Welcome to the
#MoyraStrong Foundation
At the MoyraStrong Foundation, we believe no family should have to navigate a complex medical journey alone.
Founded in honor of our daughter, Moyra, our mission is built from lived experience. We understand the overwhelming challenges that come with epilepsy, rare genetic disorders, and complex medical conditions—not from reading about them, but from living them every day. We know the sleepless nights, the endless appointments, the insurance battles, the uncertainty, and the fierce love that drives parents to keep fighting for their children.
Moyra's life inspired this foundation. Though her time here was far too short, her impact was immeasurable. She taught us about resilience, courage, joy, and the power of hope. Through her legacy, we are committed to helping other families access the resources, support, and advocacy they need when they need it most.
The MoyraStrong Foundation works to provide assistance for medical equipment, therapies, treatments, and other essential needs that are often denied, delayed, or inadequately covered by insurance. We also strive to raise awareness, educate communities, and advocate for families facing the challenges of rare diseases and complex medical conditions.
Whether you're a family seeking support, a healthcare professional, a donor, a volunteer, or simply someone who wants to make a difference, we welcome you to join us in our mission.
Together, we can ease burdens, create opportunities, and remind families that they never have to fight alone.
Welcome to the MoyraStrong family.
"Built from lived experience to support families navigating epilepsy, rare genetic disorders, and complex medical conditions."
💜🌻 Because every child deserves hope, every family deserves support, and no one should face the journey alone. 💜🌻
Empower. Advocate. Support.
Upcoming Events
The Vision Behind MoyraStrong
The MoyraStrong Foundation was created in honor of my daughter, Moyra Nichole Danaher, whose strength, joy, and light continue to inspire us every day. Moyra was born with a rare genetic disorder that caused severe epilepsy and complex neurodevelopmental challenges. Despite these hardships, she lived with a radiant smile, a brave spirit, and a heart that touched everyone she met.
Moyra’s journey taught us how isolating and overwhelming it can feel for families navigating rare epilepsies and neurodevelopmental disorders. She also showed us how much love, advocacy, and support matter in making life fuller, even in the hardest circumstances.
Through the MoyraStrong Foundation, we want to carry forward her legacy by supporting children and families living with rare epilepsies and neurodevelopmental conditions. Our mission is to provide resources, raise awareness, and create a community where no family feels alone in their fight.
We are honored to walk alongside dear friends at Olivia’s Light, another foundation born out of love. Moyra and Olivia both faced the same rare diagnosis, and heartbreakingly, both girls passed away too soon. Our families have come together in grief, love, and purpose—committed to building something bigger than ourselves, so their lights will never fade.
MoyraStrong exists so that every child like Moyra and Olivia is seen, supported, and celebrated. Their stories are not just of loss, but of resilience, hope, and a reminder that even the smallest lives can leave the biggest impact.
- Marya Danaher, President of MoyraStrong Foundation
Our mission is to create a supportive community while raising awareness about neurological disorders. Together, we can make a difference in the lives of those affected by these conditions.
Our Team
Meet the dedicated individuals behind the MoyraStrong Foundation. Each member brings unique skills and passion to support our mission of helping those in need.
Marya Danaher a.k.a. Moyra's Mom
Founder / President
Marya Danaher is the founder and president of the MoyraStrong Foundation, created in honor of her daughter, Moyra Nichole Danaher. She is also the author of Moyra's Big Purple Day, a children's book inspired by Moyra's journey that promotes awareness, understanding, and inclusion for children living with epilepsy and rare disorders.
Above every title she holds—Founder, President, advocate, or children's book author—Marya is, first and forever, Moyra's Mom. As Moyra's primary caregiver, she spent two and a half years navigating the world of rare disease, epilepsy, complex medical care, hospital stays, therapies, and advocacy, fighting every day to give her daughter the best life possible.
After Moyra's passing in October 2024, Marya made a promise that her daughter's story would continue to make a difference. That promise became the MoyraStrong Foundation, dedicated to supporting families facing epilepsy, rare genetic disorders, and complex medical conditions through resources, advocacy, education, and hope.
For Marya, this foundation is more than a nonprofit—it is the continuation of Moyra's legacy. Every family helped, every fundraiser, every book shared, and every act of service is done in her daughter's honor.
"I am, and always will be, Moyra's Mom. This foundation isn't just my mission—it's my promise to my daughter that her light will continue to shine in the lives of others."
Sean Danaher a.k.a. Moyra's Dad
Vice President
Sean Danaher serves as Vice President of the MoyraStrong Foundation and is the father of Moyra and Evan. As a member of the board, he supports the foundation's mission of helping families affected by epilepsy, rare genetic disorders, and complex medical conditions. He assists with fundraising efforts, community events, and initiatives that honor Moyra's legacy while helping ensure other families have access to resources and support.
"Serving on the MoyraStrong Foundation Board is deeply personal to me. As Moyra's father, I know firsthand how difficult it can be to obtain the equipment, therapies, and support a child with complex medical needs requires. I serve on this board to help other families facing those same challenges. By honoring Moyra's life through this foundation, I hope we can make the journey a little easier for others and ensure her legacy continues to make a difference."
Linda "Suzie" Taylor
Secretary
Linda "Suzie" Taylor serves as Secretary of the MoyraStrong Foundation. She is Moyra's aunt and a proud mother of three. Throughout Moyra's life, Suzie played an active role in supporting her care and was a source of love and encouragement for both Moyra and her family. She is dedicated to preserving Moyra's legacy by helping the foundation provide hope, support, and resources to families facing epilepsy, rare genetic disorders, and complex medical conditions.
"I am Moyra's aunt, and helping care for her changed my life. Watching her strength and the love that surrounded her inspired me to continue making a difference in her honor. Serving on the MoyraStrong Foundation Board allows me to help keep Moyra's memory alive by supporting families who are walking a similar path."
Heather Strauser
Director
Tabatha Limbert
Director
Jennifer Young-Doseck
Director
Patrick Ollhoff
Director
Mandy Jackson
Director
Derek Ricker
Director
Matthew McBride
Treasurer
Matt McBride serves as Treasurer of the MoyraStrong Foundation. He holds an Associate's Degree from ITT Technical Institute in Maintenance Management and brings both professional experience and personal perspective to the foundation. As the father of a daughter who experienced seizures, Matt understands the uncertainty and challenges families can face when navigating complex medical needs. He is committed to helping ensure the foundation remains financially strong so it can provide meaningful support, resources, and hope to families who need it most.
"As the father of a daughter who experienced seizures, I understand how overwhelming the journey can be for families. I wanted to use my time and skills to help others facing similar challenges. Serving on the MoyraStrong Foundation Board allows me to honor Moyra's legacy while helping provide families with the support, resources, and hope they deserve."