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 |
|---|---|---|---|
Florida Care Notebook
|
Epilepsy Foundation, Florida | II |
This Web page contains forms and tools for parents, including seizure action plan , medical ID care, seizure log, medication list, medical history, and family resources. |
|
Washington Epilepsy Care Organizer – English and Spanish
|
Washington State Department of Health | II |
Helps parents organize their child’s medical documents, contact information records, etc. Includes user-friendly forms in English and Spanish. |
New York Care Book- English and Spanish
|
Epilepsy Foundation, Metropolitan New York | II |
Includes care plans, log forms, seizure action plans, medication list forms and other tools to help parents manage their child’s epilepsy. In both English and Spanish. |
Epilepsy and Seizure Disorders: A Resource Guide
|
Dartmouth-Hitchhock Medical Center | II |
A resource guide for parents. Includes charts and forms and quick tips. |
