September 2008 Archives

September 26, 2008

Autism Awareness and the Potential for Partnership

From the Associated Press:

More than a dozen of the world's first ladies on Friday called for enhanced research on autism worldwide.

Ban Soon-taek, wife of the U.N. Secretary-General Ban Ki-Moon, said "not too long ago, those with autism were set aside. Today this reality is still prevalent in some parts of the world."

Panama's first lady, Vivian Fernandez de Torrijos, emphasized that early intervention is key.

U.S. first lady Laura Bush also sent a note for the event, calling autism "a global health issue."

The event was a part of global initiative unveiled today by Autism Speaks. In just three years, Autism Speaks has grown to become a major player in the disability advocacy world. Bob Wright, a former vice chairman for General Electric and chief executive officer of NBC and NBC Universal for more than 20 years, is one of the founders of the organization.

Without a doubt, more needs to be known about autism, and Autism Speaks has worked hard to make sure that more parents and educators understand cognitive developmental milestones for children. Many children can be helped earlier if the adults around them recognize the signs of autism spectrum disorders.

At the same time, other disability organizations have worried that single-minded focus on one particular disability, like the current flurry of attention around Down syndrome, distracts organizations from working together on common goals. I recently wrote an article about this phenomenon. An excerpt:

Groups that advocate on behalf of specific disabilities are proliferating, fueled by a medical establishment that can trace disorders down to their very genes and a communication system that can easily connect people around the globe.

But some advocates worry that too much focus on autism or Down syndrome, even on the presidential-campaign trail, could distract from efforts to support common issues that affect many groups.

The issue is of particular concern in education, because many of the accommodation, inclusion, and differentiated-instruction efforts in schools have the potential to cut across several diagnostic boundaries.

“What’s good for kids with autism is good for a lot of kids with developmental disabilities,” said Colleen Horton, the director of public policy for the Texas Center for Disability Studies, a part of the University of Texas at Austin. To suggest a label is all that needs to be known about a child “doesn’t do justice to the kids,” she said.

I interviewed Peter V. Berns, the executive director of The Arc of the United States for that article, but wasn't able to include him in the written piece because of space constraints. But one joint activity that he drew attention to was the widespread condemnation among disability groups of the use of the word "retard" in the movie Tropic Thunder. "There was an extraordinary coming together of organizations," he told me. Alison Singer, an executive for Autism Speaks whom I interviewed, referred to the same effort in our conversation.

So that's one good example of partnership that worked well. But should there be more joint efforts like this? Or are there already many examples of successful common advocacy?

September 25, 2008

Universal Design for Learning

The Center for Learning Disabilities sponsored an online chat on universal design for learning with Patti Ralabate, a special education expert for the National Education Association. The chat is packed with links to great resources on this topic, which advocates creating lessons and classroom materials that are flexible enough to accommodate different learning styles.

Once upon a time, when lawmakers on Capitol Hill were still discussing the reauthorization of No Child Left Behind, several education and disability advocacy groups came together in support of a provision that would promote universal design in the education law. It was noteworthy for being one of the few items that those many groups agreed on when it comes to educating students with learning differences. I wrote a story about the effort that you can read here.

September 23, 2008

A Disability Czar for Obama?

In January 2008, two representatives from Barack Obama's campaign held a conference call (pdf) with disability advocates to talk about the candidate's platform on a variety of issues. It's several months old at this point, but because disability issues are a bigger part of the campaign than they once were, I though it'd be interesting to share the transcript with those who may not have seen it yet.

Rep. Janice Schakowsky, a Democrat from Illinois and a co-chairwoman of the campaign participated in the conversation, along with Michael Strautmanis, Obama's chief counsel and the father of three children, one of whom has autism.

(Funny note: this story in the Chicago Reader suggests that Strautmanis is helping Obama lock up the Latvian-American vote, as a Latvian-African-American.)

Some of the conference call compares Obama's policy proposals to Hillary Clinton's, which is no longer relevant at this point. However, what caught my eye was a proposal from Obama to create "an assistant to the president for disability policy." The call also mentioned that Obama has two senior advisers who have children with disabilities; though only Strautmanis was mentioned, I'm assuming the other is political strategist David Axelrod, who has a daughter with developmental disabilities caused by severe epilepsy.

You can find out more about Obama's disability policy proposals here (pdf). It is comprehensive, but the elephant in the room continues to be the precarious state of the economy. My colleague Alyson Klein at the Campaign K-12 blog has a recent post on how the proposed $700 billion economic bailout of Wall Street may affect both the Obama and McCain campaigns.

September 22, 2008

Virginia Spec. Ed. Proposals Shelved

In April, I blogged about a proposed plan in Virginia to change regulations on special education so that parents would not have to be notified before a student's special education services were terminated.

At the time, I said that I didn't think the plan was going to go far, which didn't require much insight on my part: Gov. Tim Kaine had already said he was against any such change. And now, the changes have been officially ruled out.

The proposed rules changes drew 77,000 comments--the most ever for a rules change, according to a state official.

September 18, 2008

Coordinated Early Intervening Services

Project Forum, a federally funded project of the National Association of State Directors of Special Education, has released a new publication (pdf) on coordinated early intervening services. Districts are allowed to use part of their federal special education dollars on early intervening services for children who are not in special education, but who need extra academic or behavior help to do well in school.

In addition to Project Forum's excellent efforts, please check out a recent article I wrote on CEIS, as well as a blog post that discussed the topic.

September 17, 2008

Palin Says Special Needs Will Be a Priority

Her speech was heavy on economic-policy prescriptions, but on Monday in Golden, Colo., Republican vice presidential candidate Sarah Palin also outlined the issues she would focus on if she and John McCain are elected: energy, government reform, and "special needs."

From the speech:

I've told Senator McCain a few things I've learned as a senator governor and as a mom. Ever since I took the chief executive's job up north, I've pushed for more funding for students with special needs. It's touched my heart for years, especially about 13 years ago with the beautiful addition to our extended family of a nephew with autism. And now, my family and I, we have added special perspective with the birth of our beautiful baby boy, Trig, just four months ago. ...


We can join so many American families that know that some of life's greatest joys sometimes come with some unique challenges. We're going to make sure that government is on their side too. And part of that effort is going to involve making sure that our most dreadful diseases have our most effective efforts.

Too often, government gets in the way when innovators take on cancer or Parkinson's or Alzheimer's to find a cure...our administration will lead the effort to find new treatments and new cures.That's going to be a commitment in our administration.

It's well known at this point that Sarah's son Trig has Down syndrome.

The video clip begins mid-speech, but her comments on special needs are made with about 9:45 minutes left to go in the segment, and continue in more depth beginning around 5:25. (Those who are interested in hearing the entire speech can see part 1 here.)

During Palin's tenure as governor of Alaska, funding for children with severe disabilities who need specialized care has indeed gone up. (Not down.) Those children make up a relatively small part of the special education population, however. The state does not provide funding to school districts specifically for special education students with less severe needs, but does give an additional block grant to districts that they can use at their own discretion for special education, gifted education, education of English language learners, and vocational education.

Just like with McCain's speech at the Republican National Convention, I'm left wondering why there was no mention of the Individuals with Disabilities in Education Act. The opening was right there, but Palin made a quick pivot from talking about people currently living with disabilities to curing diseases.

Also, the disability advocates I've had the opportunity to interview seem to care less about government obstruction, and more about just having enough funding to explore the topics they consider important. One research avenue, federal funding of embryonic stem cell research, is something Palin opposes, as do many social conservatives and President Bush. McCain, however, says he does support federal funding of such efforts. (Skip to question #8)

It would be nice if special education and research priorities could be explored more closely during the debates. But with the economy sucking all the oxygen out of the room right now, I'm a little skeptical.

September 16, 2008

Tune In to Online Chat on Adolescents with Behavioral Disorders

On Wednesday, Sept. 17, between 1 and 2 p.m., I'll be moderating an online chat with Professors Lee Kern and Richard White on effective strategies for adolescents with behavioral disorders.

This is a follow-up to an article I wrote earlier this month on the topic. Kern is leading a new federal effort that will develop a set of "best practices" for dealing with these students' special needs, and White is the president of the Council for Children with Behavioral Disorders, a division of the Council for Exceptional Children.

No special equipment is needed to join the chat, just a computer with an Internet connection. When the chat is over, I will update this post with a transcript for those who cannot join live.

Edited to add: Here's the transcript.

September 12, 2008

New Americans with Disabilities Act Measure Could Affect Kids, Too

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Yesterday, the Senate passed by unanimous voice vote a measure designed to expand the Americans with Disabilities Act, passed into law in 1990. Now, it joins a similar bill that passed overwhelmingly in the House earlier this year. After differences are, presumably, ironed out in a conference committee and a final bill passes, it will go to President Bush for his expected signature.

Supporters of the legislation say that changes in the ADA are needed to push back against court rulings that have inappropriately narrowed the definition of an "individual with a disability." Though most of the news coverage has framed this as a workplace issue (as have disability advocacy organizations cheering this vote), there's important news here for schools and students, too.

But, of course, nothing in federal law is simple. So first, a little background ...

Most people involved in special education know about the federal Individuals with Disabilities Education Act, which guarantees certain protections to students with disabilities. It requires schools to develop individualized education programs for such students that will give them a free, appropriate public education.

But other federal laws also provide protections to students with disabilities, and one of them is Section 504 of the Rehabilitation Act of 1973, called "Section 504" for short. Unlike with the IDEA, the feds don't provide any money to schools to implement Section 504, but they still have to follow it. The two bills passed by the House and the Senate say explicitly that everything they have changed with regard to the ADA also applies to Section 504.

Every student who is eligible for the IDEA is also covered by Section 504. But a small number of students could possibly be eligible for Section 504 protections but would not be covered by the IDEA. Some examples might be a child with attention deficit hyperactivity disorder and a child with diabetes. Such students may need some accommodations, but perhaps not the full array of services that could come with an IEP.

Where it gets complicated is knowing just which children should be getting Section 504 protections, as I wrote earlier this year. Since the time the ADA was passed, the Supreme Court has adopted some pretty tight restrictions, including a 1999 decision that if a person with a disability could be brought up to the standards of an average peer through "mitigating measures," ADA protections no longer apply.

This means that a child with diabetes who controls the disease through insulin injections is using a mitigating measure and may no longer be eligible for Section 504 services. The same is true for a child with ADHD whose behavior is controlled by medication, or a child with a visual impairment who uses glasses. Basically, treating your disability could possibly mean forfeiting ADA protection, according to that Supreme Court decision and several more court decisions that followed.

With these two bills, Congress has swept away the concept of "mitigating measures" as a way of losing protection. As Sen. Tom Harkin, a Democrat from Iowa and the chief author of the ADA, said in a press release:

With today’s vote, we have restored the promise of the ADA, which was signed into law 18 years ago. The protections afforded under this historic law have been eroded and the result is that people with serious conditions like epilepsy or diabetes could be forced to choose between treating their conditions and forfeiting their protections under the law. That is not what Congress intended when we passed the law, and this bill is the right fix."

So what could this mean for children? Potentially, more of them could be eligible for Section 504 in schools. How many more, though, is an open question. It's a fairly small number of children who are Section 504-protected students; in my article, a researcher estimated from surveys that it's about 1.2 percent of children in schools are on Section 504 plans, compared to about 12 percent covered by the IDEA. The federal government doesn't require districts to track students receiving 504 accommodations as closely as students covered under the IDEA.

The early assessment offered by Perry Zirkel, a Lehigh University professor and my go-to source for special education law information, though, is that the new law could be "highly significant." Stay tuned!

September 10, 2008

Q&A with Dan Habib, Filmmaker

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Last week, I had the opportunity to interview Dan Habib, a former photojournalist who made a documentary about his son Samuel, now 8, who has cerebral palsy, and his family's efforts to ensure Samuel is fully included in school and home life. At right, you can see Dan and Samuel in a 2006 tee-ball game; Samuel is using a special walker to get around the bases.

From humble beginnings, Including Samuel has now been viewed by packed crowds around the country since its release last fall. The film bypasses some of the ponderous language that surrounds special education, and boils the issue down to its essentials: What is the right thing to do for this one child?

And, though the movie is just an hour long, Habib includes other voices, like a student for whom the regular school environment was not the right choice, and a teacher who candidly said that she felt that she lacked the right training to have students with disabilities in her classroom.

I wrote a column for Education Week about a nonprofit organization that is translating the documentary into Arabic to be shown to youth with disabilities in Iraq. But I also wanted to share some of Habib's thoughts on inclusion and education.

What are your feelings about full inclusion?

I feel full inclusion is vital not only for Samuel but for our society. Several years ago, my wife, Betsy, and I attended the University of New Hampshire Institute on Disability leadership series to learn more about being effective advocates for Samuel. We heard from disability rights advocates like Norman Kunc, who spoke about his “right to be disabled.” Norman said if offered a pill to cure his cerebral palsy, he would not take it. “If suddenly I got cured, I would have to start my identity all over again,” Norman said. “I like who I am, I like the work I do.” The leadership series helped us to see Samuel's disability as an intrinsic part--but just one part--of who he is.

I want people to get to know Samuel for all his wonderful and complex personality traits--not just as "the kid in the wheelchair." That will happen only if Samuel is fully included in our school, community--in everything we do. My hope is that this film will inspire the public, especially anyone connected to education, to talk about inclusion in a more informed and innovative way.

In the film, inclusion is handled differently by everyone who encounters it. Do you think this is a good thing, or should the process be more standardized?

Today, inclusion is still happening inconsistently throughout the country. It varies state to state, town to town and classroom to classroom.

Joe Petner of the Haggerty School (featured in the film) says we should not have to reinvent inclusion every time we try it; that for inclusion to be successful, it has to be a transferable model, not dependent on extraordinary leadership or funding. He says the most important factor in making inclusion work well is a community's commitment to the spirit of inclusion; the details will fall into place if that overall commitment is there. Administrators need to set the tone that inclusion is always the preferred path--it is written that way in [the Individuals with Disabilities in Education Act].

But inclusion can only work well if teachers and students have the proper supports in place to do it well. That includes training, technology, well-trained paraprofessionals, and planning time.

What kind of response did you get from Samuel's educators when you expressed your desire for him to be fully included in school life? Did you find universal acceptance or did it require a bit of "pushing" on the part of your family?

We don't expect Samuel's teachers to have all the answers. And we know it won't always go smoothly. We just want them to say, "let's work together to figure this out." So far, all of Samuel's teachers have really wanted to make it work, and they understood that inclusion is the right thing for all children. Like us, they believe all kids benefit from inclusion, because it teaches them that the real world has people of all abilities, and that disability is part of the natural diversity of our society. And they have told us that it has made them better teachers, because they've honed the skills they need to reach every child.

When we pushed to have Samuel's therapy (physical, occupational, speech) integrated into the class activities so that Samuel would not be pulled out of the classroom, some of the therapists were surprised, but not resistant. They said, "We haven't done that before, but we can try." That is what we ask for: that they try to the best of their ability..

I empathize with teachers and specialists that don't have support from the administrators. That makes it almost impossible to do inclusion well.

samuel_classroom_color.jpg

3-year-old Samuel with a friend in his preschool classroom.


What kind of advice would you give to parents so that they can also learn how to advocate appropriately for their children?

First, decide what you want most for your child. Then map out a path to get there. We have a magnet on our refrigerator that says, "The purpose of our lives is to be happy." We believe that Samuel's happiness is directly tied to his acceptance and involvement in our community. And the school is the hub of the community. If he is not fully included there, how can he be fully included in community? Because the neighborhood kids go to school with Samuel, they know the subtle ways he communicates, and they feel comfortable playing with him in our neighborhood. That makes him happy and feel accepted by his peers. That builds up his self-esteem, which all kids need--especially those with disabilities.

I'd also tell parents that the IEP (individualized education program) is a very powerful legal document. Play an active role in crafting that document so that it contains everything you believe sets up your child--and his/her teachers and therapists--for success in school. Then, stay involved to make sure the IEP is implemented.

We try hard to be team players with the school staff, and avoid antagonist relationships whenever possible. We try to get involved in other volunteer aspects of our school. But a parent recently sat next to me on a panel and said, "I will never apologize for advocating for my child. I get one shot at doing this right." That was powerful.

What advice would you offer principals and teachers when they are working with parents of students with disabilities? I hear so often about "pushy" parents or uncaring staff members, and it just seems like there has to be a way to get everyone on the same page.

Creating an IEP can be a traumatic and emotional process for parents, because it details all of the obstacles your child faces. Be empathetic to the pain this process can cause a parent.

Come into the relationship as a sincere problem-solver. Show that you see the child as a child, and not a case to manage. Get to know that child's strengths and personality traits. Make it clear that you presume competence, regardless of that child's "label." If you show that you genuinely want to include and teach the child, most parents will respond with a collaborative approach.

As the child gets older, offer to involve him/her in the IEP process. Samuel is almost 9 and we expect to have him attending some or all IEP meetings before long (though he would probably rather be hanging out with his friends). Most of what makes for a successful parent/school relationship is not about money or technology. It is about mutual respect, communication and a shared belief in the child.

And it never hurts when we bring cookies to the IEP meeting.


September 09, 2008

Georgia State Supe. Smarter Than a Fifth Grader

And now, the Georgia Academy for the Blind, located in Macon, the Atlanta Area School for the Deaf in Clarkston, and the Georgia School for the Deaf in Cave Spring get to benefit from Kathy Cox's smarts.

Cox, who was first elected in 2002, said the toughest question she fielded during her appearance on the Fox Network's trivia game show was which country, besides Nicaragua, borders Costa Rica. But after she answered correctly--Panama--the rest of the competition was smooth sailing.

The Atlanta Journal-Constitution has an article on Cox's triumph, as does as the New York Times.

September 08, 2008

Disability Advocacy Makes the Front Page

Once upon a time, this election season looked like it was going to be a quiet one for disability-rights advocates. But the selection of Sarah Palin as the Republican vice presidential nominee sent newspaper reporters scrambling to put together articles that ask members of the disability advocacy community What It All Means.

Here's a collection of some of the articles that were produced soon after Palin joined the ticket:

"Palin Candidacy Puts Spotlight on Special Needs" (USA Today)

"With Palin, Special Needs Get Spotlight" and "Parents of Special-Needs Children Divided Over Palin's Promise to Help" (The New York Times)

"Palin's Pitch to Parents of Disabled Raises Some Doubts" (The Wall Street Journal)

"Candidacy is a Chance to Shed Light" (The Boston Globe)

"Trig's Promise" (Newsweek)

I'm sure that's just a sample. If you see links to others worth sharing, please add them in the comment section.

September 08, 2008

Don't Forget the Paralympics!

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The summer Paralympics, an elite athletic competition for those with physical and cognitive disabilities, are currently underway in Beijing. You can follow them online through Universal Sports; a broadcast of highlights is scheduled for Oct. 18 on NBC.

The Paralympics should not be confused with the Special Olympics, which is open solely to athletes with intellectual disabilities. Special Olympics events are held year-round in many different countries, while the Paralympics are held every four years in the same city that hosts the Olympic Games.

September 05, 2008

Dear Palin Education Junkies....

I can tell that I'm getting a lot of traffic to the blog from people who are Googling "Sarah Palin" and "special education" because of the rumor that the governor cut special education funding in the state. Here's my lengthy blog post on that issue.

For those of you who are visiting for the first time: feel free to check out the place and stay a while! And, in case you haven't already seen it, I also invite readers check out an article written by my colleagues Sean Cavanagh and Alyson Klein that delves more comprehensively into what we know about the governor's education record during her relatively brief time in office.


(Education Week articles are generally available to subscribers only, but the site is hosting an "open house" through Sept. 7.)

September 05, 2008

Another Disability Shout-Out....and a Missed Opportunity?

Sarah Palin wasn't the only speaker who appealed to families of children with disabilities during the Republican National Convention. During John McCain's acceptance speech, he also directed attention to a family in the audience whom McCain believes his policies would help.

I fight for Jake and Toni Wimmer of Franklin County, Pennsylvania. Jake works on a loading dock, coaches Little League, and raises money for the mentally and physically disabled. Toni is a schoolteacher, working toward her master's degree. They have two sons; the youngest, Luke, has been diagnosed with autism. Their lives should matter to the people they elect to office. They matter to me.

Could that have been a time for McCain to slide a quick sentence mentioning his support for more federal funding for special education? He's already on record with this. It might have made a nice counterpoint to Palin's declaration that parents of children with disabilities would find a "friend and advocate" in the White House with her.

September 04, 2008

Gov. Palin's Budget for Special Education

In her well-received speech before delegates at the Republican National Convention last night, Gov. Sarah Palin of Alaska made an explicit appeal to families of children with disabilities:

...in April, my husband, Todd, and I welcomed our littlest one into the world, a perfectly beautiful baby boy named Trig. From the inside, no family ever seems typical. That's how it is with us.

Our family has the same ups and downs as any other—the same challenges and the same joys. Sometimes even the greatest joys bring challenge. And children with special needs inspire a special love.

To the families of special-needs children all across this country, I have a message: For years, you sought to make America a more welcoming place for your sons and daughters. I pledge to you that if we are elected, you will have a friend and advocate in the White House.


As many know by now, Palin's son Trig has Down syndrome.


But, while Palin was governor, did she slash special education funding from the state's budget? That was the latest charge that was flying around the Internet soon after her speech, and a reader has posted the same criticism of Palin on this blog. I've seen the same critique from posters on several Web sites now, all of whom seem to suggest that while Palin courts the disability community on the one hand, she's cutting the budget for needed services on the other.

From what I can tell, however, these charges against Palin are false, driven by a misreading of the budget documents for the state.

The "proof," as has been presented, is the part of the fiscal 2007 budget for the Alaska Department of Education and Early Development, which includes funding for the Alaska School for the Deaf, students who are patients at the Alaska Psychiatric Hospital, and the Alaska Challenge Youth Academy, a statewide, boot-camp-style program. The budget that year was $8,265,300.

But the next year, fiscal 2008, the budget is shown as $3,156,000, leading to the accusation that Palin cut the department's budget.

The difference in funding, however, is because the Alaska Challenge Youth Academy moved to a budget line item of its own. In the fiscal 2009 budget, you can see that the academy alone has a budget of $6,082,100. When you add that to the $3,156,000 that is being spent on all the other projects, it adds up to $9,238,100--an approximately 12 percent INCREASE in spending on all those particular programs, put together, since fiscal 2007.

It should also be noted that Alaska spends far more on education than just these few programs indicate. Education is typically one of the biggest parts of any state's budget, and in Alaska lawmakers plan to spend about $1.2 billion for fiscal 2009.

More accurate information about Palin's education record may be found at the newspapers in her state. The Anchorage Daily News, for example, ran a story in March about her approval of a large spending increase:

Gov. Sarah Palin has quietly signed into law the biggest rewrite of the state's education funding system in a decade, despite hints that she might veto the package.

Palin had said last week the package was incomplete. Lawmakers responded with a threat to override any veto.

She signed the bill Thursday without ceremony, applauding lawmakers' efforts in a news release.

The legislation phases in increases to per-pupil spending, increases to students with special needs and adjustments to cost factors that compensate school districts outside Anchorage for their steeper costs. It's expected to add an extra $180 million to school districts over the next five years.

Edited to add: I'd be remiss if I didn't include the reporting of my own colleague, Sean Cavanagh, who covers Alaska as one of his beats. He wrote earlier this year that the legislature and governor approved a bill that raises spending for students with special needs to $73,840 in fiscal 2011, from the current $26,900 per student in fiscal 2008.

Added 9/5: It's the blog post that keeps on growing! Reader "Sunny" asked in the comments why Palin was originally reluctant to sign the education bill, as stated in the Anchorage Daily News article I quote above. A short article I found in the newspaper's archives suggests that she didn't want to sign the bill because she wanted more money for schools included in it:

Gov. Sarah Palin says she will approve an education funding bill despite some qualms that schools could be shortchanged next year.

Palin hinted on Thursday that she could veto the bill, which was based on recommendations from this summer's Joint Legislative Education Task Force and had widespread support from lawmakers.

Palin wanted to raise the base student allocation, currently $5,380 per pupil, by $200, but the Legislature only approved $100.

September 03, 2008

Open House!

All of the stories on Education Week are available to non-subscribers until through Sept. 7. This gives those of you who haven't yet committed to subscribing a chance to read all our stories about response to intervention, Reading First, the presidential campaign, and anything else that strikes your fancy.

While I'm in promotion mode, let me also point out to fans of this blog that you can follow On Special Education in an RSS reader by clicking on the orange icon under my picture, on the right, that says "Get RSS." (My RSS reader of choice is Google Reader.)

And while you're browsing through the archives, please be sure to check out all of the other Education Week and Teacher Magazine blogs as well. They are always available to non-subscribers.

Happy reading!

September 02, 2008

The Good Behavior Game

Happy back-to-school! I know many of you may have been back for a week or two, but Labor Day seems to be a true sign that the lazy days of summer have come to a close.

I recently learned about a classroom management technique with younger kids that is quite successful, but so simple I can hardly believe that it shows such positive results: the "good behavior game." From the summer 2008 newsletter from the American Institutes for Research:

To play the game, the teacher breaks the classroom into teams of between four and seven students. The game is played while children are working individually. When a rule is broken, the teacher immediately identifies the behavior--such as a child leaving his or her seat without permission. The student's team receives a checkmark, while members of the other teams are praised for "working quietly." At the end of the game, each team with four or few checkmarks receives a reward.

Easy, right? Well, researchers with AIR followed a study of 1,200 19-to-21-year-olds who were in first and second grades in Baltimore in the mid-to-late 1980s. Some of their teachers were using the behavior game, some were not. The kids whose teachers used this method of controlling classroom behavior were much more successful than their counterparts in several facets of life: 19 percent of the "behavior game" kids used illicit drugs, compared to 38 percent in the standard classroom. When it comes to comparing use of school-based support services related to behavior, drugs, or alcohol, 17 percent of the behavior game kids did, compared to 33 percent of youth in standard classrooms.

AIR researcher Sheppard Kellam, who began studying the results of the good behavior game when he was at Johns Hopkins University, say it's critically important for young kids to be able to "learn to learn." Good behavior isn't innate, and positive peer pressure does work.

Apparently the good behavior game is well-known enough to have a great deal of research behind it. I'm curious to know if teachers have used it and how it works for them.

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