Toolkits / Care Books
Toolkits are sets of information, collected together by category, to facilitate the ease of understanding how to successfully interact with various aspects and elements of epilepsy and those affected by epilepsy.
Featured Resource
Epilepsy and My Child Toolkit
by National Epilepsy FoundationThe Epilepsy & My Child Toolkit: A Resource for Parents with a Newly Diagnosed Child provides parents with a general introduction to epilepsy and addresses the most common concerns a parent has when their child is newly diagnosed with epilepsy. They are one of our most valuable assets in the on-going effort to enrich the lives of children living with epilepsy.
| Title | Author | Phase | Description |
|---|---|---|---|
Epilepsy and Seizure Disorders: A Resource Guide for Alaska’s Parents
|
UAA Center for Human Development, University of Alaska Anchorage | II |
A resource guide for parents in Alaska. |
Wisconsin Care Notebook
|
Wisconsin Seizure Control Network | I |
A toolkit with forms to help parents keep track of their child’s medical information, special needs, and services. |
West Virginia Spread the Word Informational Resource Guide
|
West Virginia University Children’s Hospital; National Epilepsy Foundation | I |
An information resource guide for parents of children with epilepsy. Includes forms and other tools. |
New Jersey Spread the Word Family and Physician Toolkit
|
Epilepsy Foundation, New Jersey | I |
A toolkit that provides resources and tools for parents |
