Set Your Bookmarks to the New IDEA Site

IDEA Website

The Office of Special Education and Rehabilitative Services will automatically direct users from the Building the Legacy: IDEA 2004 site to the new Individuals with Disabilities Education Act (IDEA) website starting April 30, 2018.

OSERS launched the new IDEA website in June 2017 in order to provide updated department information regarding the IDEA to the public including students, parents/families, educators, service providers, grantees, researchers and advocates.

IDEA website users are encouraged to bookmark the new IDEA website: https://sites.ed.gov/idea.

While the Legacy site will redirect users to the new IDEA site on April 30, content from the Legacy site is available for reference on the new IDEA website on the Building the Legacy: IDEA 2004 historical reference page.

The Legacy site was developed in 2006 as a result of the 2004 reauthorization of the IDEA. The site was developed and updated mostly between 2006 and 2011. It had not received updates since 2013.

OSERS determined it would leave the Legacy site live after the new site launched to provide stakeholders ample time to compare the two sites, adapt to the new site and provide feedback to OSERS.

OSERS has made updates to the site based on the feedback it received from stakeholders since the initial launch of the new IDEA website.

OSERS will continue to gather feedback about the new website in order to enhance and add content to the new IDEA website to ensure the new site remains current.

Stay tuned for video tutorials highlighting features of the new site in the coming months. Comment below if you have feedback regarding the new IDEA website.

“Voices from the Field” Interview with Melissa Herzig and Melissa Malzkuhn

Visual Language and Visual Learning (VL2),
a National Science Foundation Science of Learning Center at Gallaudet University


Melissa Herzig

Melissa Herzig

Melissa Herzig is the Research and Education Translation Manager and the Director of Translation at the National Science Foundation Science of Learning Center on Visual Language and Visual Learning (VL2) at Gallaudet University. She co-founded the PhD Program in Educational Neuroscience (PEN) at Gallaudet and is its Assistant Director. Her role is to facilitate two-way communication between researchers and educators.

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Melissa Malzkuhn

Melissa Malzkuhn

Melissa Malzkuhn, digital strategist and creative director at Gallaudet, directs the university’s development of research-based creative and translational products, including bilingual storybook apps designed for early language acquisition for Deaf children. She leads the VL2 Storybook Creator program that provides training for and facilitates the development of bilingual storybook apps in multiple languages. As founder and Creative Director of Motion Light Lab, she leads projects intersecting creative literature and digital technology to create immersive learning experiences.


ED: How did you begin your career in early learning and early literacy?

Melissa Malzkuhn (MM): I have master’s degrees in deaf studies and fine arts/visual narrative, which have given me the opportunity to do a lot of creative and innovative work, while focusing on the importance of narratives. When I started working at Gallaudet in 2008, I led efforts as managing editor of the world’s first peer-reviewed sign language journal, Deaf Studies Digital Journal, which provides articles in American Sign Language (ASL) with printed English. It was fun and challenging to figure out technological capabilities in publishing a visual and spatial language. That led me into my current role with VL2, which is to create innovative resources that help families and teachers promote evidence-based approaches for promoting language and literacy in young children. My work utilizes touchscreen technology to promote a bilingual experience for families with young deaf children. That’s my journey in a nutshell. I also come from a deaf family and I grew up with rich ASL stories. I’m grateful for my access to language, narrative, and word play since birth. My experience has led me to believe in the importance of ASL literacy. The challenge is that since ASL is an oral language, stories are passed on through generations, but can easily disappear. My motivation is to document ASL literature, but to also innovate ways in how we view and interact with ASL storytelling. I’m also the mother of a deaf 5-year-old, so watching his language and literacy development has had real implications for my work.

Melissa Herzig (MH): I’ve always enjoyed working with children and thought I’d be a teacher. I also had a natural curiosity about how the body and the mind worked. I majored in biology in college. After graduating, I worked as a research assistant in language and cognitive neuroscience labs and learned the science behind cognition and language. I started a master’s program in teaching and learning and bilingual education and learned more about language and literacy development. As I began to spend time in classrooms, I found a huge disconnect between what we know from research and what was happening in classrooms, so this became my passion: better connecting research and education. I also better understood the urgency of focusing on early language development in young children. I pursued a doctorate with a strong focus on literacy and motivation. In my current position, I direct the Translation in the Science of Learning Lab. This lab is responsible for translating VL2 research discoveries for applications in various learning environments that deaf children experience. We produce publications and resources for parents, educators, medical professionals, and policy makers as well as offer training for educators on bilingual education and language policy. I am also a mother of three hearing children who have grown up in a bilingual (ASL and English) environment, which has had a positive impact on their development.

ED: What is early sign language acquisition and why should parents of young children know about this?

MH: We know from brain research that there is a critical period for language to develop. For deaf children, there is a serious risk of language deprivation during this critical period. We also know that, for deaf children, including a visual language like ASL in the early years is critical to their later development of strong English literacy and language skills. Most deaf children are born to non-deaf families and many of them don’t have all the information they need to make important decisions about promoting language and literacy development. Research demonstrates that multiple modes of communication have a positive impact on all children’s language development. Sign language helps the child’s brain progress through the normal developmental milestones by activating the part of the brain that spoken language activates. Parents of deaf children are made to think that they must choose ASL or English, but they need to know that they don’t have to choose; they should try it all, and use it all! Bilingualism, regardless of the languages used, makes children’s language and literacy development stronger. Readers can check out our Early Education Literacy Lab website for more information on the latest research in this important area.

ED: How has your work improved the quality of early learning and influenced approaches to teaching early language and literacy?

MM: I’ve been developing bilingual and interactive storybook apps for deaf children using our VL2 Storybook Creator platform. Anyone can create storybook apps using this platform. Its research-based design has three modes:

  1. Watch Mode—the storyteller signs the story from beginning to end with images of the story in the background;
  2. Read Mode—the traditional book where you go from page to page and read the text, and the reader can click to have an individual page or a word signed to them; and
  3. Learn Mode—a list of vocabulary words from the story appear, and the reader can learn and explore words in both text and sign.

This has been a wonderful tool for both educators and families. These are engaging stories for children, and also support parents in learning sign language and sharing reading time with their child. Our goal is to support young deaf children who are learning to read and reading to learn.

MH: This tool has helped boost bilingual teaching in the classroom with deaf children. Teachers have long lamented the scarcity of bilingual resources, so it is a welcome addition to the classroom. We’ve also developed resources to help teachers use the storybook apps, including lesson plans that go along with most storybook apps. Resources provide ideas for how to use the storybook apps for guided, shared, and independent reading and teaching of ASL and English grammar. The best way to help deaf children read is through stories, getting the whole picture, and building background knowledge—not to just focus on English print. We think these visual and interactive storybooks are essential.

MM: Through the VL2 storybook creator program, we’ve collaborated with a number of countries to develop translated versions in their signed and written languages. We’ve worked with Norway, Russia, Japan, Italy, and the Netherlands. On top of this, there is tremendous interest to bring our platform to more countries and to more schools in the U.S. This is really groundbreaking work! Technology has finally caught up to our needs in this area; use of this technology can support literacy for deaf children in a way that hasn’t been an option in the past.

MH: We conducted a usability and efficacy study and found that a diverse group of children were accessing and using the apps, from beginning signers to fluent signers. We also found that participants do learn new English vocabulary words from the stories. The users really liked how the tool allowed for individualization. They can move through the story at their own pace and choose what works for them (watch the story, read the story, click “play” to see videos that aid with comprehension).

ED: What are some of the challenges you have experienced in this work and what strategies have you tried to overcome them?

MH: Overall, one of the major challenges is getting findings from the research base into the hands of families when they are making decisions about early language development. There is a misconception in the medical and education fields that children need to learn spoken language in order to read. This is not true. Visual sign can activate the brain in the same place as oral language. Strong language foundation in any language is best. Strategies we’ve used for countering the misconceptions include sharing our work through research briefs, websites, and presentations. Through our translation lab, we are continually creating resources to translate the research base for families and teachers.

MM: Another challenge is the huge demand for more ASL and ASL/English content because there is limited capacity in the field. We are striving to expand the number and type of visual storybook apps to cover more subject areas and topics. Through collaboration with others, we are building a global digital library of a variety of visual books that teachers and families could access.

ED: What suggestions do you have for others interested in supporting early literacy development in young children?

MH & MM: Reading is fun, signing is fun, and the bridging of two languages in bilingual education is natural. And start early. The earlier we introduce both languages, the better. Language play is so important, and finding ways for all children to be creative with language helps develop the important skills that foster strong literacy skills.

And finally, family involvement is crucial. We encourage schools to engage families in a meaningful way, potentially providing ASL classes at family-friendly times, and encouraging language immersion at home. We’ve developed a VL2 parent package to address this, with helpful FAQs and tips for families on developing language and literacy.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Melissa Herzig
Posted by
PEN Associate Director and Strategic Focus Areas 4 Leader, Gallaudet University
Melissa Malzkuhn
Posted by
Digital Innovation and Media Strategies Manager, Gallaudet University

ED Welcomes OSERS Assistant Secretary Johnny Collett

Johnny Collett

Johnny Collett

The U.S. Department of Education welcomed Johnny Collett, the new U.S. Department of Education assistant secretary of the Office of Special Education and Rehabilitative Services (OSERS), on Jan. 16, 2018.

Collett, a former high school special education teacher, has served as the program director of Special Education Outcomes at the Council of Chief State School Officers (CCSSO) and as the Kentucky state special education director. Collett has also served as an assistant division director and exceptional children consultant both at the Kentucky Department of Education.

Collett will lead OSERS towards its mission to improve early childhood, educational, and employment outcomes and raise expectations for all people with disabilities, their families, their communities, and the nation.

OSERS comprises the Office of Special Education Programs, which administers the Individuals with Disabilities Education Act (IDEA), and the Rehabilitation Service Administration, which administers titles I, III, VI, and VII, as well as Section 509 of the Rehabilitation Act of 1973, as amended by title IV of the Workforce Innovation and Opportunity Act (WIOA). OSERS’ Office of the Assistant Secretary administers a number of special projects.

“Voices from the Field” Interview with Melody Arabo

Melody Arabo

Melody Arabo

Melody Arabo is the 2017–18 Teaching Ambassador Fellow for the U.S. Department of Education (ED) and was honored to serve as the 2015 Michigan Teacher of the Year. She has been a third grade teacher at Keith Elementary in the Walled Lake Consolidated School District since 2002. She has a bachelor’s in elementary education and a master’s in teaching and curriculum, both from Michigan State University. Melody is a wife, mother of three, speaker and presenter, author, and bullying-prevention advocate.


ED: How did you begin your career in education?

Melody: I never planned to be a teacher. I was planning to go into marketing and advertising. I had big plans to live in a city and take a train to work. When I was 19, I found out about a paraprofessional job at a local elementary school. They were looking for someone who spoke Chaldean, which I do, so I applied and was very lucky to get the job. It changed my career trajectory. I loved the school and the principal, and really loved the kids. I quickly realized what a positive impact you can have so quickly on young learners. I enrolled in an associate’s degree program at our community college focused on elementary education and then moved to Michigan State University to complete my bachelor’s (and eventually my master’s) degree in teaching and curriculum.

As a paraprofessional, I worked with kids in kindergarten through second grade, which I enjoyed. But during my year-long student teaching internship, I ended up in a third grade class. I realized I loved kids in third grade. They are independent enough to tie their own shoes and blow their own nose, but are still young enough that we can shape their learning, curiosity, and engagement. After student teaching I landed a job as a third grade teacher in the same district where I started as a paraprofessional, and have been teaching there since 2002.

ED: How did you become interested in the School Ambassador Fellowship program here at ED?

Melody: In 2015, I was honored to be the Michigan Teacher of the Year and spent the year working outside of the classroom. My biggest take away from that experience is that the educator voice is really lacking in critical policy discussions. I wanted to figure out how I could help increase teacher leadership and expand the role of the teacher voice in policy making. When I heard about the School Ambassador Fellowship program it seemed like a perfect next step, so I applied. The program enables outstanding teachers, principals, and other school leaders to bring their school and classroom expertise to the Department and exposes them to the heart of the national dialogue about education. In turn, school ambassador fellows are better equipped to facilitate the learning and input of other educators and community members.

In 2016, I was a part-time fellow for one year. This meant that I still had my classroom in Michigan and engaged and worked with ED remotely. It was an intense year, because I was staying involved at the classroom-level while being engaged in state- and federal-level activities. I am now the lead fellow here in DC and a big part of my work is with the part-time campus fellows, located around the country, who are still working in classrooms and schools. We have a fantastic group of 2017–18 fellows and my role is largely to support and connect them to work going on here at ED. I also have the goal of strengthening ED’s outreach to, and engagement with, educators. To accomplish this, we have been hosting monthly conversations on important educational issues to engage educators in the field. For example, one of our recent monthly topics was STEM (science, technology, engineering, and math), particularly how teachers are incorporating STEM in the classroom. For each conversation, we pose a question about the topic via Twitter to generate conversations among educators, encouraging them to share examples of innovation. We then collect their input and feedback, and develop a toolkit of resources around that topic. Additionally, we are tapping into teachers by asking them to write for ED’s Homeroom Blog on each of the monthly topics. I also work with our fellows to promote and encourage teachers to sign up for ED’s monthly newsletter developed for teachers, The Teachers Edition. We have involved each of the fellows in Teach to Lead, an initiative that expands leadership opportunities for teachers and further develops their ideas.

ED: What are some of the challenges you have experienced as a teacher and what strategies have you tried to overcome them? 

Melody: I am a general education teacher, but I am also a parent of children with special needs. Through struggling to navigate special education as a parent, I have realized that I am ill prepared to teach children with disabilities and see there is a huge need to bring the special education and general education worlds together. We really need to rethink teacher training; general education teachers need more training on how to teach children with disabilities and to work with special educators. I realize now that if I had known more about some of the best practices in special education, such as positive behavioral intervention and supports (PBIS); how to do functional behavior assessments (FBA) and behavior plans; universal design for learning (UDL); and response to intervention (RTI), I could have had a more positive impact on not only students with disabilities in my class, but could have better met the needs of all of my students.

In my experience, co-teaching isn’t used widely. Children with disabilities are often pulled out of classrooms for their special services and I think that because of this we are missing an important opportunity to bring special educators and general educators together. After my twins began having challenges, I became more active in the disability community and realized how limited my experiences had been in a classroom. I never had a student with autism, cerebral palsy, or other more noticeable disabilities. As a parent, I’ve realized how important it is for children with disabilities to be included in general education classrooms and schools. As a teacher, I’d really like to learn different strategies and different techniques that would benefit all of the students in my class. I think we can do this by better connecting the professionals; it is a disservice to children to have those two worlds—special education and general education—segregated.

ED: What suggestions do you have for improving the quality of early learning and education?

Melody: I believe one of the most important things we can do is to raise the importance of the educator’s voice in making policy decisions. Teachers need to be part of the conversation. The educator’s voice is there but typically only in the policy discussions. Educators need to also be part of the decision-making process, since they are the ones who know what’s realistic and what’s not. I also hope that more educators will become policy makers. From the parent perspective, I think family engagement is critical and we need to do a better job making information easily accessible for families. When my kids were first diagnosed with developmental delays, I mainly relied on other parents, which was wonderful because it created a support network for us. I believe we need to do more to connect families with other families when making educational decisions—families are more powerful and informed when they are connected.

My specific advice for educators interested in becoming part of important local, state, and national conversations is to start looking for leadership opportunities in your community, district, and beyond. Develop your leadership skills, brand yourself as expert in an area, and let policy makers know. For example, based on your expertise and experience you could be an Individuals with Disabilities Education Act (IDEA) expert, or a STEM expert, or an expert in best practices for increasing positive social emotional and behavioral skills. Engage in social media by following other teacher leaders, ED, state-level policy makers; develop your own website and blogs; and build an audience. It is okay if your audience is small at first, but you have to put yourself out there to engage. I really like the teacherprenuers initiative, where teachers think of themselves as innovators but also take on entrepreneurial leadership outside of the classroom. I would love for this to be part of teacher training. It is really empowering for teachers that think this way and have already begun engaging outside of their classrooms. So I encourage teachers to think like a teacherprenuer. This can be as simple as having a business card or presenting at a conference, and will begin to shift their idea of what it means to be a teacher and a leader.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Melody Arabo
Posted by
Melody Arabo, 2017–18 Teaching Ambassador Fellow for the U.S. Department of Education.

Challenges and Barriers to Successful Employment for Man with Visual Impairment

By Louis Herrera

Louis Herrera

Louis Herrera

I was born with normal eyesight, and at the age of three and a half it was determined that I had a visual impairment. By the time that I was about seven years old, I had lost most of my eyesight.

At the inquisitive age of four, I wanted to know how things work and how a box could have different voices coming out of it. Learning about radios was the beginning of a path to a career in the technology industry.

At the age of 15 I built my first computer at a time when components were starting to decrease in size.

Jerry-Rigged IT Systems

In the early 80s, I went to work for a Fortune 500 aerospace company. I was hired as an “experimental employee” because they had never hired a blind person before.

Back then there was hardly any assistive technology to speak of. Several companies were starting to develop a screen reader for MS-DOS, but in many cases these screen readers only worked with some specific programs.

Some of us with visual impairments, in order to maintain our jobs, had to be creative and figure out a way to generate speech output.

For me, I used an old Votrax speech synthesizer like a printer driver. Every time I wanted to know what was on the screen, I executed a print command that would convert the data on the screen to a format that Votrax could read and then speak aloud in probably the worst speech synthesizer voice that one would want to hear. Nevertheless, I was able to get the job done.

As technology continued to evolve in terms of processing speed and better video graphics, it paved the way for the beginning of a graphical user interface, which today is commonly known as Windows. This progress made it difficult for the blind user to keep up with the new changes because the screen reader at that time could not accommodate off-the-shelf hardware and software improvements. Partially-sighted people had to modify video settings to accommodate their visual requirements.

Mobile Devices

As technology continued to move towards a touch screen environment with no real interaction solution for the blind consumer, it seemed as though the blind and individuals with various degrees of visual impairment would not be able to move away from conventional mechanical user interface technology like the flip phones with the tactile keypad.

Once multilayered technology was introduced to hardware and software developers, companies like Apple and Google started to develop a user interface that consisted of gestures and tapping concepts that allowed for the interaction and execution of commands and operations.

As part of their Universal Access initiative in 2007, Apple introduced VoiceOver, a screen reader output interface for the iPhone 3GS. Apple demonstrated that touch technology could be made accessible for everyone, and in today’s work environment mobile technology is something that we all depend on.

We still have to deal with third-party applications that have the potential to be used by the visually impaired community, but we can’t use these apps because the developers either are not familiar with accessibility coding guidelines or choose to make apps more visually appealing in the hope that screen readers will provide a level of accessibility for the blind or visually impaired user.

One of the first barriers that we had to deal with had to do with educating the developers on what text-to-speech technology is and how it differs from speech recognition. This has been a problem for a long time and will continue to be a problem that affects us because developers believe speech recognition programs meet our needs. The reality is that these programs make it possible to receive speech input, but they do not read what appears on the screen.

In the case of smartphones, many app developers feel that built-in artificial intelligence (AI) programs are the same as the devices’ built-in screen readers (Apple’s Siri vs. VoiceOver, Android’s Google Assistant vs. TalkBack, Windows’ Cortana vs. Narrator) and that the built-in AI programs are all the visually-impaired user requires. Unfortunately, these AI programs are voice-driven search services that will in most instances provide audio feedback, but they are not screen readers that function without internet connectivity.

The issues described above are quite common in the desktop environment as well. The best way to resolve this issue is by requiring developers to submit their applications to a level of accessibility compliance verification before an application is deployed.

Technology in the Workplace

While technology has come a very long way and has made it possible for the blind and visually impaired to be competitive employees, there are many road blocks to still overcome for equality in the workplace.

Even with all the new advances in technology and software development today, blind or visually impaired professionals are still encountering barriers with their ability to carry out their job duties.

For example, the idea of providing PDF file attachments so that anyone, regardless of the platform being used, should be able to open the file can sometimes be an issue for some of us that use screen readers or screen magnification tools.

Often because of company policy, we are issued a computer equipped with a common commercially-available PDF reader, which does not do well making PDF images accessible. Some companies, like my employer, have smart printers/copiers that can scan a document and generate a PDF image that is not easily converted to text that can be read by the screen reader. Sometimes it is easier to print the image file and then use an optical character recognition tool to scan and read it. This is time consuming and a waste of paper.

Another on-the-job issue that we face is a lack of quality interaction and support with Information Technology (IT). While the IT staff is able to maintain and support staff using the general issued computers and software, they often don’t have the knowledge or experience to install, configure and maintain the adaptive technology.

If the IT specialist installs the specialized adaptive software, many times they do not install it correctly causing the program to fail to operate properly or at all due to the lack of the resource requirements needed for the software to run efficiently.

This is like keeping a car engine pristine with four flat tires.

In many cases, permission to update the software as needed is denied due to company policies, which leaves the assistive technology unable to keep up with the many updates and changes that the operating system and other programs the IT department regularly update to keep the hardware and software running at peak performance.

Support in the Workplace

My previous job as well as other companies will hire an assistive technology specialist to install the needed software and provide specialized scripting for the software to run on the company created software.

The software runs great until the first major update the IT specialist pushes to all computers on the network. This can affect scripting performance that was created so that the disabled user could fulfill his/her job. Often the assistive technology user has to make due with inadequate software accommodations until the company will bring in the assistive technology specialist again at a substantial fee to reinstall the scripts or create new ones if needed.

These costs and roadblocks could be minimized if employers include the employee who will be using the assistive technology so that he or she can provide input during the discussion and planning phase up to the point that it gets delivered and installed.

Developing and implementing all-inclusive collaborative meetings to address assistive technology needs will yield a more positive interactive communication and success among all participants.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

“Voices from the Field” Interview with Julie Sarama & Doug Clements

Julie Sarama and Doug Clements

Julie Sarama and Doug Clements

Julie Sarama is Kennedy Endowed Chair in Innovative Learning Technologies and Professor at the University of Denver. Her research interests include developing and evaluating research-based educational software and other technologies, using learning trajectories in standards, assessment, educational technology, curriculum and professional development, developing and evaluating research-based curricula, and asking successful curricula to scale using technologies.

Douglas H. Clements is Kennedy Endowed Chair in Early Childhood Learning and Professor at the University of Denver. Previously a kindergarten teacher and preschool teacher, he has conducted research and published widely in the areas of the learning and teaching of early mathematics and computer applications in mathematics education. His most recent interests are in creating, using, and evaluating a research-based curriculum and in taking successful curricula to scale using technologies and learning trajectories.

Doug and Julie have collaborated over the past 20 years on research and implementation projects focused on improving early math development in young children.


ED: How did you begin your career in early learning and early math?

Doug: I was always interested in math and was planning on being an engineer but after I graduated, I decided to go into early education. My first job out of college was teaching kindergarten. As a teacher, math was the shining star for me. I was so interested in young kids’ thinking around math. When I went back to school to get my doctoral degree, I focused my dissertation on preschoolers’ thinking about early math. How do young kids learn math ideas and skills? How do they think about early math? What are the best ways to teach early math?

Julie’s background was in teaching high school and middle school math. In the 1990’s we became involved in a National Science Foundation (NSF)-funded project on developing a kindergarten-through-fifth-grade math curriculum. We had developed some of the technology for the kindergarten piece of the curriculum, but weren’t able to complete it since the project ran out money. Thankfully, NSF soon came out with a call for a focus on early math, and then we had the opportunity to really start our work on early math and began developing what we call our Building Blocks project.

Julie: Previous efforts around early math focused on activities or developing ideas that sounded cool but weren’t based on research. Alternatively, we focused on identifying (from the research base) the specific features that help young children in early math. In the first year of Building Blocks, we worked on identifying the early math learning trajectories for young children. Doug reads everything from everyone; he looked at studies from a variety of related fields (developmental science, cognitive science, mathematics education, early childhood education, etc.). We pulled from all of those areas to help us develop these learning trajectories. What do kids learn, when do they learn it, and what can we do to help them progress? In the end, we developed an assessment and curriculum to help teachers understand learning trajectories. Later we were very lucky to receive funding from NSF and the U.S. Department of Education’s Institute for Education Sciences for our TRIAD project. This allowed us to develop the needed professional development materials and scale-up approaches for our work. Through TRIAD we were able to help early childhood teachers across multiple sites (e.g., Boston, Buffalo, and Nashville) understand the learning trajectories and how to implement the assessment and curriculum. This was especially important given many early childhood teachers often report they went into early childhood so they wouldn’t have to teach math!

ED: How has your research improved the quality of early learning and influenced approaches to teaching early math?

Doug: Everyone can write more cute activities that might touch on basic math concepts, but with the growing consensus on the ways young children learn to understand mathematical concepts and engage in mathematical thinking, we believe that understanding the early math learning trajectories is critical for early childhood educators to teach early math.

Julie: Learning trajectories have three parts:

  1. a learning goal (i.e., target, benchmark, expectation);
  2. a developmental path along which children develop to reach that goal; and
  3. a set of activities matched to each of the levels of thinking in that path that help children develop the next higher level of thinking.

The idea behind a learning trajectory is that these are the stepping stones to get you to your goals. Each of these stepping stones represents a significant change in the way kids think; they are the developmental progressions or descriptions of kids’ behavior that give us a hint of where a kid is developmentally. The activities that follow are critical to help move children from one stepping stone to the next.

Through our TRIAD project we taught early childhood teachers to understand how young children think about math; how to identify where kids are with their mathematical thinking; and then to provide instruction or activities that take the kids to the next level of mathematical thinking. We found that teachers when given this framework and the learning trajectories became excited about teaching math. When they saw their students’ growth along the learning trajectories, it was transformative. Teachers often tell us “I had no idea young children could learn this or think like this.”

ED: What are some of the challenges you have experienced in this work and what strategies have you tried to overcome them? 

Doug: The biggest challenge is the perception that math doesn’t belong in early childhood and that we don’t need to teach it yet. Another challenge is the false dichotomies that our field creates such as academics versus non-cognitive skills, or teaching math versus teaching literacy. We know we can teach math and literacy and social-emotional skills in early childhood. We know that early math skills are fundamental to children’s overall learning. Along with one of our post-doctoral researchers, Alissa Lange, we found improvements in oral language in classrooms that implemented Building Blocks. The learning is connected.

Julie: An effective strategy for overcoming the negative perception about math in early childhood is getting out there and talking about it. You really need a Doug! He travels a lot, spreading the word and accepting speaking engagements to all different kinds of groups about the work we are doing. Writing research articles isn’t enough. You also need your champions. The teachers we trained in our TRIAD project continue to implement Building Blocks without any coaching or support. We went back two years later and were shocked and delighted that they had all increased their fidelity of implementation, meaning they were implementing Building Blocks the way it was intended. Six years later, the teachers who were still teaching continued to implement Building Blocks. It is important to share their experiences.

[Check out this video report on the successful implementation of Building Blocks in Boston]

ED: What suggestions do you have for others interested in supporting early math development in young children?

Julie: When you focus on math, either alone or as part of a STEM (Science, Technology, Engineering, and Math) initiative, be sure to focus on the learning trajectories, not just math activities or projects, and embed math growth.

Doug: Professional development (PD) is critical and you need to start-off thinking about the PD as lasting for at least year. We know that a math day or a math workshop won’t change classroom practices, yet this is what we continue to offer to teachers. We need to be honest and start planning alternatives. Through foundation funding we developed a website with resources that support teachers to better understand learning trajectories. The website is called Learning and Teaching with Learning Trajectories (LT2), and is a great free resource for programs wanting to get started in thinking differently about early math.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Julie Sarama and Doug Clements
Posted by
Julie Sarama is Kennedy Endowed Chair in Innovative Learning Technologies and Professor at the University of Denver. Douglas H. Clements is Kennedy Endowed Chair in Early Childhood Learning and Professor at the University of Denver.

My story: The Benefits of Working with Agencies like the Washington State Department of Services for the Blind

Odyssey Sea

Odyssey Sea

By Odyssey Sea

Getting a job right after I graduated was a very exciting and scary experience. Luckily, I had Washington State Department of Services for the Blind (DSB) staff to help me along the way because without their help, experiencing new things would have been difficult. At first, I was nervous. I wasn’t sure what I wanted to do after high school. Luckily DSB staff stepped in and helped me figure out some things. I am getting job experiences with different companies like the Museum of Flight and at PAVE, a nonprofit that assists young adults like me. PAVE also assists parents, families and anyone connected to a child, youth or young adult with disabilities.

Reasonable accommodations were part of this experience. Some of the new experiences that worked for me were asking for accommodations such as getting a larger keyboard so it would be easier to see and type. Another accommodation I had was using an iPad to use the speech to text feature. This helps me get my thoughts in order instead of typing them out.

DSB also helped me get situated to find the right resources such as how to use shuttle services. It took a while to fill out all the paperwork but in the end, it was very simple to figure out and the wait was worth it.

They have helped me find job experiences which have helped me get to the job and do the work, stay busy and get ready for the real world.

I encourage you to try to get the help from agencies like the DSB or any other agency that will help you get a job. They will guide you all along the way!


Background on YES Programs that Assisted Odyssey

Programmatic Information:

Youth Employment Solutions (YES) II is a six-week program in Seattle, Wash., designed to provide valuable work experience and learning to high school students, age 16 through high school graduation. Accepted candidates are provided five weeks of paid work experience at internships created for them in cooperation with Seattle-area businesses. Positions are assigned to students based on their interests, abilities, and experience.

YES II is a residential living experience that provides students the opportunity to refine their daily living skills, such as planning, purchasing and preparing meals, and maintaining their own personal effects and common living quarters at the YES residence. Additionally, students learn skills in using public transportation techniques for travel to worksites. They are encouraged to participate in community social and recreational activities.

Washington State Department of Services for the Blind (DSB) provides training, counselling, and support to help Washington residents of all ages, who are blind or visually impaired, pursue employment, education, and independent living. Our goal is “Inclusion, Independence, and Economic Vitality for People with Visual Disabilities.”


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

A Vocational Rehabilitation Success Story: Joseph Cali

Note: October is National Disability Employment Awareness Month

Joseph

Joseph Cali

The New Jersey Division of Vocational Rehabilitation Services (DVRS), which receives Federal funding from the Office of Special Education and Rehabilitative Services’ Rehabilitation Services Administration (RSA), is pleased to share Joseph’s success story in honor of National Disability Employment Awareness Month (NDEAM).


Following an automobile accident in 2006 resulting in paralysis, Joseph spent several months in physical therapy and rehabilitation and now uses a motorized wheelchair. Joseph went on to obtain a Bachelor’s degree in Psychology and a Master’s degree in Rehabilitation Counseling in 2014—both from Rutgers University. Joseph also acquired specialized certificates in physical rehabilitation, supervision, and management.

When Joseph connected with the Vocational Rehabilitation program at DVRS, he was working part-time as an Adjunct Professor at Brookdale Community College. Joseph sought assistance from DVRS with modifying his van to independently travel to work and obtaining full-time employment. With the support of DVRS, Joseph took part in a pre-driver and behind-the-wheel driving evaluation to assess his driving needs. DVRS also supported the funding of modifications to Joseph’s van along with the necessary driving instruction.

On the employment front, DVRS certified Joseph as eligible for the Schedule A hiring authority with the federal government. After attending a federal job fair, Joseph interviewed with the Social Security Administration, who hired Joseph as a Claims Adjuster in Neptune, N.J. Joseph now works full-time and reports being satisfied with his career path and the services he received from DVRS. A special congratulations to Joseph who recently shared that he is engaged and will be getting married soon!

For more information about DVRS, please visit New Jersey’s Career Connections.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Chris Pope
Posted by
WIOA Implementation Team Facilitator Rehabilitation Services Administration U.S. Department of Education

Advocacy: The Foundation for My Success

Note: October is Learning Disabilities/Dyslexia/Attention Deficit Hyperactivity Disorder (ADHD) Awareness Month.

Carla Priest

Carla Priest

Carly Priest is a rising senior at the College of the Holy Cross in Worcester, Massachusetts, where she studies history and English. In her free time she dives for the Swimming and Diving Team, works in a local kindergarten, and writes for the school newspaper. Carly attends the National Center for Learning Disabilities (NCLD) conference as a representative for Eye to Eye, where she has served as a mentor, intern, camp counselor and Diplomat. 


Everyone has a different path to figuring out who they are. My own journey is far from over!  As a senior in college, I continue to learn about myself every day, but the ability to advocate for the resources I need continues to make all the difference. I share my story as a different learner to remind others who struggle with learning and attention issues, as I do, that success is not only possible, but critical. In learning differently, we have something unique and important to offer the world.

From kindergarten through eighth grade, I was seen as the “wacky” kid. Even though I was the “wacky” kid who had difficulty with spelling and a hard time following sequential instructions, no one suspected a learning disability because I loved to learn. Even with my love for learning, thinking back on my early education, I vividly recall feeling hopeless in the classroom. I had no words to communicate how I struggled!

My elementary school was a small public charter school that centered on a nature-based education model. The school’s kinesthetic and experiential approach to education allowed me to learn with my body, oftentimes outdoors. This emphasis on learning in motion, along with alternative instructional methods, ultimately mitigated my learning challenges enough to get by until high school.

Although mostly unnoticed through elementary school, my learning differences became apparent when I transitioned into a traditional high school. Within the first few months, my English teacher, sensing something was wrong, suggested we look deeper into what was going on. Evaluations revealed my visual processing disorder as well as attention deficit. It was good to finally have a diagnosis, but as I quickly realized, finally having a “name” for the difficulties I had always experienced was only the first step in the ongoing journey. Even though my diagnosis meant I suddenly received several types of accommodations, I still didn’t understand why I had accommodations, how they would help me, or when I should use them. I still needed to figure out what kind of tools would allow me to succeed.

Things dramatically changed for me in high school once I became involved in mentoring a younger student through Eye to Eye. Eye to Eye is a nonprofit, art-based mentoring program for students with learning and attention issues. Each art project focuses on developing students’ self-esteem, self-advocacy skills, and helping them understand how they learn and what they need to succeed.

More than anything, mentoring with Eye to Eye taught me so much more about myself. I learned that different accommodations could be helpful in different situations. I started to understand that extended time on tests was important, but in my case, it was far more important to have a testing environment with limited distractions. I looked for strong allies at school and found them. When I realized I processed information much better if my body was in motion, a psychology teacher encouraged me to walk around the back of the classroom during lectures, and would toss me baseballs to keep me focused and engaged in class. With these newfound allies, I was able to explore new ways of learning. With newfound confidence, I embraced my capacity to think differently, and began to explain to others what my “labels” meant. If I could self-advocate, success in college would not only be possible, but (as my allies assured me) inevitable.

Research shows that self-awareness and self-understanding are keys to success for young adults with learning and attention issues. A Student Voices study by the National Center for Learning Disabilities shows that young adults with learning and attention issues who are successful after high school have three things in common: a supportive home life, a strong sense of self-confidence, and a strong connection to friends and community. My community of support and allies, including my family, Eye to Eye, and my teachers, helped me develop and grow in these areas.

Now that I am in college, advocating for myself has become more important than ever. I speak to each professor about which accommodations I need and when I’ll need them. I am able to customize learning in a way that works for me. In addition to college, I have even had opportunities get involved in advocacy on a larger scale through an internship with the U.S. Department of Education as well as working with the National Center for Learning Disabilities in the areas of self-advocacy and personalized learning.

As I began to understand how I learned differently and developed the ability to communicate those differences to others, I laid a foundation for my future. Every learner should have the same opportunity to understand how they learn differently and embrace those differences. If we do not help our students access the resources they need, we will lose out on the intelligence, creativity, and passion of so many students with learning and attention issues who fail to see their future as one full of opportunities for success.


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Carla Priest
Posted by
A student at College of the Holy Cross and a Diplomat with Eye to Eye

Our Highs are Higher

Carrie Woodcock and her family posing in front of a lovely rural stream

Carrie Woodcock and family

Carrie Woodcock is director of the Maine Parent Federation and a parent of 10-year-old Sami who has Down syndrome.


This summer, I attended a conference alongside doctors, nurses, physician assistants, therapists and other medical professionals, all of whom work with children with special healthcare needs and disabilities. I was there to represent parent voices as the director of the Maine Parent Federation, an OSEP-funded Parent Information Center. I am a big supporter of, and was very excited for, the keynote presenter that day, Dr. Brian Skotko.

Dr. Skotko is a genetic specialist and co-director of the Massachusetts General Hospital Down Syndrome Program. He has also gone on to facilitate the creation of many such clinical programs throughout Massachusetts. I was first introduced to him at the annual Massachusetts Down Syndrome Conference. I was so impressed with our first encounter that now, whenever I attend events at which he’s speaking, I always attend his sessions—regardless of their subject matter—and  always walk away having learned something new.

At the conference we attended this summer, Dr. Skotko discussed the impact of a Down syndrome diagnosis on the immediate family. He and his staff had conducted some of the first surveys of parents, siblings and individuals with Down syndrome. To say that I was thrilled that a physician and sibling of an individual with Down syndrome himself took this opportunity to raise awareness for family engagement, a crucial subject many times overlooked by medical professionals, was an understatement. His data were brought to life by his personal experiences, and were overwhelmingly positive. They indicated that a large majority of surveyed immediate family members love and are proud of their family member with Down syndrome.

During a question and answer period following the presentation, a professional in the front of the room challenged some of the data Dr. Skotko had presented. She brought to his attention that perhaps the data were positively skewed because parents and family members would have guilt associated with speaking negatively about their experiences and, ultimately, their own family member. Well, I am not one to hold my tongue, but I did have to pause to ensure I reigned in my “mommy” emotions and represented the parent voice in an assertive yet positive way.

In that moment, memories from my 10 years of being a mom to my precious gift rushed back. Some of the first feelings to come back to me were those that I have been ashamed to admit as a parent. For example, the diagnosis at my daughter’s birth had me thinking that I would always be a parent to a child living at home. The hours in the hospital enduring her open heart surgeries had brought me emotionally to my knees, wishing my child was healthy. I recalled the times her anxiety caused bathroom accidents in public places, which had me wishing for normalcy. Listening to friends talk about their gifted and talented children had me feeling like an outsider. I remember feeling sad because the birthday party and play date invites were few and far between, if at all. For a second I thought that maybe this woman was right; maybe I do sugar coat my family’s reality because I am too ashamed to admit otherwise.

But in the next moment, I saw Sami’s hand reaching for my mom’s face, days after open heart surgery. This was the first expression of her personality shining through. I remembered my toddler son translating her words and being so proud that he was the only one who could understand her. We celebrated her first everything and then celebrated her first everything all over again when she regained a lost skill. I recalled the way that, no matter where we are, she makes people smile, no matter what kind of day they may be having. And the oh-so-many little things in life I would have completely overlooked were it not for her.

I gathered my thoughts, raised my hand, and explained this concept to the group. In fact, the professional that asked the question was right; the challenges are hard and often. We do have doubts about our ability to parent and yes, horrifyingly enough, we will ask “why me?”

However, we celebrate and appreciate all that is positive. We do this in a way that is bigger than any outsider could know, and we do it time and time again. The impact has been so positive—my family completely changed for the better the moment Sami came into our lives. In addition to the daily joy we experience with her, all of us are dedicated to her cause, and the cause of others. My professional career has shifted from sales and marketing to assisting families with their own special loved ones. My husband, who was and still is a physical education teacher, has brought her spirit to the way he interacts with his students, including those with special needs. Lastly, but perhaps my proudest family accomplishment, is how Sami refers to her 13-year-old brother as her hero. No matter the circumstance, he shows no embarrassment towards her, only love and admiration.

I summed up my comments that afternoon, and I’ll leave the same simple thought for you here. “You see, our lows may be lower at times, but our highs are more often, and they are always so much higher. We wouldn’t dream of trading it for anything!”


Blog articles provide insights on the activities of schools, programs, grantees, and other education stakeholders to promote continuing discussion of educational innovation and reform. Articles do not endorse any educational product, service, curriculum or pedagogy.

Carrie Woodcock and daughter, Sami.
Posted by
Director of the Maine Parent Federation and a parent of 10-year-old Sami who has Down syndrome.