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UNPRECEDENTED CLASS ACTION CIVIL RIGHTS COMPLAINT
Children with Diabetes Sues CA School Districts for Denial of Glucose Monitoring and Insulin Administration At Schools
“(OCTOBER 11, 2005, Oakland, CA) - Four elementary school-age students, along with the American Diabetes Association, filed an unprecedented civil rights complaint today in U.S. District Court for the Northern District of California seeking class action relief against the California Superintendent of Public Schools, the California Department of Education, members of the California Board of Education, the San Ramon Valley Unified School District, the Fremont Unified School District, and their Superintendents and Boards of Trustees. The suit asks the Court to compel public school officials to comply with federal law by providing the assistance that California students with diabetes require to manage their diabetes during the school day.
"The complaint alleges that the state and the local districts violate Section 504 of the Rehabilitation Act (Section 504), the Individuals with Disabilities Education Act (IDEA), the Americans with Disabilities Act (ADA) and applicable federal regulations in their failure to ensure the health and safety of public school students with diabetes in Kindergarten through 12th Grade by providing insulin administration, blood glucose monitoring, proper care in emergency situations, and other appropriate diabetes care.”
For more information, contact:
Julia Epstein, Disability Rights Education & Defense Fund, (510) 644-2555
Great News for South Carolina's Children with Diabetes!
New law allows students to carry their own medicines: Medication won’t require a visit to the school nurse By DEVON MARROW. S.C. children suffering from chronic illnesses soon will be able to carry relief in their pockets.
A new law slowly making its way into South Carolina’s classrooms allows children who suffer from such illnesses as asthma and diabetes to carry and administer their own medicines. ... Lexington 4 is the first school district in the Midlands to officially revise its policy to include the 4-month-old legislation. Until now, most school districts have required that only school personnel, usually nurses, give medicines to students. ... For 8-year-old Trevor Collins, having diabetes means an insulin shot in the morning and evening. ... As a Frances F. Mack Primary School student, the second-grader also needs to check his blood sugar level before he joins his classmates for lunch... The State.com, December 9, 2005.
Federal laws may require that schools and day care facilities participating in the National School Lunch, School Breakfast, and Child and Adult Care Food Programs accommodate children with medical conditions such as diabetes. Regardless of the law, knowledgeable school staff are essential in providing a safe school environment for children with diabetes. Here are some key points to keep in mind. Retain all diet prescriptions on file. Diet prescriptions should only be changed by the physician or appropriate health professional.
U.S. Department of Education - Print this page (word document)
Individualized Education Program (IEP)
The reauthorized Individuals with Disabilities Education Act (IDEA) was signed into law on Dec. 3, 2004, by President George W. Bush. The provisions of the act became effective on July 1, 2005, with the exception of some of the elements pertaining to the definition of a “highly qualified teacher” that took effect upon the signing of the act. This is one in a series of documents, prepared by the Office of Special Education and Rehabilitative Services (OSERS) in the U.S. Department of Education, that covers a variety of high-interest topics and brings together the statutory language related to those topics to support constituents in preparing to implement the new requirements. This document addresses only the changes to the provisions of IDEA regarding individualized education program (IEP) team meetings and changes to the IEP that took effect on July 1, 2005. It does not address any changes that may be made by the final regulations.
1. Revises language regarding members of the IEP team.
The term “IEP team” means a group of individuals composed of:
2. Identifies when IEP team meeting attendance is not necessary.
A member of the IEP team shall not be required to attend an IEP meeting, in whole or in part, if the parent of a child with a disability and the LEA agree that the attendance of such member is not necessary because the member’s area of the curriculum or related services is not being modified or discussed in the meeting. A parent’s agreement shall be in writing. [614(d)(1)(C)(i), (iii)]
3. Authorizes excusals from IEP meetings.
A member of the IEP team may be excused from attending an IEP meeting, in whole or in part, when the meeting involves a modification to or discussion of the member’s area of the curriculum or related services if:
The parent’s consent shall be in writing. [614(d)(1)(C)(ii), (iii)]
4. Adds new provisions for making changes to the IEP.
In making changes to a child's IEP after the annual IEP meeting for a school year, the parent of a child with a disability and the LEA may agree not to convene an IEP meeting for the purposes of making such changes and, instead, may develop a written document to amend or modify the child's current IEP. [614(d)(3)(D)]
Changes to the IEP may be made either by the entire IEP team or, as provided in Section 614(d)(3)(D), by amending the IEP rather than by redrafting the entire IEP. Upon request, a parent shall be provided with a revised copy of the IEP with the amendments incorporated. [614(d)(3)(F)]
5. Encourages consolidation of IEP meetings.
To the extent possible, the LEA shall encourage the consolidation of reevaluation meetings and other IEP team meetings for the child. [614(d)(3)(E)]
6. Authorizes alternative means of meeting participation.
When conducting IEP team meetings and placement meetings pursuant to Sections 614, 615(e), and 615(f)(1)(B), and carrying out administrative matters under Section 615 (such as scheduling, exchange of witness lists and status conferences), the parent of a child with a disability and an LEA may agree to use alternative means of meeting participation, such as video conferences and conference calls. [614(f)]
 Topics in this series include: Alignment With the No Child Left Behind Act; Changes in Initial Evaluation and Reevaluation; Children Enrolled by Their Parents in Private Schools; Discipline; Disproportionality and Overidentification; Early Intervening Services; Highly Qualified Teachers; Individualized Education Program (IEP) Team Meetings and Changes to the IEP; Individualized Education Program (IEP); Local Funding; National Instructional Materials Accessibility Standard (NIMAS); Part C Amendments in IDEA 2004; Part C Option: Age 3 to Kindergarten Age; Procedural Safeguards: Surrogates, Notice and Consent; Procedural Safeguards: Mediation and Resolution Sessions; Procedural Safeguards: Due Process Hearings; Secondary Transition; State Funding; and Statewide and Districtwide Assessments. Documents are available on the OSERS Web site at: www.ed.gov/about/offices/list/osers/index.html.
Page Updated 023/06/2006