My Nonprofit Reviews

Our journey started on November 15, 2018 when our then 4 1/2 year old son was diagnosed with epilepsy. His preschool had to call 911. This day was terrifying and we had no idea what we were about to embark on. I remember leaving the doctor's office trembling, scared, and lost. I am a social worker so I knew there had to be an agency that could help us. I found ESF and they have helped support us since the day we contacted them. It means everything to us to know other families who are experiencing what we are and an agency that helps connect us together. ESF also provides information, support, advocacy and knowledge. We have participated in events and the awareness walk. This agency is critical for families. This I can not say that enough. We so appreciate all they have done and what we can do in the future to give back. Continued awareness, advocacy, and services are needed for families who have a child diagnosed with epilepsy. Thank you to all at ESF!