Showing posts with label FAQs. Show all posts
Showing posts with label FAQs. 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."

Wednesday, October 7, 2009

Autism x 6: How Do We Do It?

We've been getting this question a lot recently in emails. And it is a question that we've been getting from day one. My wife is the glue that holds us together and works hard to make our family feel more 'normal'.

We both grew up not knowing what a special needs family was. The last few years have been a crash course, near literally. We are not perfect or have any unusual talents that help us make it though each day. We just plug along and do the best we can.

Some days it is overwhelming and maybe we escape with too many DVD rentals or midnight snacks, but you do what you have to do to maintain your sanity.

No one asks for challenges like these precious angels bring to a family. However, we figured that God must really want to straighten us out to have given us six children with Autism. I feel they are here mainly for us to learn from them, instead of the other way around.

We used to complain a lot more (i.e. not enough money, need a home of our own, etc) but we are getting better. Hey! It looks like the children are doing a good job with us after all.

They are the special ones. Me? I'm just the Dad.

Monday, October 6, 2008

Autism X 6, FAQs

Frequently Asked Questions. In case some of you haven't heard what FAQs are. So, the past few days I've done a bit of lurking on blogs that have been talking about our documentary. I'm wondering if they watched the same one that I saw last Wednesday.

So I've decided to create a recurring post, called simply "FAQs". To make them easy to find, I will have a 'label' category of just the FAQs post. I hope to clear up a large number of misconceptions, misquotes and misinformation about us.

Question: Why did you keep having children when you knew they had Autism.

Answer: All of the children were born before we knew anything. We were first told that Bobby should be evaluated for a 'communication disorder' when he was 11 1/2, Mary, our youngest, was almost 5 months old. This was May 2005.

Question: How old were the rest of the children at that time?

Answer: Emma - 7, Nephi - 6, Sarah - 3 and Ammon - 1 1/2

Question: Wasn't Sarah the next child that you thought may have Autism?

Answer: We were concerned that something may be going on with Sarah. (May 2005). That summer Robin's parents visited us for their vacation. We live in Utah, they live in Minnesota. Robin's mother suggested that maybe something was wrong with Sarah's hearing. She didn't talk, but we weren't overly concerned because Nephi did not talk until he was 3 1/2. Sarah wasn't that old yet.

Question: So when did you find out about Sarah's Autism?

Answer: After Robin's mother's concerns we asked people at church and other friends what they thought. Some also suggested that something may be wrong. We were told of a pre-school in our school district where Sarah could be evaluated. This was August 2005. Two special education teachers visited with Robin and Sarah. They told Robin that they thought she was Autistic. We were shocked, we had no idea what Autism was. We thought she was like Nephi, just a slow talker. We didn't know yet that Nephi had Asperger's Syndrome. Looking back now, we figured that we were too close to the situation and had no idea that something serious was going on.

Question: Come on, you had no idea? No Doctors said anything?

Answer: No, not a single one. We suspected nothing ourselves until Bobby's school said he may have a 'communication disorder'.

Question: So you knew that Sarah had Autism in August 2005.

Answer: No, the preschool said they thought she was. They said they would need to do testing and evaluations once she was enrolled in the pre-school. The determination from the school was in December 2005. They said Autism. However, she did not have an official Doctors diagnoses until October 2006.

Question: Why did it take so long to get the Doctor diagnoses for Sarah?

Answer: John had just started working for a company with great pay and benefits when Sarah's school suggested Autism. (August 2005) We both took it hard, but it affected John's work performance as well. In December 2005 the pre-school said that Sarah HAD Autism. John's father died a few days later, after a long illness. It was a bad month. John asked for a lighter workload, but was told that he should take care of his family problems... at home. John's supervisor said that John had quit. This was not true. But, he had neither the physical or mental strength to fight it out. So we had no insurance for official Doctors diagnoses. We had to wait until Sarah's medicaid kicked in and then wait months for a Dept. of Mental Health appointment.

To be continued...