Share your experience and help others
We’re proud to partner with the Child Neurology Foundation to conduct a survey to understand caregivers’ experiences raising children with neurologic conditions.
This Needs Assessment Survey is designed to identify stressors and areas of greatest need in our community. The results will be shared with the Pediatric Epilepsy Surgery Alliance (along with other advocacy partners and healthcare providers) so we can better serve our families.
Caregivers of children with neurologic conditions can complete the brief survey through May 3rd at: https://www.surveymonkey.com/r/PESA-24 or use this QR code:
Deadline: May 3, 2024
about the author
Audrey Vernick is our Director of Patient and Family Advocacy. She is the parent of a child who had hemispherectomy for seizures caused by stroke. She holds a level 2 certification in Special Education Advocacy Training from the Council of Parent Attorneys and Advocates and is certified by The ARC in future planning. She also serves on the International League Against Epilepsy’s Social Work and Social Services Section.