Team 1 — ICAN

President

Jaime Buzzeo

Born with Microphthalmia, Jaime understands firsthand the challenges of growing up without seeing others who looked like her or having a community that shared her experience. When she became President of ICAN in 2026, following Ryan McGrady's leadership, she embraced the opportunity to help build the support system she wishes to have known during her childhood. Jaime is dedicated to ensuring that every individual and family affected by Anophthalmia and Microphthalmia can find connection, resources, and a sense of belonging within the ICAN community.

Treasurer

Ryan McGrady

For many years, Ryan has been a driving force behind ICAN, dedicating countless hours to supporting the community and helping lead the organization's programs and annual conference alongside Erin Rosenberg. His commitment has helped shape ICAN into the resource it is today. While stepping back from his leadership role, Ryan will continue to be an active part of the ICAN family as Treasurer, attending conferences, and supporting individuals and families on their journeys.

Director of Development

Jonah Remz

As a father of a child (Bodie) with unilateral Anophthalmia, Jonah brings both personal experience and deep passion to his fundraising efforts for ICAN. Discovering ICAN provided him and his wife, Jenna, with a supportive community and the knowledge they needed to advocate confidently for their son. Inspired by the connections and encouragement they found—especially after attending their first ICAN conference—they asked themselves, “How can we help other families experience the same support?” Since then, Jonah has been dedicated to giving back and helping ensure that other families feel empowered, informed, and connected on their journey.

Director of Development

Jenna Silver

As a mother of a child (Bodie) with unilateral Anophthalmia, Jenna understands the emotions, questions, and uncertainties that many families face following a diagnosis. Through her family's journey, she discovered the power of community, connection, and shared experiences. Inspired by the support her family found through ICAN, Jenna has dedicated her time, energy, and compassion to helping other families feel less alone as they navigate their own paths.

Jenna is passionate about ensuring that every parent knows there is a network of people who understand and care. Her commitment to ICAN is rooted in the belief that no family should have to navigate Anophthalmia or Microphthalmia without support, encouragement, and hope for the future.

Director of Social Media

Kellie Hansen

Kellie has been a part of the community since 2022 when her daughter Kennedy was born with unilateral Microphthalmia. Feeling lost in the early days post diagnosis, she happened upon the MAPS Facebook page and her life was considerably changed for the better. She has solicited advice from strangers who have since become friends and sincerely understands the value and importance of the bonds created throughout this community. She is incredibly passionate about empowering her daughter to embrace her uniqueness and grow confidently into the bright star she was meant to be.

Kellie understands the magnitude of seeing others like you and being able to relate to individuals experiencing similar challenges. With this condition being so rare, she is dedicated to running our social platforms to be a safe place to share challenges and wins, stories and questions, and to relate to one another on a level most might not understand. She wants you to know you are not alone...we are all in this together!