Showing posts with label Family Info. Show all posts
Showing posts with label Family 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."

Friday, January 8, 2010

Sorry for Being Gone

Well, I'd imagine that we've lost just about every follower that we had for this blog by now. But, I quess that it will give me a place where I can write and not worry too much about what I say.

The car contest was a BIG flop. So much for 6 weeks of work to create the video. Some people were very helpful watching it a bunch, but that was about it... a few people. Got a lesson in knowing how many people were able to help us, I thought I was more known about or something. Boo Hoo...LOL!

I and Robin have been hanging out a LOT more on Facebook the past month. I've also been doing a lot of Twittering and on the business site: LinkedIn.

I've decided that I will leave this blog just for family stuff only, and of course when I can get to it. I've been very busy launching my business expansion. Here are some links to find the other places I hang out. Be my friend there if you like.

Facebook
Twitter
LinkedIn
YouTube

Dad

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.

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, July 17, 2009

I'm Coming to a Town near You

Life is settling down to somewhat of a routine once again and I'm back to blogging and Autism advocating. I've added videos back onto our YouTube page and will be adding more as I'm able.

As I travel in my 18-wheeler doing my new job as a trucker, I make stops all over the USA. I would like to meet as many of you as I can. As I receive assignments to know where I'm going, I'll post to this blog what truck stops I expect to stay at at the end of each driving day. If you live in the area I'll be staying, send me an email at: autism_bites@yahoo.com with a subject of: truck stop visit. Include your phone number, I'll call to set up a time and we can get together. I'd like to take pictures too and include them in this blog if you don't mind.

Let me know what you think and any suggestion you may have.

Dad

Sunday, June 14, 2009

Life on the Road

This is just the second time I've been home since May 28th when I started my final "on the road" training to be a truck driver of a 74' tractor and trailer. I've been to WI, MI, IN, UT and CA, then of course through the states in between. Two things have been the hardest so far: trying to sleep on the bed in the sleeper of a moving truck as it bounces along the Interstate roads and getting a sore butt while driving for 9 - 10 hours straight.

Two more weeks and I'll be assigned my own truck and I'll be able to better establish a routine for me and my family.

Dad

Saturday, May 23, 2009

Things Are Looking Up



I like many have been struggling with earning what our family needs lately. Last year was going well until November when the economy took its hit. I've tried to continue to earn with our internet businesses, BUT it wasn't making it. I sent out nearly 100 resumes in the last couple of months and only got a few nibbles. So after much discussion between Robin and I... prayers etc. we decided that I should go through the training of becoming a over the road trucker.

The accelerated class I started 2 weeks ago had 42 students, yesterday just 13 were left that passed all the requirements. I was in that group, of course ;) By the end of this coming week I'll be hitting the road for an additional 14,500 miles with a driving trainer to learn the actual on the road experiences. It will be somewhat difficult for Robin and the children, but I have to earn for our needs of course. Please pray for her especially and the family generally if you would. After I get settled into the job I'll be back on this blog and some of our other online hangouts.

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.

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

Friday, November 21, 2008

It's The Most Wonderful Time of the Year




First Ammon got it, then Sarah was the next day and then last night Robin had it. So far the rest of us are OK, but we'll see what the weekend will bring. **UPDATE** Saturday: Mary had it last night and Bobby has it today, and on his birthday too. Poor boy...

Dad

Monday, November 10, 2008

Trying to Be More Like Jesus

On Sunday, November 9, 2008--yesterday--we did something we have rarely attempted over the last couple of years or so...we all went and stayed at church, ahh!!!!

It was a special occasion. The children's group at our church, called the Primary, put on their annual sacrament meeting presentation. Our "sacrament meetings" are when the entire congregation gathers together in the chapel for one hour church service, this is in addition to a couple of hours of classes. The children ranged in ages from 3 to 11, and even though our group of kids is kind of small--we have a lot of empty nesters and senior citizens in our congregation--it's always a BIG deal. After all, hearing kids sing and gave little talks during church service is absolutely precious. Those beautiful young faces looked like little angels up there.

Our youngest, Mary, 3, was wearing an all white ruffled dress that kind of bounced and flowed along with her as she moved. She has been able to join and stay with the Primary most of the time with the help of a bag of books the leadership put together to help encourage and calm her down. But, apparently there was just too much stimulation with the entire congregation and their visitors like grandparents and aunts and uncles and cousins to keep Mary with the program, literally and figuratively! First, she wanted to draw, then she wanted to sit on my lap, then she kind of wanted to join her class, but when she started climbing the steps to the stand, she turned around and smiled like a little showman. She then started jumping up and down on the stairs, beaming all the while as she made a louder and louder thumping sound. After whispering a few times to get down, she had to be fetched. She didn't last much longer and Bobby, 14, had to chase after her into the hallway.

Ammon, who just turned 5, always loves being in the chapel when we sing hymns, he loves music. But, when we're not singing, we lose him quickly. I think we almost got through to the passing of the sacrament--the bread and water in our religion, to help us remember the body and blood of Jesus Christ who sacrificed Himself for us so that we can receive a remission, or forgiveness, of our sins--when John had to take off into the hallway with Ammon and Sarah. Sarah lasted the longest, was pretty calm and quiet until she kept bouncing and making her sounds that got too loud and distracting.

So, after the passing of the sacrament, they started the Primary program. Mary was supposed to be one of the first speakers, she'd be repeating a couple of sentences with help from a leader. She made it back to the chapel by then, but kept going here, there and everywhere, and Bobby ended up having to follow her out again. So, Mary didn't make it to the pulpit--like she cared anyhow little stinky winky....

Nephi, 9, did an amazing job singing. He forgot his glasses, so he couldn't read the visuals for the lyrics, but he moved his mouth almost the whole time during the songs. He also did a good job reading.

Emma was asked to write a short little talk, and we realized that maybe we should have remembered to look at it before hand, some of it that is....She talked of her family. She said that she and all her brothers and sisters have autism, then she mentioned the severity of each kids autism. She said that we're a very close family, how sweet. She then said that mom and dad get mad and yell sometimes, but they still love us! She then said that Extreme Makeover Home Edition called us and wants us to apply, that we really need a new house because it's little and the babies destroy it, but we can't get on the show because we're renters. She then mentioned our documentary and that everyone should watch it when it reruns on Discovery Health and TLC. We're very proud of her, spoken from the depth of her heart, nothing genuine held back, and with the charisma of a true spokes person.

Near the end of the program, they did a little presentation of the special needs primary children. Unfortunately Sarah was in the hallway screaming her head off, so she didn't make it and Mary was AWOL with Bobby. A 10 year old boy started counting, this is huge for this child because he has classic autism and has been making huge strides in his language the past couple of years. This boy also said "Jesus!"

Then, one of the leaders talked a bit of how special these children are, and I think it may have included some talk of tolerance, patience, respect, and how much like Jesus these children are. We believe in our religion that kids and people with mental challenges are innocent, that they were already perfect in Heaven before they came to earth, but that they needed to come to earth to get a body more than anything, that and to be a learning experience and example to the rest of us, to help the rest of us become better and make it to Heaven too. The leaders tried to encourage and help Ammon hold up a picture of Jesus Christ in the garden of Gethsemanie. The children then sang "I'm Trying to Be Like Jesus". This song is my favorite of all the children's songs in our religion. It was so touching. I usually tear up when I hear this song, but there was just too much going on for me to soak it in--and before the song could end, Ammon dove head first from the dividing wall on the stand, then ran off, that boy!!!!

Here is a link to the song "I'm Trying to Be Like Jesus" by Janice Kapp Perry--I think it's sung by Felicia Sorenson though...

Sincerely,

Robin Kirton

Saturday, November 8, 2008

Ammon Turns Five

Ammon's birthday was yesterday. He still tries to touch the candles instead of blowing them out, but he has made so many improvements this past year. Just this morning when he was out of breakfast cereal he came to me with the bowl and shook in in front of me. As if to say, "Hey my bowl is empty!" It was cute.

This year he has gone from no words to at least a dozen. Maw (Mom), Be Be (Baby) he usually uses this to bring attention to his needs, he's the Be Be. And so far we haven't received calls from school that he has bitten someone. Overall great progress for the little guy.





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

Thursday, August 21, 2008

Back to Minnesota for a Wedding

Sorry guys, I've been pulling all nighters getting ready to put up a new business website. Not done yet however.

Then we've been doing a lot of running around getting the gang ready for school this next week. ALL of our pumpkins will be in school for the full day! We'll miss them, BUT we will sure be able to get a lot more done around the house.

Oh yeah, THE WEDDING... My oldest son, Ben and I made the trip alone. Robin stayed home and went crazy with the children.

The lovely bride is my sister's daughter, Deanne (you can see that see gets her looks from my side). Her soon to be husband, Tony.



This is me and my sister Sherri...



My sister-in-law said she had better not see any pictures of her, this is one of her daughter Shannon. Not sure who the other lady is (wink, wink). The other picture here is of my other cute little niece, Maria.


Then there was this young man I kept running into. He was always texting. I never really got a good look at his face because he was always looking down. But, I'd swear he looks a lot like my eldest son, Ben.





I gave my Mom one of our AutismBites t-shirts. Mom has always been one to tell you like it is, this shirt definitely reflects that.



The main reason we went was for Ben to finally meet his Grandmother 'in the flesh'. The wedding gave us a good excuse to make the four day there and back driving worth it.

Dad

Thursday, July 24, 2008

Spongebob and The Great Giggle Box

A couple of nights ago, the night after our PARTY FOR THREE, Mary, 3, woke up crying. I sort of woke up from it, but then staggered to bed when I saw John awake. I assumed he was going to deal with her. In time, I kept hearing John moan and groan as Mary kept crying. John was too tired to be very patient, and was letting her cry for a time seeing if she would fall asleep again, like she usually does.

Well, Mary kept crying and John was losing it. So, I got up and told him to go to bed, I'll deal with her. I asked Mary "You wanna hold mama?" She said "Mama hold you." Sometimes mom is the only thing that will make a child happy. We had to put on a Spongebob DVD because that's Mary's current obsession. It used to be Blue's Clues and Elmo. She won't watch Blue anymore, and Elmo not so much, it's almost always "Bah Bob on DVD!" now. As John and I were talking in the middle of the night while I was changing Mary and getting her ready to sit with me, from down the hall we heard a little "Hee hee!" We kept hearing it over and over again and were looking at each other like "Uh oh." So, John got Sarah, 6, our little giggle box, and brought her into the living room to change a rank bomb in her pants. He then went to bed as me and the little girls had a slumber party. Sarah bounced and frolicked around giggling like there was no tomorrow. She likes to get real close right in my face and roar with laughter, nearly making me deaf in the process. I tried to sleep in the recliner, but couldn't get comfortable enough. Mary finally passed out cold and laid down on the couch. Sarah was still bouncing off the walls in a jovial frenzy with more "Hee hee!"'s in my face. I was so wasted, I'd had enough. So, I replayed Spongebob and made sure the room was safe--the dividing wall up and the bathroom locked--then I went to bed.

A few hours later, I came into the living room to check on them. Sarah was leisurely sitting in my recliner, and as I looked at her in the dimly lit room, she looked right at me as her mouthful of teeth emerged, her eyes lit up and twinkled and she went "HEE HEE!"

She started to nod off about then, but then perked up again. She giggled all the way to the bathtub and in the bathtub. Later, when I called her name a few times to tell her I needed to dry her hair, she said "Say ah, Say ah." She's never said her name so clearly before!!!!!

Here's Sarah after she got home from school yesterday....














By the way, Ammon, 4, is progressing so well in his communication. After he had his after school snack, he comes up to me and sticks his finger in my face with gooey and chunky brown stuff on it--and I didn't give him chocolate. Hey, at least he didn't wipe it on his clothes and not tell me about it. For that, I totally couldn't get upset with him, I was just SO PROUD of my boy!!!

Sniff sniff...

Mom

Wednesday, July 23, 2008

A Party For Three

Hi folks!

Please forgive me for not writing much lately, I'm just so tired most of the time, argh. Well, I just had to tell you about some of our latest adventures with the little ones around here....

We were invited to a neighborhood block party yesterday evening. We were looking forward to it. So, although I could picture in my mind how it was going to be with our little ones once we got there, we chanced it anyhow. After all, we like being social, we really like our neighbors and we don't get out much. We made sure not to forget to put their autism bites shirts on as well since we may not already know everyone there.

So, we put Ammon, 4, in the stroller, Mary, 3, walked with Nephi, 9, and Sarah walked with me holding the side of the stroller as we moseyed down the street. We went into the back yard where we saw two guests that had arrived so far, and the children immediately went into a frenzy on the teeter totter and trampoline as these guys looked on in awkward silence. However, Sarah, 6, went straight for the flower garden until the dogs came excitedly running out. Sarah then screamed loud enough for the entire neighborhood to hear, which made the dogs even more excited as they ran up to her this time going "Ar ar ar ar ar!!!" So, Sarah continued to scream bloody murder. The dogs soon ran off elsewhere while Sarah was still shaking in her sneakers, but then...."Ar ar ar ar!!!!" again. The owner of the home then came out and loudly exclaimed something like "Don't run from the dogs or yell and scream because that just makes them get louder and more agitated!" Well, I stood there stunned. Well, it was private property and a happy event, so I kept my emotional reaction to myself and quietly started taking off with Sarah and Ammon as fast as I could. As I was leaving, the wife of the home kindly told me that they put the dogs in the house. I said something like "Oh, it's okay. She pulled up some of your flowers too."

So, I took them to our favorite hamburger joint, Arctic Circle. I prayed mightily to God that they would behave there, especially since it was just them and myself. On the way in, Ammon ran around some cars in the drive through, but we otherwise made it in alright. Ammon immediately went to the play land, and Sarah sat at the high table patiently waiting--I think God is very generous with tender mercies, especially when they are much needed.

A young family was sitting in the booth Ammon usually sits with us at. He tried to sit with them and started going for their food when I said "Nuh uh, Ammon" as he smiled slyly, then went off to the play land. Sarah and Ammon soon inhaled every last morsel of their fries and chicken rings. With Ammon, when he finally joined us, he started scooping his food up with his hands. I looked away for a moment and when I looked back, it was ALL gone. I looked to see if it was on the floor, then noticed that his cheeks were stuffed full as he was quickly and carefully chewing it all before it went down the hatch.

They soon were playing, and then Ammon was playing with the door. A 7 yr old boy with high functioning autism next to us told me that my son was at the door. I thanked him for telling me, that he's a good helper. Ammon had vanished right before that in what seemed like an instant. The 7 yr old boy's mom and I started visiting and by the time Ammon ran to the drive through for the third time, I had it. I gave Sarah what was left of my pop so she wouldn't fuss and I scooped up Ammon and we went to the car....Back at home, I watched them play outside in the back yard. In a first, Ammon kept coming up to me with a big sweet smile and taking his hands behind my back and butt to try and bring me to the swing where I had to swing him for like an HOUR. He was quite the laughing, happy boy as Sarah frolicked around the yard trying to eat dirt and unripened fruit from the trees.

...We may very well have to wait for the next life to be able to have and go to parties like everyone else. Oh well, this life is real short compared to eternity anyhow....


Robin Kirton.....the mom