This article is reprinted from the A.T. Quarterly, Volume 1, Number 3 (1990)
United Cerebral Palsy Associations (UCPA), Inc., working in cooperation
with Susan Goodman, an attorney and a parent of a child with a disability, has successfully
secured a new policy letter from the Office of Special Education Programs (OSEP) that clarifies
the right of a child with a disability to assistive technology devices and services under P.L.
94-142, the federal mandate for a free appropriate public education.
The letter issued on August 10th states clearly:
State agencies, advocates, and parents should take steps at the local and state level to ensure
that this important OSEP policy clarification translates into real benefits for students in the form
of access to assistive technology in the schools.
In addition, if students in your state are having problems with accessing assistive technology
in your school system, write Judy Schrag, Director, Office of Special Education Programs, 330
C Street, S.W. Washington, DC 20202-2736. Let her know about what is happening to families.
If you are interested in receiving a copy of the letter or a list of action steps, please contact the
RESNA TA Project Office.
Working together with special education administrators, parents, therapists, nonprofit
providers and staff from the "Tech Act" states, this policy memo could open many new and
exciting opportunities for children to access assistive technology services with EHA.
(Editor's note: this new column has been added to the newsletter to inform states and
organizations about changing policy in the area of AT services.)
The A.T. Quarterly was a newsletter developed by the RESNA TA
Project under a contract with the National Institute on Disability and Rehabilitation Research
(NIDRR), U.S. Department of Education (ED). The content, however, does not necessarily reflect
the position or policy of NIDRR/ED and no official endorsement of the material should be
inferred.