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 Understanding AD/HD
Press Release: June 1, 2006
Bilingual publication on special education rights released;
Booklet targets parents of Hispanic children with AD/HD
Landover, MD --- The National Resource Center on
AD/HD, a CDC-funded program of the patient advocacy group Children and
Adults with Attention-Deficit/ Hyperactivity Disorder (CHADD) and the
National Alliance for Hispanic Health (the Alliance) released today a
free bilingual booklet, Educational Rights for Children with
Attention-Deficit/Hyperactivity Disorder: A Primer for Parents. The
booklet is a joint publication by the two organizations to increase the
availability of information about laws protecting educational rights of
eligible children with AD/HD. This new publication will serve as an
important tool for Hispanic/Latino parents of children with AD/HD to
ensure free appropriate public education (FAPE) for their children.
"Hispanic children with AD/HD have unique needs," said Jane L.
Delgado, PhD, MS, president and CEO of the Alliance. "Our hope is that
this guide will help Hispanic parents face the challenges they meet when
their children are diagnosed with AD/HD and who may be eligible for
services in the public school system." According to the National Survey
of Children’s Health (NSCH), 7.8 percent of children ages four to
17 have a history of AD/HD; that figure correlates with the national
incidence of the neurobiological disorder. Typically, symptoms of AD/HD
arise in early childhood, although the disorder may not be diagnosed
until later.
The 52-page Spanish/English booklet guides parents through the process
of identifying the disorder for their children, and understanding
federal laws that assure specialized education and related services for
eligible children with AD/HD. Written in a question and answer
format, the booklet responds to the most frequently asked questions
parents have about AD/HD and includes case studies, a flow chart
illustrating the step-by-step process to evaluate a child for especial
education services, a list of available resources, and a glossary.
"Developing informational materials in English and Spanish is a
critical part of our outreach efforts to the Latino community and we're
pleased to have this opportunity to partner with the Alliance on this
important publication," said Phyllis Anne Teeter Ellison, PhD, president
of CHADD. "It’s CHADD’s responsibility to ensure information
about the diagnosis and treatment of AD/HD is available to everyone
affected by the disorder, especially in terms of educating our
children."
Publication of the Primer was made possible by a cooperative grant
from the Centers for Disease Control and Prevention, which funds the
National Resource Center on AD/HD (NRC) through CHADD. Single free
copies of the guide are available on request by calling the NRC at
1-800-233-4050 or the Alliance's Su-Familia Helpline at
1-866-783-2654.
About the National Alliance for Hispanic Health (NAHH)
The National Alliance for Hispanic Health is the nation's oldest and
largest network of Hispanic health professionals. The nation's action
forum for Hispanic health, Alliance members deliver services to over 12
million persons every year, making a daily difference in the lives of
Hispanic communities. For more information, visit the Alliance's website
(www.hispanichealth.org) or
call 1-866-SU-FAMILIA (1-866-783-2645).
About CHADD
CHADD (Children and Adults with Attention-Deficit/Hyperactivity
Disorder) is the nation’s leading non-profit organization serving
individuals with AD/HD and their families. CHADD has more than 14,000
members in 200 local affiliates throughout the U.S. Local CHADD groups
offer support for individuals, parents, teachers, professionals ad
others. For more information on the National Resource Center on AD/HD,
visit the Center's site at www.help4adhd.org or call
1-800-233-4050.
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