Marcus, a hard-working father of four children, describes the determination of his nine-year-old son building a full-size Batmobile by dumping out all of the Legos he had accumulated over the years and designing it on his own. Despite the fact that his son was told his family could not afford the expensive kit, he persisted by deciding he could make what he wanted using photos he found online. Imagine the pride and satisfaction of accomplishing what others would not even fathom undertaking.
Now, fast forward to six years later and see that same, determined, bright, teenage boy spending countless hours every day of the week to grasp the most basic and fundamental skills in reading, spelling, and writing. Who was there to help? Did anyone, such as staff, recognize a problem or diagnosis to help him excel as he brilliantly did with those Legos? If so, was there anyone trained in effectuating this assistance? Unfortunately, this was not the case for Adam. Fortunately, he did not give up and even without proper assistance managed to complete as many tasks he could.
This story pertains to the student in California’s Office of Administrative Hearings’ (landmark decision, (July 2017)). The names are fictional. This case demonstrates the dangers of districts not providing appropriate training with regard to Specific Learning Disabilities (SLDs) by pertinent staff including teachers all the way up the principal. A lack of training withholds our children’s federal right to a Free Appropriate Public Education (FAPE).
The 2017 Guidelines (CDG) state, “Although the problems experienced by students with dyslexia may originate with neurobiological differences, the most effective treatment for these students and for those who struggle with related reading and language problems is skilled teaching. For that reason, it is critical that educators receive accurate and current information about evidence-based instructional strategies.”
In the case mentioned above, the court voted in favor of Adam, that 15-year-old teenage boy, hereby granting and ordering a long list of remedies. The Court recognizes the failures of the District but does not blame it per se. It further states that “school districts may be ordered to provide compensatory education or additional services to a student who has been denied a FAPE but … the award must be fact-specific.” Compensation may not always get to the student directly in monetary form but instead in services.
The court further states, that the IDEA can satisfy the compensatory remedy by staff training. The decision goes on to discuss the importance of appropriate goals and services to meet Student’s unique needs in the areas of reading, spelling, and writing. For Student’s needs in this case it would be one hour per day of instruction in Orton-Gillingham, or the Slingerland method each school day or the equivalent thereof. These are the methods most effective for dyslexia.
The CDG suggests standards for reading teachers that have been developed by the International Dyslexia Association (IDA) and the types of educators who can serve students with dyslexia and includes a list of salient personnel to obtain and use this knowledge. It emphasizes, “There is a great need for all educators and related service providers to be prepared to meet the needs of students with dyslexia, including speech-language pathologists, school psychologists, school counselors, school administrators, and paraprofessionals.”
Yes there is a way to help our children. Fortunately, in California, the decision along with CDG guidelines will help rectify wrongdoings mostly unbeknownst to district personnel. With this knowledge, now is the time to be informed and help our students overcome these tremendous barriers to an appropriate education. It is more expensive for districts not to abide by these words of wisdom. As a single mother of a 6-year-old boy struggling with similar obstacles, I feel blessed knowing that he can and will have appropriate services.
If he does not, I have the knowledge to pursue and advocate for him. With diligence, adherence to authority and guidelines, and patience we can do right by our children with SDLs and there will be no one left to blame.
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