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Transcript of LIVE Q & A with Gary Mayerson
How To Compromise With Your School District Without Compromising Your Child
Navigating the IEP process can be an overwhelming experience. Join nationally renowned attorney Gary Mayerson as he answers live questions from parents and explains what parents can do to secure effective and appropriate programming.
Gary Mayerson is the founder of Mayerson & Associates, a law firm in Manhattan that was formed more than a decade ago as the very first law firm dedicated exclusively to serving people with autism. To date, Mr. Mayerson and other lawyers at his firm have helped more than 1,000 families in more than 30 states, as well as military families stationed abroad. He also is the author of How To Compromise With Your School District Without Compromising Your Child (DRL Books 2005). In addition, Mr. Mayerson is a long-time board member of Autism Speaks and serves as the Director of the Autism Speaks Federal Legal Appeals Project, a pro bono initiative at the federal level.
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Family Services Office Hours – 8/17/11
Office Hours, a new resource available on the web at www.autismspeaks.org will easily connect families to a wide variety of autism-related resources, including Family Services’ Toolkits, and the Autism Speaks Resource Guide, an online national database of autism providers and resources searchable by state and zip code. Family Services’ Office Hours is designed to quickly provide access to resources that are available and free to the entire autism community.
“Having a family member with autism can easily lead to feeling isolated without knowing where to turn. In addition, most families have little free time to search for reliable information about autism, yet they may be in need of timely information. Office Hours offers a quick connection to the Autism Response Team(ART) who can assist you in getting the information you need as quickly as possible,” states Marianne Sullivan, Assistant Director of National Outreach and Resources.
The Office Hours resource is staffed by ART coordinators who are specially trained to connect families affected by autism to resources.
In addition to Office Hours, ART is available by telephone during usual business hours at 888-AUTISM 2 (888-288-4762). You can also reach ART by email at familyservices@autismspeaks.org.
Here is the transcript:
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IEPs, iPads and Bullies: 10 Tips From a Dad Who’s Been There
James Vaughan’s 11-year old son, Kian, is entering the 6th grade in the Weber County public schools in Utah. Kian, who has high functioning autism, has been mainstreamed in public school since the second grade and has made great strides. James attributes the progress to the successful partnership he and his wife have cultivated with the folks at Kian’s school. James is one of many parents sharing his story, tips and team on MyAutismTeam. We recently spoke with him to learn how he has partnered with his public school to create a positive and safe learning environment for Kian. Here are 10 tips we gleaned from speaking with James. Hopefully some of them will help you. You can post questions and comments directly to James’ wall by clicking here .
(10) Get the Official Diagnosis As Early As Possible
Dr. Megan Farley of the University of Utah diagnosed Kian. We didn’t get the official diagnosis until December of last year when he was 10 because we had been worried about saddling him with the label of autism. In retrospect I would say the right time to get a diagnosis is “as early as possible”. Having the official diagnosis in hand, along with some written recommendations from the doctor enabled us to secure even more services for Kian including technology assistance [see #9]. When we decided we wanted a diagnosis we had to be very persistent with our pediatrician to get a referral. He kept assuring us that Kian would outgrow some of his developmental challenges, but in the end agreed to give us the referral when we were persistent.
(9) Be Firm, But Flexible
My wife and I always make sure that every concern we have about Kian is thoroughly understood by our partners at the school, particularly during the IEP process. Talking about his speech delays got us speech therapy. Talking about his challenges interacting with other kids led to social skills therapy, and so on. It’s important to make sure they understand and address each issue. I’m the kind of person that doesn’t take “No” for an answer, but you have to be flexible. There have been times we’ve requested something for Kian that the school hasn’t been able to accommodate. But rather than saying “No” they’ve always said, “I don’t know if we can do that, but here are other options we can do.”
(8) Communicate Frequently All Year, Even After the IEP
The open communications continues after the IEP, otherwise it’s not a real partnership. We regularly check in with Kian’s teachers and aide to make sure we are helping each other. We also keep the focus of the communication on Kian’s development. We let them know things we are trying at home that are working, and notify them of any changes that could impact Kian’s performance in school that day. We’ll say, ” You may see some distraction today – here’s why… .” That helps them understand how to interact with him. Similarly, we want them to tell us about the challenges they are having with Kian at school so we can then work on those issues at home. The more we are open with each other on a regular basis, the better the job we do meeting Kian’s needs. It keeps everyone focused on the goal of his development.
(7) Speech Therapy, Social Skills and 1-on-1 Aides
Before the second grade, Kian was in the school’s alternative kindergarten and first grade program. There, he had a strong speech program and one-on-one time. He flourished. Now, in the mainstream curriculum, he has an aide and is pulled out of class for 30 minutes each day for either speech therapy or social skills integration. That one-on-one time has been critical, and the special attention from the aide makes it easier to accommodate Kian in the classroom.
(6) Ask If Your Child Can be Tested Differently
When the teacher stood up in front of the class and read off questions for the students to answer in writing, Kian couldn’t really respond to this normal classroom testing, but it was not due to a lack of understanding of the material. When we asked, “Can Kian be tested differently?” the school was happy to do so. He now gets tested on computer where he can type his answers — something he can do quite well.
(5) Seek Out Alternatives for Stressful Situations
Going out to recess was more traumatic than fun for Kian. If that is the case for your child, ask if there alternatives. We asked and Kian was able to stay in the classroom during recess so he could read or do some other type of project.
(4) Get Involved If You See Bullying & Teasing
It’s not surprising that a child struggling with social interaction will get teased and sometimes bullied, but it’s certainly not acceptable. If you see it, GET INVOLVED IMMEDIATELY. My wife is a spunky lady. When she sees bullying going on she makes sure that the students and parents involved know about it and are educated about it. But she does it in an understanding way. She explains how kids are different from each other. We’ve increased awareness about bullying at the PTA. PTA is a great thing. You’re mingling with other parents and making them aware of the issues. When other parents become aware of the issue, they then talk to other parents, who in turn, talk to their kids. We’ve received phone calls out of the blue from other parents saying, “I learned about the teasing my child was involved with. You won’t have a problem with that again.”
(3) Start With The Goal of Building a Real Partnership
One of our goals from the outset was to form a strong, open partnership with the people at the school, from the Principal to the teachers and aides, to the Special Education Director. Kian’s challenges were a lot bigger than we could handle on our own. We let them know how much we’d appreciate their help looking out for Kian and making sure his needs were met. We committed to be totally transparent and open with them and to help reinforce the right behaviors at home.
We certainly didn’t want our son to be a distraction to the teachers and other students, but we also wanted to make sure he had everything he needed to develop and grow. The principal of our school recently told me why they’ve always been so open to finding solutions for Kian saying, “You cared, you really showed it was about forming a partnership with us, and you were always up front about the issues before they became a situation.”
(2) Reduce Homework and Leverage Technology
After spending a day with Kian, Dr. Farley immediately suggested a reduced homework load for Kian and suggested we use a computer or other technology to help him type his homework. 20 minutes of normal homework was taking him 1-2 hours to do (partly due to challenges with handwriting). Our school district had a special foundation that was able to provide Kian with an iPAD. He uses the ipad to keep a calendar of his assignments and to type out his work rather than writing everything out by hand. He also receives a reduced amount of homework. Again, this is setting him up to be more successful each day rather than falling behind.
(1) Reach Out to Other Parents
In the autism community, the biggest contributor to hopelessness is not knowing who to talk to and where to go for advice. I like what MyAutismTeam is doing because they make it easy to connect with other parents near me and see which providers they recommend and what kinds of activities they are doing. It’s a great tool to get those relationships started and then be able to expand on them. My wife and I started a program in Utah called FAAST (Families of Autism and Asperger’s Standing Together) that meets monthly. I posted an upcoming meeting on my wall on MyAutismTeam the other week and ended up meeting another parent that way.
- Interview Conducted by Eric Peacock, GM of MyAutismTeam
How To Compromise With Your School District Without Compromising Your Child
Join us on August 17th at 7 pm EST as Gary Mayerson discusses parent advocacy and answers your questions about what you can do.
Navigating the IEP process can be an overwhelming experience. Join nationally renowned attorney Gary Mayerson as he answers live questions from parents and explains what parents can do to secure effective and appropriate programming.
Gary Mayerson is the founder of Mayerson & Associates, a law firm in Manhattan that was formed more than a decade ago as the very first law firm dedicated exclusively to serving people with autism. To date, Mr. Mayerson and other lawyers at his firm have helped more than 1,000 families in more than 30 states, as well as military families stationed abroad. He also is the author of How To Compromise With Your School District Without Compromising Your Child (DRL Books 2005). In addition, Mr. Mayerson is a long-time board member of Autism Speaks and serves as the Director of the Autism Speaks Federal Legal Appeals Project, a pro bono initiative at the federal level.
Boynton Beach Grandparents Raise Funds for Autism Speaks
This is a guest post by Autism Speaks Board Member Gary Mayerson. Mayerson is the founder of Mayerson & Associates, the first and only law practice in the nation dedicated to representing children and adolescents with autism spectrum disorders.
From its very inception, Autism Speaks has recognized the importance of family support, and the role of the extended family. Indeed, Autism Speaks was founded by two highly motivated grandparents, Bob and Suzanne Wright.
On February 15, 2011, approximately 150 Boynton Beach grandparents attended a luncheon fundraiser for Autism Speaks, raising more than $10,000 in the process. They came to listen to Autism Speaks Board Member Gary Mayerson speak about the epidemic-like statistics, and the many ways in which Autism Speaks is addressing the problem.
We wish to thank everyone who attended and, in particular, the following committee members who organized this worthy event: Gerri Ackerman, Elaine Baranoff, Luba Ditkowitch, Ellen Feller, Harriet Fried, Carolyn Holland, Shirley Meltzer, Mara Lee Nozetz, Rita Rosen, Patty Rosenfeld, Phyllis Spieler, Dee Silverman, Ruth Schwartz, Renee Telsey and Sylvia Zeidman (Gary Mayerson’s mother in law).
In Memoriam: Dr. O. Ivar Lovaas (1927-2010)
Editor’s note: On August 2, 2010, Dr. O. Ivar Lovaas passed away. We sincerely thank Dr. Lovaas for all of his contributions to the autism community.
In 1981, with the publication of Dr. Lovaas’ pioneering work, Teaching Developmentally Disabled Children (popularly known as “The ME Book”), the landscape of the world of autism was quite different than it is today. In 1981, the prevalence of autism in the general population was reported to be only 4 in 10,000, hardly the 1 in 100 world epidemic that autism represents today. While considered a relative rarity at the time, a diagnosis of autism in the 1960’s and 1970’s was considered by most to be the beginning of a countdown to institutional care. To add insult to injury, Bruno Bettelheim and others were disseminating and perpetuating the notion that autism was caused by cold and unfeeling “refrigerator mothers” and other forms of inadequate parenting. For much of the latter part of the last century, families of children with autism had little, if anything, to hope for.
Dr. Lovaas, who had already been working with children with autism for decades, knew better. Dr. Lovaas knew instinctively that poor parenting was not to blame. However, finding the root cause of autism was not Dr. Lovaas’ chosen mission. Instead, Dr. Lovaas focused his energy and attention on developing effective teaching strategies. Dr. Lovaas believed that children with autism could “learn to learn.” Back in the day, this was considered by many to be an unreachable star.
Just as Thomas Edison’s numerous lightbulb failures paved the way for Edison’s ultimate success, Dr. Lovaas painstakingly identified the “serious mistakes” that he and his colleagues at UCLA had made over the course of two decades in attempting to teach children with autism and other severe developmental disabilities. Dr. Lovaas knew that the first step to finding an effective, core intervention would be to identify and eliminate the various approaches and strategies that had been tried, but which were demonstrably ineffective. Dr. Lovaas then worked tirelessly to break down the large and general problem of “disability” into manageable and separate behavioral units. Through years of trials, Dr. Lovaas further refined his behavior modification techniques and approaches. Over time, Dr. Lovaas’ work in the field became recognized to the point that for many, “Lovaas” became synonomous with the term “Applied Behavior Analysis.”
During the 1980’s, Dr. Lovaas and his colleagues at the UCLA Young Autism Project further refined their behavioral approaches, and they were fortunate enough to receive an important grant from the NIH allowing a most unusual and intensive approach that had never before been attempted—a forty hour per week one-to-one teaching program. In 1987, the results of Dr. Lovaas’ study, entitled Behavioral Treatment and Normal Educational and Intellectual Functioning in Young Autistic Children, were published in the Journal of Consulting and Clinical Psychology, a respected peer review journal.
While there certainly was some controversy over the precise “design” of Dr. Lovaas’ study, there had never before been a study reporting such a favorable outcome—many of the students who had been receiving a 40 hour per week intervention program for approximately 2-3 years had recovered function to the point that they were considered virtually indistinguishable from their typically developing peers. A 1993 follow-up study appearing in the American Journal on Mental Retardation confirmed that some six years later, all but one of the children in the “best outcome” group had retained the gains reported in the 1987 study. In 1998, the Surgeon General’s Report on Autism referred to Dr. Lovaas’ 1987 study as a “well designed study” that “….demonstrated the efficacy of applied behavioral methods [ABA] in reducing inappropriate behavior and in increasing communication.” Vindication!
In 2002, Dr. Lovaas asked me to write a chapter on ABA litigation for his then upcoming update to The ME Book, Teaching Individuals With Developmental Delays (Pro-Ed). Dr. Lovaas told me in the charming Norwegian accent that he never seemed to lose despite living in this country for many decades that his greatest wish was that every parent, whether residing in California, New York or Alaska, would have access to effective autism treatments. Dr. Lovaas regularly spoke of the need for insurance reform, as he knew full well the devastating impact autism can have upon the family. The dedication appearing in Dr. Lovaas’ latest book speaks volumes as to his empathy and compassion for the family: “This manual is dedicated to all parents of children with developmental delays in recognition of the heavy burdens they carry, and the models they provide for all parents to follow.”
I last sat with Dr. Lovaas and his lovely wife, Nina, at the Autism Speaks’ benefit concert in Los Angeles, headlined by Paul Simon and Jerry Seinfeld. Dr. Lovaas was truly pleased to see how far public awareness of autism had come. He also has a special appreciation for Jerry Seinfeld’s jokes, ostensibly because so many of them are based on the nuances of human behavior.
Dr. Lovaas’ pioneering work has not only helped, but has profoundly changed the lives and futures of thousands of affected children and their families. Dr. Lovaas’ work continues to have a profound impact on the professional development of today’s autism professionals. Perhaps most importantly, where once there was darkness, Dr. Lovaas brought light and genuine hope.
The autism community clearly has lost a giant.
This guest post is by Gary Mayerson. He serves on the board of Autism Speaks and is the founder of Mayerson & Associates, the first law firm in the nation dedicated to representing children and adolescents with autism spectrum disorders.







