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Journal of Social Work in
Disability & Rehabilitation
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Everything You Never Wanted
to Know About Special
Education … and Were Afraid to
Ask (I.D.E.A.)
Sandra Altshuler PhD, LICSW
a
a
School of Social Work, Eastern Washington
University , 203 Senior Hall, Cheney, WA, 99004, USA
Published online: 23 Sep 2008.
To cite this article: Sandra Altshuler PhD, LICSW (2007) Everything You Never Wanted
to Know About Special Education … and Were Afraid to Ask (I.D.E.A.), Journal of
Social Work in Disability & Rehabilitation, 6:1-2, 23-33, DOI: 10.1300/J198v06n01_02
To link to this article: http://dx.doi.org/10.1300/J198v06n01_02
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Everything You Never Wanted to Know
About Special Education . . .
and Were Afraid to Ask (I.D.E.A.)
Sandra Altshuler
SUMMARY. Social workers who work with families and children are
often unaware of the legal protections afforded to educational experiences for children, particularly to children with disabilities. Yet, all
social workers, regardless of their practice setting, should be aware of
the important educational rights to which children with disabilities and
their families are entitled, as codified in the original legislation, P.L.
94-142, and its subsequent revisions. This legislation is currently entitled
the “Individuals with Disabilities Education Act,” or the “I.D.E.A.”
Provisions included in the I.D.E.A. are covered with which all states
that receive federal educational funding are mandated to comply.
Reviewed are the 13 “disabling conditions” that allow for students to
qualify to receive special educational services, as long as one of the
conditions is adversely impacting their educational success. It concludes with recommendations for social work advocacy regarding this
legislation. doi:10.1300/J198v06n01_02 [Article copies available for a fee from
The Haworth Document Delivery Service: 1-800-HAWORTH. E-mail address:
Sandra Altshuler, PhD, LICSW, is Associate Professor, School of Social Work,
Eastern Washington University, 203 Senior Hall, Cheney, WA 99004 (E-mail:
saltshuler@mail.ewu.edu).
[Haworth co-indexing entry note]: “Everything You Never Wanted to Know Special Education . . . and
Were Afraid to Ask (IDEA).” Altshuler, Sandra. Co-published simultaneously in Journal of Social Work in
Disability & Rehabilitation (The Haworth Press, Inc.) Vol. 6, No. 1/2, 2007, pp. 23-33; and: Disability and
Social Work Education: Practice and Policy Issues (ed: Francis K. O. Yuen, Carol B. Cohen, and Kristine Tower)
The Haworth Press, Inc., 2007, pp. 23-33. Single or multiple copies of this article are available for a fee from
The Haworth Document Delivery Service [1-800-HAWORTH, 9:00 a.m. - 5:00 p.m. (EST). E-mail address:
docdelivery@haworthpress.com].
Available online at http://jswdr.haworthpress.com
2007 by The Haworth Press, Inc. All rights reserved.
doi:10.1300/J198v06n01_02
23
24
DISABILITY AND SOCIAL WORK EDUCATION
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Website:
© 2007 by The Haworth Press, Inc. All rights reserved.]
KEYWORDS. Students with disabilities, the I.D.E.A., social work
advocacy, educational rights
INTRODUCTION
The educational experiences of all children have significant impact
on their overall well-being. Social workers who work with families
and children are often unaware of the legal protections afforded to
children, particularly to children with disabilities. All social workers
who work with children and families, regardless of their practice setting, should be aware of the important educational rights to which
children with disabilities and their families are entitled (Altshuler &
Kopels, 2003).
The U.S. Congress enacted a veritable revolution in 1975, when it
passed the Education for All Handicapped [note: I will use the term
handicapped when it is historically accurate to do so] Act (P.L. 94-142),
that provided sweeping rights to such students. Previous to the 1975
Act, schools were permitted to exclude students with any type of perceived handicaps, based on the principle of in loco parentis; e.g., that
schools were free to make educational decisions acting in place of
parents (Allen-Meares et al., 2000, and Washington & Welsh, 2000).
Indeed, all that was required for exclusion was a request by a teacher,
parent or administrator, stating that the child’s handicap was making
it too difficult either for the child or peers to learn, or for the teacher
to teach. Further, there were no agreed-upon definitions about what a
handicap was or was not; therefore, any person could claim that a student
had a handicap, thereby justifying exclusion. These practices led to
widespread private placements of students with handicaps if their
parents could afford such services and widespread exclusion from
accessing any benefits that public educational settings offer to all other
students.
In 1975, P.L. 94-142 mandated that all handicapped children were
entitled to receive special education and related services specifically
designed to meet their needs and provided financial support to ensure
its mandates. One of the primary purposes of the original legislation
was to ensure that children with disabilities between the ages of 3 and
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Sandra Altshuler
25
21 were not excluded from public schools. At the time of its passage,
more than half of children with disabilities in the United States did not
receive appropriate educational services, and one million children with
disabilities were excluded entirely from the public school system [20
U.S.C. § 1400(c)(2)]. P.L. 94-142 also provided protections for the
rights of parents, children, and educational institutions regarding its
requirements. While P.L. 94-142 was designated as permanent legislation, Congress was required to reauthorize the federal financial support
for it on a periodic basis (theoretically, every three years). During each
reauthorization process, Congress was able to modify the requirements of
the law.
Thus, P.L. 94-142 was reauthorized in 1990 and renamed the Individuals with Disabilities Education Act (P.L. 101-476), commonly
referred to as the I.D.E.A. One of the major changes instituted in 1990
was the law’s emphasis on comprehensive, coordinated, interagency
early intervention services for infants and toddlers (Allen-Meares et al.,
2000). The most recent amendments to the I.D.E.A. were adopted in
1999, and expanded definitions of disabilities, including addressing
the needs of homeless children and children with disciplinary problems
(Altshuler & Kopels, 2003). All of these changes, while significantly
impacting the rights and protections of children with disabilities and their
families, also retain the basic rights and protections that have been
extended to them since the law’s 1975 origin (Altshuler & Kopels, 2003).
“P.L. 94-142” and the I.D.E.A. are terms often used interchangeably by
professionals and lawmakers.
Throughout its history, states have developed policies to comply with
the I.D.E.A. based on their varying interpretations of the law. Unfortunately, states’ policies may not always comply with the requirements of
the law. In fact, a recent study by the National Council on Disability
found that all states are out of compliance with the law’s requirements
in some manner (National Council on Disability, 2000). Therefore, this
article must, by necessity, cover the mandates found only in the federal
law, and may not reflect individual states’ interpretation and policy development. Because of the detail that can be included in every provision
of this law, this article will review only the basic protections provided,
including the legal definitions of educational handicaps, so that all social workers will be in a strong position of advocacy for their clients, no
matter what setting they are placed. For more details about any of these
provisions, the student is encouraged to review the law itself and its
accompanying revisions.
26
DISABILITY AND SOCIAL WORK EDUCATION
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Provisions of P.L. 94-142
Zero Reject/Child Find: One of the most important messages of P.L.
94-142 is that all children with disabilities fall within the provisions of
the law. No child may be rejected or excluded from accessing education
based upon the existence of a disability. Furthermore, P.L. 94-142 requires every state to identify, locate, and evaluate all children with disabilities residing in that state [34 C.F.R. § 300.125]. This “child find”
principle applies to all children with disabilities, regardless of the severity of the disability or their attendance at private schools. In 1999,
Congress clarified that the child find requirements also apply to highly
mobile children with disabilities and specifically define highly mobile
children with disabilities to include those who are migrant or homeless
(Altshuler & Kopels, 2003). Congress also explicitly required that school
districts take a more active role in searching out and finding these families and children, rather than leaving the burden of self-identification up
to the families themselves.
Free and Appropriate Public Education (FAPE): The original law
stated that children with disabilities are entitled to receive a free and
appropriate public education, commonly referred to as a FAPE. As
Altshuler and Kopels (2003) explain, the term FAPE means that special
education and related services are provided at public expense and without charge to parents; meets State defined standards; includes education
from preschool through high school; and are provided in conformity
with an individualized education program [34 C.F.R. § 300.13].
Least Restrictive Environment (LRE): This provision of the law requires
that students with disabilities receive a FAPE, to the maximum extent
possible, with non-disabled, general education students (Allen-Meares
et al., 2000). Special education services can be considered a continuum of
services, from consultative services on one end, spanning to institutional
care on the other end. The extent to which a student’s day is restricted
from the typical interactions with their non-disabled peers is how the
level of environmental restriction is determined. The overall purpose of
the LRE provision is to ensure that schools minimize the amount of time
a student is not with their non-disabled peers.
Nondiscriminatory Evaluation (NDE): Children with disabilities were
protected from nondiscriminatory evaluation through a requirement
that a multidisciplinary team must complete a wide range of non-biased
assessments specific to children’s suspected disabilities before placement into special education can occur (Altshuler & Kopels, 2003). The
NDE must be completed by professionals qualified and knowledgeable
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Sandra Altshuler
27
in the relevant disability being evaluated. The NDE cannot use a single
assessment, or a single discipline, as a sole determinant for placement
into special education; it must be comprised of a variety of valid, standardized, non-biased assessment instruments administered by more than
one professional [20 U.S.C. § 1414 (b)]. Some states refer to the NDE
as a case study evaluation (“CSE”). Regardless of its terminology, the
NDE/CSE must be fully re-done every three years, to ensure continuing
appropriateness of placement.
Multidisciplinary Team (MDT): The MDT, as defined, is comprised of
a variety of professionals from a variety of disciplines, who administer
and evaluate the standardized assessments for determining eligibility
for special education placement. However, the MDT does more than
simply assess and evaluate. The MDT attends meetings, often called
Multidisciplinary Conferences (MDCs), at which eligibility, placement
and educational decisions are made. As such, in addition to the professionals who are performing the evaluations, the MDT is comprised of at
least one of the student’s general education and special education teachers; a representative from the local educational administration (LEA)
who is familiar with both the general curriculum and the available resources; and the student’s parents [20 U.S.C. § 1414 (d)(1)(B)]. This is
true regardless of the student’s age (e.g., 3-21), although after age 14, it
is expected that the student would also become a member of the MDT.
Individualized Education Program (IEP): A FAPE is ensured, and
children with disabilities are protected from inappropriate educational
services, by the mandate that schools must create an Individualized Educational Program. This plan, known as an IEP, is designed specifically
for each student receiving special services, a plan that must be reviewed
and rewritten yearly to reflect current functioning and progress toward
educational goals (Altshuler & Kopels, 2003). As Turnbull and Turnbull
(1998) delineate, the IEP is required to have a number of components
[20 U.S.C. § 1414 (d)(1)(A)]:
1. A statement of students’ present levels of educational functioning
and how the disability impacts their ability to progress within the
general curriculum;
2. A statement of measurable annual goals and short-term objectives
that address the students’ educational needs that result from their
identified disability;
3. An outline of the specific special education services, related services, supplemental services, and program modifications that will
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28
DISABILITY AND SOCIAL WORK EDUCATION
be made in order to achieve the measurable annual goals, including their frequency, duration and location;
4. Any modifications in standardized testing (while this is beyond
the breadth of this chapter, it is important to point out that this provision in P.L. 94-142 is contradicted by provisions in the No Child
Left Behind Act (P.L. 107-110), which specifically disallows any
such exclusion or modification for students with disabilities) and
how students will be appropriately assessed for educational progress;
5. A statement of how students’ progress toward the annual goals will
be measured and how their parents will be regularly informed; and
6. When students reach the age of 14 (and older), a statement of transitional service needs and agency linkages, if appropriate.
The 1990 Amendments that provided for early intervention services
also revised requirements for an individualized educational program
specifically designed for infants and toddlers. One revision was the requirement of an Individualized Family Service Plan (IFSP) that must be
developed for any child identified with a disability younger than 5 years
old. As the name indicates, the primary distinction between an IEP and
an IFSP is the requirement that the family be included in any individualized program for such children [20 U.S.C. § 1436]. In addition, all IFSP’s
must define the specific steps involved in transitioning the child to their
next educational setting.
Parent Involvement/Procedural Due Process: Every iteration of the I.D.E.A.
from its inception has attempted to ensure parental involve- ment and
participation in the special education process. Under the cur- rent law, a parent
may be defined as a birth or adoptive parent, a legal guardian, a surrogate
parent, or someone acting in the place of a parent (e.g., foster parents) [34 C.F.R. §
300.20]. The general idea (not the legal technicalities) of procedural due process
has to do with fairness and the ability of the parents to legally disagree with
decisions being made about their children. In effect, the federal government has
defined exactly how state and local educational agencies must include parents
throughout the entire process, and, the legal procedures by which parents can
ensure that their, and their children’s, rights are being protected. The I.D.E.A.
delineates a series of requirements for State Educational Agencies (SEAs) to involve
parents in decision-making about policies and procedures for special education. For
example, all SEAs are required to create Advisory Panels for special education that
are primarily comprised of parents and teachers of students with disabilities, and
individuals with disabilities (in addition to a myriad of educational and
administrative professionals)
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Sandra Altshuler
29
(Turnbull & Turnbull, 1998). The I.D.E.A., in conjunction with the
Family Educational Rights and Privacy Act (FERPA), addresses issues
regarding students’ educational records, including access, confidentiality,
and privacy.
In ensuring fairness of the process, the school district is required to
follow a specific series of steps from the moment that it decides to investigate the potential for a student to qualify for special education. The
school district is required to provide to parents a 10 day written notification of any type of MDC and make clear efforts to ensure that parents
can attend such meetings. The parents must receive a copy of minutes
from the proceedings for all meetings. The school district is required to
provide parents with both written and verbal explanations of parents’
and students’ procedural safeguards under the I.D.E.A., and all written
communication must be in the parents’ native language. The school district must obtain written informed consent from the parents before initiating any and all components of the NDE/CSE and must obtain written
informed consent from the parents again before the child will ever be
placed into special education. In other words, providing consent for the
evaluation does not mean that parents must, should or otherwise feel obligated, to provide consent for placement into special education. School
districts must make efforts to ensure parent participation in the yearly
review and development of the IEPs.
Finally, in cases where there is a disagreement between the school
district and the parents, the I.D.E.A. provides for an abbreviated court
procedure, commonly called due p ...
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