Rate Your School District on Special Ed

Sites like Special Ed Ratings are only as good as the ratings people provide. So search for your school district and share your thoughts to help other families. The site is at www.specialedratings.com.

And Now a Word from Your Child's Special Education Teacher

Thanks to Google Plus, I've discovered a new blog and a a great advocate. Dennise Goldberg writes for the Special Education Advisor, and this post caught my eye: "Secrets from Your Child's Special Education Teacher." I highly recommend it.

Take a look at the Special Education Advisor website, and you can follow them on Facebook.  Dennise is on Twitter as @specialedadvice and Google+.

ADA Turns 20

Today President Obama celebrated the 20th anniversary of the Americans with Disabilities Act. Read his remarks.

New Members of President's Committee for People with Intellectual Disabilities

President Obama has appointed an impressive group of advocates to the President's Committee for People with Intellectual Disabilities. The web post includes short bios.

National Family Caregivers Month

NATIONAL FAMILY CAREGIVERS MONTH, 2010

BY THE PRESIDENT OF THE UNITED STATES OF AMERICA

A PROCLAMATION

Every day, family members, friends, neighbors, and concerned individuals across America provide essential attention and assistance to their loved ones. Many individuals in need of care -- including children, elders, and persons with disabilities -- would have difficulty remaining safely in their homes and community without the support of their relatives and caregivers.

Caregivers often look after multiple generations of family members. Their efforts are vital to the quality of life of countless American seniors, bringing comfort and friendship to these treasured citizens. However, this labor of love can result in physical, psychological, and financial hardship for caregivers, and research suggests they often put their own health and well-being at risk while assisting loved ones. Through the National Family Caregiver Support Program, individuals can help their loved ones remain comfortably in the home and receive assistance with their caregiving responsibilities. This program provides information, assistance, counseling, training, support groups, and respite care for caregivers across our country....

Our businesses and companies can also contribute to families' ability to care for their loved ones in need. By offering flexible work arrangements and paid leave when caregiving duties require employees to miss work, employers can enable workers with caregiver responsibilities to balance work and family obligations more easily. Such efforts impact countless lives across our Nation, easing concerns and contributing to the well-being of individuals and families as they go about their daily lives.

During National Family Caregivers Month, we honor the millions of Americans who give endlessly of themselves to provide for the health and well-being of a beloved family member. Through their countless hours of service to their families and communities, they are a shining example of our Nation's great capacity to care for each other.

Signed Oct. 29, 2010, by President Barack Obama. Read the whole thing.

Looking for GOOD News!

Taking a glance at my Google Reader today, I was once again reminded how much negative news we hear each day in the area of special education and disability policy. Just today, I see:
- "Autistic Boy Abused by Bus Driver"
- " 'Drop Your Disabled Kids at Shelter,' Indiana Parents Told"
- "Special Education Attorney Convicted of Defrauding Parents"
- "Behavior Specialist with Bogus Credentials to Serve Prison Time"

I'm on the lookout for some positive news, and I need your help. Tell me about a teacher or school that's doing a great job for students with special needs. Or how much fun your child is having for Halloween. Or an elected official who "gets it." Or anything -- but it has to be good news. Add a comment here or email me.
I'll start with a news item from work, where we (Children's National Medical Center) hosted a Halloween party for kids on the oncology/hematology unit. These photos of kids who are spending the holiday in the hospital will make your day. View photos here.

Apple Highlights Apps for Special Needs

Apple has created a section titled "Useful for Everyone: Right from the Start" that lists 72 applications for the iPhone and 13 for the iPad to help people with special needs develop skills in areas from emotional development to communication to life skills. Many parents and consultants have identified useful apps for people with special needs, but this seems to show an increased focus by Apple to meet the needs of -- or should I say "market to" -- people with special needs. If the tools like iPhones and iPads are expensive, the apps are not. Read more.

What technology tools and applications have you found helpful?

School District Sues Family for Legal Costs of Special Ed Lawsuit

When you hear "lawsuit" and "special ed," you probably assume parents are suing a school district, right? Not this time.

A school district in Texas is going after a family who sued to improve their autistic child's education program. The family gave up after nearly four years of fighting, and now the school district is going to federal court to try to force the family to pay the estimated $250,000 that the suit has cost taxpayers. A teacher at the school says pressure is building to drop the lawsuit. "I think the lawsuit should end," he said. "I think the community should demand that it ends. I think there should be a major uproar because if they are going to sue this parent when is it going to be your turn next."

Watch the news story from Fox 26 in Houston. Thanks to Disability Scoop for the scoop.

A New Direction

I want to say thank you to my loyal readers -- everyone who has submitted suggestions, commented on my posts, challenged my opions, and shared my blog with others over the past few years. As any parent of a child with special needs will understand (and, really, any parent of any child will understand), I'm feeling a bit overwhelmed with my "outside" activities beyond my 9-to-5 job (if only it were 9-to-5!). I love my job, and I love all of my volunteer activities -- maintaining this blog, advocating for people with disabilities as a board member of The Arc of Montgomery County, coaching young hockey players and serving as communications director for the American Special Hockey Association, and playing hockey myself.

In addition to that, my wife and I are working hard to ensure that our daughter receives the level of education and instruction that she needs and is entitled to. I'm not going to go into the details here, but I'd be happy to talk to parents or other advocates about some of the issues we're dealing with.

For all of those reasons, I'm going to be blogging less often. Honestly, I feel guilty whenever an issue comes up and I don't have time to properly comment and analyze it here. So starting today, I'm enhancing the news feed on this page -- showing the most recent items from some of my favorite news sources -- Disability Scoop, Disability News by Patricia E. Bauer, Autism Speaks, and some that specialize in special education law. That will keep this blog timely in a different way, and when I feel strongly about something or have an urge to post, I will. I encourage you to follow these and other sources to get the news you can use to advocate for the people you care about and all families affected by disabilities.

You can also follow me on Twitter, at twitter.com/mmiller20910 -- I will post news related to special needs several times a week. And please follow special hockey at twitter.com/specialhockey and at facebook.com/specialhockey. That's always a good source of inspiring news about athletes with special needs and the volunteers who are helping them win on and off the ice. And feel free to shoot me an email any time. Thanks!

Internet "Equalizer" for People with Disabilities

A recent article from Agence France-Press explores how Facebook, email, online chats, and other technology are helping to crate :a virtual world of equality" for people with disabilities. Pacific Diversified Services, an organization that promotes inclusion, trains clients in basic computer skills and to safely use social networks. "It really adds to their sense of acceptance in the community," the program's director says.

Read "Internet an Equalizer for People with Disabilities."

Open Letter to Special Needs Professionals

Last week Pia Prenevost -- blogger, developmental psychologist, NICU nurse, and full-time advocate for her son -- posted "An Open Letter to Special Needs Professionals" on a blog called The Thinking Person's Guide to Autism. If you are a parent, teacher, therapist, or anyone who knows someone with a family member with special needs, I encourage you to read her letter. It's particularly appropriate as the school year begins. It reads in part:

"I just wanted to...caution you. Or warn you. Please, tread carefully. You see, what you might not realize as you look at me, talk to me, tell me your opinions, our options, our lack of options, and your predictions of our outcomes is that; well ... you see that heart? The slightly broken, definitely bruised one? Yeah, that’s my heart.

"Now, I realize that as you look at me you might see a confident parent, or an angry parent, or a happy-go-lucky parent. You might think that I understand everything, or nothing, or that I have all the experience in the world because I have done this before, or that I know the rules, or that I don’t know the rules and that is for the best. You might believe that I am high maintenance, or overreacting, or maybe neurotic, or disengaged and uninterested. Or that I don’t really care, or maybe I care too much...

"Some of 'us' parents -- the ‘special’ ones -- can be a pain in the ass. I know that. We know that. But we are fighting a fight we never planned to fight, and it doesn’t end. We don’t get to clock out at the end of the day. We don’t get a vacation from it. We live it, everyday. We are fighting without knowing how to fight it, and we depend so much on you to help us. We are your harshest critics. We are our own harshest critics too. We are genuinely fearful, and driven, and absolutely devoted. And we also know, we need you. So please, be careful with us. Because as hard and tough as we may look outwardly, our hearts are fragile things."

Yesterday Pia posted a summary of reactions to the piece on her blog, The Crack and the Light. Thanks for sharing, Pia.

Autism-Related Risk of Divorce Exaggerated?

While no one would question the fact that raising a child with a disability presents additional challenges to parents, allegations that parents with a child with autism are much more likely to get divorced may not be accurate. Studies have claimed that raising a child with autism significantly increases the rate of divorce, but a new study reported on WebMD says 75 percent of parents of children with autism remain married.

If you consider that about half of all marriages end in divorce, could it be that parents actually stay together at a higher rate when dealing with autism? Interestingly, as many as 66 percent of divorces involve couples who do not have children at all. You could speculate that not having children leads to loneliness (as one study claimed) or that the lack of responsibility makes it easier to break up.

Instead of examining statistics, I think more work should be put into helping couples improve their relationships -- both for the good of their marriage and their child. Dr. Robert Naseef of alternativechoices.com gave a presentation just last week on "Living with Autism in the Family: Taking Care of Everyone's Needs." Dr. Naseef debunked the myth of the high divorce rate, saying, "Citing autism as the reason for a marriage failing can be seen as yet another reasons for saying why autism is awful. Exaggerating the negative does not help us." And he offered the following tips:

For men:

- Learn to listen without trying to fix.

- Tell her what she is doing well.

- Do something to give her a break.

- Find romance in everyday life.

For women:

- Tell him to just listen -- that's all you need.

- Tell him what he is doing well.

- Tell him what he can do for you.

- Find romance in everyday life.

Do you have other tips, or sources of useful information?

Wheelchairs and Burritos: Court Says Chipotle Violated ADA

Maybe it's because I'm a fan of Chipotle, but I'm not sure how I feel about a recent ruling against the restaurant for violating the Americans with Disabilities Act -- because it's counters are too high for people in wheelchairs to see the food. I've noticed before that the walls are too high for even some short people, like children, to see the ingredients, but no one is denied any food. The people who sued want Chipotle to lower their walls, but I wonder if it would be an acceptable compromise to offer a menu with photos so people could choose their ingredients. Another chain, Qdoba, is set up the exact same way. Read about the San Diego case from 10News.

What do you think?

20th Anniversary of ADA

I have not been very good about keeping this blog up to date. Has anyone noticed?

The biggest news story since I last posted is the 20th anniversary of the Americans with Disabilities Act (ADA). Patricia Bauer at Disability News has a good summary of media coverage.

Read more on the anniversary:

Autism Speaks blog

President Obama's executive order on Increasing Federal Employment of Individuals with Disabilities

ADA at 20: A Nation Transformed, in which Senator Tom Harkin refers to the ADA as the "Emancipation Proclamation for people with disabilities."

Proposed rule by Department of Justice to ensure web access to people with disabilities

More federal resources from ADA.gov

Are you encouraged or discouraged about where we are as a country when it comes to the rights of people with disabilities?

Department of Education Adds Two Special Ed Officials

Sue Swenson, former commissioner of the Administration on Developmental Disabilities, has been appointed Deputy Assistant Secretary of the Office of Special Education and Rehabilitative Services, and Melody Musgrove will be the Director of the Office of Special Education Programs. Read more from Education Week.

Transition Tips for Parents of Adult Children

Disability.gov has new resources for parents who are planning for their child's transition to college, jobs, and adulthood. Read Preparing for Post-Secondary Education.

2010-11 White House Fellows Include Gallaudet Professor

From a White House media advisory today, Gallaudet faculty member Kubby Rashid, who is deaf, has been chosen as a White House Fellow.

"Kubby Rashid has been a member of the Gallaudet faculty since 1994, including a stint as Chair of the Department of Business. In addition to teaching, Dr. Rashid was active in faculty leadership and administration, and was co chair of a major initiative to reconfigure all academic programs at the University. Dr. Rashid served on the board of the World Deaf Leadership Program, guiding development projects for the deaf communities in South Africa and Thailand. She has also worked with individuals from many developing countries, helping deaf people learned to develop leadership skills and advocate for themselves. Dr. Rashid has previously been involved with the National Deaf Business Institute and taught several years for NDBI and Merrill Lynch's summer program for Deaf Business owners and would-be entrepreneurs. She was the first coordinator of the Bernstein Leadership Institute's Deaf Women's Leadership Program, and implemented the program and curriculum that form the core of the DWLP today. In 2008 she was appointed by Governor Martin O’Malley to a six-year term on the Board of the Maryland School for the Deaf and also serves as a Board member of Discovering Deaf Worlds, an NGO dedicated to helping deaf people in developing countries."

L.A. Official Justifies Cuts for Students with Disabilities: Special Ed "Takes Away from Regular Kids"

Many think it; few say it.  Los Angeles Unified School District is closing 200 classes and a campus for students with disabilities.  The explanation from Superintendent Ramon C. Cortines: "You have to look at it in perspective. When you fund some of the special ed things, you're taking from regular kids."

As reported in the Los Angeles Times, to help close a $640 million budget gap, LA is cutting back on a campus for blind students, closing a special-needs center, and eliminating 200 classes.  As in any district, parents of "regular kids" are also not happy -- other cuts are being made to the arts, music programs, and libraries, not to mention more than 1,000 layoffs.
 
About 13 percent of students in the L.A. school district have an identified disability.  Now more of these students will be put in larger classes, commute farther to school, and in some cases will have no bus transportation at all.

Yes, the city and the state are facing a tremendous budget problem.  But if you agree with me that Superintendent Cortines should not pit "special ed things" against "regular kids," email him at superintendent@lausd.net.  (The defender of "regular kids" is pictured above.)

DC Admits Bungling Inclusion Plan; Vows to Press On

As I've pointed out before, truly exceptional services for children with disabilities -- especially preschoolers -- are few and far between.  When parents find services that are appropriate to their child's specific needs, they will do anything possible to access them.  So when quality services are taken away, with little thought about either the students or the parents, bad things happen.  People get mad.  Children don't get the services they need.  Even if there are short-term savings to denying children the services they need, the long-term costs are astounding.

As an example, yesterday the Washington Post reported that the District of Columbia's top special education official admitted that his department mishandled its plan to "reintegrate" students with special needs into the public school system.  (Read "DC Special-Ed Official Issues Apology: Initiative Mishandled, Parents Say; System Tried to Move Kids from Private Schools Back to Public Schools.")

The backlash from parents in DC should come as no surprise.  I recently reported on a similar plan in Maryland to move preschool children with special needs from an exceptional "non-public" school to the county's public elementary school in the name of inclusion -- seemingly with little regard for quality.  While county officials and parents have only positive things to say about the preschool that's been serving these children for decades, the county claims the students will be better served in large schools without specialized instructors or services.   Montgomery County Superintendent Jerry Weast has made the laughable assertion that this move has nothing to do with saving money.

The problem in both the District and Montgomery County is twofold -- the plans themselves are flawed, and officials have not been honest and open with parents about their plans to make radical changes in the way they serve students.  Richard Nyankori, deputy chancellor for special education, has taken an interesting approach of bad-mouthing the private schools that many parents are so thankful for.  He said, "I can't overemphasize that some students enrolled in private schools are not getting what they deserve."  That may be true for a portion of students, but when parents are actively fighting to get their students into those schools and to keep them there, that argument loses a lot of steam.  And the District has offered no evidence of its newly discovered ability to meet needs it has historically been unable to meet.

When the city says the public school system "now has the capacity to serve more students with disabilities," that doesn't mean they have teachers with better qualifications, training, and experience.  It means they have budget problems and don't want to pay for private schools, even if those schools are more suited for many children with special needs.  I know many families who have spent thousands of dollars in legal fees to make the case for their children to receive an education in a private school setting, because the public schools have failed to meet their children's needs.  Are we to believe that these schools have drastically improved their ability to meet these needs?  Or are the District and other school systems asking parents to accept a lower level of quality and specialization for their children?

Despite bungling this situation enough to attract national attention, Nyankori has vowed to continue the "reintegration" plan.

I think there's a simple solution for the District.  Let the public schools show they can provide excellent instruction for kids with special needs, and let them compete with the private schools.  If parents value inclusion -- and many do, very much -- then the public schools should be able to attract their share of students.  In the meantime, they have a tough case to make.  The reason that more than 25 percent of special-needs students are in private placements is because the District has been unable to provide the level of education required by federal law.  The burden should be on DC schools to prove they can offer the specialized instruction that's needed.  Parents should not be asked -- or required -- to risk their children's educations and future success because the District doesn't want to pay for private school.

As the trend toward "inclusion," "reintegration," or whatever you want to call it continues -- often at the expense of students with the greatest needs -- what can we expect in New York City, the nation's largest school system, which is seeing record increases in the number of special needs students?

Disability Community Reacts to Supreme Court Nominee

From JFActivist:

The Bazelon Center for Mental Health Law congratulates President Obama on his nomination of Solicitor General Elena Kagan to replace Justice John Paul Stevens on the Supreme Court. "The advancement of legal protections for people with disabilities has always been a bipartisan effort.We need strong leaders on the courts to ensure that disability rights laws have the broad remedial effect Congress intended," said Robert Bernstein, Ph.D., executive director of the Bazelon Center.  "We hope General Kagan will be such a leader on the Supreme Court."

Read more.

Dr. Stanley Greenspan, Pioneer in Autism Therapy, Leaves Legacy and Lessons

I was sad to read today that Dr. Stanley Greenspan, the founder of "Floortime" and the Developmental, Individual Differences, Relationship-based model (DIR) approach to developmental therapy, had died.  His books, his lessons, and his therapeutic models will benefit children for generations to come.  If you haven't seen how children with autism do (or do not) learn, it would be easy to write off Dr. Greenspan's approach as simple "play therapy."

But the brilliance of Dr. Greenspan's model is in its apparent simplicity.  While some therapists, teachers, and parents will continue to debate the relative effectiveness of applied behabioral analysis (ABA) and DIR/Floortime, anyone who has met more than one person with autism knows that it is a wide spectrum.  As with any other learners, there is not one method that works equally well with all children with autism.

My daughter has received both ABA instruction and Floortime therapy (in fact, through Dr. Greenspan's office).  What has worked best for her has been a combination.  In lay terms, Dr. Greenspan's approach recognizes that a child cannot learn unless they are engaged in an activity.  So instead of forcing a child to do something he doesn't want to, the child gets to direct the activity.  For example, if the child shows interest in a ball, the therapist (or parent) can use that ball to initiate engagement.  Dr. Greenspan valued social skills, playdates, emotional awareness, and relationships -- helping children develop life skills while expanding their cognitive understanding.  He saw every child as a unique human being with feelings, needs, interests that could be leveraged to help them learn.

Whether you are interested in DIR/Floortime or want to learn about how children with autism learn, get Dr. Greenspan's book "Engaging Autism," co-authored by Serena Wieder.  In it, he writes: "Often we look for a way to reach a child – the magic key that will unlock the hidden door – when all the while the child is showing what he needs by his actions and the way he’s processing what comes his way....

"The child may have a disorder or a set of problems, but he is not the disorder. He is a human being with real feelings, real desires, and real wishes."

Read tributes to Dr. Greenspan.  For more information about DIR/Floortime, visit the Interdisciplinary Council on Developmental and Learning Disorders at www.icdl.com/.  Mike Frandsen, who reports about autism for the DC Examiner, wrote a nice article about Dr. Greenspan.

Sec. Duncan Calls on Teachers to Raise Achievement of Special-Needs Students

Speaking to 6,000 special educators at the annual conference of the Council for Exceptional Children Wednesday, Education Secretary Arne Duncan called on teachers to improve the achievement levels of students with special needs.  He said that while we have made progress in expanding educational opportunities for all children, "a significant gap between our aspirations and reality" for students with disabilities. "The graduation rate, postsecondary education rate, and employment rate are all increasing, but they are still, frankly, far too low."

"Even in my lifetime, public schools virtually ignored children with disabilities. Many children were denied access to public schools, and those who attended didn't get the individualized instruction and appropriate services they needed and deserved.

"Over the past 35 years, we've made great strides in delivering on the promise of a free, appropriate public education for children with disabilities. Thanks to the advocacy and hard work of people and organizations like the Council for Exceptional Children, six million students with disabilities are in school—and millions of them are thriving.

"Yet unfortunately, many children with disabilities are not getting a world-class education. The President and I are committed to doing everything in our power to make that bedrock American promise of equal educational opportunity a reality. With the reauthorization of the Elementary and Secondary Education Act, we have a historic opportunity to move closer to fulfilling that promise for all students."

Read his full remarks, "Keeping the Promise to All America's Children."

Back from a Break: Disabled Hockey Festival

I haven't updated this blog in a while, partly because my attention shifted last week to managing communications and another blog for the 6th Annual USA Hockey Disabled Festival in Laurel, Md. I've mentioned before that I volunteer with the American Special Hockey Association, which is similar to Special Olympics for ice hockey (because SO doesn't offer hockey) for people with developmental disabilities. But special hockey was just a part of the festival, which also included sled hockey, deaf and hearing-impaired hockey, and amputee hockey. The festival included several games with the USA Warriors, a program for wounded soldiers who are using hockey as part of their physical and emotional recovery.

Please read and share the festival blog, even with your friends who aren't hockey fans.  One of the best articles about the festival was from the local Gazette newspaper, which really explored the therapeutic benefits of hockey for children with autism, Down Syndrome, and ADHD. Read "Disabled Hockey Festival Ready to Score: Coaches, Parents Say Players Feel Part of Something Beyond a Disability."

Sled hockey

One of the USA Warriors, a double amputee who's an inspiration to his teammates and opponents.  Read about the Warriors, "The Warriors Way," from USA Hockey magazine.

Duff Goldman of "Ace of Cakes" on the Food Network, designed and delivered a special cake for the festival. While he was there, he asked to try out sled hockey and got to play alongside members of the USA Sled Hockey Team, which just won the gold medal in the Paralympics in Vancouver.  A future episode of the "Ace of Cakes" will feature his participation.

To learn more about special hockey, visit us at www.facebook.com/specialhockey, follow us on Twitter at www.twitter.com/specialhockey, or visit www.americanspecialhockey.org.

Puppy "Not a Pet, but a Friend" to Twins with Autism

As Autism Awareness Month begins, take a look at this touching story about how a dog is helping twins with autism.

Health Care -- Thoughts?

Are you looking for a long analysis of the health care bill? You won't find it here. I want to know what you think.

Quoted in Disability Scoop, Liz Savage, director of health and housing policy at the Disability Policy Collaboration, said "I think everyone in the disability community is thrilled because everything that we fought for was included."

So are you thrilled?

Light It Up Blue for Autism!

Autism Speaks is asking people to be creative by deciding how to "Light It Up Blue" during Autism Awareness Month in April. They're asking bloggers to post in blue during the month, and when they contacted me they recognized that my blog is already blue (just a coincidence). So the best thing I can do is challenge you to Light It Up Blue and let me and our readers know how you're doing it. Some ideas from the Light It Up Blue website:

- Wear your Autism Speaks puzzle piece pin every day throughout the month of April, and tell people about autism if they ask about it.
- Change your Facebook profile picture to the Light It Up Blue logo and tag at least 10 of your friends.
- Post on your blog about how you are “lighting it up blue” to raise autism awareness.
- Add the Light It Up Blue logo to your e-mail signature … and type your e-mails in blue!
- On April 2, wear blue clothing and ask your co-workers, schools and friends to wear blue too. Take pictures and add them to our Flickr gallery.
- Bake puzzle piece shaped cookies and frost them with blue icing, then bring them to your school, work, or place of worship to raise autism awareness.

In honor of the third annual United Nations World Awareness Day on April 2, the Empire State Building will have a special lighting on the evening of April 1. If the Empire State Building can "go blue," the sky is literally the limit.

Children with Special Needs Left Behind -- Again

I have a confession to make.

Many people have told me my blog is one of their most important resources to keep up to date on disability issues. The blog was even named one of the top resources for special education teachers.

But I have to confess that the only reason I started this blog -- and the only reason I keep it going -- is to support my daughter and people like her. Yes, it may help inform other people, raise awareness, and support important changes. But it's really all about her. My only expertise in education is from my attempts to navigate the system as a parent.

My 6-year-old daughter has autism and a seizure disorder, and she is non-verbal. She's also a student, and as a student she has a legal right to an appropriate education.

I try not to be partisan in this blog, but as a Democrat, it was easy for me to criticize the Bush Administration's policies in education (and so many other areas). It's harder for me to acknowledge that under the leadership of Secretary Arne Duncan, the Obama Administration's education policies appear to be more of the same (or worse), at least as they relate to children like my daughter.

My wife reminds me that our family is in the minority -- most children in the United States are not disabled. For most of them, focusing on the need to increase test scores and get into the best college makes sense. Unfortunately, the single-minded focus on test scores and academic achievement means that my daughter and others like her are positioned as obstacles to progress, as opposed to welcome members of the education system. They are undervalued, underserved, underfunded, and "left behind" in the truest sense of the term.

I'd like for my daughter to attend college one day, but today her schoolwork is focused on teaching her to care for herself, to pay attention to her surroundings, and to match shapes and colors. If you are a parent of a typical child, maybe even a child in a Gifted and Talented program, imagine these two scenarios:

1. Your child's school is judged solely on students' academic performance -- test scores and college readiness. The higher your students' performance, the more federal and state money and other benefits your school will receive. You are punished for low test scores. Do you want my daughter to attend your child's school?

2. Your child's school is judged on students' academic performance and its ability to incorporate children with disabilities, children who are still learning English, and others with special needs -- so they can learn from typical peers, and vice versa. The federal and state governments reward your school and provide incentives for incorporating these students and teaching them important life skills. Now do you want my daughter to attend your child's school?

Occasionally, Secretary Duncan does talk about special education. What he says is that more students in special education should graduate. That's nice for the children who have the ability to achieve at that level. But what about the many children who don't? Are non-diploma students who also have a right to an education on his radar at all? Or they mere obstacles to his legacy as a reformer?

Sadly, when asked about special education, even after being in office for more than a year, Secretary Duncan punts the question. It seems that he hasn't considered these questions himself, and you have to wonder if he considers special education a necessary evil that comes with his job. Education Week reported recently, "Rep. Robert E. Andrews, D-N.J., asked [Duncan] how the department would like Congress to revamp assessments for English-language learners and students in special education. A number of schools in his districts are not meeting the achievement targets in the NCLB law because of those groups of students, he said. Secretary Duncan said that he thinks that might be the toughest question the department has to tackle in reauthorization of the ESEA. He said he has tapped Alexa Posney, the assistant secretary for special education and rehabilitative services, and Thelma Melendez, the assistant secretary for elementary and secondary education and a former English-language learner herself, on how best to measure those students’ progress."

It's good that he's asked his assistant secretaries to look into "the toughest question" regarding reauthorization. But when you roll out a comprehensive reform plan, isn't it time for some answers? And some leadership?

Obama Plan and Special Ed

I'll have more to say soon about the Obama Administration's proposal for education reform ad its impact on special ed. For now, read Disability Scoop's summary, "Obama Education Overhaul to Up Ante for Students with Disabilities."

In Education Vote, Politics Wins; Kids Lose.

If you've followed my blog over the past few months, you've read about the proposed budget in Montgomery County, Md., that would eliminate a proven program for preschoolers with disabilities, replacing it with a flawed, experimental program that was created without the involvement of parents or the county's partners who have successfully provided these services for 35 years.

Parents vocally expressed their opposition to this plan. Many pointed out that Superintendent Jerry Weast blatantly violated a Board of Education policy that new programs must be presented in time to be reviewed -- before showing up in a budget.

Today, the members of the Board of Education unanimously approved that budget.

Unanimously, they voted against a proven program that parents have relied on to give their children a chance to succeed.

Unanimously, they told parents of special-needs children that they do not value their opinions and experiences when making major changes to the services the county offers.

Unanimously, they told Dr. Weast that he can unilaterally create, change, or shut down any program he chooses -- and they will rubber stamp his decisions.

Unanimously, they threatened the future well-being of our county's youngest and most at-risk children.

UPDATE: I've created a Facebook group to encourage people to ask Montgomery County Executive Ike Leggett to overturn this decision and preserve MPAC's services for children who need them. Before March 1, email him at ocemail@montgomerycountymd.gov or call his office at 240-777-2500 and urge him to overturn the realignment of preschool services and to preserve MPAC.

President's Special Ed Funding Increase Not Enough, Some Say

President Obama's proposed budget includes $250 million in new special education funds, but some advocates say it's not enough. The budget proposal has nearly $12 billion in special ed funding for states, which is $250 million more than last year.

"But despite the increase," Disability Scoop reports, "the federal contribution toward the cost of special education would remain steady at about 17 percent. And that’s a problem for special educators who want the president to stick to his campaign promise of fully funding the program."

Deborah Ziegler of the Council for Exceptional Children said: “We are disheartened to see the president did not use this opportunity to fulfill his campaign commitment to fully fund special education and early intervention programs. Another opportunity to make progress toward fully funding IDEA has, sadly, been missed.”

When the Individuals with Disabilities Education Act was passed in 1975, Congress committed to funding 40 percent of the cost of educating students with disabilities, with states covering the rest of the cost. But the government has typically provided less than 20 percent of the cost.