From the Mail Bag: Fall Autism Gossip 2


Neighborhood

By Admin, Section From The Streets
Posted on Wed Aug 23, 2006 at 08:11:07 AM EST

It's back to school time! Anyone in the Springfield R-12 District interested in exploring the possibility of starting a SEPTA-Special Education PTA? Please email the gossip at drrethman@yahoo.com

The Family Bridges (Bringing Relevant Information Delivering Genuine Enthusiasm To Systems of Care) meeting for Greene County will be Tuesday September 5th (first Tuesday of each month) from 6-8 p.m. Their membership includes families dealing with severe emotional disorders, behavioral disorders and those with co-occurring diagnoses. The Greene County Bridges meeting is at North Point Church, visible on the north side of I-44 just west of the Humane Society. Childcare is provided, as is a potluck dinner! Call 872-9594 for more information or email them at thefamilybridge@aol.com.  

Ann Boushey will be at The Second Annual Authors' Fair at the Library Center September 9th 10-Noon. She will be there with her new book: Talking Teenagers: Information and Inspiration for Parents of Teenagers with Autism or Asperger's Syndrom e. Her previous book on autism is a part of the library collection and available for check out--Parent to Parent: Information And Inspiration For Parents Dealing With Autism Or Asperger's Syndrome.

At the September 19th ANJEL (A Natural Journey toward Empowered Lives) meeting the guest will be Dr. Pierce from a local vision clinic. ANJEL meets at Campbell United Methodist from 6:30-8:30 p.m. Activities are always provided for the children in attendance so please RSVP your children with Lisa Slattery at 882-4063. You can also reach her at icanlaff@sbcglobal.net

Families 4 Families - Greene/Christian Network holds monthly meetings in Springfield. Families 4 Families is a support/advocacy network for Families with Children/Youth with Severe Emotional Disorders (SEDs). Lynn Prince and Kathy Lutz, Co-Coordinators You can reach them by email at families4families.greene@gmail.com. Their website is very informative: www.families4familes.org.  

The Southwest Missouri Walk for Autism Research will take place on Saturday, October 21st at JFK Stadium, Springfield, Missouri. You can register a team and find out more information about getting invovlved at www.autismwalk.org OR by calling the Walk office at 866-500-6227 OR contact Elizabeth Aley, local Co-chair at 724-0331 and/or autismwalk@cebridge.net.  

MPACT's Annual Conference is September 15th, 2006 from 9:00-4:00 a.m. at St. Louis. The cost for a parent is $50.00, both parents $75.00. See attached flyer (created in Adobe Acrobat). You may also register on-line at www.ptimpact.com

The Network has taken over the information dissemination duties of Disability connections. To receive email updates from them on a range of disability topics call them at 895-7464 or email them at sdasn@aol.com. The following is a forward from The Network from the Missouri Planning Council for Developmental Disabilities The Partners in Policymaking Application for 2007 is attached--I think. If not the application can be accessed at: www.mpcdd.com. 

Lorman Education Services will be presenting a one-day seminar, Understanding Individuals With Asperger's Syndrome Or High Functioning Autism, in Springfield on Friday October 20th, 2006. {The Day Before the Walk} The speaker is Beverly Bishop. She is the author of the Future Horizon Book, My Friend With Autism. The cost for the day is $299.00. For more information visit their website, www.lorman.com; email them at customerservice@lorman.com; phone 866-352-9539.

The August edition of Town and Country has a very good article about autism. 

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Father, Son Document Autism
By Sean Ludwig - Southeast Missourian

David and Taylor Crowe just can't sit still.

Whenever the father and son have a spare moment, they are always doing something productive. 

David, an orthodontist who lives in Cape Girardeau, and Taylor, his autistic son, are currently involved with projects aimed to educate people about autism.

Not only are they working on bringing to life The Tailor Institute, a not-for-profit organization dedicated to autism research, but they also are putting the finishing touches on a new DVD that will help people understand autism. 

Autism is a spectrum disorder. It can range from the low-functioning, which can include mental retardation, all the way to genius-level intellect with social difficulties consistent with autism, David said.

The Tailor Institute, which received a $200,000 grant from the Missouri Department of Economic Development, is attempting to advance the systems of care and services for high-functioning autistics. The organization has conducted interviews with parents, physicians, therapists and educators. It is developing educational materials and will begin conducting more research in the fall. 

In 2000, the Crowes finished "Growing Up With Autism," a 20-minute VHS tape that shows Taylor's development growing up and ways to cope with the disorder. The DVD is a new, extended version of "Growing Up With Autism" and it runs about an hour with bonus materials. 

The old video showed Taylor up to age 19. The new version incorporates how the 25-year-old lives with his disorder as he attends the California Institute of the Arts in Valencia, Calif.

"The target audience is educators, families, parents, siblings and people that either are new to the diagnosis of autism or want to learn more about it," David said. 
Taylor said the video was important because autistic people can misinterpret things like teasing and joking.

"Some of the teachers I had as a kid would say stuff to me that 

made me think they wanted to kidnap me," Taylor said. "One said if I didn't 

get my work done, I'd never go home. They were teasing. I didn't know that."

Taylor said for this and several other reasons, educators need to be educated on autism.

He also said all autistic people should have a "circle of friends," and encourages them to have a variety of friends, all of whom are familiar with autism. 

"Autistic people need friends, too," Taylor said. "I have a friend with Asperger syndrome who says I'm his chief number one friend. The reason is because he never had a circle of friends."

The first version was produced by Showcase Productions (now Showcase Technologies) and began being distributed in 2003 by the Council for Exceptional Children's Division on Developmental Disabilities. More than 3,000 copies of the video have been sold. 

Tom Emmendorfer, who works at Showcase Technologies, is producer and editor of the DVD project and has spent more than 100 hours shooting footage, editing and conceptualizing ideas. Emmendorfer said they aim to have the project finished by early September.

"I see the potential Taylor has to offer the world," Emmendorfer said. "I see the gift he has and it's neat to be a part of that."

Taylor, who is high functioning, is studying animation at CalArts and intends to graduate in May 2007. He aspires to work at Dreamworks Animation.

When Taylor isn't studying or painting, he gives speeches at autism conferences. His next speech is at the 2006 Texas State Conference on Autism in September.

"I don't enjoy rehearsing and all," Taylor said. "But I know it's something I have to do to help other people with autism." 

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

SMALL POND 
author unknown to me

If you have a child with autism, which I do, and if you troll the Internet for information, which I have done, you will come across a certain inspirational analogy. 

It goes like this: Imagine that you are planning a trip to Italy. You read all the latest travel books, you consult with friends about what to pack, and you develop an elaborate itinerary for your glorious trip. The day arrives. You board the plane and settle in with your in-flight magazine, dreaming of trattorias, gondola rides and gelato. 

However, when the plane lands you discover, much to your surprise, you are not in Italy -- you are in Holland . You are greatly dismayed at this abrupt and unexpected change in plans. You rant and rave to the travel agency, but it does no good. You are stuck. After a while, you tire of fighting and begin to look at what Holland has to offer. You notice the beautiful tulips, the kindly people in wooden shoes, the French fries and mayonnaise, and you think, "This isn't exactly what I planned, but it's not so bad. It's just different." Having a child with autism is supposed to be like this -- not any worse than having a typical child -- just different. 

When I read that, my son was almost three, completely non-verbal and was hitting me over a hundred times a day. While I appreciated the intention of the story, I couldn't help but think, "Are they kidding? 

We are not in some peaceful countryside dotted with windmills. We are in a country under siege -- dodging bombs, trying to board overloaded helicopters, bribing officials -- all the while thinking, "What happened to our beautiful life?" 

That was 5 years ago. My son is now 8 and though we have come to accept that he will always have autism, we no longer feel like citizens of a battle torn nation. With the help of countless dedicated therapists and teachers, biological interventions, and an enormously supportive family, my son has become a fun-loving, affectionate boy with many endearing qualities and skills. In the process we've created, well, our own country, with its own unique traditions and customs. 

It's not a war zone, but it's still not Holland . Let's call it Schmolland. 

In Schmolland, it is perfectly customary to lick walls, rub cold pieces of metal across your mouth and line up all your toys end to end. You can show affection by giving a "pointy chin." 

A "pointy chin" is when you act like you are going to hug someone and just when you are really close, you jam your chin into the other person's shoulder. For the person giving the "pointy chin" this feels really good, for the receiver not so much - but you get used to it. 

For citizens of Schmolland, it is quite normal to repeat lines from videos to express emotion. If you are sad, you can look downcast and say "Oh Pongo." When mad or anxious, you might shout, "Snow can't stop me!" or "Duchess, kittens, come on!" Sometimes, "And now our feature presentation" says it all. 

In Schmolland, there's not a lot to do, so our citizens find amusement wherever they can. Bouncing on the couch for hours, methodically pulling feathers out of down pillows, and laughing hysterically in bed at 4:00 am, are all traditional Schmutch pastimes. 

The hard part about living in our country is dealing with people from other countries. We try to assimilate ourselves and mimic their customs, but we aren't always successful. It's perfectly understandable that an 8-year-old boy from Schmolland would steal a train from a toddler at the Thomas the Tank Engine Train Table at Barnes and Noble. But this is clearly not understandable or acceptable in other countries, and so we must drag our 8 year old out of the store kicking and screaming while all the customers look on with stark, pitying stares. But we ignore these looks and focus on the exit sign because we are a proud people. Where we live, it is not surprising when an 8-year-old boy reaches for the fleshy part of a woman's upper torso and says, "Do we touch boodoo?" We simply say, "No we don't touch boodoo" and go on about our business. It's a bit more startling in other countries, however, and can cause all sorts of cross-cultural misunderstandings. And, though most foreigners can get a drop of water on their pants and still carry on, this is intolerable to certain citizens in Schmolland who insist that the pants must come off no matter where they are, and regardless of whether another pair of pants are present. 

Other families who are affected by autism are familiar and comforting to us, yet are still separate entities. Together we make up a federation of countries, kind of like Scandinavia. Like a person from Denmark talking with a person from Norway, (or in our case someone from Schmenmark talking with someone from Schmorway), we share enough similarities in our language and customs to understand each other, but conversations inevitably highlight the diversity of our traditions. "Oh your child is a runner? Mine won't go to the bathroom without asking permission." "My child eats paper. Yesterday he ate a whole video box." "My daughter only eats 4 foods, all of them white." "My son wants to blow on everyone." "My son can't stand to hear the word no. We can't use any negatives at all in our house." "We finally had to lock up the VCR because my son was obsessed with the rewind button." 

There is one thing we all agree on: we are a growing population.

10 years ago, 1 in 10,000 children had autism.

Today the rate is approximately 1 in 250.

Something is dreadfully wrong. Though the causes of the increase are still being hotly debated, a number of parents and professionals believe genetic pre-disposition has collided with too many environment insults -- toxins, chemicals, anti-biotics, vaccines -- to create immunological chaos in the nervous systems of developing children. One medical journalist speculated that these children are like the proverbial "canary in the coal mine" here to alert us to the growing dangers in our environment. While this is certainly not a view shared by all in the autism community, it feels true to me. 

I hope that researchers discover the magic bullet we all so desperately crave. And I will never stop investigating new treatments and therapies that might help my son. But more and more my priorities are shifting from what "could be" to "what is." I look around at this country my family has created, with all its unique customs, and it feels like home. For us, any time spent "nation-building" is time well spent.

< Greene County Clerk of Circuit Court Michael Carr Under Criminal Investigation | The Urban Permaculturist: Food Not Lawns Issue, Late Summer 2006 >

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From the Mail Bag: Fall Autism Gossip 2 | 170 comments (170 topical, 0 hidden)
Autism (none / 0) (#1)
by Anonymous on Thu Aug 24, 2006 at 08:29:48 AM EST
   I am so glad to see so much information
available about autism. As more information
comes out the myths can be shelved. The help
that comes from just sharing a story from
parent to parent is a boon. It also helps
others who come into contact with Autistics.
   Also what shines through is the love these
parents have for their children. What we once
considered a burden has become a connection to
a larger life than itself. Along the way we
learn about autism but also too these children
teach us as well.

From the Mail Bag: Fall Autism Gossip 2 | 170 comments (170 topical, 0 hidden)
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