
Setting the Research Agenda for Autism Speaks- An interview by Diane Twachtman-Cullen, Ph.D., CCC-SLP
Meet the new, eminently qualified scientific leader of Autism Speaks.
Click here to read the interview.
|

Diane Twachtman-Cullen, Ph.D.

Liane Holliday Willey, Ed.D.
|
Autism Spectrum Quarterly News Brief
Autism Spectrum Quarterly Editors Judge the Autism
Tissue Program’s Undergraduate Juried Poster Contest:
And the Winner Is . . .
To raise awareness of their brain donation
program, the Autism Tissue Program
(ATP) sponsored a poster contest in which
undergraduate students were asked to create a
poster to highlight ATP’s important message.
The editors of ASQ were asked to judge the
entries. Because of the number of entries submitted,
the choice was diffi cult, but the editors
of ASQ are pleased to announce that they have
indeed selected a winner. The winning poster
was submitted by Teri Baker of Eugene, Oregon,
and was on display at the 36th annual meeting
of the Society for Neuroscience held in Atlanta,
Georgia from 10/14/06 through 10/16/06. The poster will also be displayed in clinics and at
conferences, nationwide. We at ASQ extend
our heartiest congratulations to Teri.
ATP is a national brain tissue donor program
that gives over 42 scientists, worldwide, the
opportunity to research the causes of, and
treatments for autism, by making available to
them precious, post mortem brain tissue. This
brain tissue research allows these scientists to
understand the basic neurobiology of autism
so that advances in preventing and curing
this disorder may be possible. This research also assists in the development of improved
day-to-day treatments and educational interventions,
appropriate medications, and a new
understanding of the genetics of autism.
You can help if you are the parent of a child
or children with autism, are related to someone
with autism, or have autism yourself. The
ATP is encouraging entire families to consider
donating brain tissue for research. In addition,
researchers also need brain tissue from people
without autism for scientific comparison. To
learn more about the program and to register,
please visit www.memoriesofhope.org or call
1- 877-333-0999.
|
Teri Baker Writes about Ragan
Ragan McKaye, my youngest daughter, was a
darling child with an innate sweetness about her that was hard for
anyone to resist. Ragan had the most engaging “DQ” smile to go
with the twinkle in her eye. But in spite of her liveliness of spirit,
Ragan was unable to share her thoughts, her fears, or her pleasures
with her family, because of her autism.
Ragan didn’t talk until after her eighth birthday. Her speech was
echolalic, with a long phase of perseveration thrown in for good
measure. In spite of her diffic ulties with language, Ragan never lost
her sense of humor. She found the funny in most every situation,
including her own mistakes. Ragan was one of the few children I’ve
known who could laugh at herself.
Despite the obvious outward signs of her autism (vocal/physical
stims; awkward gait; anxiety), Ragan always tried to act as normally
as possible, for as long as she could, when she was in public.
Ragan’s two older sisters, Erin and Morgan, never hesitated to take
their little sister out for a “Sisters’ Saturday Shopping Day”. These
once-a-month outings often included a movie. Sometimes Ragan
wouldn’t be able to sit through the film, in which case one of her
sisters would walk through the mall with her until the film was over.
Or they would sit in the car and wait. Erin and Morgan were never
detoured by Ragan’s disability. Quite to the contrary, they never
failed to find a way to include her as much as her endurance level
would permit. I think that how we loved Ragan makes it easier for
us to miss her, because we embraced her so fully.
I was Ragan’s teacher, and I was always on task. From the time
Ragan got up in the morning, until she went to bed at night, I was
her constant instructor. In hindsight, I am not sure I had as much fun with Ragan as I could have had, although, we did have fun and
funny moments together.
I remember the time I had Ragan help me wallpaper the ceiling in
our bathroom. That was when I taught her the meaning of words
and phrases like: push, push up, pull, pull down, hold, don’t move,
and wait just a moment longer. Ragan was almost
always up to lending a hand with any task, and
did so with a smile on her sweet face. She was an
inspiration to her family and her community.
Long ago—many years before Ragan died—I
realized that this youngest child of mine was a
gift. I hope I have honored her gifts, because in
the end it was Ragan who was my teacher.
|
Bio
Teri Baker, mother of Erin, Morgan, and Ragan, was divorced
one year before Ragan’s death. Her two older daughters lived with Ragan
and Teri so that they could watch Ragan while she was at work. Teri
worked in the mornings; Erin and Morgan worked in the afternoons
(Erin and Morgan own a martial arts school). It was through their experience
with their sister, Ragan, that Erin and Mo expanded their school
to accommodate children with autism. At present, Teri works in the
Springfield School District as a special education teacher’s aide, working
directly with children with autism. She is an American Heart Association
certified BLS CPR Instructor, and is enrolled at Western International
University in its undergraduate program in Behavioral Science. Teri also
sits on the advisory board for the Northwest Health Foundation, which
awards two-year fellowships to local autism researchers. Despite her very
busy schedule, Teri is also a volunteer leader for Autism Speaks.
|
|
|