Cranio Cutie is a 501(c)(3) that is served by a board of Directors. Cranio Cutie board members are volunteers who willingly give up their time to forward the mission of Cranio Cutie.
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Megan Ward, President
Megan is the founder and President of the Cranio Cutie Foundation. She is the mother of two children, Annie and Silas. Megan understands the impact Craniosynostosis can have on the whole family, since her daughter, Annie was diagnosed at birth. Megan is a graduate of Kansas State University and has her Masters in Social Work from University of Kansas. She loves spreading awareness, supporting families of children with Craniosynostosis and partnering with the Craniofacial Clinic and Children’s Mercy Hospital in Kansas City. Contact Megan. Penny Lyons, Vice President
Penny Lyons has served as the Vice President of Cranio Cutie since its found in 2014. Penny attended Oklahoma State University and has served on many boards and volunteered at many community and charity events. Penny lives with her husband Steve in Baldwin City, KS and has 2 grown children and 2 grandchildren. Cam Brennan, Board Member
Cam is a husband and father. He is pleased to serve on the Cranio Cutie board because of his relationship with The Ward’s and their sweet little Daughter Annie. He also runs a social media consulting company and a podcast network. Hannah Carlisle, Board Member
Hannah is a home health nurse excited to serve on this board. She see's the impact a community can have on the outcomes from medical procedures and diagnoses, both good and bad. Working with Cranio Cutie, it is her desire to help cultivate a positive community for all of those involved. Her family has been involved in the organization since it began and shares the same desire to be a positive influence on the world around us. Christy Hoskins, Board Mem
Christy Hoskins is a wife and is a mother to three children, Jacob, Grace, and Elijah. Christy worked in financial services for 15 years prior to staying home with her children. Christy witnessed first hand the impact on a child and family that comes with Craniosynostosis diagnosis. She seeks to create community awareness as well as support families of children with Craniosynostosis. Rob Wonnel, Board Member
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