Showing posts with label Autism Info. Show all posts
Showing posts with label Autism Info. 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

Tuesday, November 17, 2009

Beating Up Autistic Kids


I just read a story from Texas where teachers are hurting children with special needs in the name of discipline.

On the Facebook forum I answered questions from a concerned parent: I do not have an autistic child but ... My children attend a school that does have autistic and other special needs students. What is the best way to handle a situation where a student with special needs does harm someone else or does bully or spit on someone? I know it happens but do not know what parents of special needs children think is proper procedure. If my son spit on someone or bullied someone or hit someone they would be disciplined and possibly suspended and I am wondering what is acceptable punishment for special needs students. I am sorry if this upsets anyone but I really want to know?

I said: "I have my methods that work very well, however I will probably upset some 'gentler' folks. I use what has been termed in the past as 'tough love'. Bottom line I don't let them get away with anything. It probably helped that I had 4 NT children in a first marriage. I treat our 6 ASD pumpkins like I would an NT child and do not let them get away with bad behavior because they are 'disabled'.

At our school they use a two hand to one arm hold on a child to guide them away from a situation and to a classroom set aside for children having problems. An aide or teacher is there to help direct their emotions away from things harmful or disruptive.

For a school to allow a child to be physically harmed in the name of discipline is criminal and arrests and jail time need to be given. If a parent did the same thing it's abuse and the state steps in. School districts and teacher must be held to the same standard. If I can help in any additional ways please let me know. That goes for anyone else reading this too."

What do you think?

Dad

Sunday, October 18, 2009

Created a New Tote

When Robin and I got the ideas for our t-shirts, we were only thinking about how they would help our lives. However, when other parents and families of Autistic people heard about them they wanted us to make them available to anyone. Thus our Autism Bites t-shirts were born.

Since that day I've had a few requests to add to the choices available. I was recently contacted by a parent and a group of teachers that wanted a tote bag with a face and saying combonation that we did not have. Here is what they wanted -



Its a great idea and one that can be used for any disorder, not just Autism. Christmas is approaching, if you can't find what you like in what we are offering let me know and I'll see what I can do. Thanks!

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

Tuesday, September 29, 2009

Autism X 6: A Year Later

On October 1st Discovery Health channel will be showing our family story... again. During this past year it's been aired about 8 - 12 dates that we know of. It was shown in Australia and in England as well. Discovery Health did not tell us about the Australia showing (they don't have to). We found out from a number of emails from some new Aussie friends.

The show in England had a bit of lead up advertising and media attention. Robin was interviewed by a woman's magazine, we asked for a copy like we always have done with the other media, but we didn't get it. The most amazing thing for us was that we did not get a single response to the documentary from anyone in England. Maybe something was lost in the translation. Not sure.

We've had all the range of responses as you might expect. People wondering how we do it, other wondering WHY we did it. We received email from well wishers and others calling us the foulest names possible. Some have told us we deserve a Extreme Home Makeover show, and others said we don't know how to clean up a home. We've been accused of using our kids for financial gain, but the truth is we are worse off financially then a year ago -- just like the rest of the country.

But we are glad that the show was made and the other documentary, Keys to Unlocking Autism, that we were a part of. Awareness is the key and the beginning steps to making the life's of persons with Autism better. But even though the term 'Czar' is getting a bad rap lately -- we need one. An Autism Czar to coordinate the efforts correctly, as much as possible.

We call ourselves 'Autistic Parents', other parents know what we mean. Some goofs have thought we were saying we are Autistic too. We know how to handle the joys as well as the crap, literally, being parents to six children with Autism. And we're still plugging away a year later.

Dad

Friday, September 11, 2009

Autism x 6: Update to Our Main Website



I've made changes, updates and have refocused the meaning of our website: AutismBites

Autism with six children is still not the best part of the day, however we want to focus more on the positive. We've found that certain things work for us and make life A LOT better. Maybe it can help your family too.

Updates are on the main page, about us and links. Who can tell me first, the major change made to our blog?

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

Sunday, April 26, 2009

Chicago Police Officer Beat Autistic Teenager

Another story of an Autistic person not being understood. Two posts below this one is a link to a training video for police officers. Please post the HECK out of this link!

The boy in the above story sounds a lot like a 16 year old version of my Ammon (5). Like Ammon, he was watching cars drive by and when someone came up to him to see what he was up to, he ran off. That is EXACTLY what Ammon would have done.

Just because someone does not recognize a policeman's authority does not deserve a belt to the head needing EIGHT staples! I'm hoping that there is more to this story then some rogue policemen whacking teenage Autistic kids.

I LOVE my children with Autism, and do not want to change them just to make ME feel better. It's stories like these that make me want to find that elusive 'Autism Cure' so they will better understand the world.

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, April 13, 2009

New Law Enforcement and Autism Training Video

Last week Robin and I attended the Autism Council of Utah (ACU) It was the second I had been to and it is always well attended by various state agencies, other public and private groups and parents.

One of the highlights was the showing of a DVD geared toward Law Enforcement and Autism. SaharaCares developed the video that can be used to train police officers on how to recognize signs of Autism, and gives constructive suggestions for dealing with people that have Autism.

I hope that this can go out to police departments all over the country. Too often we heard of some Autistic person having a bad experience in this area. After watching the video tell me if you too teared up like I did.

The website link with video, click here

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.

Saturday, January 17, 2009

Autism Gospel, According to John

From a recent post at a group I belong to, it was asked about how neighbor kids and their parent relate to your Autistic child.

I said: it is very difficult to find parents and children that are accepting of an ASD child. We have discovered who our real friends and family are since getting our dx on the children in Oct 2006. We have everyone we know falling into one of 3 groups. Accept us, hate us or ignore us. The largest for our experience is, ignore us. Then hate us, and the smallest is accept us. Unfortunately a lot of family and friends are NOT in the accept us group.

But, like I said, you really find out about people when Autism comes into your life. It hurts for awhile, but we have made new friends and 'family' to replace the old. Find local groups to be a part of, learn from and develop friendships in groups like these and work on developing a thicker skin.

I feel that we, and all Autistic parents, were chosen by God to care for these special spirits he has entrusted us with. And where much is given, much is expected. We have children of light that must not be hidden, but should be placed on a hill for all to witness and enjoy. If ignorant and uncaring people cannot see that they are indeed special, and not in the typical 'special' label way, then that is their failing.

I really believe that the rise in Autism is part of the preparation for Christ's return. If someone cannot be accepting of a child or adult with a disability, then they can have no part in his kingdom. He must separate the wheat from the chaff, the good from the bad. We and our families are his servants doing some sifting.

Now, I'm not saying that I'm some saint or that I'm perfect. But, I do feel that we have been given a task and there may be some suffering, like the early Christians, for us to bear. If we stand strong, do not wilt and move forward with conviction we will be able to increase the acceptance and tolerance of people with Autism. "...when ye are in the service of your fellow beings ye are only in the service of your God."

I'll get down from the pulpit now; I hope that I have not offended anyone. I just feel very strongly about our roles as parents of Autistic children.

Dad

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

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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

Wednesday, December 3, 2008

Study Shows Families' Financial Strain From Autism

More than half a million U.S. children have autism with costly health care needs that often put an unprecedented financial strain on their families, national data show.

Compared with parents whose youngsters have chronic health care needs but not autism, those with autistic children are three times more likely to have to quit their jobs or reduce work hours to care for their kids. They pay more for their kids' health needs, spend more time providing or arranging for that care, and are more likely to have money difficulties, the study found.

"This is the first national survey that looked at the impact on families of having kids with special health care needs," said lead author Michael Kogan, a researcher with the government's Maternal and Child Health Bureau.

The results are from a nationally representative 2005-06 survey of nearly 40,000 children with special health care needs. These children have a broad range of chronic conditions, including physical and mental illness, requiring more extensive than usual medical care.

A total of 2,088 children with special health needs had autism, which translates to about 535,000 kids aged 3 to 17 nationwide, the study authors said.

The study appears in December's Pediatrics, being released Monday.

Autism typically involves poor verbal communication, repetitive behaviors such as head-banging, and avoidance of physical or eye contact. Affected children often need many more types of treatment than kids with other chronic conditions, including speech and behavior therapy and sometimes medication. Kogan said that may explain the disproportionate strain on their families.
Jacquie Mace, whose 12-year-old son, Austin, has autism, said the study presents a "very realistic" picture of the challenges affected families face.

Mace said she spends "easily $15,000 to $20,000 out of pocket" yearly on supplies for behavior treatment she provides for her son.

She's still working to pay off a $7,000 bill for dental work Austin had last year. He has to be sedated and hospitalized for dental care because he can't sit still in a chair, Mace explained. Austin's health insurance doesn't cover any of it, she said.

Some states require insurers to cover certain autism treatment while similar proposed measures are pending in others, including Illinois.

Mace hasn't had to quit her job helping local families find autism resources, but knows of many parents who've had to leave work to care for their autistic kids.

She is divorced — another common casualty, she said, of the challenges of caring for autistic kids.

Story link: http://www.iht.com/articles/ap/2008/12/01/america/MED-Autisms-Costs.php

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For we that are parents of children with Austism, this story falls into the catagory of: 'about time others figured this out'. Since we have not had anyone come forward to help with the creation and financing of the AutismBites Foundation (see AutismBites website link for more info:
http://www.autismbites.com/foundation.html) we have come to the conclusion that we will have to do it by ourselves. The process and grants to families in need will unfortunately be much slower, my goal is to start helping families this Spring.

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