October is Learning Disabilities/Dyslexia/Attention Deficit Hyperactivity Disorder (ADHD) Awareness Month
Lena McKnight was born in Norfolk, Virginia and raised in Harlem, New York. She attended public school in New York City until 10th grade and later enrolled in a YouthBuild program where she achieved a High School Equivalency Diploma. Lena then went on to graduate with an associate’s degree and later a bachelor’s degree in Theatre and Sociology in May 2017. Lena has served as a Student Advocate for 10th graders through the Harlem Children Zone and remains involved with YouthBuild. She now works full time and devotes her career to serving kids in her community. Lena is committed to using her voice to have a positive impact on the field of education and on society at large.
Assistant Secretary Johnny Collett and Deputy Assistant Secretary Kim Richey visited Strong Foundations Charter School during the 2018 Back-to-School Tour.
October is Learning Disabilities/Dyslexia/Attention Deficit Hyperactivity Disorder (ADHD) Awareness Month.
Seven years ago, one of my former students came to visit me and see the school I helped to found, Strong Foundations Charter School, a public charter school formed to provide excellent reading instruction to all students.
My former student was home from college where he majored in music and also played in two successful bands nearby. As we walked through the halls, he saw the elementary students working, some of whom were in Orton-Gillingham class—a structured reading approach to help students learn to read. I remarked that if he had been in a school like this, he might not have had to struggle so much with reading when he was younger.
His reply was bittersweet to me. “If I had been to a school like this, I might have been able to be your friend sooner.”
Douglas Rawan II, a sixth-grader with dyslexia
Note: October is Learning Disabilities/Dyslexia/Attention Deficit Hyperactivity Disorder (ADHD) Awareness Month
My name is Douglas Rawan II. I am 11-years-old, live in Massachusetts, and I have a story about dyslexia.
It starts back in fourth grade when I began to feel different than my friends in school. Making jokes was the way I would cover up having no confidence in school. No one knew that inside I felt stupid. I remember one day when my mom asked me to do some reading and writing, and I threw pencils on the floor and my book. I remember my mom looked really sad. Inside I knew it would be too hard, but I didn’t know why. Since Kindergarten, my mom hired tutors to help with reading, but nothing changed at school. I also had a hard time focusing at school until one day I came home and told my mom that I asked the assistant principal for a standing desk. My parents didn’t even know what that was.
Note: May is Better Hearing and Speech Month.
Infancy and early childhood are important times of life for all children, but more so for those who have delays in development. These delays may be from genetic conditions, disabilities, various risk conditions, or unknown reasons. While families may be the first to recognize a difference in their child’s developmental progress, professionals trained and licensed in early childhood intervention have the skills and knowledge to detect a developmental delay and to then provide intervention to remediate and/or minimize its impact on a child’s development.
Will Eiserman, Director, Early Childhood Hearing Outreach (ECHO) Initiative at Utah State University.
Will Eiserman is the Director of the Early Childhood Hearing Outreach (ECHO) Initiative, at the National Center for Hearing Assessment and Management, Utah State University. As Director of the ECHO Initiative, he has led a national effort to assist Early, Migrant, and American Indian/Alaska Native Head Start programs in updating their hearing screening and follow-up practices. Working in close collaboration with a team of pediatric audiologists and other Early Hearing and Detection Initiative (EHDI) experts, Eiserman has been responsible for the design of training systems, mechanisms for tracking and follow-up, and evaluation strategies associated with early and continuous hearing screening activities. His career has focused on a variety of efforts to improve early intervention systems for children with special needs, and on meeting the psycho-social needs of children with craniofacial disfigurements and their families. Eiserman’s perspective is influenced by his extensive international and cross-cultural experiences that include work in Ecuador, Vietnam, Costa Rica, Russia, and Indonesia.
Note: April is National Autism Awareness Month.
Carolyn Hayer with son Chris and their family
Carolyn Hayer is the Director of Parent and Professional Development at the Statewide Parent Advocacy Network (SPAN) in New Jersey, a federally funded Parent Training and Information Center.
There was a time when I couldn’t even say the word out loud. It was too painful, too devastating to utter. I wanted to believe that if I didn’t say the word, it didn’t exist. But it does exist; it’s real, and it’s beautiful, and it’s challenging all at the same time. And whether I say the word or not, my son Chris has autism.
Note: April is National Autism Awareness Month.
The Bae family during trip to England
Just like any other school day, Eugene, my son with autism, left on the bus this morning to go to a day program provided by our school district. For the last 20 years, he and I wait for the bus by sitting on our front porch. As he steps on the bus, he shouts at me with his happy high-pitched voice, “Bye Mom!” This is our ritual to begin each new day, to meet that day’s challenges, emotions, promises, and hopes.
In June this year, he will age out from the district program. I cannot help being emotional whenever I think about his first day of preschool and the journey that Eugene and our family have been on since then. On that day, I cried in the car for two hours after separating from my miserable, crying child.
Note: October is Learning Disabilities/Dyslexia/Attention Deficit Hyperactivity Disorder (ADHD) Awareness Month.
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.
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.