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About

Finding Inspiration in Every Turn

Our Vision

Hunter’s Heart Foundation envisions a world where every child with Duchenne Muscular Dystrophy (DMD) can pursue a fulfilling and limitless life. We are unwavering in our commitment to:

  • Empowering boys and girls with DMD and their families through unwavering support and comprehensive resources

We firmly believe that every child with DMD possesses the potential to reach their full potential, and we are steadfast in our dedication to transforming this vision into a tangible reality.


Our Mission

Hunter’s Heart Foundation is a non-profit organization dedicated to enriching the lives of children battling Duchenne Muscular Dystrophy (DMD). We achieve this mission by providing comprehensive support and resources, championing research and treatment advancements, and raising public awareness about DMD.

A world beyond wheels race

Our Story

HHF came to life on January 14, 2021.  Our goal is to offer high-engagement programs designed to help individuals and their families. To bestow hope, education, and advocacy to thrive despite the challenges they are facing.

Our Team

Hunter’s Heart Foundation believes in the idea of leading by example. We are fortunate  to have a leadership team that strives to embody this principle in everything we do.  This starts with being “heart” focused which means caring deeply about the people we serve and the work we do. Our goal is to do our work to the best of our ability to help those in need, especially the thousands of people who struggle with DMD.

Karen Guillemno

Karen Guillmeno

Founder

Rashana Lauderdale

Rashana Lauderdale

CFO

Tenisha Ford

Tenisha Ford, AMFT

Board Member

Carla Pickett

Board Member

Jazmine

Jazmine Oliver, MD

Board member

Leslie Parque

Leslie Parque, M.A,

Board Member

Dr. Leigh Ramos-Platt

Board Member

Sima Perez

Sima Perez

Board member