Founders

Catrina Byrge’s granddaughter, Brie, was diagnosed with Polymicrogyria at three weeks of age. She sought to find out more information about PMG and was appalled at the lack of information and support that was available. She came to the realization that an organization such as PMGA was greatly needed. With over 20 years of nursing experience, as well as prior experience working for nonprofit organizations, Catrina had a clear vision for the PMGA Organization and helped to create the mission we continue to focus on today. She served a three-year term as President and Chief Executive Officer from 2012 to 2015.

Brandy Davis, is the mother to Brie, who was diagnosed with Polymicrogyria shortly after she was born. Brandy’s experience as a Finance Coordinator for a major national nonprofit organization for children in the Northeast Florida area and her heart for helping children gave her the expertise to help create the PMGA Organization. Her strong desire to bring about awareness of PMG and to assist other families struggling with PMG related issues was the reason she worked so tirelessly to create this organization. She served a four-year term as PMGA’s Vice President and Treasurer from 2012 – 2016.

Mel Rush, is the mother to Luke, who was diagnosed with Polymicrogyria while she was still pregnant (extremely rare) due to Luke’s enlarged skull on ultrasounds. Mel’s experience with PMG is different than most because she knew and had some resources available to her and Luke at birth. However, even with that knowledge, she soon found that it was only a drop in the bucket. There was so little information available, and what she did find was mostly technical medical papers that she didn’t understand. It is Mel’s greatest wish that when someone else tries to find answers, that PMGA will be there to help them find the information and resources they need. As a dedicated teacher, Mel has a very special place in her heart for children. She served a two-year term as PMGA’s Secretary from 2012- 2014.

Brie was Brandy’s daughter and Catrina’s granddaughter. She, along with all those affected by PMG, were the founder’s inspiration to create the PMG Awareness Organization with the hope that one day, a cure will be found. Until then, PMGA will work together to bring about awareness, to support research, to educate the public and to advocate for all those whose lives have been or will be affected by Polymicrogyria in the future. Together, we can all make a difference!