Board of Directors & Officers
Meet our talented and passionate team, driven and focused on moving forward the mission to drive research and raise awareness around HNRNPH2 genetic mutations.
TRISH FLANAGAN - CO-FOUNDER, BOARD DIRECTOR & PRESIDENT
![]() Trish is a passionate co-founding member of the Board of the Directors for The Yellow Brick Road Project and mom to Morgan, touched by an HNRNPH2 mutation. A seasoned Early Childhood Educator, she earned her Bachelors Degree of Science from Penn State University majoring in Human Development and Family Studies with an Early Childhood focus. Her first role working with children was within the Child Life Program at Westchester Medical Center in NY providing play experiences to children as well as offering psychosocial support to their families. She went on to earn her Masters Degree in Early Childhood Education from the College of New Rochelle and resides and teaches in the suburbs of New York. |
HAIM FARKASH - CO-FOUNDER, BOARD DIRECTOR & VICE PRESIDENT
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PAULA TYSON – CO-FOUNDER, BOARD DIRECTOR & SECRETARY & TREASURER
![]() Paula Cole Tyson is a dedicated co-founding member of the Project and devoted mother to Lillie, a beautiful little girl impacted by an HNRNPH2 genetic variation. She is currently a Compensation Consultant and Analyst at ChaseCompGroup. Before joining the firm in 2011, she worked independently for consulting and other service firms, assisting in client relations, account management, and accounting functions. Prior to her independent work, she worked for a private company for six years in personnel management and client relations and began her career as an analyst and consultant for Watson Wyatt (now Towers Watson) in the areas of human resources and organization effectiveness. She obtained her Bachelor’s degree in Romance Languages from the University of Georgia, graduating Magna Cum Laude. |
ROBERT GLENN – BOARD DIRECTOR, HEAD OF TECHNOLOGY
![]() Robert "Bobby" Glenn is devoted father to Rose and member of the board of directors. He studied Molecular and Cellular Biology at the University of Colorado, Boulder, but ultimately found his passion working in various roles in business development and marketing in the tech industry. Robert was first introduced to HNRNPH2 when his daughter, Rosie, was diagnosed in 2019. He's watched his determined daughter work hard for every little achievement, and is so proud of her accomplishments. As the Director of Marketing and Communications, Robert is committed to leveraging his experience for raising awareness for HNRNPH2, along with other orphan diseases. His goal is to raise funds in order to further develop research into this new genetic mutation. |
STACY PADDON – BOARD DIRECTOR, INTERNATIONAL OUTREACH COORDINATOR
![]() Stacy Paddon is determined to help her daughter Cady and all those affected by HNRNPH2 mutations to live the best lives they can. She currently works for the Business Intelligence team at Christie's auction house in London, having previously spent time in the company's Human Resources office where she managed European recruitment. She has previously held management positions at the National Trust, the Vancouver 2010 Olympic and Paralympic Winter Games Organizing Committee and ING Insurance. She holds a Bachelor of Journalism degree from Carleton University with Combined Honours in Political Science and is a Chartered Insurance Professional. |
NEENA KANTARIA – BOARD DIRECTOR, COMMUNITY ENGAGEMENT & FUNDRAISING
![]() Neena Kantaria is the loving aunty to Amara (her niece), who has an HNRNPH2 mutation. She is deeply passionate about making a meaningful difference in the lives of those impacted by this ultra-rare condition. Neena currently works as the Director of Strategic Operations for TEAM Services Group and holds her Master’s in Project Management from USC. In addition to her professional career, she is committed to raising awareness and ensuring HNRNPH2 remains in the spotlight— believing that visibility is the first step toward progress. She actively leads fundraising efforts and champions opportunities that bring global attention, resources, and support to the HNRNPH2 community. |