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Special Education

The costs of special education are skyrocketing as are the number of  students diagnosed as having special needs.  In the last fiscal year Massachusetts spent more than 1.7 billion dollars on special education — that’s up half a billion dollars since 2002.

Much of that money is going for the record high number of students diagnosed as having an “autism spectrum” disorder. About 1,000 autistic children are enrolling in Massachusetts public schools each year. Some parents have hired attorneys to make sure school districts comply with the law that requires all students receive a “free and appropriate” education.

We look at how schools are funding special education programs and how parents are fighting for the education of their children.

Listen to the full show:
listen

Plus, in our web specials: Living with autism…

Radio Boston: Special Education in Massachusetts
Airdate: November 16, 2007


Web Specials…Here is a list of resources for parents interesting in learning more about Special Education in Massachusetts:

For an overview go to the Massachusetts Department of Education , you can also visit their resources link for more about specific disabilities.

To learn how you can help your special needs child or to find an advocate contact the Massachusetts Advocates for Children.

To learn more about autism visit the National Autism Center.


Living with Autism: “Love just costs something, sometimes.”alexa2.jpgMeghna Chakrabarti writes: That’s what Ali Watt told me when I went to visit the North Shore Education Consortium. Ali’s daughter, Alexa, is a student there. Alexa is 15 and has severe autism. She doesn’t talk much. Mumbles and groans and sings, more than anything. She’s tall and beautiful, too.

Alexa is Ali’s only child. Though she loves her daughter without condition and with total conviction, Ali still struggles with the mystery of autism. When we talked, a bewildered look sometimes flashed across her eyes. Her daughter’s true soul is somewhere in there, she believes. It’s just fronted by the ferocity of the severe autism. So, there’s a lot of frustration, Ali told me, both hers and Alexa’s.

Faith, family, and words, have brought Ali a measure of serenity. In 2004 she wrote Hurricane Dancing: Glimpses of Life with an Autistic Child, a book of poems Ali had penned over the years.

She read one of the pieces for us:
poem.mp3

alexa1.jpgWith the bewilderment comes also unanticipated moments of amusement and joy. Ali couldn’t stress this enough. I got a taste of what she meant when I went on a walk with Alexa. She sang the whole time… “walking in a winter wonderland… walking in a winter wonderland.” Autism, Ali says, means finding the balance between the wonder, and the wondering.

Hearing Things (2000)
by D. Alison Watt

“Alexa, this is Doug.
Do you remember our friend
Doug?
Say hello to Doug!”
She looked at him then looked at me
downright disbelieving.
He walked away
and to his back
she said hello:
“Quack, quack, quack.”


Links to Massachusetts Autism Resources:Autism Society of America, Massachusetts chapter

Doug Flutie, Jr. Foundation for Autism

Massachusetts Advocates for Children: Autism Project

Massachusetts Department of Education: Autism Special Education

Comments
  • Meghna says:
    November 16th, 2007 at 5:31 pm

    FROM THE RADIO BOSTON EMAIL IN BOX:

    Hi,
    Â
    My experience is more with moderate special needs rather than severe special needs.  I am a learning disabilities specialist currently in private practice although I have taught in the school setting also. I think a major issue with respect to the population I deal with, is that regular education teachers are very often not prepared by their training and supervision experiences to provide for the students who are included in their classes although many schools mandate inclusion.  I think one thing we all need to think about is overhauling teacher preparation programs.  As my professor at Northwestern University said, there is no such thing as specal education, only good teaching and not so good teaching.
    Â
    -Kalyani Krishnan

    Language and Learning Specialist
    Coordinator of Follow-up Evaluations
    Institute for Learning and Development

  • Meghna says:
    November 16th, 2007 at 5:32 pm

    FROM THE RADIO BOSTON EMAIL IN BOX:

    Name: Sarah Commerford

    Subject: special education

    Message: As a parent of two children with special needs, and as
    professional special education advocate, I can say with certainty that
    while the costs of educating children with special needs is indeed
    high, the long term strain on the state and federal prison, mental
    health and welfare system would be far higher without continued early
    intervention and intensive, direct instruction for school aged
    children with disabilities.

    There are no easy answers, but compromising special education
    programming on the premise that it costs too much is short sighted and
    can never be an option.

    Sarah Commerford, M.Ed.

  • Meghna says:
    November 16th, 2007 at 5:33 pm

    FROM THE RADIO BOSTON EMAIL INBOX:

    Every society that values human beings intrinsically must make hard
    decisions about how to accommodate the wide variance in human ability
    and native circumstances. For an isolated tribe in the amazon a
    seriously disabled or impaired child might be allowed to die as an
    infant since the material wealth and resources of the society simply
    can’t support the child’s needs.
    Our society is rich beyond the imaginings of previous generations:
    we absolutely have the material abundance to provide for the needs of
    all the disabled — child and adult. That we choose not to — day after
    day — as individuals voting down school budget overrides and
    corporately on the part of the great wealth holders of our country — is
    more than a shame, it is a crime.


    —————————————–
    David Pfarrer

  • Meghna says:
    November 16th, 2007 at 5:34 pm

    FROM THE RADIO BOSTON EMAIL INBOX:

    I have yet to hear anyone talk about the fact that many of the
    conditions that require “special education” have clinical diagnosis and,
    therefore are more like having a disease that requires medical care than
    simply an extention of the fundamental education model. This does not
    mean that they shouldn’t have everything available, but it does suggest
    that one way of funding this is to require “health insurance” to cover
    these conditions as well. If they really things that can be diagnosed
    then we whould a pooled sharing of the societal reponsibility to provide
    for these conditions. It isn’t The Solutions but it might help to fund
    things without putting all of the burden on the “property tax” as it is
    now. There must be a better way to fund these costs in a way that
    doesn’t put them in a competition with meeting the basic mission of our
    eduction system. This is a false competition that serves noone in the end.

    I four eduction system is less and less effective at delivering the core
    eduction to the majority of students we will not be competitive in the
    world and will have a decline in our quality of life. This will make
    much more difficult to provide anything to anyone!

    Just my 2 cents….

    Thanks,

    Scott Samenfeld
    Arlington, MA

  • Meghna says:
    November 16th, 2007 at 5:34 pm

    ANOTHER ONE FROM THE EMAIL INBOX:

    Name: Peg Anderson

    Subject: Special Ed

    Message: I went through this with my son. In 1990 he had problems
    adjusting to school. He was diagnosed with ADHD. In order to serve
    my sons interests I was the mother from hell. I made sure that I knew
    my rights and the law. My son had his own Aid from second through
    sixth grade. He had many plans over the years. I had cooperation in
    elementary and middle school however in High School the principal say
    no need to obey the end plan. I found that they had broken the law and
    used that as club to beat them into doing what they should have done.
    I am from a very wealthy school system. If I had not been as
    aggressive and downright rude my son would not have made it. When
    school systems claim that they want to help special needs children my
    experience is that they want to help them in a way that is cheap and
    convient for them not the child. My son made it through to the othe
    side. He is a senior at UMASS Dartmouth and doing very well.

  • Meghna says:
    November 16th, 2007 at 5:35 pm

    FROM THE RADIO BOSTON EMAIL INBOX:

    Name: Marcia

    Subject: SPED violations

    Message: Please check with the MA Department of Education. Newton’s
    audit revealed all sorts of compliance violations, and I’m sure other
    communities did as well. It’s not a questions–it’s a fact and it’s
    published for public consumption.

  • Meghna says:
    November 16th, 2007 at 5:36 pm

    FROM THE RADIO BOSTON INBOX:

    Name: John Craig

    Subject: special ed

    Message: Hi
    The moral tragedy here is that there is very little outrage that
    there is an epidemic happening! Why are there so many kids on the
    spectrum? We have to look at ALL possibilties. Not just gloss over
    vaccines and vaccine additives and rely on three foreign studies
    which are flawed. Environmental insults of all kinds are not being
    taken seriously. In the history of humankind, there never has been a
    “genetic epidemic”.
    Thanks
    John Craig
    PS The 1 in 150 # from the CDC I think is for full blown autism.

  • Meghna says:
    November 17th, 2007 at 12:17 pm

    FROM THE RADIO BOSTON EMAIL INBOX:

    There is no question that extensive investment should be made in high-functioning children who will eventually either contribute to the community or cause problems. This is sound economically and ethically.

    However, we might do well to question our goals with regard to lower-functioning children. I recall hearing a story on NPR awhile back about a family (this story was presented by the father) who had reluctantly put their 13-year-old autistic son in a group home after years of struggle within the family. Sometimes their son was violent, and had to be restrained. Finally they accepted that this was not good for him, as well as not good for them. At first the transition was difficult. But when their son began to return for home visits, they found that he was not only happier, but that he was more sociable and had begun learning his alphabet. The option of a higher quality of life in an institutional setting might be a more enlightened goal than what we have now.

    Sincerely,
    Natalie Gillihan

  • eprince says:
    November 17th, 2007 at 3:19 pm

    Excellent show! As a special education administrator who is responsible for leading the meetings that determine eligibility, it’s difficult to see how many parents have been led to believe that special education is the only way that a student can get a quality education. Many academic weaknesses are not disabilities and there are many, many schools and teachers who are dedicated to improving academic skills for ALL students. In our district we see that having rid ourselves of substantially separate classrooms for students with more significant learning disabilities has been a phenomenal success in improving their academic abilities. This model is not necessarily less expensive, and in some ways it is more expensive; but it is the best way for teachers to work together to improve their practice. The further away a student is from their peers and the general education setting, the less opportunity they have to learn from a variety of experts in the curriculum.

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