Educational Resources

Educating a student with Batten disease presents unique and significant challenges to the child or teen’s family, his or her teachers, and to school administrators. Many are not familiar with Batten disease due to its rare occurrence and are unsure how to best meet the special needs of the student.

BDSRA provides materials and support services to help school systems learn more about how they can best serve students with Batten disease. Enhancing the student’s quality of life is our first and foremost goal.

Here is a sampling of some of the concerns raised by parents of children who have Batten disease:

“I’m confused as to what an Individualized Education Plan (IEP) should include for my child — where do I start?”

“My child is young — are there educational services for preschoolers with Batten disease?”

“My school isn’t following the IEP that we set up for my child — what should I do next?”

“My child has severe behavioral issues — how should the school address these?”

“I’m concerned about my child’s inability to fight infection and school environments are notorious for spreading germs — what are your recommendations during flu season?”

You can request the Juvenile Neuronal Ceroid Lipofuscinosis (JNCL) and Education books by reaching out to Patrick Kotnik, by phone at (614)973-6013 or email at patrick@bdsrafoundation.org. BDSRA and families contributed to the content that will be in the book by participating in an extensive online survey.

School Accommodations

The student’s special needs in the classroom will depend on where he or she is in the arc of the disease process and will vary greatly due to individual differences. Our premiere school resource, the “Teach and Be Taught” manual helps in educating members of the child’s education team: the family, teachers, principals, therapists, aides, bus drivers, other students and members of the child’s school and community network. It contains specific recommendations and suggestions for making a variety of accommodations in the school setting.

To order the “Teach and Be Taught” manual and contact Patrick Kotnik, by phone at (614)973-6013 or email at patrick@bdsrafoundation.org.

Although there is no known cure for Batten disease, the progression of the disease is well-documented and somewhat predictable, thus serving as the foundation for the guide content (although there are individual differences, as in any disease process). We encourage parents and caregivers to share as much information as possible pertaining to the child’s medical condition, his or her abilities, strengths, and limitations. Regular communication is a key component to optimizing your child’s success in the classroom.

Information & Advocacy in the School Setting

BDSRA staff can help you advocate for your child or teen in the school setting. To request help with a school issue or concern, contact Patrick Kotnik by phone at (614)973-6013 or email at patrick@bdsrafoundation.org. or by phone at 614-973-6013. We can assist families by writing a letter of support to the school staff and/or by being part of a school team meeting via phone conferencing.

Learn More about Batten disease & Share With Others

In addition to the “Teach & Be Taught” manual and information about Batten disease is available on our web site.  Stay connected to BDSRA on social media and help us to raise awareness by sharing BDSRA posts and tweets!

Helpful Links and Resources

Parents and Caregivers may join the BDSRA Closed Facebook by clicking here.  Our Batten families are experts and can provide timely advice and tips that have worked for them.  Keep in mind that individual differences and varying state laws and regulations may affect your child’s school situation.