Our Story

Jeffrey Irwin has served as Executive Director of the Epilepsy Association of Western New York (EAWNY) since 2013, leading the organization’s efforts to empower, educate, advocate for, and support individuals and families affected by epilepsy and seizure disorders throughout Western New York. He oversees programs and services that promote independence, improve quality of life, increase access to critical resources, and foster greater understanding of epilepsy within the community.

A lifelong Western New York resident, Mr. Irwin earned his master’s degree from Canisius University and brings extensive experience in nonprofit leadership and community-based services. He is dedicated to strengthening collaborative partnerships, expanding public awareness, reducing the stigma surrounding epilepsy, and ensuring that individuals living with epilepsy have access to the education, support, and advocacy they need to thrive.

Outside of work, Mr. Irwin enjoys traveling, spending time outdoors, hiking, and exploring new places with his dog, Paxten.

A New York State Licensed Clinical Social Worker, Cheryl Best has been a dedicated member of the Epilepsy Association of Western New York since 1985. She provides counseling, education, advocacy, and support to individuals and families affected by epilepsy and seizure disorders, helping them navigate challenges such as adjusting to a diagnosis, anxiety, depression, relationships, grief, parenting, career concerns, self-esteem, seizure safety, and building resilience. Cheryl also connects individuals with valuable community resources, including healthcare providers, financial assistance, transportation, scholarships, OPWDD services, and recreational and vocational programs.

In addition to counseling, Cheryl conducts weekly outreach visits to the Epilepsy Monitoring Unit at Golisano Children’s Hospital, facilitates virtual support groups and social events, and works to ensure individuals and families feel informed, connected, and supported. She considers it a privilege to have served the epilepsy community for more than 40 years and continues to be inspired by the strength and resilience of the individuals and families she meets. Outside of work, Cheryl enjoys spending time with her husband, their two grown children and their spouses, hiking, boating, gardening, painting, and caring for her beloved cats.

Alexandra Franco supports clients through advocacy, education, and community outreach, helping people feel informed and connected throughout their care journey.

For more than 22 years, Renay has served the Epilepsy Association of Western New York as Information Services Coordinator, Race Director, and former Epilepsy Conference Director. She is dedicated to advancing the Association’s mission by increasing epilepsy awareness, reducing stigma, and improving community safety through education. She provides seizure recognition and first aid training for schools, organizations, families, and community members, helping ensure that individuals living with epilepsy are better understood and supported.

In addition to coordinating community outreach initiatives and special events, she researches, writes, and produces the Association’s annual newsletter, The Epigram, connecting the community with educational resources, advocacy efforts, and stories of hope. Her work reflects a longstanding commitment to empowering individuals and families affected by epilepsy through education, awareness, and support.

Outside of work, she has been happily married to her husband, Joe, for 41 years and is the proud mother of two sons and grandmother of two grandchildren. She enjoys traveling, attending live concerts, reading, and spending time with family and friends.

Lynn has been a dedicated member of the Epilepsy Association of Western New York since 2007, advancing the organization’s mission by providing compassionate support, education, and guidance to individuals living with epilepsy and seizure disorders and their families. Before joining the Association, she spent 16 years working in a residential program supporting individuals with developmental disabilities, including many affected by epilepsy.

Drawing on more than three decades of experience, Lynn empowers individuals and families with the knowledge, resources, and support they need to navigate the challenges of epilepsy with confidence. She provides education, answers questions, addresses concerns, and connects people with services that promote independence, enhance quality of life, and strengthen community support. Lynn proudly serves individuals and families throughout Chautauqua, Cattaraugus, and Allegany counties.

Nancy Brown serves as the Administrative Assistant at the Epilepsy Association of Western New York (EAWNY), where she plays an essential role in supporting the organization’s mission of improving the lives of individuals and families affected by epilepsy and seizure disorders. By coordinating daily operations and providing administrative support across programs, services, and community outreach efforts, Nancy helps ensure the Association remains responsive, organized, and accessible to those who rely on its services.

Outside of the office, Nancy enjoys planning her next travel adventure and exploring new destinations. She also treasures spending time with her family, whose support and encouragement inspire her commitment to helping create a welcoming and compassionate experience for everyone who connects with the Association.

Allie Roesch has worked in the mental health and human services field since 2012, bringing extensive experience supporting individuals and families through life’s challenges. She joined the Epilepsy Association of Western New York in July 2024 as a Support Counselor and Community Advocate, where she advances the Association’s mission by providing compassionate counseling, education, advocacy, and resource navigation for individuals living with epilepsy and seizure disorders. Her work helps empower people to better understand their condition, overcome barriers, access essential services, and improve their quality of life.

In addition to her role at the Epilepsy Association, Allie serves as a Care Advisor at PinnacleCare, helping clients navigate complex healthcare decisions with empathy and expertise. Outside of her professional roles, she enjoys traveling, spending time with her husband, and exploring new adventures with their rescue Standard Goldendoodle, Craig.