are a testament to their determination and persistence. One such
goal that each of them hope to achieve, along with steering their children on the road to recovery,
is to encourage individuals to obtain a better appreciation for individuals with autism.

"Individuals with autism have a sincere desire to connect with others," said Denise
Skinner, whose son Nathan received an autism diagnosis; "However, for that connection to take
place, they need to be accepted for who they are. Unfortunately, there is a stigma that exists
which says that individuals with autism do not want to connect with others, which is completely

Trying to remove this stigma has taken on increased importance in our society, especially
considering the fact that more individuals are receiving diagnoses of autism.

Advocacy organizations, celebrities and political figures have contributed in various
ways to raise the awareness of individuals diagnosed with autism and its related disorders, and
thereby reduce the stigma. Each has dedicated its efforts to informing the public of the
challenges in dealing with an autism spectrum disorder, and providing resources to aid parents in
taking care of their autistic children.

One such group, Autism Speaks, provides a weekly 100-day kit that provides aid to
parents taking care of their children in the days immediately following an autism diagnosis.
Components of the kit include how to establish a competent team of therapists, as well as how to
protect your home from your child's unpredictable behaviors.

Another organization, the Interactive Autism Network Project, focuses on removing the
isolation that families experience with an autism diagnosis, by connecting them with researchers
whose goals are to gain a better understanding of autism and share said understanding with these
families. The network's goal is that this research will help improve social services for people
with autism spectrum disorders.

Celebrities who have spoken out against the autism stigma have done so through the lens
of their own personal experiences. Actresses Jenny McCarthy and Holly Robinson Peete have
children with autism, and they have used their fame as a springboard to share their experiences
with the management of the disorder.

Both have written books, with McCarthy detailing her experiences in helping her son
overcome his autism diagnosis in her book "Louder than Words: A Mother's Journey in Healing
Autism." Peete, along with her husband Rodney, also have a son with autism, and have
contributed a pair of books about better understanding autism, titled "My Brother Charlie" and
"Not My Boy!: A Father, a Son and One Family's Journey through Autism."

In addition, both McCarthy and the Peetes have founded non-profit organizations to raise
awareness for autism. McCarthy founded, along with her former husband, Jim Carrey,
Generation Rescue, a non-profit organization dedicated to empowering parents of autistic
children and giving them the tools necessary intervention. The Peetes have since dedicated their
joint charity, the HollyRod Foundation, to greater autism awareness.

The government has directed their efforts towards research and treatment of autism. In
2000, then-president George W. Bush approved the Children's Health Act, with sections
dedicated to the funding of additional research and information on autism and pervasive
developmental disorders. In 2001, U.S. Reps. Chris Smith R-N.J., and Mike Doyle, D-Pa.,
founded the Congressional Autism Caucus to raise national attention for autism. In 2006, then-
president Bush would sign the Combating Autism Act in 2006. This act would allow for an

estimated $920 million for the next five years to go toward combating autism through biomedical
and environmental research, awareness campaigns, surveillance and early identification.

In 2007, then-Sen. Hillary Clinton introduced the Expanding the Promise for Individuals
with Autism Act, which dedicated $350 million in federal aid to improving autism treatments,
interventions, and services for individuals with autism spectrum disorders.

Along with the additional federal funding dedicated to autism treatment, research and
intervention, the Expanding the Promise for Individuals with Autism Act allows for the creation
of a task force that meets with Congress and the President and gives updates on the status of
biomedical and behavioral autism research. This act also allows for grants and protections for
families dealing with autism and other developmental disabilities. The House version of this act
is now in the House Energy and Commerce Committee, while the Senate version remains in the
Senate Committee on Health, Education, Labor, and Pensions.

Currently, President Obama is pledging to dedicate even more funding to autism
research, promising $210 million that will go toward funding studies that will help in increasing
autism awareness.

Pledging money toward research is an admirable goal. However, it is likely that little of
those funds will go toward funding for autism treatment programs, Son-Rise or otherwise. This is
because the majority of additional autism funding goes toward research.

Many parents say they would greatly appreciate any form of governmental assistance for
their Son-Rise program, especially if that assistance came in the form of additional funding.

"I would love to have government support for my Son-Rise program," said Becky
Givens. "Even though I have my own agency, we struggle with finances."

Of course, should the government decide to fund programs like Son-Rise, it could lead to
increased government stipulations for these programs, a scenario that would not sit well with
Karey and Kelley Rogeny.

"While government funding would be great to offset costs and provide assistance for
early intervention, taking on government funding ties you to government regulation, meaning
that strings will always be attached to said funding," Kelley Rogeny said.

Though opinions diverge as to how far they should go, allowing the government to
contribute in some capacity to autism treatment programs, specifically in offsetting costs, would
prove a boon to parents. This is especially so considering that an autistic individual can
accumulate $3.2 million costs over his or her lifetime, and that autism costs society $35 billion a
year in direct and indirect expenses each year, according to an April 2007 report in the Archives
of Pediatrics & Adolescent Medicine.

However, while more attention is being paid to autism awareness, understanding and
research thanks to the efforts of notable individuals in government and the arts, not enough
notice is being given to the inherent complexities that exist in autism. This lack of attention to
these intricacies makes it problematic for meaningful action to be taken. One such individual
who emphasizes this is Erin Healy of the Bureau of Autism Services in Pennsylvania.

In her report titled "Improving Autism Policies beyond the Enigma," she observes that
the inherent complexity in an individual autism diagnosis means that there are no federal
standards for diagnosing and treating autism or its related disorders. Although extensive research
has yielded greater understanding of autism and possible treatment solutions, the lack of a
definitive federal standard will result in families losing resources spent on treatments that have
little scientific support, according to Healy.

In addition, while young children with autism spectrum disorders are likely to obtain
some form of early intervention, adults on the autism spectrum are far less likely to get help.
That is because adults lose their access to special education services. The lack of assistance
forces them to fend for themselves, with not always favorable results. This is even more
devastating if there has not been early diagnosis and treatment

Finally, the services provided by the government for autism treatments, specifically
Medicaid and other services, require the families to fit specifications such as income brackets, or
go through special education programs. In addition, the programs offered tend to either focus on
autism spectrum disorders directly, while others tend to adopt a one-size-fits-all approach, which
ignores the unique aspects present in autism.

The inherent complexities that are present in autism, whether they exist in its treatment
programs, or research, mean that finding a straightforward means to comprehend and ultimately
overcome this disorder will prove difficult. This lack of understanding, however, should not have
to translate to fears surrounding the perceived limitations of autism.

"Autistic children are not crazy," Marie said. "They simply have trouble understanding
the world around them. They have tremendous potential, so do not sell them short simply
because you do not understand them."

"What I wish people knew about autism," David Borshiansky said, "is that the things that
they do that we may not understand actually do have a purpose, and we can use these things as a
starting point for getting to know more about them."

"In particular, we can use this information to change our view of autism as a cold and
unfeeling way of being by considering that these 'behaviors' or 'isms' are often means of coping
with an unpredictable, or even hostile, world."

Select Son-Rise Family Stories Jason Townsend-Rogers

Barbara Fernandez: Proving that Son-Rise is effective for parent and child alike

Barbara Fernandez and her 8-year-old daughter Anna have much in common. They both
have short, black hair, slender figures, black eyes and a curiosity to experience the world around

Barbara and Anna Fernandez also share one more thing: Both of them have been
diagnosed with autism, and both of them have seen it affect their lives.

The Son-Rise program has helped in uniting two distinct individuals who happen to share
a common diagnosis, while also proving that its methods are effective regardless of age.

"The Son-Rise program has helped me to recover off the spectrum, to the point where I
can feel normal both inside and out," she said.

Specifically, Barbara has been diagnosed with a higher functioning form of autism
known as Asperger's syndrome. She credits her personal experiences, coupled with the tools
provided by the Son-Rise method, in allowing her to reach her daughter.

Achieving that connection proved difficult at first because Anna, diagnosed at 3 years of
age, proved initially distant.

"She was emotionally disconnected from me," Barbara said. "We lived in the house
together, but we essentially had no relationship."

This disconnection extended to Anna's social behavior.

"Anna was socially isolated and would spend most of her time lying down, looking out
the window and making bird sounds," Barbara said. "She would also spend lots of time with her
dog, along with toys and electronics."

Anna's speech was also limited. Her first word was "cup" and she said nothing else after
that. She refused to have any type of conversation with Barbara, preferring instead to run away.

Anna's situation was complicated further by the fact that she also suffered from
claustrophobia. Her discomfort of being in enclosed spaces would lead to tantrums, so much so
that her mother ultimately decided against taking her anywhere.

The determination to reach her daughter led Barbara to seek the services of DAN (Defeat
Autism Now) doctors and to employ the gluten-free/casein-free diet. However, the results of this
diet were far from successful.

"We tried the diet, but it did not really help or work much. In fact, we tried many other
diets, with most of them yielding only subtle results." Barbara said.

Barbara found out about the Son-Rise program through an article in Mothering magazine,
a parenting publication. The article was part of a series that covered alternative autism
treatments. The article intrigued her, but she still had doubts.

"Doing this program meant that I had to invest a lot of my money and time, so if the
program did not work, it would be a huge gamble," she said.

"Also, $2,500 and a week's worth of time is a huge investment, especially considering
that other autism treatment programs are similar to this one in some way and do not always

Objections aside, Barbara said her time with the Son-Rise program has paid dividends for
her and her daughter.

"My biggest change with the Son-Rise program is that I have become more
understanding and patient," Barbara said.

Anna smiles more frequently than she once did, Barbara noted. She has a more positive
attitude, has improved her mastery of sentences and words and spends far less time "isming," or
stemming, which describes an autistic child's repetitive body movements that stimulate the
senses, such as flapping hands or slapping fingers.

"She now has an average of five- to six-word sentences and can say 12-word sentences as
well," Barbara said.

However, Barbara said, Anna's greatest improvement is her increased level of empathy.

"She now says 'I love you, mom!' to me," Barbara said.

These advances were possible through Barbara's efforts, along with her five-person
volunteer team. Barbara regards her volunteers highly because, she believes, they are important
to the Son-Rise experience.

"My volunteers are like props in that each one you bring in has different qualities. Each
of them is delivering the Son-Rise program in a different way," she said.

Barbara said that she hopes success stories like hers will get greater attention.

"I think that those people who draw the unlucky card of autism should receive some type
of assistance, as autism is something that can be cured, treated and helped."

Becky Givens: An ABA therapist embracing the warmth of Son-Rise

If knowing is half the battle when it comes to autism, then Becky Givens' level of
knowledge has allowed her to be more prepared than most when it comes to facing the
challenges inherent in this condition.

The source of this knowledge is due to Givens' time as an Applied Behavioral Analysis
therapist a therapy that involves using behavioral methods to measure behavior, teach
functional skills and evaluate progress.

Becky's experience as an ABA therapist proved especially advantageous when deducing
the early condition of Isaiah, her dark-skinned, brown-eyed 4-year-old son.

"I have been training children in autism for over 20 years, so I knew that he had autism
when he was 12 months old," she said. "However, we lost him when he was 9 months old. At
that time, he did not respond but instead stared at us blankly. He also failed to hear our voices."

Isaiah's autistic conditions were complex. He was self-injurious and non-verbal, lacked
eye contact with everyone except Becky, had no level of interaction and cried frequently. To
make Isaiah's living environment more favorable, Becky moved to a new house, which did little
to change the situation.

The move, she said, actually made his condition worse.

"The chemicals in the environment were making him sicker," she said.

In response, Becky tried modifying his diet and giving him various supplements.

"We started out by giving him Max GXL, a supplement that would boost his gluteus-iron
level. This resulted in a lot of positive changes, such as him being able to brush his teeth," she

She then tried azithromycin, an antibiotic that improved his speech. Becky noted that this
medicine, along with the Max GXL, contributed positively to his development.

"He could talk with the antibiotics, but adding the Max GXL made him a different child,"
she said. "He was able to hold a pencil and do lots and lots of things."

These positive results with azithromycin were unexpected, Becky admitted.

"I gave it to him one night, and he said 'Good morning,' to his brother Joshua the next
day," she said.

Becky's meeting with the Son-Rise program occurred at a conference in Orlando, where
she met Raun Kaufman. She was unfamiliar with the program despite the amount of time she
spent working with autistic children. "That conference changed my life," she said.

Becky has been a Son-Rise parent with Isaiah since June 2008. She has a series of paid
assistants, who are mainly college students. Becky pointed to Isaiah's improved speech,
increased willingness to let others engage, and a greater attention span as indicators of the
program's effect on him.

These positive results tend to clash with Becky's ABA training. She said it was difficult
to adapt to the differences in practice between Son-Rise and ABA.

"My biggest concern was that I was trained in not allowing the child to run the house,"
Becky said.

However, despite the fact that ABA and Son-Rise have their differences, Becky also
noted some similarities between them as well.

"For ABA therapy, we do certain things that we also do in Son-Rise. For instance, we
don't reinforce negative behavior."

As Becky continues with her Son-Rise training, she hopes the two schools of thought can
eventually merge into one, specifically having a Son-Rise philosophy achieve ABA results.

Becky is aware of the role that biomedical treatments have had in supplementing her Son-
Rise experience. She hopes that people see her success with the Son-Rise program, through the
eyes of a dedicated ABA therapist, will inspire other professionals to take a second look at cases
of autism.

"Kids with autism can recover," she said. "We professionals have programmed them to
think that this is not the case, which is absolutely not true."

Greg Milk: "I love and swear by Son-Rise"

In reflecting on his Son-Rise program experiences, Greg Milk came to a singular
realization: It was never about his children, it was always about the reactions of him and his

The serene looks given by Greg's kids, 5-year-old Caleb and 9-year-old Trinity, whom
Greg affectionately refers to as "his goats," were best reflected in their faces. While Trinity and
Caleb, two African-American children who each possess brown eyes and short black hair,
reacted to their autism diagnoses calmly, Greg and his wife were anything but.

"Trinity and Caleb were happy, almost in a state of peace," Greg said. "My wife, Isis, and
I, were the ones that were expressing concern."

Concerned about their condition, Greg and Isis Milk set out to obtain answers. They
initially tried Applied Behavioral Analysis therapy, a decision that Greg quickly regretted.

"It was almost like dog training," Greg said. "Every time Trinity would do something,
they would tell her 'no, no, no' and then forcibly show her the correct action. What they did kind
of weirded me out."

The Milks then tried Relationship Development Intervention therapy, which focuses on
relationship training that encourages the child to form bonds with his or her parents. To Greg,
this "made more sense" than ABA therapy.

One treatment method that did not make much sense to them was adopting the gluten
free/casein free diet. "We tried it for two years straight, almost becoming diet monks, but we did
not see any remarkable results," he said.

The Milks learned about the Son-Rise program when Isis read "Son-Rise: The Miracle
Continues" during a trip to the library. After reading about what the Kaufmans had gone through
for Raun, she discussed the program with Greg, who agreed to apply the book's principles to
their children.

"My wife and I love and swear by this book," Greg said.

The Milks have been Son-Rise parents since February 2009. Greg manages the program
with Caleb and Trinity while Isis works. Caleb gets 25 hours a week of Son-Rise time while
Trinity receives his full attention on the weekends.

Greg said the time spent with Caleb has resulted in him achieving greater eye contact and
an increased attention span. Nevertheless, he noted, one of the greatest changes that has occurred
since applying Son-Rise program principles has come from within himself.

"I love my kids more now," he said, "and I am more accepting of them."

To Greg, this greater acceptance and ability to connect with his children is far more than
any specific "goals" that are set on a timeline.

"People tend to look for quantitative results," he said. "When you hear three years, you
are instantly expecting results. Results might come, they might not; for me, it is all about
connecting with my kids."

Greg does not actively seek volunteer assistance in his Son-Rise program, preferring to
think of himself as an "artist" and see the results of his efforts first-hand.

He would appreciate, however, if the government played a more active role in funding
the Son-Rise program.

"There needs to be funding for families who have income that can't support their autistic
children," Greg said.

Denise Monert-Feliciano: "There is more to Son-Rise than just the technique."

Lack of eye contact and hearing, running in circles, and delays in speech are common
traits in children with autism, and they were present in Denise Monert-Feliciano's then 2-year-
old son, Joshua.

When observing the actions of her son, who possesses brown skin, black eyes and wavy
black hair, Denise was quick to notice that something was wrong, even though her occupational
therapist and pediatrician thought otherwise.

"I would continually ask them whether or not he was autistic," she said, "and they would
reply, 'No, we have seen autistic children before.'"

This skepticism did not stop Denise from looking to help her son, and once he received
his autism diagnosis when he was 3, she immediately began looking for treatments that would
benefit him.

Denise tried ABA therapy for a year, hoping that it would help Josh's development. The
results said otherwise, much to her disappointment.

"I was not happy with what was going on," she said. "I was not happy with the results
and the progress. I could see that my child was not motivated, and he looked like he was in a
depressed and tired state all of the time."

Undaunted, Denise continued researching. She came upon a Web site called "Kyle's Tree
house," a 501c3 organization that had been put together by Jenifer and Jeffery Westphal, who are
from Newtown Square, Penn., to help their autistic son, Kyle. Denise noted she had visited this
site one year earlier, but that something stood out with this return trip.

"This time, there was an actual video of Kyle talking and telling about the Son-Rise
program, as well as how to reach these children," she said.

The video proved inspirational for Denise, who then ventured to the source of the Son-
Rise program, the Web site for the Autism Treatment Center of America.

"The more I read about Son-Rise, the more Ijust knew that it was what we were going to
do," she said. "If I hadn't found this program on the Internet, I am afraid to even think about
where we would be."

Denise and her husband, Rico, have been Son-Rise parents for two years, starting after
returning from the Son-Rise Start-up Program at the end of February 2008. Her team consists of
her and her husband, along with three other volunteers, and they adhere to a 45-hour-a-week
program designed to help Joshua achieve his potential.

Denise describes her dedication to Son-Rise as "relentless," believing that applying the
program's principles of love, respect and acceptance should be done in and out of the playroom.

"We don't just do Son-Rise in the room. We live Son-Rise, and I think that makes a
difference," she said. "The Son-Rise program also encourages us to work on ourselves because
the better we are, the better attitudes we have, that will ultimately reflect on our children,
whether they are autistic or not."

Denise uses a video camera during her son's playroom sessions to monitor his actions,
noting such factors as eye contact and interactions with others. She then uses these reactions to
dole out feedback to the people that work with her on a frequent basis.

Denise makes sure that she pays those who contribute to her cause because she finds that
it helps in maintaining consistency and stability in her program.

"We have found that paying people is easier and more effective because we can help
dictate the hours and it is more of a set schedule in terms of training," she said.

These efforts by Denise and her team have strongly affected Joshua for the better, who is
now a happy child who possesses considerable energy, Denise said.

Denise also has observed that Joshua has greater eye contact than before, along with an
increased willingness to interact with others and greater speaking capabilities.

Denise said that she hopes that more individuals will look at stories like hers and draw a
different impression of autism.

"I want people to know that autism is not a tragedy," she said. "Recovery is possible, and
the way to achieve that recovery is to do it in a loving and accepting manner."

The Borshianskys: "Eidan is once again curious about his environment"

"Let's wait and see."

So said the very first pediatrician Jennifer and David Borshiansky consulted in an attempt
to figure out what was wrong with their son, Eidan. The Borshiankys needed answers as to why
their then 4-year-old son, the eldest of their children who is thin, wears glasses, and possesses
green eyes, was choosing not to speak, look at others, and have little interest in his environment.

Unwilling to accept this passive response, the Borshianskys sought out the counsel of
geneticists, developmental pediatricians, neurologists and medical officials who would be willing
to give them clues to their son's condition.

"We were hoping to receive a treatable diagnosis, rather than an incurable disorder like
autism," David Borshiansky said.

Jennifer and David Borshiansky also had to manage his cerebella hypoplasia and
hypotonia. The former left him with underdeveloped motor skills, while the latter meant he
possessed less muscular strength than other children his age.

Treating Eidan's aliments required the Borshianskys, of Scottsville, Va., to seek the
assistance of their state's early intervention program, which allowed him to receive aquatherapy,
vision therapy and hippotherapy, in which a therapist uses horse-style movements to assist in
sensory input.

The Borshianskys supplemented Eidan's early-intervention program with digestive
enzymes, nutritional supplements, shots and hyperbaric oxygen treatments. These would help in
caring for Eidan's other symptoms, but would prove ineffective in treating his autism.

The Borshiankys initially sought the services of an applied behavioral analysis specialist
to treat Eidan. They were not satisfied with the results, however, because they felt that the
regimented structure of ABA therapy did not fit in with Eidan's needs.

"We discontinued the therapy because the methodology did not respect Eidan in the way
that we wanted," David said.

"While the ABA therapist that worked with Eidan genuinely loved him, she would also
get very frustrated with him at times and manipulate him in a way that was too rough for our

The Borshianskys felt that the ABA therapy failed them because its practices did not
approach Eidan by accepting him, wanting his best, and working with him so that he is able to
achieve it.

After trying ABA therapy, the Borshianskys tried to focus their efforts on spending
individual time with Eidan, using the lessons learned from their ABA therapist. However, this
effort also proved disappointing.

"In the end, everything was expensive and disappointing," David said.

The Borshianskys then sought a program that could help them better understand Eidan's
autism diagnosis. Finding the right solution was important because their insurance was also
proving insufficient in terms of financing Eidan's various treatments and medical tests.

The Son-Rise program seemed to be a viable solution when they learned about it from
Suzanne Evans Morris, a speech therapist who did some work with the Autism Treatment
Center. Morris was referred to the Borshianskys by a therapist who knew Dr. Stanley Greenspan,
a psychiatrist who invented floor time therapy. They said they were excited about the program,
but hesitant about the financial commitment and the time and effort it required.

"An ideal Son-Rise program runs 10 to 12 hours a day, seven days a week, for an average
of three to five years," David noted. "Additionally, the training involved a costly weeklong trip
to Massachusetts that was well beyond our means, especially after years of medical expenses."

The Borshiankys turned to their family and friends for support, which allowed them to
obtain enough moral and financial backing to attend the Son-Rise Start-up program in
Massachusetts and return home with the resources necessary to start the program.

Since attending that start-up session on the last week of February 2008, the Borshiankys
have been dedicated Son-Rise practitioners. Their team, which includes them and three
volunteers, aims to equip Eidan with the social skills necessary to survive in an unpredictable

"Our goals are to develop the social fundamentals that form the basis for all learning and
are generally understood to be deficient in people with autism," David said.

Achieving this goal requires the Borshiankys and/or their volunteers to spend 50 to 60
hours a week with Eidan in a distraction-free playroom, allowing those inside to focus their
attention exclusively on Eidan.

Thanks to the program, Eidan has changed from a child who lacked curiosity and interest
in the world and the people in it, to a happy, vocal and fulfilled individual, his parents say.
Indeed, David praised the program for helping with improving his eye contact and allowing him
to walk independently.

"Also, Eidan is no longer non-verbal, and he has shown interest and curiosity about his
environment and he is now playing with toys that he has ignored for years," David said.

Additional Family Stories Jason Townsend-Rogers

Melinda Clerico: Son-Rise helped break the language barrier

Melinda Clerico has made it clear that the Son-Rise program has greatly enhanced the life
of her 4-year-old son, Riley Sheridan, and she is particularly effusive when recounting his
greatest achievement.

"Language, language and language," she said with pride in her voice.

Her singling out of language is fitting, considering that Riley's lack of speech initially
served as a key barrier during his early development.

"Other than language, the early stages of life for Riley were mostly normal," she said.
"He was a stiff baby and cried fairly often. He also had an affinity for me and no one else."

Yet everything changed 10 months later.

"Around 10 months after he received his MMR (measles, mumps and rubella) shots, he
lost the only word that he had ball," she said. "After that, he became a super stiff baby, needing
to be held even more. There were days that he was never out of my arms."

Riley was literally at a loss for words.

"His tears became the norm for him, as if they were his only words, yet they were never
accompanied by 'Mommy', 'Daddy', or 'I love you'," she said.

Riley also had problems adapting to his environment. He had to cover his eyes when
entering light and cover his ears when dealing with sounds. When Riley was 14 months, Melinda
expressed even more concern when, during a visit to the pediatrician, Riley could not identify
certain parts of his body.

"I asked the pediatrician why he could not find his nose," she said. "I have four other
children and they could all find their noses, but for Riley, no nose, ears or eyes."

Riley's situation forced Melinda to dedicate all her attention to him.

"All of this, plus much more, equaled no time for anything else," she said. "I couldn't
leave him and we couldn't go anywhere, so we didn't."

However, her extra time with Riley did not yield any additional clues as to how to handle
his condition. "We had no tools to deal with or understanding of whom or what he was," she

Melinda first attempted to alter Riley's diet. Going on advice that she had received from
her in-laws, Melinda put Riley on a gluten free/casein free diet and gave him cod liver oil. With
this change in diet, Riley became less agitated and held his dad's hand for the first time.

She also gave Riley a weighted vest and a stabilizing pressure input orthorsis (SPIO), a
flexible compression bracing system that helps with stability. The SPIO, along with the weighted
vest, helped in improving Riley's physical awareness by making him more cognizant of his
limbs and stabilizing his core and joints. Despite this progress, Melinda was still concerned that
he could not go anywhere easily.

Reading Jonathan Levy's book "What You Can Do Right Now to Help Your Child with
Autism" helped her better understand Riley's condition. She read and reread it and then showed
it to her family members.

Levy, a certified Son-Rise Family Trainer who has worked with autistic children since
1993, used his book to condense the Son-Rise method into 10 easy-to-understand principles, a
practice that Melinda quickly embraced.

"It was our first autism book, and it has shaped everything we did," she said. "It is very
simple, gracious and respectful of you and your child."

Newly inspired, Melinda placed several calls to Jan Marie Gundacker, a Son-Rise Family
Counselor, and after completing some forms her Son-Rise journey began. Her approach to the
Son-Rise Program is more family-based. She admits to never having a volunteer, an idea that she
herself finds "a bit scary," but finds that the lack of volunteers does not mean Riley lacks outside

"My other son, Gabriel, who is 5, is his number one therapist. He has taught Riley
everything," she said. "We have also had team members from Riley's school, such as the director
of the developmental playschool, come to play with Riley every week."

After adopting this approach, Riley has since become patient and can go to the store or
library without any difficulty. Melinda said that these gains complemented Riley's substantial
language progress.

"He went from 15 words at 2 years of age to 78 by June of 2008," Melinda said. At this
time, Riley was 2 years and 11 months old.

"After returning from the Son-Rise Start-up Program, a five-day training session that
gives parents the tools to start their home-based Son-Rise programs, Riley blossomed to 350
words in two weeks and now has a vocabulary well over 2,000 words," Melinda said.

The Rogenys: We did not want to be spectators in Zane's development

Every parent wants the best for their children, even when adversity threatens to limit their
promise. In Zane Rogney's case, his diagnosis of autism meant that there would always be a
ceiling on his potential.

"There was never a hope of anything more than teaching Zane to cope or gain skills that
would help him to be successful," Kelly Rogeny said. "There was no hope of healing or recovery
for him."

This was not enough for Karey and Kelley Rogeny, who were willing to do whatever it
took to see their 8-year-old son reach his potential.

They first tried taking Zane to speech therapists, occupational therapy and early
intervention. This meant Zane spent much of his early development under the care of
professionals, which did not please the Rogneys.

"We felt like spectators during this entire time," Karey said.

Karey and Kelley believed that they had to take a more active role in their son's
development. The first step in this process, they decided, was in altering his diet.

"We found with Zane that there could be biomedical imbalances due to the nutrition that
he is getting, so we removed gluten, casein, dyes and preservatives from his diet," Karey said.
"We also removed soy and sugar. In fact, after taking out sugar, we decided to take it a step
further and instituted the GAPS protocol, which is similar to a specific carbohydrate diet that
limits all carbohydrates."

Dr. Natasha Campbell McBride originated the GAPS protocol. It emphasizes a three-
pronged approach that includes diet, detoxification and supplementation. Applying this three-
way approach, McBride states that all dairy products be eliminated from the diet of an autistic
child, as she has seen that their removal has resulted in children that have better eye contact and
communication, as well as corrections in eczema and asthma.

McBride's other parts of the GAPS protocol include implementing supplements such as
Vitamin A & D in the form of fermented cod liver oil, which can help in building strong bones in
children and in the development of the brain and nervous system, and eliminating all sources of
exposure to toxic chemicals. This can include actions such as avoiding swimming pools with
chlorine in them and only purchasing items made out of cast iron or stainless steel, rather than

The Rogneys originally heard about Son-Rise through a local friend of theirs who had
attended the start-up program. The Rogneys researched Son-Rise and then decided to move

They said that given how much they had spent on speech and occupational therapy and
with diet alterations and specialist visits, Son-Rise had proven a good investment.

Still, one challenge the Rogenys have faced in their Son-Rise program is maintaining a
steady set of volunteers.

"Our Son-Rise program is not consistent as some of our volunteers have come and left.
Most have come for projects, others for service, but none have stayed on permanently," Kelley

Fortunately, the Rogenys have friends who ably contribute their time and efforts to
Zane's development, which has made it easier for Karey to focus on his job and take care of
Zane at the same time.

Since adopting the Son-Rise program, the Rogneys said they have seen the positive
strides Zane has made.

"There has been a large growth in attention span for Zane since Son-Rise," Kelley said,
"He also has greater eye contact and has become more comfortable in his own skin."

Zane enjoys the company of others a lot more since Son-Rise, Kelley adds, but he still
faces some minor challenges with social flexibility.

Challenges aside, Kelley hopes that Zane's progress will inspire other parents with
autistic children to view their situation more positively.

"So many think that there is nothing that you can do about autism, when that is not the
case," Kelley said. "There are many solutions that exist. The problem is that these solutions are
not common knowledge, thus parents choose not to pursue them or do anything about it."

Marie Trempe's Son-Rise Story Jason Townsend-Rogers

Marie Trempe: "First seek to understand, and then be understood."

Narottam Cecil's defining characteristics are his boundless energy and cheerful spirit,
traits that ably complement his slender figure, brown hair, blue eyes and gentle, caring smile. He
loves running around, bouncing on his trampoline, laughing and telling stories, especially when
they are about his favorite topic dinosaurs.

Narottam was not always this way, however, as obstacles more formidable than any
dinosaur or imaginary monster threatened to limit the energy this 10-year-old's ebullience would
bring into the world.

It all started at 21 months, an age at which many parents are merely concerned with
readying their children for new experiences and environments. Narottam's mother, Marie
Trempe, had a far more serious matter on her hands. At 21 months, Narottam suffered from
neuroblastoma, a cancer of the nerve cells, along with opsoclonus myoclonus syndrome, a rare
autoimmune disorder.

"Basically, his immune system was attacking the tumor, and then it went into overdrive
and started attacking the brain, thinking it was the tumor because the brain and the tumor are
both made up of nerve cells," she said.

"Narottam lost his speech and he could not walk because his immune system was
attacking the brain stem and the cerebellum," she said. "As these two parts deal with language
and emotions, Narottam would get rage attacks."

"He could not walk or talk and was shaking all over. His eyes were also moving all over
the place."

Marie was able to find a physician to treat Narottam's cancer, as well as another one who
cured him during its remission stage. Now, Narrottam's cancer no longer threatens his life.

However, that victory failed to prepare Marie for what would happen next.

"Because of what happened with Narottam's auto-immune disorder, he could not talk, so
when he returned to school, people saw some 'autistic-like' behaviors," she said. "They thought
that these behaviors were leftovers from the opsoclonus myoclonus syndrome, as they affected
his brain."

These behaviors led Narottam, 7 years old at the time, to be diagnosed with Asperger's
syndrome an autism spectrum disorder in which an individual has difficulties in social
interaction, combined with restricted and repetitive patterns of behavior and interests. This
diagnosis, along with his frequent visits to the hospital, made it difficult for him to keep and
retain friends.

"When Narottam was 4 or 5, he had no problem playing with kids his age," she said. "At
that time, kids are still innocent. Once those kids got older, though, they became more
sophisticated socially and they and Narottam grew apart."

Narottam's interest in dinosaurs failed to captivate his older peers. The fact that he did
not share in the pursuits of his older friends did not help matters.

"Narottam is not as physical as the other boys," Marie said. "The Opsoclonus myoclonus
impeded the development of his gross and fine motor skills. He does not like sports. As he grew
up, his interest in dinosaurs became narrower. He would know everything about them!"

Knowing everything about dinosaurs would be invaluable for anyone aspiring to be a
paleontologist, but it did not endear him to other children his age.

"Other kids would think that Narottam talks too much," Marie said. "They would also
tease him, but he would not realize it as he is not as socially perceptive as they are."

"He would laugh with the other kids, not knowing that they are really laughing at him."

These challenges, brought on by a combination of Narottam's complicated health and his
autism diagnosis, represented a significant hurdle for Marie to overcome.

"I was a little lost after everything that we went through," Marie said.

Her quest to find answers for Narottam's condition led her to seek the services of various
specialists. That, along with the dietary changes she made that consisted of removing specific
minerals and additives, brought mixed results.

The dietary changes led to positive gains. Already health conscious, Marie only had to
make incremental changes to Narottam's eating habits.

"Considering everything that I had already done regarding his health, I did not have to
change anything in his diet after realizing that he had autism," Marie said.

"Narottam was already on a sugar-free diet," Marie added. "I made sure to never give
him any processed food, or anything that contained white sugar or white flower."

Marie also eliminated acidic foods from his diet, including tomatoes, potatoes, eggplants
and bell peppers. Narottam's diet after these changes would consist mainly of gluten free/casein
free foods.

Along with these foods, Marie also employs medicinal herbs to supplement his diet.

"I give Narottam ayurvedic herbs, which are an ancient medicine from India," she said.
"These herbs help with his immune and nervous systems, along with his brain."

In addition to these dietary changes, Marie also employs craniosacral therapy. This
involves the use of a soft touch to enhance the craniosacral system, which includes membranes
and cerebrospinal fluid that surround and protect the brain and spinal cord.

Marie's visits to various specialists were not as constructive because she ended up
meeting specialists who focused more on the disease and less on the person.

"I first tried visiting a DAN (defeat autism now) doctor," Marie said. "Not only are they
extremely expensive, but they mainly deal with the problems rather than the child."

"The allopathic doctors that I visited were so used to treating children a certain way, that
when someone that is different shows up, they do not know what to do."

This realization forced Marie to take the lead in managing her son's health.

"Much ofNarottam's healing has come from my research on the Internet," she said.

This research has also led to Marie finding a neurologist who researched Opsoclonus
myoclonus disorder.

Marie's visit with the first doctor led to mixed results. While she credits him with
diagnosing his Opsoclonus myoclonus correctly, she was surprised that he possessed limited
experience in treating his condition.

"The neurologist who first diagnosed Narottam had never met a child that had
Opsoclonus myoclonus before," Marie said.

This led Marie to do her own research to find a neurologist that did research on this
disorder. Marie had to fight with her insurance in order to get them to approve his treatments
because he was out of state.

"It took a month and a half for them to give their endorsement," Marie said.

The ordeal that Marie had to go through to treat her son revealed the challenges of the
medical process, specifically how difficult it is to find treatment for an unfamiliar diagnosis.
However, this instance also reinforced her determination, as well as how far she was willing to
go to help her son.

"You really are on your own in this process," she said. "However, I am lucky to have an
amazing husband who stuck by us and fully supported us and in that I live in a wonderful
community where people are extremely supportive. Also, I am the type of mother that never
takes no for an answer."

This resolve and persistence would serve Marie well when it came to finally seeking the
key to figuring out Narottam's autism.

Marie first heard about the Son-Rise program when a friend of hers, Marie Glasheen,
visited the Option Institute in Massachusetts. While there, she saw the movie "Son-Rise: The
Miracle of Love."

Marie then invited Glasheen's daughter to babysit at her house. Once she arrived, she
presented Marie with a copy of the movie and a Son-Rise flier. At that moment, Marie knew that
she had struck gold.

"This program blew my mind," she said. "It was exactly what I wanted. A program based
on love and care. Other programs that I have tried have tended to force children to do things, a
method that I do not agree with."

Programs that help children with autism should focus on getting to know them, and not
vice versa, Marie said.

"Steven Covey once said that you should first seek to understand, and then be
understood," Marie said. "Many autism programs tend to focus on applying this saying in
reverse. That is why I found Son-Rise so great. It encourages you to go into the world of an
autistic child to try and understand them."

Marie called Brian Nelson, a family counselor with the Autism Treatment Center of
America, to learn more about the program. Brian instructed her on various Son-Rise techniques,
including how to use Narottam's motivations in a positive way. Marie found this delivered
instant results once she applied it.

"The day before his FCAT, I wrote a letter to Narottam and signed it 'T-Rex of the
Canyon,'" Marie said. "That letter motivated Narottam to focus for the test and he ended up
scoring higher than he had ever before."

That experience encouraged Marie to go forward with the Son-Rise program. She sped
through the transition thanks to a stable community of friends, discounts from the Option
Institute and help from her parents, who assisted in planning fundraisers that would help in
paying for the program's costs.

Marie has since dedicated a year and a half to the Son-Rise program. The results of her
efforts have led to a calmer, more patient child, one that is more flexible and willing to engage
with his environment, she said.

"Narottam used to have a lot of outbursts and tantrums every night before I started the
Son-Rise program," Marie said. "That has since stopped. His eye contact has increased
tremendously, and he is far more flexible than he was before. He used to have blinders on him
and he does not have that anymore."

These blinders refer to Narottam's laser-like focus on dinosaurs. Marie is trying to
encourage Narottam to appreciate the lives of others, and to be able to discuss topics other than
whether T-rexes are the most powerful beasts on the planet.

Crucial to Narottam's progress, Marie believes, are the addition of volunteers to her
program. Marie has three volunteers that she believes greatly enhance Narottam's Son-Rise

"Volunteers are great for the program as it allows other people to get to know Narottam
and see how great he is," Marie said. "Narottam also gets to learn about different types of
personalities, and he will also behave differently depending on the volunteer."

As Narottam continues to make progress, Marie hopes that more people will gain a
greater understanding and appreciation for individuals with autism.

"Autistic children are not crazy," Marie said. "They simply have trouble understanding
the world around them. They have tremendous potential, so do not sell them short simply
because you do not understand them."

Alternative Autism Treatments

The Son-Rise program is unique among methods of autism treatment, emphasizing child-
centered therapy and distraction-free settings over rote repetition. Yet it is not the only means of
therapy for children with autism spectrum disorders. Four distinct treatments are listed below,
and additional information on these and other therapies can be found at the National Autistic
Society at

Applied Behavioral Analysis (ABA Therapy)

The most familiar of the autism treatment methods because of extensive research and
scientific analysis, along with its being the only form of autism treatment recognized by
the Food & Drug Administration.

Teaches social, motor, verbal behaviors and reasoning skills using careful behavioral
observation and positive reinforcement, as well as prompting; when children perform a
specific behavior correctly, they are rewarded.

More information can be found at asp

Relationship-Development Intervention Therapy (RDI Therapy)

New, trademarked therapy developed by a husband-and-wife team of clinical
psychologists, Steven Gutstein, Ph.D., and Rachelle Sheely, Ph.D.

The program's central focus involves improving quality of life through the enrichment of
social skills, adaptability and self-awareness. This progression encompasses six main
objectives, which are emotional referencing, social coordination, declarative language,
flexible thinking, relational information processing, along with foresight and hindsight.

More information about can be found at

TEACCH (Treatment and Education of Autistic and Related Communication
Handicapped Children)

*Eric Schopler, Ph.D, who is a professor of psychiatry and psychology at the University of
North Carolina, Chapel Hill, founded the program in the 1970s. The program is unique
for establishing the "Culture of Autism," a distinctive approach to interpreting the various
characteristics associated with autistic individuals.

Key attributes of this culture include a preference for processing visual forms of
information above all else, along with difficulties in combining ideas, organizing
materials and activities and strong sensory preferences and dislikes.

The program's main goals include skill development while achieving a sense of
confidence, self-efficacy and a conscious engagement in fulfilling activities. Achieved
through employing the "Structured Teaching" method, which includes concepts such as
creating a personalized plan, rather than relying on a structured curricula, and including
visual supports in daily activities.

More information can be found at

Growing Minds Autism Program

This program was founded by Steven R. Wertz, who worked with the Option Institute for
23 years, from 1983-1998, as a senior teacher. He holds certification in both Son-Rise
program training and Applied Behavioral Analysis therapy.

Some of the program's key principles are that systematic education must be a part of
treatment for autistic children, effective therapy for autistic children must include
nurturing relationships for their parents and teachers, and programs must be tailored to fit
both the parent and the child rather than the parent or the child.

The Growing Minds Program advertises itself as an "alternative" to Son-Rise by offering
to balance social development with skill development, offering access to a broad
selection of methodologies and providing less of a financial strain.

More information can be found at

Helpful Information Related to Autism

Autism Treatment Center of America, Home of the Son-Rise Program:

Autism Speaks:

Autism Society of America:

Autism Network Project:

Centers for Disease Control and Prevention (Autism Spectrum Disorders):

The Option Institute:

Kyle's Tree house:

Locating a DAN (Defeat Autism Now) Doctor: Ic.htm

Relate to Autism:

Son-Rise: A Miracle of Love Movie (accessible on YouTube):

Son-Rise: The Miracle Continues by Barry Neil Kaufman:
Kaufman/dp/0915811618/ref=sr 1 1?ie=UTF8&s=books&qid=1271816323&sr=1-1

What You Can Do Right Now to Help Your Child with Autism by Jonathan Levy: