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Archive for June, 2011

Autism in the News – 06.21.11

June 21, 2011 1 comment

Four parents of autistic children sue Philadelphia School District (Philadelphia, Penn.)
Four parents have filed a class-action lawsuit on behalf of their autistic children, alleging that the Philadelphia School District is illegally moving the children from school to school based solely on their disability. Read more.

Joplin Tornado Destroys More Than Buildings (Joplin, Mo.)
On May 22, 2011 an EF5 tornado, jokingly referred to in the movie Twister as “the finger of God,” tore through Joplin, Missouri. Almost 30% of the city was destroyed, including one of the two main hospitals. Read more.

Beechwood College Cardiff Art for Autism photo gallery (UK)
Beechwood College, near Cardiff, has launched a national art competition to showcase the creativity of young people with an Autistic Spectrum Disorder (ASD). This entry is from James Bowler, 18., from Bury in Greater Manchester. Read more.

Hamilton Theater welcomes film-goers who have autism (video) (Hamilton, N.Y.)
For a child with a sensory processing disorder, going to the movie theaters can be overwhelming and disorienting. Read more.

RF team earns autism group’s top-fundraiser title (River Falls)
For the past two years, the River Falls-based Cruisin’ for Carter team has earned the title of No. 1 fundraising group of the Walk Now for Autism event, held to benefit the nonprofit organization Autism Speaks of Minnesota. Read more.

Autism in the News – 06.20.11

Autism Center in Joplin, Mo. Hopes to Rebuild (Joplin, Mo.)
The Ozark Center for Autism in Joplin, Mo. says it remains committed to rebuilding its nationally-renowned program after the center was demolished by a deadly tornado that struck the city of Joplin last month, the Associated Press reports. Read more.

Autism bill passes state Legislature unanimously (Staten Island, N.Y.)
A bill that would provide health insurance for screening, diagnosis, treatment and therapy for individuals with autism passed the state Legislature unanimously on Friday, a crucial step for families seeking enhanced care for their children, said a Grant City mother. Read more.

Autism never got in the way of Naples grad Ian Liebentritt, on or off the court (Naples, N.Y.)
Ian Liebentritt was just 13 years old when Greece Athena High School’s Jason McElwain, who was diagnosed with autism at a young age, stepped into that national spotlight after playing in the team’s final regular season game. Read more.

Carroll youth coordinating golf outing, raising awareness of autism (Carroll, Penn.)
Michael Collier knows what it’s like to sometimes be misunderstood. As someone who has a form of social autism called Asperger syndrome, Michael admits he has trouble interacting with others, whether it be by failing to notice social cues or struggling to carry on a conversation. Read more.

Two Elk Grove boys skate for autism (Elk Grove, Calif.)
Two Elk Grove youngsters took to the highway for a remarkable journey on specialized skateboards to highlight the challenge of autism. Read more.


Diagnosing Autism Spectrum Disorder

June 20, 2011 48 comments

Parents are usually the first to notice the early signs or “red flags” of autism spectrum disorder.  Maybe it was something different they noticed about their child at birthday party, or the child not developing like a sibling. What was the experience that led you to seek professional advice for your child?

How did you feel when you or your child received an autism diagnosis? What were your initial steps? What advice would you share with someone who has been recently diagnosed? 

The Autism Speaks 100 Day Kit and the Asperger Syndrome and High Functioning Autism Tool Kit were created specifically for newly diagnosed families to make the best possible use of the 100 days following their child’s diagnosis of autism or AS/HFA.

Please join us Wednesday, June 22nd at 5 pm EST for ’100 Day Toolkit’ LIVE Facebook chat with the Family Services Staff. 

Ernie Els Featured on ESPN’s ‘Outside the Lines’

June 20, 2011 7 comments

On June 19, Father’s Day, Ernie Els was featured on ESPN’s Outside the Lines, discussing his son, Ben, who diagnosed with autism at 4 years old, changing his family. Tom Rinaldi describes a father and son’s journey far beyond the golf course. Click on this Outside the Lines‘ screen shot watch segment.

Els for Autism
“It is several years since our son Ben was diagnosed with Autism. We suspected for a few years that something was not quite right. There’s a process that every kid goes through. Crawl at nine months, walk at 12 months, and then start talking and so on. With Ben we started thinking: ‘Why is he not crawling? Why is he not walking? Why is he not looking me in the eye?’ Things like that. We soon discovered he was quite severely touched by Autism. We established the Els for Autism Foundation in 2009 with the goal of funding an Autism Center of Excellence, the first of its kind in the world. Autism hits families hard and I’ll be fighting for the rest of my life to try and help others in the same situation. I hope you’ll share an interest and join me in this fight.”  - Ernie Els

Congratulations to Denny Hamlin on his NASCAR Sprint Cup Race Win

June 20, 2011 2 comments

Congratulations to Denny Hamlin for claiming his first victory of the season in Sunday’s Heluva Good! 400 at Michigan International Speedway. Denny was able to hold off Matt Kenseth, crossing the finish line a mere .281 seconds ahead! Way to go Denny!

Click here for more on the Heluva Good! NASCAR Sprint Cup Race.

Denny Hamlin  piloted the No. 11 FedEx Autism Speaks Toyota at the FedEx Autism Speaks 400. and you can check out his Die-Cast Car here!

Family Services ’100 Day Tool Kit’ LIVE Facebook Chat

June 20, 2011 6 comments

Join us Wednesday, June 22nd at 5 pm EST for an online Facebook chat with the Family Services Staff. Using the 100 Day Tool Kit as our guide, we will focus on what you can do during the first 100 days following your child’s diagnosis and the steps you can take to get stated.

IACC releases 2009 Portfolio of grants

June 17, 2011 1 comment

The Interagency Autism Coordinating Committee (IACC) recently released their annual report on the portfolio of autism research funding for 2009. The report reveals that over $314 million dollars was spent on autism research from both federal and private sources. This report comes at a crucial time when the Combating Autism Act of 2006 (CAA) is under consideration for renewal. The CAA instigated the formation of the IACC which helps guide the appropriate use of federal funds for autism research.

So what was funded in 2009? The IACC breaks down funding into seven categories that stem from the key questions in the IACC’s strategic plan. The questions are listed in the figure below. In 2009, almost one-third of the funding (32% of total) went toward identifying risk factors for autism spectrum disorders (ASD).This category also received the greatest funding in 2008. The second and third most funded categories were investigations of the underlying biology of ASD (20%) and the development of treatments or interventions (20%). The categories receiving the least funding were services research (3%) and studies on autism during adulthood (<1%). The IACC noted these categories as special targeted areas for increasing funded projects in future years.

2009 included significant funding from the American Recovery and Reinvestment Act (ARRA) that Congress authorized earlier in the year. The National Institutes of Health used Recovery Act money to fund autism research with $64 million dollars that supported 141 new projects, which accounted for 33% of NIH’s autism research in 2009. The ARRA grants were targeted to address the IACC’s strategic plan questions and an analysis of those grants separately looks similar to the overall portfolio of grants. The greatest percentage of funding was allocated for studies of risk and underlying biology and least for services studies and understanding adult outcomes. The ARRA infusion of federal funds significantly increased the dollar amount of federal funding for autism research over 2008.

Overall, funding for autism projects increased by 21% from 2008 to 2009, much of this due to the ARRA funding.

The analysis also included a breakdown of funding by federal and private organizations. By far NIH supported the greatest number of projects (516) and granted the most money ($197 million) overall. The second and third biggest supporters of autism research were private organizations. The Simons Foundation granted $51 million over 98 research projects in 2009. Autism Speaks supported 220 projects with $23 million dollars raised from generous donations of families and loved ones who want to see better lives for all who struggle with ASD.

These numbers show the impact that foundations such as Autism Speaks can have on the direction of autism research as they typically support ideas deemed too “risky” for NIH funding. Indeed, a recent analysis conducted on Autism Speaks’ grants showed that for each dollar invested in research, investigators leveraged $10 more in additional funding. Researchers were able to use our early investment to further their studies and advance our collective understanding of autism.

Autism Speaks’ Chief Science Officer, Geri Dawson, Ph.D., says “Although we are pleased that funding increased for ASD research, we are still in great need of increased funding so we can make faster progress. Notably, the current IACC report shows that more funding needs to be directed toward research on adults and services. Basic scientific discoveries need to be translated into real world solutions that impact the daily lives of people struggling with autism.”

The timing of this report is critical. As previously mentioned, the CAA is now up for renewal. Without this support we would not have the IACC , which brings together stakeholders from the federal government, private research organizations, and community leaders to consider the needs of the community as a whole so we can best invest research dollars to solve pressing questions that actually impact the lives of real people.

Last month, new reauthorization bills were introduced with strong bi-partisan backing in the Senate by Senators Robert Menendez (NJ-D) and Mike Enzi (WY-R), and in the House by Autism Caucus Co-chairs Rep. Chris Smith (NJ-R) and Rep. Mike Doyle (PA-D). President Obama has pledged to sign a CAA reauthorization into law this year. The Combating Autism Reauthorization Act of 2011 (CARA) would extend the CAA – which includes funding for critical research, services and treatment, and contains measures to ensure cost-efficient planning and coordination of these efforts – for three years at current funding levels.

As Autism Speaks co-Founder Bob Wright stated last month upon the introduction of CARA, “Bi-partisan support for any legislation today is rare, and reflects our elected leaders’ understanding of the severity of the challenges we face. It is imperative that CAA is reauthorized, so that the vital work in research, treatment and services can continue.”

The numbers in this report are just one way to quantify the investments that are being made in our understanding of autism spectrum disorders, from risk factors to the effective delivery of services. We will continue to keep watch and advocate for more research that is aimed at improving lives today and transforming lives tomorrow.

The entire report is available for download here.

Accommodation

June 17, 2011 7 comments

This is a guest blog post from Autism Speaks Science Board member John Elder Robison, author of Look Me in the Eye: My Life with Asperger’s and Be Different: Adventured of a Free-Range Aspergian.

Should we change, or should others change for us?  Should workplaces change for us?

We (by we, I mean anyone) must be able to present ourselves in such a way that the people we engage think we are nice/interesting/capable or whatever they need to continue the interaction.  If we fail to do that, we will not move forward in a relationship with that person.  That may mean we don’t make a friend, or we don’t get a job, or we don’t get admitted to a school. Whatever it is, it’s a lost opportunity.

Obviously no one can succeed with every engagement of another person, but each of us must look at our total tries, and our success rate.  If the success rate is low, we have to ask ourselves why.

In my last post, I talked briefly about Asperger people who fail to get jobs for whatever reason, and then allege discrimination.  Some neurodiversity voices ask for an end to that discrimination, and for greater acceptance.

I have asked for greater acceptance myself.  I think that is a noble goal, but not one we will see attained anytime soon.  When I look at how I was treated in childhood, how my 21-year old son grew up, and what I see today I see some change but not much.  It leads me to wonder how much acceptance and accommodation we might reasonably expect.

I think what happens is that the philosophical desire for more broadminded treatment flies in the face of evolutionary human development.  We have thousands of years of experience that tells us a person acting a certain way is a bad person; a threat.  We are conditioned to reject people who exhibit those behaviors.  What arethose behaviors, you ask?   There is no single, simple answer.  We just seem to be programmed to pick up certain unspoken cues and interpret them that way.

The problem folks like me have is that our Asperger’s causes us to exhibit innocent but non standard behaviors that get interpreted as bad.  I’ve written on this before, urging people to think twice when a person says or does something unexpected.  I think that works in some situations, especially with people who are exposed to kids with differences or AS in the family. For the great majority of people, though, the message does not get through or it gets ignored.

That’s why I say we are 1% of the population and we can’t expect the other 99% to change for us.  Laudable as the goal of change may be, they just don’t care.  Note than I am not saying the 99% are normal and we are abnormal. I understand the 99% have many issues of their own.  I’m just observing that the odds are stacked very heavily against us, when it comes to getting them to change in all their collective diversity, indifference, ignorance, and whatever else.
What about discrimination?  I won’t say there are not people who discriminate against autistic people.  I’m sure there are.  That said, when we fail to get a job or make a friend, I still maintain that failure usually stems from our behavior (unexpected or unacceptable), and not from arbitrary discrimination against the underlying cause (Asperger’s.)
I cannot control what other people think about “my kind.”  Prejudice or discrimination is something I cannot change, and frankly, I would not want to do it for my benefit through force of law.  Why?  Because if someone does not want me around, that is enough.  I am out of there.  I am not going to stay where I am not wanted.
I want to be in control of my life.  That means I work on changing my behavior as needed to fit in.  I have full control of my actions, so I know success is achievable for me by that route.  I don’t wait around for others to change, because that is frustrating and often unsuccessful.
What about accommodation for sensory issues?  Several people asked my thoughts on that.  Examples might be moving to a quieter work cubicle, or getting different lighting.  I think many sensory accommodations are reasonable and doable for employers.  I am absolutely in favor of any subtle changes in the workplace that make folks like us more comfortable.
At the same time, I recognize that kind of accommodation has its limits.  If the accommodation would require major changes in the workplace, and that same workplace is acceptable to everyone else, I’d get a different job.  But that’s just me.  Through my life I have chosen to vote with my feet in situations like that.  Others would fight for change and I can respect that, even though I would not do it myself.
In our society, we have chosen to let government dictate the tradeoffs by which some people are inconvenienced for the benefit of people with disabilities.  An example of that would be handicap parking spaces.  By having those spaces we allow those who need them to access facilities they could not otherwise visit. But the non-handicapped person who needs a space pays a price for that accommodation even as it sits unused and he has nowhere to park.
Disability rights advocates fight those battles on many fronts.  I applaud their efforts and successes, but I do not wait for such accommodations to improve my own life.  Since I want action now, I make my own way as best I can.  That is the sometimes hard reality we all face, every day.  We can hope and work for societal change, but we still have the chance to make the best of the life we have today, because today will never come again and I don’t want to spend it waiting.  I want to be acting.

Autism in the News – 06.17.11

June 17, 2011 5 comments

Cary man creates iPad app for individuals with autism (Cary, Ill.)
After 25 years of working in special education, Victor Morris wanted to assist individuals with disabilities even further. Read more.

Finally together, Wendrows try to heal (Detroit Free Press)
Julian Wendrow waited in the house, too nervous to greet his children in the driveway. He hadn’t seen his son and daughter — hadn’t even spoken to them — in 106 days. Read more.

See. Touch. Learn. iPad app for Autism, Special Needs (Stamford, Conn.)
Brain Parade, a pioneer in innovative mobile, education solutions, announced today that they are slashing the price of the picture card libraries for their See. Touch. Learn. product to $0.99 (USD) for a limited time. Read more.

‘Face blind’ sufferers see world like this. But now there’s hope (UK)
A Scottish eye expert has developed what he says is the first treatment in the world for people who suffer from face blindness. Read more.

Ross mum’s advice on summer trips with autistic children (UK)
Ullapool mother Morven Da Forno is fully aware that while the summer holidays represent six long weeks of freedom for many, for children with autism it is a break in routine which can prove upsetting and disorientating. Read more.

Autism Speaks Live Chat with Rodney Peete

June 17, 2011 9 comments
6:54
Hi, I’m Rodney Peete, Co-Founder of The HollyRod Foundation. I am so excited to be here to chat with you and I share our story. I hope that I can help you along your journey
6:55
Comment From Rae

how did your son’s inital diagnosis effect your relationship with your son?

6:55
Hi Rae!
6:56
My son’s initial diagnosis really started to drive a wedge between us because I didn’t know what autism was
6:56
As he started to withdraw and become more non-verbal I didn’t know how to interact with him. Mostly it was because I did not know about autism so I needed to educate myself
6:56
I was heavily in denial about his condition and diagnosis
6:57
I probably, like many fathers, thought I could fix him.
6:57
I used my own methods of connecting with him and they never worked
6:58
Comment From Phyllis

Any advice for me I have a 17ry old son with autism and am going thru a divorce, he blames me for everything?? Makes me sad.

6:58
Hi Phyllis I know this must be a difficult time for you
6:58
Due to my denial, my wife gave me an ultimatum. I got on board or out of the house
6:58
I had to choose between my family and my own ego
6:59
Once I chose correctly we were able to move forward as a family
6:59
The most important thing, in going through this divorce is your 17-year-old son
6:59
Comment From HEIDI

RODNEY- ALTHOUGH WE’VE COME ALONG WAY , IM STILL SO SCARED FOR MY 18 YR OLD SON- WHO IS ON A 4TH GRADE LEVEL- I THINK MORE SO, AFTER HEARING WHAT HAPPENED TO JOHN TRAVOLOTA’S SON- TO HAV FEARS???

7:00
Hi Heidi
7:00
Our son is 13 now and we are thinking about his adulthood and it is a scary time
7:01
We need to do a better job as a society working with children who become adults with autism, whether is be jobs, education, housing, integrating into mainstream society.
7:01
These all need to be dealt with
7:01
No matter what age, you must continue to be an advocate for your son
7:01
Comment From Adam

Hello Rodney. Go Trojans!!!

7:01
Fight On Adam!
7:03
Comment From Tom

How old was your son when he was diagnosed

7:04
hi tom Rj was diagnosed at age 3
7:05
Comment From Robert

Rodney , Having a son with Autism also i have learned to love all the little things the way he says hi daddy or “Tickle Me” love the book and keep spreading the word

7:05
Yes Robert, it is about small wins
7:05
I can remember the first time my son said, ‘I want some french fries’ from the backseat. I thought it was the same as us winning the championship game!
7:06
Comment From Erin

How do you make sure you have a great relationship with your other children? I find it difficult to make sure there is enough time for everyone and am always afraid someone will feel left out!

7:06
Eric, yes it is very difficult
7:06
RJ has two brothers and a sister
7:07
What we have done is make sure we have educated his brothers and sister about autism, about his abilities so they become advocates for him. They are part of his therapy. Everything they do in interacting with him has helped us engage everyone in this fight
7:08
We are getting so many questions which is so exciting!
7:08
We are trying our best to answer them all – keep them coming!
7:08
Comment From Greta

Can I just get off topic for a second and tell you how excited I am to see you here! My son, Austin, is 5 and was just diagnosed – he’s very high functioning, and I’m very grateful for that. But I am a huge Dallas Cowboys fan (born in Dallas) but I grew up in Mesa. We’re the same age. :) Anyway, I just bought your Kindle version of your book for my husband. I am looking forward to reading it after he’s finished. Thanks for everything you and your family do.

7:09
Thank you Greta- we are all in it together!
7:09
Comment From Ric

Was it hard to play football and to raise your child?

7:09
YES Rick – Thanks God I had a rock for a wife
7:10
She rolls up her sleeves at every stage- talked to every doctor, really jumped in with both feet, while I was away playing football!
7:10
I like most dads wanted my son to follow in my footsteps
7:11
I saw my teammates bring their kids in the locker room. When I brought my son in, he didn’t really understand the gravity of what was going on
7:11
I really had to come to grips, that it was about him, not about ME. Once I did that, our relationship flourished
7:12
Comment From HEIDI

RODNEY IM SURE UR OVERWHELMED WITH COMMENTS, IS THERE ANY STRUTURE TO LIVE CHAT???? IM CONFUSED??

7:12
Heidi, there are just so many coming in, and we are trying our best to answer them all. THANK YOU ALL for being here
7:12
We still have 45 minutes!
7:14
I wrote a book last year called, ‘Not My Boy!’
7:14
The reason I called it that, was because that is how I felt at the diagnosis. ‘No way, Not my boy!’
7:14
Understanding the journey we were about to go on, I became very selfish
7:15
I made it all about me, when really it was about him. I did not pay attention to therapy or other families who would try and talk to me. I wouldn’t even talk to my wife!
7:15
It drove a serious wedge in our relationship. She was onboard and I wasn’t.
7:16
I think part of me was embarrassed because I didn’t know how to handle in in public, but what I realized later, is that he has gifts, just like every other kid. We must pay attention to the give HE HAS, not the gift we want him to have
7:17
Here is a link to by book, if you are interestedhttp://www.facebook.com/autismspeaks?sk=app_225711834125562
7:18
I turned a corner through an embarrassing moment
7:18
We had a collective meeting with all of my son’s therapists and I was asked to show them how I was interacting with my son at home
7:19
When I attempted to do this, everything was completely wrong. RJ gave me NO response
7:19
When the therapist interacted with him, he laughed, joked and smiled. They were connected. At that moment, I knew if I was going to have a relationship with my son, I had better educate myself and accept this.
7:19
I had better be onboard 100%
7:19
Comment From Elizabeth

How did you and your family handle the looks and stares and ugly little comments that can really make you feel bad?

7:20
Elizabeth, that was a great question
7:20
Although part of you wants to lash out at the people that are staring and passing comments
7:20
We try to use those moments as teachable moments in educating people about autism.
7:21
I talk about a moment in my book, when our son was in the 4th grade and he was not getting invited to playdates and birthday parties and his twin sister was
7:21
A lot of it was, the kids and the parents didn’t understand what was going on with RJ
7:21
we called a meeting with his classmates and hosted an ‘Autism 101′ with Holly and myself
7:22
we let the students ask questions, ‘Why doesn’t he say hello?’
7:22
ALL questions were asked and we took the ‘scary’ out of autism
7:22
we told them that there are some things RJ is Good at and some things he is bad at
7:23
He is bad at making friends, BUT he is good at giving the capitals to every state
7:23
The kids got it
7:23
They came back with, ‘I am good at soccer, but stink at math!’
7:23
It was the kids that educated their parents about RJ
7:23
From that moment on, he had a great group of friends, that he still has to this day
7:26
My wife and I founded The HollyRod Foundation
7:26
It is all about helping families and raising their quality of life. Once our son was diagnosed, we moved our focus to that
7:27
We began speaking about autism and how it affected our family. When we received a diagnosis, we had no outlets. We want to provide the light at the end of the tunnel
7:27
Comment From Alyssa

My husband hides behind his work as the excuse why he hasn’t really connected with our 2 autistic boys. Any ideas you have that I could use as a first step to building a relationship?

7:27
You can learn more about us here, http://www.hollyrod.org/
7:27
HI Alyssa
7:27
I was the same way.
7:28
The first step is trying to understand where he is coming from
7:28
I did not hear my wife the first 2 years after the diagnosis. She didn’t want to hear about my feelings about being a father and what I expected about my feelings for my son
7:28
I wouldn’t approach it as you need to interact with you son
7:29
Approach it as, it is okay you are feeling like this. But you need to connect with your son. Get to know him first
7:30
Comment From Mike S

isnt it true that 50 percent of married couples with a child who has autism get divorced? i think its not fair to walk away from each other because of that?? i have a 7yr old with autism been married 9 yrs

7:30
Hey Mike
7:31
I don’t know if that statistic is accurate
7:31
But i do know, that sometimes one parent takes the lead, while the other lags behind, which sometimes causes friction
7:32
It is important for both parents and the whole family to be educated and onboard. It is okay whatever all happens, as long as the family is involved
7:33
I am so impressed with all of the parents and families members on this chat. It is amazing how the community has come together and I am thrilled to be a part of it!
7:34
Comment From Lena

Hi Rodney! Our sons are the same age? How are you and Holly handling puberty? I was told that our boys are more intense than other boys their age.

7:34
ohhhh Lena, you’ve got that right!
7:34
My son is going through puberty right now
7:35
and it is definitley having some effects on his emotional state
7:35
He is certainly now interested in girls!
7:35
I have to to be honest, it scares me!!
7:35
I have had ‘The Talk’ with him several times
7:36
but until he has experienced, ‘hanging out’ or ‘holding hands’ or anything like that, I won’t know how he responds
7:36
He gets very giddy and excited when his sister’s friends come over!
7:37
Comment From Guest

Do you have any advice on how to handle meltdowns public?

7:37
This is a difficult one, because you don’t always know when they are coming
7:37
Every child is different
7:38
What works for us, is we always have candy
7:38
Some people think it hypes a child up, but it works for us in public places
7:38
Whatever works, works!
7:38
Comment From REST

How can I help my husband accept and understand our 12 yr old Aspergers son?

7:39
Hi REST
7:39
I recommend my book- I cover denial, anger, and everything in between
7:40
Sorry! here is the right link to ‘Not My Boy!’http://www.amazon.com/Not-My-Boy-Familys-Journey/dp/1401323618
7:40
Comment From Mary Len

How old is RJ now and what kind of school environment is he in?

7:40
Hi Mary Len
7:40
RJ is 13
7:41
Last year he graduated 6th grade in a mainstream school
7:41
with his twin sister!
7:41
6th grade was very difficult because he was reading at 4th grade level. He managed, with a shadow, to do very well
7:42
There was a high level of anxiety when thinking about Middle School
7:42
We decided to give him a break and create a home school program for him for a year
7:42
He will enter 7th grade Middle School in the Fall and thankfully, he will be able to have a shadow with him
7:43
There was a lot of anxiety with him in 6th grade with him
7:43
He couldn’t keep up with his friends academically, which created behavioral issues that were not good for him
7:43
He took the rigid pressure of going directly to 7th grade, and he is back to being a happy excited, flouring kid
7:44
It is OKAY that he goes at his pace, not someone elses
7:44
It is about, the child, and what is best for him
7:46
Comment From anne

do you know where families can go who have an adult child with autism and get financial help for services that medicaid no longer covers, like dental

7:46
Hi Anne
7:47
This is a question that so many families face
7:47
Holly and I are frequently asked about this
7:47
Autism Speaks developed, the ‘Transition Tool Kit’
7:47
The Autism Speaks Transition Tool Kit was created to serve as a guide to assist families on the journey from adolescence to adulthood.
7:48
It covers housing, employment, advocacy, and an array of other topics
7:48
Comment From Demi

I heard yall tried the non glutien diet how has that worked for your son?

7:48
Hey Demi!
7:48
We did try the non gluten diet
7:49
It helped him, especially when he was younger, with focus
7:49
He is allergic to peanuts
7:49
With his diet over the last 10 yeas we have monitored it for him and it has been very helpful
7:50
Comment From Kathy

Rodney, I have two boys both with Autism, one is 8 the other is 6. You are so right, we have to educate society and ourselves to be able to help every child with Autism. Everyday is a blessing and a battle but you begin to appreciate the little things that are accomplished. I thank you and Holly for all of the wonderful things you have brought to help with the fight for a cure. Thank You

7:50
Thank you Kathy
7:50
Comment From Keisha

I saw the episode of The Talk that you did with Holly and Joe. It was so awesome. I think I need to buy your book for my husband. Somethimes we end up on opposites sides in dealing with our 12 yr old’s Autism

7:51
Hi Keisha – that was a great show too!
7:51
A many thanks to CBS and ‘The Talk’
7:52
Thank you for allowing Holly to have a voice
7:53
Comment From Paula

Is your son aware of his diagnosis? I haven’t told my son yet. I think he knows he is different though. The school is pressuring me to tell him. I just can’t bring myself to do that.

7:53
Here is a link to ‘The Talk’s’ Show with Autism Dads!
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hi Paula
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Yes, my son is aware
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We thought it was important that he understood what autism was
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He needed to know what he was going through
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Around 6 or 7
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It is important for kids understand what is in front of them
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Now that he is 13, he blames autism!
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Now he thinks it is funny!
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Once, he left pizza under his mattress for 2 weeks
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and he blamed autism!
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When I asked him why!
7:57
It was my pleasure to be here today to chat with all of the families. It is very clear you are all passionate and are trying to find the best way to advocate for your child
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Remember, we are in this together
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I encourage you to visit autismspeaks.org for more resources and information
7:58
My best advice would be, continue to educate the public
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The more people understand, the more acceptance our kids will have
7:58
Thank you so much – I wish I could stay longer!
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