Showing posts with label Media. Show all posts
Showing posts with label Media. Show all posts

Tuesday, January 12, 2010

Autism x 6 - How It All Started


This is the story in our local newspaper that started us on the road to "fame".


Autism x 6: Family's kids all have the disorder
By Angie Welling
Deseret Morning News
Published: Sunday, June 3, 2007 12:21 a.m. MDT

MURRAY — One minute they're sitting, the next they're gone. Off the couch and onto the rocking chair, into the corner of the room, anywhere but where they were.

The children move quickly, often too fast for their parents — or even the camera's lens — to catch them.

This speed, this constant flash of children, is why the Kirton house looks like it does: a veritable maze of locked doors and makeshift barricades that are designed to keep kids in, or out, of certain areas. It is why the Kirton parents can keep talking through just about anything, hardly raising their voices while 8-year-old Nephi has yet another "meltdown" as 5-year-old Sarah, aka "Tigger," bounces madly on the couch beside them.

After all, if John and Robin Kirton focused too much on these incidents, who would catch 3-year-old Ammon, lovingly referred to as "The Destroyer," before his little hand finds its way into his dirty diaper? And where, during all of this, are the older children, Bobby and Emma, or the baby, Mary?

Life with six children is tough. Life with six children with autism practically defies description.

The stress has landed the family in juvenile court, following an offhand comment from a frustrated mother, and cost John Kirton his job and the family's medical insurance. But it has also helped the Kirtons — who now market their own "Autism Bites" T-shirts — recognize the healing power of laughter.

"We use sarcastic humor to diffuse our stress," Robin Kirton said with a smile. Added husband John: "If we didn't laugh, we'd cry."

Dubious distinction

In Utah, 1 in every 133 children has autism, according to a recent study that placed Utah's rate about 12 percent higher than the national average. University of Utah researchers found that the rate is even higher for boys, at 1 in 79.

Even with such high state rates, having six children from the same family on the autism spectrum is extremely rare, said Judith Pinborough Zimmerman, Ph.D., assistant professor in the department of psychiatry at the U.

"What tends to happen is sometimes families, if they have one child with autism, they tend to stop having other children," she said. "Geneticists refer to it as stoppage."

Autism is characterized by impaired social, communicative and behavioral development. It is a spectrum disorder, with symptoms and characteristics ranging from mild to severe. Common characteristics include resistance to change, a difficulty expressing needs, tantrums, difficulty socializing with others, an obsessive attachment to objects, over- or under-sensitivity to pain and a preference for being alone. There is no medical cure for autism.

Autism cannot be detected by medical tests; diagnoses are based primarily on observation. Its causes are unknown, though research indicates that genetics can be a factor, while many believe that environmental factors and even childhood vaccines may be to blame.

The Kirtons note all of these factors when questioned about the cause of their children's autism. They also point to John's age as a possible factor, as he was over 40 when all of his children were born. (Bobby, the oldest boy, is Robin Kirton's son from her first marriage.)

The Kirton's own research, through Internet searches, online discussion groups and local autism conferences, has led the family to believe it may lead the nation in the number of children with autism. It's a dubious distinction to John and Robin Kirton, but they also see it as an opportunity to educate others about the disorder and, maybe one day, start their own nonprofit organization to raise money for other families with autistic children.

This week, researchers from the Utah Registry of Autism and Developmental Disabilities, a joint project between the state health department and the U. medical school's department of psychiatry, will visit the family's home to draw blood from each family member as part of an ongoing study into the role of genetics in autism.

'Dangerous thoughts'

John and Robin Kirton bristle when asked the all-too-familiar question about their family: Why didn't they, as many parents do, stop having children?

Depending on their mood, the Kirtons respond with humor, frustration or defensiveness. Regardless, the answer remains the same — all of the Kirton children were already born when Bobby's fifth-grade teacher told John and Robin she suspected the boy suffered from Asperger's syndrome, a mild form of autism.

According to the Utah Registry of Autism and Developmental Disabilities, signs of autism-spectrum disorders are often the most obvious in 3 and 4 year olds, while more mild forms are often not diagnosed until later in childhood.

After observation tests confirmed Bobby, now 13, was a high-functioning autistic, the Kirtons began to become concerned about their other children. Sarah's diagnosis came next, then Ammon's.

"That's about when my grieving period started," John Kirton said.

The Kirtons sought early intervention services for the two children, each considered "classic autistic." Falling at the severe end of the spectrum, each child is still in diapers and has limited verbal skills. It was one of those early intervention workers, from a local nonprofit organization that contracts with the Utah Department of Health, to whom Robin Kirton made the comment last fall about the family's Murray home being so dirty that some days she was tempted to "burn the whole thing down and start over."

The remark was never meant seriously, said Robin Kirton. It was simply one of those "dark and dangerous and scary thoughts that crosses the minds of all parents but you don't do."

Still, within an hour, workers from the state Division of Child and Family Services were at the front door. One week later, all six children were at the Christmas Box House, where they lived for two weeks while their mother's mental state was evaluated.

"I feel like my character was, at first, so smeared," Robin said. "At the same time, I know they were doing their job. I've just had to prove myself and earn our freedom back.

"It really helped humble us. It made us appreciate the children more."

It also led to an official diagnosis for the other three Kirton children after the juvenile court judge ordered that they be tested for autism, as well. Last November, the news finally came: Emma, 9, and Nephi also have Asperger's syndrome and 2-year-old Mary has PDD-NOS, which stands for "pervasive developmental disorder — not otherwise specified."

The news, Robin said, "was hard to take." However, the diagnoses also helped the family in certain ways, she said. "For one, it helped make sense of all the stress."

'Armageddon level'

The Kirtons will be back in court late next month for what they hope will be their final court hearing. "The thing with the thing," as John Kirton refers to the state intervention, is finally winding down.

The pair has made necessary changes to their home, and John Kirton has found work driving a truck for a local excavation company. The owner is sympathetic to the family's situation and the fact that John misses at least one day of work every couple of weeks to tend to his family — the reason he lost his previous job. And although John and Robin are without health insurance, three of the children receive Medicaid and the other three are on federal SSI (supplemental security income) through Social Security.

Meantime, the couple, who celebrated their 11th wedding anniversary in late May, will continue to cope with their situation in their own ways. John blogs on their Web site autismbitestheblog.blogspot.com/ about his family and rents World War II movies because, "even though I know how it ends, I like to see the fighting and how they got there." Robin, on the other hand, steals whatever free time she can to play her favorite computer game, Snood.

Recently, while reaching the highest level in the puzzle game, Robin reached an important conclusion about her life.

"I realized that the lower levels aren't fun now, because I'm good at it," Robin Kirton said. "If I had, say, six normal kids or less kids that were normal, that would be easy for me. God knew I was up for the challenge, so he made it.

"Six autistic kids is my Armageddon level."

Monday, November 23, 2009

The Chicago Tribune Takes on Alternative Autism Treatments

Below is the blog post of Lisa Jo Rudy of About.com Guide to Autism. To use the links in the story go to her original post here. At the end of the article you will see how I feel about it.

"This week, the Chicago Tribune came out with a long piece entitled Autism treatment: Science hijacked to support alternative therapies and subtitled Researchers' fears about misuse of their work come true. In essence, the article is a condemnation of the Defeat Autism Now or DAN protocol and other biomedical treatments for autism. Among the article's statements:

Most physicians recommend intensive behavioral therapy and, if asked, warn parents away from experimental treatments.

Even so, studies have found that up to three-quarters of families with children who have autism try at least some alternative therapies.

Physicians and others in the movement -- many affiliated with the organization Defeat Autism Now! -- say their treatment protocols rest on a foundation of solid science. But the Tribune found otherwise after speaking with dozens of scientists and physicians and reviewing thousands of pages of research and court testimony.

Later this week, another article came out entitled Autism treatment: Success stories more persuasive to some than hard data. The gist of the second article: kids with autism may improve with or without therapies, so it can be very hard to know what's "really" working.

As might be anticipated, the articles have raised a storm of protest -- and an equally hefty shower of approval. Two regular About.com commenters, Harold Doherty and Autism News Beat, take opposite perspectives. Harold is disturbed by what he feels is an anti-therapy stance by the Tribune, while Autism News Beat says "It's called journalism..... Get used to it. Expect more in the coming months as the news and entertainment media's narrative switches from "alternative medicine produces miracles" to "science is being highjacked to fool parents". Age of Autism, some of whose writers are specifically presented in a negative light in the Tribune articles, are predictably vocal in their criticism.

Whatever happens next, it seems clear that the autism wars are nowhere near over. In the present battle, the Chicago Tribune has made its point of view very clear indeed. It will be interesting to see whether Autism News Beat is right that the "narrative is changing."

My guess is that consensus is a very, very long way away."

My comments:

The fights and arguments will continue to go on and on and on... until someone does a COMPLETE study of all that is out there without bias.

Is that someone the government who is joined at the hip with the AMA, FDA, the big drug companies and more? Or will it be Autism Speaks funded by well meaning parents and concerned others?

Either way those two DO have biased agendas. And that leaves parents and their children on the sidelines still waiting for the shining knight to come riding over the hill with help. I don't think it'll happen.

I think we (Autism parents) are going to have to do it on our own if we can expect to see any real results. But how to afford it? That's the 64 million dollar question.

I hope that we can joined forces to create the wealth needed to say to hell with the government and the promises of hope from others that will never be fulfilled to make a difference for our children today.

Dad

Saturday, October 3, 2009

Autism Rate Now 1 in 100, Still Autism x 6 for Us

1 in 100? It's scary, it's terrible, it's the end of the world!! Naaaah, if you have children with Autism you just learn to deal with it.

However, friends don't come over any more, family avoid you, you're in foreclosure or going bankrupt. If you are so bold as to step out into the outside world you get the "look" or stares usually followed by unsolicited parenting advise.

You may not be able to hold down a regular job. You need a lot of time off. You had the hope that there was a government program, an agency or charitable organization that could help with SOMETHING.

Then 'how life really is' sets in.

After awhile you come to realize its all up to you. You stop feeling sorry for yourself. You stop caring about the mean people, uncaring family members or government indifference to your plight.

You come to accept your life with an Autistic child(ren). Then you learn to embrace it. To appreciate their innocence.

Sure the meltdowns, the poop, the constant messy home STILL aren't that much fun -- but you deal with it. You realize your blessings and find peace in your life.

1 in 100? It's still 6 in 6 for us.

Dad

Friday, May 1, 2009

Autism Awareness Month - So What !!

So what has Autism Awareness Month done for you? Did you think more about your child and their Autism? Let me guess, you think about it all the time anyway. An 'awareness' month, has not really changed how you deal with Autism. Am I right?

What about your family? Did they come over to the house against their self-imposed avoidance of your family? No? Huh, really. You mean they didn't offer to watch the kids? Give you a break? Nothing?!? Didn't they know that it's Autism Awareness Month?

OK, ok. But, I bet you saw THAT celebrity on the talk shows again with their latest book on curing Autism. Do you wonder if it's all about adding some extra zeros into their bank account? Most of the blogs and posts believe that. I don't know, I'm not them. I hope they have a higher goal then just money.

But, there sure have been lots of newspaper stories and local TV reports. So at least some 'awareness' is going on. Right? Did you hear about some sort of new laws... or mandates that came out of Washington this month? Have we seen any real details and how it can positively affect families of Autism? No? Me neither.

I was hoping that since President Obama had lots of changes in mind, that it would include Autism. Autism IS high on his list of things to do. It says so on the White House website. There is next years Autism Awareness Month I suppose. Hmmmm, there still are a couple of days before the end of the month. Maybe we'll get a surprise Autism birthday present!

Hey! Stop holding your breath, I'm afraid you'll pass out.

We should be grateful that we have our own month. But is it for us? Are we getting any real benefit? What do you think? Is it just a bunch of lip service? To make us think that the media, government, etc. do actually care and are concerned?

If not, you need to get off the couch and DO SOMETHING about it! Every MONTH needs to be Autism Awareness Month, where things are getting done to help your situation. Not just a bunch of talk. If you as a parent or a person of Autism don't speak up and I mean really do some shouting... otherwise, we are just sheeple (people that act like obedient sheep) and be thankful for whatever crumbs fall off the 'table' of resources and finances that happen to come along. I'm just one voice, we need many more!

Otherwise, Autism Awareness Month is not for parents or persons of Autism... is it?

Dad

Friday, April 17, 2009

Fed Up With Autism Fighting

Here is a great posting opinion from Tiffany and my comments too:

Tiffany this is a fantastic post and one that EVERYONE should follow the advice of. Every family is different, each Autistic child is different from every other Autistic child. No one should tell another parent or person with Autism what they should be doing with their life... even if they think they KNOW that family from watching them on TV. ;)

Our family goal is to increase the awareness, acceptance and understanding of Autism and all of it's various aspects and effects on families.

Some have accused me of trying to make money from my children. First if they follow your post's advice they shouldn't assume they know what I'm doing and be quite. However we've made money from our situation from a 'location fee' from the film production company. This is a standard in their industry. Then we have made an income from the sales of the Autism t-shirts that Robin and I designed.

But all the other TV, radio, magazine, blog and internet interviews we have received nothing. AND I'm not asking that they do.

95% of the comments we get on our blog or from emails have been positive and supportive. And I will continue to advocate for my children until the day I die. We too did not yell, "Yipee!" when we got the diagnosis for the children. We too did LOTS of grieving, for around 1 1/2 years. I was let go from the job I had at the time because quite frankly, at the time I was useless and not able to have my head into work. Worrying and wondering about what life was going to be like with Autistic children was just too much. It was tough and still is and IS financially hard. And I'm not sorry and will not apologize for mentioning that Autism hits families in the wallet. We've received many, many emails confirming this from other families. And they too are glad that the world is starting to understand those financial hardships. Its a FACT that people need to realize.

We need to stop the fighting among ourselves. It's a waste of time, effort and emotions. Another parent may want to chelate or put their children through test after tests or treatment after treatment after treatments. Or do nothing. Another parent may not agree with either and you know what? Each one is doing right thing for THEM.

That "Autism Czar" appointment that President Obama promised? He/she should understand all the above of what you and I have said here. And have a plan for ALL families and persons affected by Autism. And we need to get the support from this Czar... NOW. Too much talk and not enough action.

My creed: Autism IS a Spectrum Disorder, CAUSED by a spectrum of reasons, needing a SPECTRUM of treatments or solutions and requiring a spectrum of funding.

Peace and Blessing to all... Nuff said.

Dad

Monday, March 30, 2009

Autism X 6 and Other Media Appearances

Mark your calendar for April 6. Unlocking Autism will be on that day, click here for times. Our producers did a great job again. This documentary shows four families that have children with Autism. You will see our family as the last profiled. That will be followed by our documentary, Autism X 6. For those times click here.

I was interviewed a few months ago and this article came out this past Sunday across the US in American Profile.

Dad

Sunday, March 15, 2009

Utah Lawmakers Say No to Autistic Kids

Thousands of parents made the trek to the State Capital building many times over the past couple of months. They attended the announcement, committee and floor votes for Clay’s Law. Just what was this landmark proposal? During the past legislative session parents were hoping to get financial relief for treating their Autistic child. What we they asking for? Large grants for experimental treatment methods? No. Did they want a free gift from taxpayers for unproven therapies? Nope. Parents just wanted their insurance companies to provide coverage for early intensive behavioral intervention for children with Autism. Interventions that were already known to be the most effective methods to help these affected children.

But, the costs would way too much for policy holders that may never need these services, opponents claimed. This proposal would have resulted in a less than 1% increase in insurance premiums. The ‘big money’ fact to consider is this: Untreated autism is estimated to cost approximately $3 million over the person’s lifetime. Intensive early behavioral intervention, the type covered by the bill, can cut this down by $1 million. That means the bill could pay for itself with the savings from just three or four children. With 1 of 79 boys in Utah receiving an Autism diagnosis the long term savings would have been tremendous.

So what will they be getting? An option to purchase a ‘rider’ type of policy before the child reaches 3 months of age. Not much help because of the fact that the average ‘severely’ Autistic child is not diagnosed until 18 – 24 months. What about the parents of children who already have an Autism diagnosis? Nothing. Chalk up another one for the insurance companies who seem to be better at taking care of themselves lately.

Dad

Saturday, February 7, 2009

Be an Autism Advocate

Making calls and emails are good starts. Do a search on the web page of your closest major newspaper and see what kind of Autism stories they've done. If they haven't done anything in the last six months... call them.

How we got started: We found out all 6 were Autistic in fall of 2006. While watching "Extreme Home Makeover" in Feb 2007 they said the family had the most documented Autistic children in one family... five. Robin and I looked at each other, "Guess we have the most". I emailed the local ABC station the next morning that we have 6 ASD kids and got an email from a reporter back right away. They were doing a story that night and wanted some footage on our family. We were on the news that night.

A month or so later I called our two major newspapers. One was more excited then the other to do our story. An interview and photos later and we were on the front page of the Sunday paper. (Check it out and add a comment to their website, that can insure that it stays available) That was June 2007.

Because of that newspaper article we were contacted by Readers Digest, People Magazine and Figure 8 Films (fro Discovery Health). People came in July for the interview, the photographer came in December. (long story). The film crew first came in Dec 2007 for the next 6 months. Each visit was 2-4 days.

The People magazine article came out in Feb 2008 and the interviews with Good Morning America, Inside Edition and Larry King soon followed. We had also been contacted by the Helen DeGeneres show and Oprah. Nothing has come of those as of yet. "Home Makeover" did contact us and wanted us to apply, but you need to own your home or have property they can build on. We rent and have no land.

Between the beginning and now I've made calls (lots) and emails to many politicians and various groups and individuals (the rich and famous). You wouldn't believe how many people who SAY they support Autism have never responded. I even sent Jenny McCarthy one of our t-shirts and never heard back.

Yes, the hours are long and there are many disappointments in trying to increase Autism awareness. But, as I tell many people, Autism IS my life. I figure it's my job and "calling" in life to do all I can. I've felt dumb standing around an event where I know nobody and try to start conversations. Then try to bring the conversation around to Autism. I've actually created a Autism business card for myself and Robin.

But, to do nothing... I feel is just not acceptable. Do something, anything... it will make a difference. If every parent will be an advocate we can make a HUGE difference for our children. So make calls, write, search and read. Do what you can when you can. We are all in this together and we need each one of us.

Dad

Friday, January 23, 2009

Our BIG Autism Day

Yesterday we met with one of the social workers at Ammon and Mary's Autism school. They called the meeting to go over a STRESS survey. We were concerned and wanted to make sure we did not miss the appointment. We had run ins with social workers in the past. But all was well and we were told that we were doing a good job in spite of having our 6 ASD pumpkins. Whew!

That was at 9am. At 11am there was a press conference at our state capitol building. Another mom of Autism that we know, got a Senate sponsor for a bill to get insurance companies to cover Autism treatments. I went to offer my support and was able to get the reporter who did our GMA followup story at the local ABC channel to talk with us (click on Autism story).

During that time Robin stayed at the children's school to help Ammon's teacher who was short staffed. She caught a ride home on their bus. The coordinating of getting Bobby over to church for a special youth meeting. Calling the school for Emma and Nephi to meet me out front instead of walking home. Getting a call from the bus assistant for Sarah to have the bus bring her back to the school (they were in front of the house) so I could get her Emma and Nephi into the car and rush to the bus stop where Mom, Ammon and Mary were waiting to be picked up. Pant! Pant!

Later in the evening I left at 6:15pm to go to a speaking event with Temple Grandin at the Salt Lake City Library, about 25 minutes drive. But, I got there early enough to get a good seat. Afterwards she signed books. I gave her a copy of the People magazine with our article and a DVD of our Discovery Health documentary. She said she had not heard of our family yet. Dang, I've got to do a better marketing job! LOL



At 10:05pm I got a call from my 26 yr old son (first marriage) to ask what I was doing to be on the news that day.

Most days aren't this busy, but it's getting to be more and more each month.

Tuesday, December 30, 2008

Bringing in the New Year with the Kirton's

I signed up to be notified whenever our latest showing of 'Autism x 6' is going to be on the Discovery Health channel. Yesterday I was doing some Autistic surfing and went to their website.

The program will be on tomorrow night, December 31st at 8pm and 11pm, Eastern time.

So if you like to hang around the house on New Years Eve or, like us, never go much of anywhere anyway. Watch us again or for the first time. I did post a video on YouTube with a January 2009 suprise from the Kirton family. Check it out.

Dad

Thursday, December 18, 2008

Easter Seals Doing a Better Job Then Autism Speaks?

There certainly is strong feelings about Autism Speaks (AS) as an organization, both good and bad. I'm glad for all the awareness they create. We're doing as much as that as we can ourselves. But what is AS doing for Mom and Dad Autism?

Many people get pretty heated when it is brought up that AS is putting their money towards research and nice salaries for company executives. Sure research is all well and good, BUT again, what about Mom and Dad? Learning about the causes of Autism are a bit of a moot point for parents financially strapped trying to help their children with Autism. Wouldn't it be nice if some organization was there for parents... NOW?

Easter Seals to the Rescue

Easter Seals has come out with a new study: Living with Autism Study. Here is some information about it:

Autism affects more than 1.5 million Americans and their families. Critical services and supports are needed to raise a child with autism, but they are few and far between.

In cooperation with the Autism Society of America, Easter Seals surveyed over 2,500 parents of children with autism and typically-developing children -- about daily life, relationships, independence, education, housing, employment, finances and health care.

The results gathered from our groundbreaking autism study paint a startling picture of the life-long fears and anxieties people with autism and their families face ... and the disparities among parents of children with autism as compared to parents of typically developing children:

• Nearly 80% are extremely or very concerned about their child’s independence as an adult.
• Only 14% feel that their child will be able to make life decisions.
• Only 17% think their child will make friends.
• They report that they’re “financially drowning,” with concerns for their child’s financial future.

Thanks to the generous support of MassMutual Financial Group, the findings are now available to you. As an Easter Seals national corporate partner and the study sponsor, MassMutual is committed to serving children and adults with autism through its exclusive SpecialCare program, a solution that gives families living with autism and other disabilities access to information, specialists, and financial strategies that can help improve their quality of life.

Millions of families are desperate for solutions and resources. Easter Seals and others in the autism community are doing their best, but current systems, structures and resources to help people with autism and their families do not adequately meet the growing need, especially for adults with autism.

Easter Seals will use these findings to raise awareness of and advocate for the life-long services families living with autism desperately need.

Story and how to get the study link

---------------------------------

Wow, isn't it about time? I think many were hoping that this is what AS should have been doing years ago. But, finally someone is, Easter Seals. Looking at their website I find that they are like AS and do ask for donations. I'm not sure about the rest of you, but I'm ready to go to an Easter Seals version of Walk for Autism. What do you think?

Dad

(Here is a cute Ammon and Mary pictures with Santa, for those who've asked for cute pictures)



Tuesday, December 16, 2008

Utah May Mandate Health Insurance for Autism Therapy

By: Heather May
The Salt Lake Tribune (http://www.sltrib.com/ci_11238552)
Updated: 12/15/2008 04:59:59 PM MST

Leeann Whiffen made a promise that when it was over -- two years of intensive therapy to free her son from the grip of autism -- she would do what she could to help other parents afford the same sort of expensive treatment.

The Highland mother says her son, Clay, is now recovered from the disorder that had muted her babbling toddler and traded his peek-a-boo play for obsessions with round shapes and tan foods. Not even his third-grade teacher would know he was once labeled autistic, she said.

But she had to take out a second mortgage on her home and put every expense she could on credit cards to free up $30,000 a year for treatment. Knowing other parents aren't so lucky, Whiffen is working to force Utah health insurance companies to cover autism therapy.

"People need to know these kids can get better," Whiffen said this week. "I can't imagine what life would have been like for him if we wouldn't have been able to do this program."

This fall, over breakfast at Mimi's Cafe, Whiffen and another mother of an autistic child, Brittany Recalde, easily persuaded Sen. Howard Stephenson, R-Draper, to sponsor the bill in the upcoming legislative session.

"It's a draconian society that would knowingly watch children grow past the window of opportunity [for treatment] without [providing] assistance," said Stephenson, who has successfully sponsored an autism treatment bill in the past.

Stephenson said "Clay's Law" is still being drafted, but would include an annual coverage cap, likely around $30,000, and a to-be-determined lifetime cap. It will also require families to contribute.

To receive coverage, the children couldn't be older than 5, since research has shown the most dramatic benefits occur the earlier the treatment starts, Stephenson said.

'Dramatic gains' » Insurers would likely only be required to cover what is known as applied behavior analysis, or ABA therapy. It provides one-on-one treatment for up to 40 hours a week at home, reinforcing communication and appropriate social behavior and discouraging negative behaviors.

Instructors break down skills like following directions and carrying on a conversation. It has been criticized for not helping children form social relationships, but according to the National Institute of Mental Health, ABA is widely accepted as effective.

Claims of an autism cure are controversial. But studies have shown 30 percent to 40 percent of higher-functioning autistic children who receive two years of intense ABA therapy "will be indistinguishable from normal children 10 years down the line," said William Jenson, an educational psychology professor at the University of Utah who supports the bill.

Leann Whiffen, of Highland, is behind an effort to require insurance companies to cover autism therapy like the kind she used for her son, Clay. Clay was diagnosed with autism when he was 2. After two years of expensive therapy (at a cost of $30,000 a year), Clay, now a third-grader, was considered cured.

"They probably still are autistic, but they've made such dramatic gains that you can't distinguish them from other kids," he said.

Other children show gains but still need special-education support, and some don't benefit. Jenson cautioned it is impossible to predict how children will respond.

The bill's emphasis on ABA is based on research by Jenson, who helped start the ABA-focused Carmen B. Pingree School for Children with Autism. He recently analyzed 19 studies published over the past 40 years and found ABA was the only intensive early intervention that provided significant improvement in IQ, language and self-help skills.

"If you waste time in that window from 18 months to 5 years with ineffective therapies, you are probably going to decrease this child's chances in making dramatic gains through adulthood," Jenson said.

Questioning the cost » Supporters expect opposition from proponents of non-ABA treatments. And the Utah Health Insurance Association is worried about cost and effectiveness, said Kelly Atkinson, executive director.

Self-insured companies and the federal government would be excluded, leaving smaller employers to bear the costs, which Atkinson predicted would be "substantial."

Insurers say states should subsidize the therapy as an educational intervention, but also question whether it is proven. Atkinson cites the work of a Brown University professor who notes that the primary study used to tout ABA included only 19 children. The professor also points to research showing other interventions work, even beyond age 5, and to a study showing only up to 4 percent of children will recover.

"We have to see the scientific data that demonstrates that this is a proven successful therapy for the majority of people who participate in it," Atkinson said.

Countering the cost argument, supporters of Arizona's recent similar mandate estimated the monthly price at $1.50 per insured customer. Proponents also argue treated children will need fewer state services in the future.

For Whiffen, there is no question the therapy was worth the money. Between the ages of 2 and 4, Clay spent up to 40 hours a week slowly learning how to talk, play with toys, sit in a chair. A video she shows is striking: In one of his first sessions, Clay lets out a sustained, guttural scream as an instructor tries to get him to place blocks in a bucket. Two years later, he sits calmly at a table, laughing and talking with his instructor about forming a triangle with the markers.

Whiffen, who had wondered if her son would ever know who she was, started noticing a difference earlier.

"He looked me in the eye, called me mom and held out his cup," she said. "It was like seeing him being reborn."

hmay@sltrib.com

My posted comments to this article:

This bill is a start and we must start somewhere. Three of my children have and do attend the Carmen Pingree school for Autistic children. ABA does work.

With 1 of 150 children having Autism it's not just 'our' problem, Santiago, it's everyone’s.

It's pay now or pay later. And the costs WILL be higher as children with Autism become adults. If you think your insurance rates may be higher with the passing of this bill, just wait 10-15 years if we don't.

Sticking ours heads in the sand won't make this problem go away.

I do have some serious problems with the age limit up to age 5. My youngest is 4. Are we to just throw our hands up and say "Oh well, I guess that's tough luck for us!?"

And this isn't just a Utah problem. It's a national epidemic. In Utah 1 of 94 boys have Autism and we are the 3rd highest in the US. A serious NATIONAL plan MUST be put together... NOW!

If ABA is the only proven method to work let's find some other methods. One method used up to age 5! It's like putting a band aid on a severed arm.

But hey, it's a start.

~ Dad

Friday, November 28, 2008

Surprise, We're Back...

When flipping channels on Wednesday, Robin discovered that our program "Autism X 6" was playing. The last we heard was that we would be on again in January side-by-side with a new Autism program that our production company has been working on.

So, I checked the listings for the next month on the Discovery Health channel and here are some additional times:

Nov 29, 1:00 pm
Dec 14, 10:00 pm
Dec 15, 2:00 am

The times are likely for the Eastern timezone, but we've been surprised before. Check local listings to be sure.

Dad

Saturday, October 4, 2008

Autism X 6, Why We Did It

I received a very sad email from a mother that has it as bad or worse then us in regards to the number and severity of her children's Autism. However she was angry that we are 'getting rich' from 'exploiting' our children. I hope that my response can help to further clarify who and what we are. Our goals and dreams we hope to accomplish by appearing in a documentary about Autism.

My response:


I'm sorry to have offended you, it sounds like you are in the same boat as us; or maybe worse. Your situation is one of the main reasons we decided to put our family 'out there' in the first place.

The average Joe out there has NO idea what it is like to raise children like we have. The medical bills, the special diets, various treatments and more. Sure some will judge and complain, but that is their problem not ours.

We'll continue to try and educate and increase the level of tolerance and acceptance toward our children. It's not much yet but we have been able to help raise nearly $25,000 for a number of charities that help Autistic families. (not for the AutismBites Foundation however) Many of the links on our website have benefited from us placing them on our site. That is our intention, to help others as well.

We don't have the pulling power of a Hollywood celebrity or have written a best-selling book. But we feel an obligation to let people know that there are many people that are having a VERY tough time raising Autistic children. Not just us or you.

We haven't been paid for any magazine, newspaper or TV interviews (that's a myth). It has made people aware of us and we've sold a number of t-shirts. But, 95% or more of the costs of those shirts goes to shipping and production for the website that makes them for us. And we're losing count of the number of free t-shirts that we've sent to families that have a difficult time affording them.

The film production company did pay us a 'location fee' to film us, and even though we appreciated it very much; it wasn't that much. We aren't rich now. The money is not rolling in like some seem to believe.

After trying to maintain a 9 to 5 job these past couple of years, I gave up. The workplaces just weren't able to have me take off for appointments, emergencies or sickness. I can understand that and harbor no hard feelings. But I still need to provide for my children. That is why I need to have a blog and website that may include some advertising, links to businesses or various offers.

I sent out our 'invitation' email to only those who kindly emailed us messages of hope and understanding. I'm sorry you got on the list by mistake. I'm sorry to have given the impression that we are doing this for money. I guess that people assume that when a sad tale is told that they are expecting a handout. We got a ton of emails from people that wanted a mailing address to send things to us. Others wanted to donate money, so our website manager put a PayPal button there. They feel good, we are very grateful and our children lack for a bit less. WIN-WIN-WIN

We aren't exploiting our children, we are showing the world how beautiful they are and how blessed we are. Our new business link on our home page has products that people buy every day. We aren't begging anyone to buy, but we hope that some will. It's my home business just like your doll hospital.

I'm sad to hear that you have no help, no respite, no breaks and no 'loot' rolling in. We have NO help, 4 hrs of respite for 2 children a week, NO breaks and NO loot rolling it. And that's OK for us too.

Sort of.

I want money to 'roll' in for my family. I want to take care of them and give them what they need and a few wants. I DO want money rolling in from MY efforts, the businesses I create and put together. I DO NOT want to barely 'get by' and barely make it each day. I want a better life for my children, they've already been given a hard road in life and they deserve better. And somehow, some way I'll work and scratch and find a way to do that for them. They are my children I love them and I don't think I need to accept a vow of poverty to be in the good graces of the rest of the world.

I wish you all the best and hope you find peace and blessings in your life.

John

Tuesday, September 16, 2008

Discovery Health Profiles the Inspiring Kirton Family in Autism x6

This is the press release from Discovery Health about our documentary.

Saturday, August 23, 2008

Autism Family on Discover Health Channel

We now have a date (not the time yet) for the documentary about our family. We believe the title is: Autism X 6. It will be shown on October 1st. We have seen the films 'rough' cut and they have shown our family just the way we are. It's not always pretty, but many of you will relate quite well I'm sure.

It will be a good idea to have your friends, neighbors, family and church members watch so they can begin to have an idea what you go through each day. Thanks for your continued support.

John and Robin Kirton

Monday, August 4, 2008

We Are So Spoiled by David Letterman

I'm usually a Jay Leno viewer as opposed to David Letterman. I received this in an email today and hope that indeed he said this. If so, my respect for Mr. Letterman has jumped dramatically.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

David Letterman wrote this; it's the David we don't often see...

As most of you know I am not a President Bush fan, nor have I ever been, but this is not about Bush, it is about us, as Americans, and it seems to hit the mark.

The other day I was reading Newsweek magazine and came across some Poll data I found rather hard to believe. It must be true given the source, right? The Newsweek poll alleges that 67 percent of Americans are unhappy with the direction the country is headed and 69 percent of the country is unhappy with the performance of the President. In essence 2/3 of the citizenry just ain't happy and want a change. So being the knuckle dragger I am, I started thinking, 'What are we so unhappy about?''

A.. Is it that we have electricity and running water 24 hours a day, 7 Days a week?

B.. Is our unhappiness the result of having air conditioning in the summer and heating in the winter?

C.. Could it be that 95.4 percent of these unhappy folks have a job?

D.. Maybe it is the ability to walk into a grocery store at any time and see more food in moments than Darfur has seen in the last year?

E.. Maybe it is the ability to drive our cars and trucks from the Pacific Ocean to the Atlantic Ocean without having to present identification papers as we move through each state?

F.. Or possibly the hundreds of clean and safe motels we would find along the way that can provide temporary shelter?

G.. I guess having thousands of restaurants with varying cuisine from around the world is just not good enough either.

H. Or could it be that when we wreck our car, emergency workers show up and provide services to help all and even send a helicopter to take you to the hospital.

I.. Perhaps you are one of the 70 percent of Americans who own a home.

J.. You may be upset with knowing that in the unfortunate case of a fire, a group of trained firefighters will appear in moments and use top notch equipment to extinguish the flames, thus saving you, your family, and your belongings.

K.. Or if, while at home watching one of your many flat screen TVs, a burglar or prowler intrudes, an officer equipped with a gun and a bullet-proof vest will come to defend you and your family against attack or loss.

L.. This all in the backdrop of a neighborhood free of bombs or militias raping and pillaging the residents. Neighborhoods where 90% of teenagers own cell phones and computers.

M.. How about the complete religious, social and political freedoms we enjoy that are the envy of everyone in the world?

Maybe that is what has 67% of you folks unhappy.

Fact is, we are the largest group of ungrateful, spoiled brats the world has ever seen. No wonder the world loves the U.S. , yet has a great disdain for its citizens. They see us for what we are. The most blessed people in the world who do nothing but complain about what we don't have, and what we hate about the country instead of thanking the good Lord we live here.

I know, I know. What about the president who took us into war and has no plan to get us out? The president who has a measly 31 percent approval rating? Is this the same president who guided the nation in the dark days after 9/11? The president that cut taxes to bring an economy out of recession? Could this be the same guy who has been called every name in the book for succeeding in keeping all the spoiled ungrateful brats safe from terrorist attacks? The commander in chief of an all-volunteer army that is out there defending you and me?

Did you hear how bad the President is on the news or talk show? Did this news affect you so much, make you so unhappy you couldn't take a look around for yourself and see all the good things and be glad? Think about it......are you upset at the President because he actually caused you personal pain OR is it because the 'Media' told you he was failing to kiss your sorry ungrateful behind every day. Make no mistake about it.

The troops in Iraq and Afghanistan have volunteered to serve, and in many cases may have died for your freedom. There is currently no draft in this country. They didn't have to go. They are able to refuse to go and end up with either a ''general'' discharge, an 'other than honorable'' discharge or, worst case scenario, a ''dishonorable' ' discharge after a few days in the brig.

So why then the flat-out discontentment in the minds of 69 percent of Americans?

Say what you want but I blame it on the media. If it bleeds it leads and they specialize in bad news. Everybody will watch a car crash with blood and guts How many will watch kids selling lemonade at the corner? The media knows this and media outlets are for-profit corporations. They offer what sells, and when criticized, try to defend their actions by 'justifying' them in one way or another Just ask why they tried to allow a murderer like O.J. Simpson to write a book about how he didn't kill his wife, but if he did he would have done it this way......Insane!

Turn off the TV, burn Newsweek, and use the New York Times for the bottom of your bird cage. Then start being grateful for all we have as country. There is exponentially more good than bad. We are among the most blessed people on Earth and should thank God several times a day, or at least be thankful and appreciative.' 'With hurricanes, tornadoes, fires out of control, mud slides, flooding, severe thunderstorms tearing up the country from one end to another, and with the threat of bird flu and terrorist attacks, 'Are we sure this is a good time to take God out of the Pledge of Allegiance?'

David Letterman

~~~~~~~~~~~~~

Dad

Tuesday, July 22, 2008

Michael Savage Autism Comments

As many of you know we like to say how we feel on t-shirts. We have come up with three shirts that tell Michael Savage exactly what we think.

Dad

Monday, June 9, 2008

John and Robin Kirton Family's NEW Autism Book

We would like your opinion as quickly as you are able. We've been thinking that it would be a good idea to tell our story in a book and we'd like your help. What information or area in our lives would you like the most to know about? Please respond with your ideas to our email address: autism_bites@yahoo.com.

We want to have the book published before our documentary is shown on Discovery Health channel in October.

Thanks,
John and Robin Kirton

Sunday, June 1, 2008

We've Joined the YouTube Website

It looks like the links are coming down on our website where we showed some of the various programs we've been on (i.e. Good Morning America, Inside Edition, etc.). We had asked to have copies on DVD of the shows sooooo... we are going to put them on YouTube.

The Inside Edition story was pre-empted in Utah by the NCAA tournament and we never saw it until our DVD arrived 3 weeks later.

Here is the link to the Inside Edition story. I'll be adding more as I can. Update: I've now added the Good Morning America story. Their website is no longer showing the video, here it is again for those who missed it.

Dad