Tag Archive for 'Families'

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Canadian kid docs on chiropractic

Over on I Speak of Dreams, Liz Ditz posted an entry showing that the Canadian Pediatric Association understands the appropriate use of chiropractic procedures with children and youths. Jump to Liz’s post, read her entry, and follow her link to the statement: “Canadian Pediatric Society Position Statement: Chiropractic care for children: Controversies and issues.”

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New Jersey task force on reading disabilities created

Seventh grader Samantha Ravelli, of Ocean City (NJ, US), is probably one of the youngest lobbyists who ever tasted success. According to Diane D’Amico of the Press of Atlantic City, Sammie (and her team, including her mother and sister) convinced their legislature to form the New Jersey Reading Disabilities Task Force.

Sammie has substantial reading problems, and her contacts with legislators inspired them to draft legislation creating the task force. Assemblymen Nelson Albano and Matt Milam and state Senator Jeff Van Drew collaborated to get it passed. It cleared the assembly in February and the senate in December 2009.

As a part of their efforts to promote awareness of dyslexia and to encourage legislators to create the task force, the Ravellis created Sammie’s Mission. Visit it and also read Ms. D’Amico’s blog post How Sammies’s dyslexia inspired a law and her news story, State Senate approves bill to form reading disabilities task force, about the events. Finally, snag a pdf of “An Act establishing the New Jersey Reading Disabilities Task Force.”

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Is inclusion right for your child?

Over on LD Experience, Kathryn Burke posted an editorial recounting some of her experiences as a parent of children with Learning Disabilities who must weigh placement alternatives. She describes an encounter with another parent who disagreed with her decision to place her elder son in a specialized school.

A parent from my son’s school, who had not heard about the lecture from me, came to greet me and ask if I could put her name on the “special education distribution list.” Another woman overheard our discussion and asked about the list, how it had started, and if she could join. I told her that I had assembled the email list from the names of individuals who had been present at events organized by the Parent Council at my son’s school, of which I was a member of the executive. I explained that the school was a specialized site within the public system for students with learning disabilities. Upon hearing this, the woman looked at me with a level of disgust as if I had grown horns, and loudly said, “I will have absolutely nothing to do with people who believe that children with disabilities should be segregated!”

Continue reading ‘Is inclusion right for your child?’

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Many dreams spoken

Yesterday was the anniversary of I Speak of Dreams, the blog that Liz Ditz maintains. Liz has used it to many sensible and helpful posts for parents, teachers, and others. She’s dug through mountains of information (including mis- and dysinformation) to make sense of issues and then reported about them clearly and thoroughly.

Liz, sorry I’m a day late, but Happy Blogiversary!

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Suggestions from advocate

Paul Rendine, who chairs the Disability Advocates of Delmarva Inc (DADI), is contributing a series of articles about disabilities to a local publication for the peninsula holding parts of Maryland and Virginia and all of Delaware. The first of the series addresses Learning Disabilities. Although the content is brief and the coverage of Learning Disabilities is not in depth, it is generally accurate and merits note because of the effort.

Link to Mr. Rendine’s article. DADI has its own Website; DADI provides scholarship support to individuals with disabilities.

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Stick to your pans

Jamie Oliver
Jamie Oliver by
really short

Via a post by “Sixty-Five” at Life Begins at Sixty-Five, I learned of an article by Alex Witchel in the New York Times featuring the famous chef, Jamie Oliver. The 35-year-old Mr. Oliver has been a one-person juggernaut in the world of cuisine. Mr. Witchel’s story is about Mr. Oliver going to a metropolitan area in West Virginia (US) noted for the high rates of obesity among its populace; there he will promote the pleasures of home-cooked food.

As Sixty-Five noted, an interesting subtext to the story is Mr. Oliver’s schooling experiences. Mr. Oliver’s success comes against a back drop of Learning Disabilities. Here’s a snippet from the Times article to illustrate:
Continue reading ‘Stick to your pans’

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Parents’ and children’s views

The US Public Broadcasting System has two articles that will be of interest to some readers of LD Blog. The titles of them tell enough about the contents, each of which has four subparts, that I can simply list them here:

Flash of the electrons to to Leila over on Special Ed and Me, whose post entitled “Inside the Mind of Someone with a Learning Disability” led me to the articles.

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Miguel might show us what’s wrong

Under the headline, “Age-Old Problem, Perpetually Absent Solution: Fitting Special Education to Students’ Needs” in the Washington Post, Jay Mathews writes about the case of Miguel Landeros:

Miguel Landeros is a lanky, well-spoken 12-year-old about to begin seventh grade in Stafford County. He is severely learning disabled, with reading, writing and math skill levels at least two years below his peers, and needs special teaching, according to a licensed clinical psychologist at the Kennedy Krieger Institute in Baltimore and other specialists.

Last February, Stafford officials refused to accept that evaluation and left him in regular classes. He performed poorly, failing all core subjects. Recently, they promised to give him more specialized services, but not the ones the experts who examined him say he needs.

I admit that education writers in general, and I in particular, write very little about learning disabilities and the many failures of federally mandated public school programs to help students who have them. I often say the cases are so complicated I have difficulty translating them into everyday language, and even then readers struggle to understand.

Mr. Mathews’ admission of a lack of understanding about special education (in general) and Learning Disabilities (in particular) is unsurprising to me. Not only is there a lot to know (and, sadly, too often educators do not even know what there is to know), but lots of people who view educational issues through the lenses of finance, policy, and social justice simply don’t get (a) the evidence available about effective educational practices and (b) the personal side of education.

Had Miguel had early access to effective instructional practices, which have usually been more readily available in special education, during his early years of schooling, he probably would have at less substantial problems as he moves into middle school. Special education has been education’s reservoir for research about effective teaching methods over the past 20-30 years.

Dan Hallahan and I cited a series of innovations that emanated from LD (e.g., systematic monitoring of progress, explicit instruction in strategies for solving academic tasks) and are now widely adopted in education. In Michael Gerber’s memorable phrase, Learning Disabilities served as blue-green algae for education, forcing us to abandon antiquated notions of classification and instruction and move toward more flexible perspectives, just as blue-green algae precipitated a change from Linnaean taxonomy to classification based on evolution.

The case of Miguel illustrates how educators reject reasonable and evidence-based methods in favor of ideologically driven policies. In place of employing powerful instructional practices and adapting instruction to individuals, schools too often explain away students’ difficulties. They make what amount to excuses!

I have not seen the thick sheaf of papers that Miguel’s mother sent to Mr. Mathews, so I don’t know if that folder contains any of the following excuses for not serving Miguel. I suspect, however, that Kelli Castellino (Miguel’s mother) has heard some of them, and likely others:

  • “He’s just a boy; they mature differently”;
  • “He’ll get it when he decides to put his mind to it”;
  • “We don’t want him to have the stigma of special education”;
  • “He just needs a little extra time to finish things”;
  • “We can’t give every child a Cadillac education.”

(Parents and teachers, please feel free to add other examples to this list. Just drop ‘em in the comments.)

In addition to the excuses, we educators often let ideology and half-truths trump the individual needs of children, which puts us at odds with parents. The innovation of the Individuals with Disabilities Education Act (IDEA) was considering students with disabilities as individuals. Based on the unique educational needs of those students determined to be eligible, educators and parents are supposed to develop individualized education programs.

I suspect that Ms. Castellino also heard that (a) the least restrictive environment is a critical concern, (b) inclusion is the approach recommended by experts, (c) accommodations are all most students really need, (d) special education identification processes are subjective and arbitrary, (e) half of the students with LD don’t really have true disabilities, and more.

Many special educators, especially those in administrative positions, seem to have bought the idea that including everyone in general education is the goal. They point to the lesser outcomes for students with disabilities (e.g., higher failure rates on competency tests and greater chances of under- and unemployment after school, just to name a couple) and argue that those results are caused by special education’s separatistic and ineffective ways. For some unknown reason, they forget that there must have been something unique about the students that contributed to them being identified in the first place.

They also ignore the fact that some of the early, ardent advocates of inclusion have recanted. Take, for example, Mary Warnock’s change of position, as noted in this entry over on Teach Effectively:

Mary Warnock, the individual most responsible for promoting inclusionary policies and practices in Britain, has said that the effort to include students with disabilities in mainstream schools has “Has gone too far. It was a sort of bright idea of the 1970s but by now it has become a kind of mantra and it really isn’t working.”

For some students, inclusive schooling is just fine, but when it becomes the de facto standard, then it butts heads directly with IDEA’s foundational idea: individualization. When inclusion is invoked in cases such as Miguel’s, ideology trumps reason.

Mr. Matthews wondered whether a charter school for students with LD would be a solution. I suspect that one based on evidence about effective instructional procedures and practices (and there is plenty of research documenting them) would be beneficial for those students. But, those same methods could be put into practice in the public schools. A major impediment to doing so, in my estimation, is our current emphasis on how special education is something to be avoided, that it’s broken, wrong, misguided, and undesirable.

Another reason that the charter might work is that it might be freed from the shackles of ideologically-driven education. But I can already hear the howls about how awful such a school would be. The ideologues would complain that it was separatist, inconsistent with the real world, too expensive, and so forth.

Link to Mr. Matthews’ article.

Gerber, M. (2000). An appreciation of learning disabilities: The value of blue-green algae. Exceptionality, 8, 29-42.

Lloyd, J. W., & Hallahan, D. P. (2005). Going forward: How the field of learning disabilities has and will contribute to education. Learning Disability Quarterly, 28, 133-136.

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Think Aloud redux

Over on Twitter, friend of LD Blog Liz Ditz retweeted this:

RT @Includekidswdis: Stop, Think, Do a program by Lindy Petersen http://is.gd/1FQ0h which can really help children with #ADHD

I took a quick look and immediately remembered the work of Bonnie Camp and her colleagues (especially Mary Ann Bash) during the previous millennium. Dr. Camp and her group developed, researched, and refined methods for teaching children with learning and behavior problems, including attention deficit disorders, to manage their behavior. The Think Aloud program was at the forefront of the cog-mod mania that swept through child clinical psychology and special education in the 70s and 80s.

THINK ALOUD is a psychoeducational training progtam designed to enhance social and cognitive problem solving skills for increasing prosocial behavior and decreasing impulsivity. Much of the program content was chosen to correct cognitive deficits displayed by young aggressive boys. (1,2) Research on verbal mediation indicated that before internal controls could be established, many children needed first to establish effective control by verbalizing aloud then fading to a silent level. The Think Aloud Program was designed to teach children a problem solving process (including problem identificaton, generation of alternative solutions, predicting consequences and evaluating outcomes), how to verbalize aloud, how to apply this process in both cognitive and social situations, then move to silent direction and control of behavior. The original research with the program was conducted in two controlled trials and one refresher program with pairs of 6-8 year old boys rated as hyperaggressive by their teachers. (3,4,7,8,9,12) The manual for this program, along with details of research findings, is presented in Think Aloud: Small Group Program (11).

The numerals in the quote are footnotes (not surprisingly). They refer to only a few of the dozens of sources Dr. Camp provides.

Although it is a bit rough as a Web site, Dr. Camp has created an Internet site for Think Aloud. It features citations for those sources as well as some of the original materials. In addition, she has made some new materials for the program available as downloads.

Link to the Think Aloud site.

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Research on chiropractic effects on LD

Somewhere someone who’s read my two earlier entries about chiropracty and Learning Disabilities probably said, “How can he say chiropractic treatment of LD is ‘bogus?’ Hasn’t he read the research?” Well, I actually did read what research I could find.

I looked for studies about the effects of chiropracty and LD. I didn’t find any credible studies demonstrating the benefits of chiropractic treatment for LD or related problems. Indeed, the studies I found used inadequate research methods (unrepresentative samples; weak measures; designs that do not permit causal inferences; etc.). I was pleased to learn that my quick review agreed with a review reported by Yannick Pauli.
Continue reading ‘Research on chiropractic effects on LD’

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