Education.com

Developing Your Child’s IEP (page 5)

By Theresa Rebhorn
National Dissemination Center for Children With Disabilities

 5. Participation with Nondisabled Children

The IDEA says that each IEP must include:

“...an explanation of the extent, if any, to which the child will not participate with nondisabled children in the regular class . . . ” (27)

As we said earlier in this publication, the IDEA strongly prefers that children with disabilities be educated in the general education class with nondisabled children. In order to support your child in this setting, the IEP team considers what your child needs in terms of:

  • accommodations,
  • modifications,
  • supports, and
  • supplementary aids and services.

Even a child with many needs should be involved with nondisabled peers to the maximum extent appropriate. Just because a child has severe disabilities or needs modifications to the general curriculum does not mean that he or she should be removed from the general education class. (28) If your child is removed from the general education class for any part of the school day, the IEP team must include an explanation in the IEP.

6. Modifications for Your Child

Sometimes a student may need to have changes made in class work or routines because of his or her disability. Modifications can be made to:

  • what a child is taught, and/or
  • how a child works at school.

Sometimes people get confused about what it means to have a modification and what it means to have an accommodation. Usually a modification means a change in what is being taught to or expected from the student. Making an assignment easier so the student is not doing the same level of work as other students is an example of a modification. An accommodation is a change that helps a student overcome or work around the disability. Allowing a student who has trouble writing to give his answers orally is an example of an accommodation. This student is still expected to know the same material and answer the same questions as fully as the other students, but he doesn’t have to write his answers to show that he knows the information. What is most important to know about modifications and accommodations is that both are meant to help a child to learn. For example:

Jack is an 8th grade student who has learning disabilities in reading and writing. He is in a regular 8th grade class that is team-taught by a general education teacher and a special education teacher. Modifications and accommodations provided for Jack’s daily school routine (and when he takes state or district-wide tests) include the following:

  1. Jack will have shorter reading and writing assignments.

  2. Jack’s textbooks will be based upon the 8th grade curriculum but at his independent reading level (4th grade).

  3. Jack will have test questions read/explained to him, when he asks.

  4. Jack will give his answers to essay-type questions by speaking, rather than writing them down.

Modifications or accommodations are most often made in the following areas:

Scheduling. For example,

  • giving the student extra time to complete assignments or tests
  • breaking up testing over several days

Setting. For example,

  • working in a small group
  • working one-on-one with the teacher

Materials. For example,

  • providing audiotaped lectures or books
  • giving copies of teacher’s lecture notes
  • using large print books, Braille, or books on CD (digital text)

Instruction. For example,

  • reducing the difficulty of assignments
  • reducing the reading level
  • using a student/peer tutor

Student Response. For example,

  • allowing answers to be given orally or dictated
  • using a word processor for written work
  • using sign language, a communication device, Braille, or native language if it is not English.

Modifications to State or District-Wide Assessments

The IDEA requires that students with disabilities take part in state or district-wide assessments. (29) These are tests that are periodically given to all students to measure achievement. It is one way that schools determine how well and how much students are learning. The IDEA now states that students with disabilities should have as much involvement in the general curriculum as possible. Therefore, more and more students with disabilities will be participating in these general assessments. This means that, if your child is receiving instruction in the general curriculum, he or she could take the same standardized test that the school district or state gives to nondisabled children. Your child’s IEP must include all modifications or accommodations that your child needs so that he or she can participate in state or district-wide assessments.

The IEP team can decide that a particular test is not appropriate for your child. In this case, the IEP must include:

  • an explanation of why that test is not suitable for your child, and
  • how your child will be assessed instead (often called alternate assessment). (30)

Ask your state and/or local school district for a copy of their guidelines on the types of accommodations, modifications, and alternate assessments available to students.

7. Location and Duration of Services

Each of the services your child needs is written down in the IEP. The IEP must also say:

  • how often your child will receive the service(s) (number of times per day or week),

  • how long each “session” will last (number of minutes),

  • where services will be provided (in the general education classroom or another setting such as a special education resource room), and

  • when services will begin and end (starting and ending dates). (31)

The IEP team should also consider whether or not your child needs to receive services beyond the typical school year. This is called Extended School Year or ESY services. (32) Some children receiving special education services may be eligible for ESY services. Ask your state and local school district for a copy of its guidelines for determining eligibility for ESY. If you or your child’s teachers feel your child needs ESY services, it should be discussed during the IEP meeting.

8. Reporting Your Child’s Progress

Under the IDEA, you must be informed of your child’s progress on IEP goals at least as often as parents of nondisabled children are informed of their children’s progress. (33) So, if typical students get regularly scheduled report cards, you should get IEP progress reports for your child, at least as often. In these progress reports look to see whether or not your child is making enough progress to reach his or her goals by the end of the year. If not, then you will want to talk to the IEP team about why enough progress is not being made and what should be done about it.

 9. Transition Services (34)

As your child gets older, you will start to plan for the future. You, your child, and the rest of the IEP team will consider many questions. What will your child do after high school? Will he or she go to college or vocational school? Will he or she work in supported employment or get a competitive job? Will he or she live independently or continue to live at home? Will you need help from other agencies to carry out these plans?

By the time your child is 14 years old, the IEP must include plans to help him or her move on from high school to life as an adult in the community. This is called transition planning or transition services. You can begin making plans for transition services earlier than age 14, if the IEP team thinks that it is appropriate. At this age, transition planning focuses on your child’s transition service needs such as his or her courses of study (for example, participation in advanced placement courses or in a vocational education program). At age 16 (or younger, if the IEP team feels it’s appropriate), your child’s IEP must include a statement of the services your child needs to prepare for life after high school, including any interagency responsibilities or needed linkages with outside agencies.

Transition planning is intended to help your child consider and prepare for post-secondary activities (35), including any of the following:

  • postsecondary education (such as a 2 or 4-year college or business school),

  • vocational training (to prepare for working in computers, auto mechanics, or hotels/restaurants, for example),

  • integrated or supported employment (such as a sheltered workshop, a job coach, or Vocational Rehabilitation services),

  • continuing and adult education (such as classes offered by your community Adult Education office or Department of Recreation),

  • adult services (such as a day program, group home),

  • independent living, and

  • participating in the community. (36)

Planning for transition is a very important area for the IEP team to consider. When the team is going to talk about transition, your child must be invited to the meeting. Services must be based on your child’s needs, taking into account his or her preferences and interests. A lengthy discussion of transition planning is beyond the scope of this Parent’s Guide. However, because it is so important, you will want to learn more about it. You will find more information on transition in the list of Resources at the end of this guide.

10. Age of Majority (37)

When a student with a disability reaches the age where one is considered to be an adult, (called the age of majority), the state may transfer to the student all the educational rights that you, as parent, have had up to this point. Depending upon your state law, this usually happens between 18 and 21. Not all states transfer rights. But if your state does, then the rights and responsibilities that you have had for your child will belong to your child at the age of majority.

Beginning at least one year before your child reaches the age of majority, you and your child will receive written notice from the school telling you of the upcoming transfer of rights (if any). When this happens, the IEP will include a statement that you have received the notice and have been told about the transfer of rights.

There are some exceptions to this transfer of rights. For example, some children with disabilities may need to have a guardian appointed to make decisions for them. Other students may not have the ability to give informed consent (38) with regard to their education. Or your child may be fully capable of making these decisions, but still want your help in these matters. In all these cases, the state can establish a way for you to continue to represent your child’s educational interests. You will need to check your local and state IDEA regulations to find out how this issue is handled.

III. Deciding Your Child’s Placement

What is placement? How is my child’s placement decided?

Once the IEP team has decided what services your child needs, a decision must be made about where services will be provided. Where your child’s IEP is carried out is called placement. You as the parent have the right to be part of the group that decides your child’s placement.

In deciding your child’s placement, the group must make sure that your child has the maximum opportunity appropriate to learn with children who do not have disabilities—in academic, nonacademic, and extracurricular activities. (39) This part of the law is called Least Restrictive Environment or LRE.

Least Restrictive Environment is explained in the IDEA as follows:

“. . . To the maximum extent appropriate, children with disabilities . . . are educated with children who are nondisabled; and . . . special classes, separate schooling or other removal of children with disabilities from the regular educational environment occurs only if the nature or severity of the disability is such that education in regular classes with the use of supplementary aids and services cannot be achieved satisfactorily.” (40)

IDEA also says:

  • The child’s placement is determined at least annually; is based on the child’s IEP; and is as close as possible to the child’s home.

  • Unless the IEP requires some other arrangement, the child is educated in the school that he or she would attend if nondisabled.

  • When looking at placement options, consideration must be given to any potential harmful effect on the child or on the quality of services that he or she needs.

  • A child with a disability may not be removed from education in age-appropriate regular classrooms just because he or she needs modifications to the general curriculum. (41)

Often, the IEP team makes the placement decision. In some places, the placement decision is made by another group of people. In either case, under IDEA, the group that makes the placement decision must include you, as the parent(s) and others who:

  • are knowledgeable about your child;
  • understand the meaning of your child’s evaluation data; and
  • know the placement options. (42)

When discussing placement, the group should consider your child’s unique needs and determine what the least restrictive placement for your child is, based upon those needs. A placement that is least restrictive for one child may not be least restrictive for another. What is least restrictive for each child is based on that child’s unique needs. This means that the school system cannot use a “one size fits all” approach to educating children who have a disability. Decisions must be based on individual needs as stated in the IEP, not on—

  • the child’s disabling condition or label (such as placement in a special class for students with mental retardation just because a child has cognitive impairments),

  • disability program categories (placement in an particular LD program just because a child needs LD services),

  • the location of staff,

  • the funds that are available, or

  • the convenience of the school district.

In making placement decisions, the group looks to another important part of the IDEA, the continuum of alternative placements. (43) The continuum includes the different options where children can receive services. These options include placements such as:

  • a general education class
  • a special education class
  • a special education school
  • at home, or
  • in a hospital or other public or private (44) institution.

A student’s placement in the general education classroom is the first option the placement group should consider. Can your child be educated satisfactorily in the general education classroom? What aids, services, and supports does your child need to make this possible? If the group decides that your child’s needs can be met in the general education class, with supports, then that placement is the least restrictive environment for your child.

View Full Article

Add your own comment

Ask a Question

Have questions about this article or topic? Ask
Ask
150 Characters allowed

Washington Virtual Academies

Tuition-free online school for Washington students.