Special Education Today

3 March 2010

Shortest Resolve in History…

Filed under: Food for thought, life — Leila @ 7:49 pm

I was so gung-ho last night. I decided that I needed to change my negative way of thinking. I was so inspired by my nephew who just moved back home last night. He’s so positive that some of it rubbed off on me. Well, that optimism lasted for less than a day. Why you ask?

Well, God just isn’t on my side.

  • I can’t buy a job to save my life,
  • I’m behind on so much stuff,
  • I hate life. Sometimes I curse the day when I wake up,
  • I just got a fucking ticket for not stopping at a stop sign. You sure can tell the state of California needs money.
  • I’ve decided that I do not believe in God the way I used to. I’ve decided he’s not in the habit of helping me out for the past couple years. So, I don’t choose to believe in him anymore.

My power of positive thinking lasted for less than 24 hours. I think I like my negative way of thinking. It obviously works for me. As a man thinketh, so is he!


Spread the Word to End the Word

Filed under: Uncategorized — Elisabeth Williams @ 6:41 pm
Spread the word to end the word March 3, 2010 is the official awareness day of the nationwide Spread the Word to End the Word campaign to discontinue derogatory use of the “r-word” and promote acceptance of people with intellectual disabilities.  The campaign is encouraging people to rally and pledge their support at www.r-word.org with the goal of reaching 100,000 pledges.



Spread the Word to End the Word is a campaign created by youth, in an ongoing effort with Special Olympics and Best Buddies International, to engage schools, organizations and communities by raising the consciousness of society about the dehumanizing and hurtful effects of the “r-word.”



The Council for Exceptional Children was one of more than 200 international organizations to sign on in support of this important campaign. CEC has also been working to get co-sponsors for Rosa’s Law in the House and Senate. Rosa’s Law, S. 2781, was introduced by Senator Barbara Mikulski (D-MD) in November, 2009. U.S. Senator Michael B. Enzi (R-Wyo.), Ranking Member of the Health, Education, Labor and Pensions Committee, is the Republican sponsor of the bill.  (See a previous CEC Policy Insider story). Representative Michael McMahon (D-NY) introduced a companion bill, H.R. 4544 in the House.  Rosa’s Law would change terminology throughout federal law from “mentally retarded” to “intellectually disabled.” Several groups in the field have already made this change.



Pledge your support at www.r-word.org and check out the many events planned all over the world to see if YOUR area has created an event to spread the word to end the word.



Pledge your support at www.r-word.org and be sure to check out the latest entry on CEC’s Reality 101, where blogger Ellen sounds off on the need for “people-first” language.

How much Does the Federal Government Spend on Special Education

Logo of the United States Government Accountab...Image via Wikipedia



The Government Accountability Office has released a report on federal education spending. You can review the entire report here. Those of us who crunch numbers enjoy these sorts of reports.

Although it is difficult to decipher in parts because special ed funds get disbursed through different programs and the federal budget is a big mess. Nonetheless, these reports are instructive. The main special ed program, the grants to states, makes up about 19% of the total federal education spending. The total of this program for Fiscal Years 2006, 2007 and 2008 was 32.3 billion dollars. This is another one of those reports that special ed professionals should save a copy of. You never know when you may be requested to quote stats!

Any thoughts about these numbers? Do they sound about right? Take a look at the report for all education programs and what we spend on them.



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Urge Congress to Fund ONLY Federal Gifted Education Program

Students at computers In 2009, less than 2 cents out of every $100 of the federal K-12 education budget was devoted to meeting the needs of the nation's gifted and talented students. Please join CEC in urging Congress to support the ONLY federal program dedicated to meeting the unique learning needs of students with gifts and talents, the Javits Act.  If our nation is to remain globally competitive, we must increase our investment in gifted education.



Representatives Gallegly (California) and Matheson (Utah) are circulating a letter to their colleagues in Congress asking for their support of the Javits Act.  The Gallegly-Matheson letter supports restoring funding to 2002 funding levels, before a series of cuts and level funding eroded the program’s reach. 



Recent research analyzing NAEP and state assessment data indicates a growing ‘excellence gap’ at the top levels of achievement between disadvantaged students and their more advantaged peers, which may take up to a century to close.  There has never been a more pressing time to recommit to our investment in the Javits Act. 



Please urge your Representative to sign on to this letter supporting the Javits Act by the March 12th deadline!  



MeMoves – Revisited

Filed under: DVD, MeMoves, calm, focus, motions, thinkingmoves.com — Patrick Black @ 10:00 am
I wrote about MeMoves a couple of weeks ago, and I wanted to come back and share some anecdotal thoughts about it!  I received my MeMoves DVD last week, and I'm loving it!  I am using it throughout the day to focus and calm my students and they are responding.  I've found that even when the students have trouble with a motion (some are quite hard!) it seems to help them get ready to work.  They are even asking to MeMoves during other times.  It's nothing concrete, but I can say that this DVD has been a great addition to my repertoire and I'm so glad that I purchased it.  Check out Memoves at http://thinkingmoves.com.

Patrick


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Ellen: Student/Child/Boy/Girl/Son/Daughter/Man/Woman/PEOPLE with Disabilities

Filed under: Blogger Ellen, Inclusive Practices — Anna @ 7:39 am

Ellen Last week I read two articles in Time and People magazines that referred to individuals with Down syndrome as “Downs,” “Downs syndrome kids,” and even “the disabled.” Say what you will about the quality of my personal magazine subscriptions, but do a search for “the disabled” on the Washington Post or the New York Times Web sites and see how much it pops up. It’s everywhere.

Today, March 3, happens to be the official awareness day of the Special Olympics’ nationwide campaign to discontinue derogatory use of the “r-word” and promote acceptance of people with intellectual disabilities. I encourage all of you to pledge your support at www.r-word.org.

Media outlets have been stepping all over themselves recently trying to report on this campaign, the “Family Guy” vs. Sarah Palin incident, and Rahm Emanuel’s misstep. As tasty as those stories are, I wish journalists would slow down their mouths and fingers long enough to process the actual language they use to describe people with disabilities. While the word “retard” certainly occurs in public discourse much more often than it should, it is indicative of a much larger and more widespread problem.

From a clinical, grammatical standpoint, I understand that terms like “the disabled” fit better in a headline and possibly flow better into a microphone than the sometimes-clunky “people with disabilities.” But it’s the “people with” part that is essential. People with disabilities are not their disability. They are people.



That idea bears repeating. The people part comes first. The creative name we have for that nifty turn of a phrase is called “people-first language.” It’s not a fad, and it’s not about political correctness. It’s about the power of language to shape our fundamental ideas about the rights and values of people.



If you refer to people with disabilities as “the disabled,” you turn them into a collective noun that qualifies them only by one characteristic: their disability. The word “people” is also a collective noun that means any group of human beings. So when you hear or read the word “people,” you have the vastness of humanity from which to pull your initial perception of the subject or object of that sentence. In contrast, when you hear or read “the disabled,” you draw upon not only the innately limited range of characteristics of disabilities possible on Earth, but the even more limiting range of characteristics of disabilities about which you personally know.



Of course, sometimes we don’t want to just say “people” with disabilities; we want to talk about a man with Down syndrome or children with cognitive disabilities or girls with attention deficit disorder. So we do: We just say “girl” or “boy” or “man” or any one of the many nouns at our disposal and we say it first. We use that noun, the noun that refers to the person, first.



It may sound simplistic or condescending or like we’re thinking too hard about it – and perhaps I am preaching to the choir here – but language is powerful. Disabilities are characteristics of people. Those characteristics do not, in and of themselves, define people. Until American education and public perception and cultural identification catch up to that idea en masse, we need to be bombarded with the “people first” message. 



As small as it is, and as awkward as it can sound, and as worked up as we may get over it, putting the person first does make a difference. People with and without disabilities are readers and listeners and viewers of an incredible amount of content, especially with the many media sources we have access to these days. We will all read about and hear of and see people first. Even if the detail of their disability comes two words later, it still comes later.



It isn’t about political correctness. It’s about the other r-word: respect.



Spread the Word to End the Word

 

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