We are a small but mighty bunch that is blooming with passion for girls and boys suffering from Rett Syndrome. We are always looking to add to our team. 

Please contact us if you would like to get involved!

Roger Brooks

Chief Operating Officer & Rett University Director

Roger has worked extensively in the retail, restaurant, and franchise arenas designing and developing training for corporations. Roger lives in Irving, Texas, with his wife and two beautiful daughters; Juliana, who has Rett Syndrome, and Olivia.


Kevin Pierce

Director of Development

Kevin joined the GP2C team in February 2018 after a 30 year career with The Boeing Company, including technical development and project management of large scale defense and space systems. Kevin resides in Huntsville, Alabama, with his wife Sonja.  Kevin’s daughter and son-in-law, Brittany and Ben Goodman, and granddaughters Blakely (who has Rett Syndrome), Andi Mac and Emmy Jo, reside in Nashville, Tennessee.

“From the day we received Blakely’s diagnosis in 2014, we have seen GP2C empowering families worldwide with the knowledge and tools needed for our daughters and granddaughters to be successful.  I’m excited to be a part of this team as we not only help families with today’s needs, but also support the exciting journey to tomorrow’s cure.”



Amei Prachthauser

Program Manager

Amei joined our team in 2014. A New Jersey native, she enjoys spending time with her son, Dominic, family and friends. Amei has nine plus years planning and executing events at some of the Southeast's leading resorts and a strong customer service background. Amei brings a genuine passion to raising awareness and helping to raise funds to support families, educate and provide research to cure Rett Syndrome. 


Jenny Tesler


Family Support and Advocacy

Jenny Tesler is a writer, blogger and active advocate for her daughter Magnolia, living with Rett Syndrome. She resides in Los Angeles, CA with her husband AJ and their two kids. You can find her writing about her family’s life adventures with Rett Syndrome at

“The Girl Power 2 Cure community has been a life line to families living with Rett Syndrome. Their focus on education, communication and living life, is truly inspiring. I am happy to be joining the team.”


Carolyn Fowler


Family Support and Advocacy

Carolyn and her husband Stephen, along with their three children Evelyn (who has Rett Syndrome), son Ellis, and newest addition Merrit, reside in the Washington DC area. Carolyn has worked for 15 years in caring for children of all abilities and as a support to their families. Once her daughter Evelyn was diagnosed with Rett Syndrome, in October of 2017, she has made it her mission to give her daughter a voice as she and her family navigate this journey. Joining the Girl Power 2 Cure Team is an honor as she joins the cause in finding a cure- for Evie and all those affected by Rett.



Kristi Henderson

Support Coordinator

Kristi is a lifelong resident of Amelia Island. She is a mother to two wonderful girls, Kenzi and Kaisen. With a strong background in customer service and office management she plans to do her part in helping Girl Power 2 Cure continue to grow and fight for a cure.

“You can’t meet one of our girls or boys without falling in love. The light in their eyes makes coming to work every day a joy. It’s a privilege to spread awareness about Rett Syndrome and to be a tiny part of finding a cure.”





GP2C is the most inspiring organization I've ever encountered! Not only does it provide funding but it provides support and LOVE!

— Rachel Dalton