About
Glanzmann Thrombasthenia: Our Board Members
Glanzmann's Research Foundation is a beacon of hope for those affected by Glanzmann Thrombasthenia (GT). Our board members, who hail from across the U.S., have personal experiences with GT, making them passionate advocates for our cause. Meet these inspiring individuals below:
Peter Zdziarski
President
Peter was one of the first patients diagnosed with Glanzmann Thrombasthenia in Massachusetts. He understands the power of community and is dedicated to ensuring that no one with GT feels alone.
Melissa Zdziarski
Support Services Director
Melissa's son, Peter, was diagnosed with Glanzmann Thrombasthenia 34 years ago. She found support in the GT community and is honored to serve on the board, hoping to make a difference for GT families worldwide.
Sherry Crutchfield
Board Member
Sherry was initially misdiagnosed with Von Willebrand's disease. After her correct diagnosis of Glanzmann Thrombasthenia, she found a family in the GT community and is honored to serve on the board.
Cris Swain
Board Member
Cris, an educator with a daughter diagnosed with Glanzmann Thrombasthenia, has found support and solace in the GT community. She is honored to contribute to the cause as a board member.
Emily Kichline
Board Member
Emily was diagnosed with Glanzmann Thrombasthenia at 2 months old. The GRF has been a major source of support and motivation throughout her life, and she is honored to serve on the board.
Aidana Plummer
Board Member
Aidana, along with her brother, has GT. She is thrilled to be a part of the Glanzmann's Research Foundation and contribute to the GT family.
Gretchen Plummer
Board Member
Gretchen, mother of two children with Glanzmann Thrombasthenia, is honored to serve on the board of the foundation started by her friend Helen Smith.