Hunt Hollis
Hunt is a happy, curly headed ten-year old who is full of life despite his diagnosis of Mitochondrial Disease. He is our inspiration and the driving force behind our efforts to improve the quality of life for children and families who have special needs.
Our Mission
Team Hunt is dedicated to serving families whose lives are affected by diagnosis of disease or disability. We support therapy programs, offer hope and create awareness of what’s possible through adventuring outside.
INSPIRED BY HUNT
The Hunt Michael Hollis Fund
The Hunt Michael Hollis Fund supports families who have loved ones with mitochondrial disease, developmental delays, and special needs through raising awareness and money to help find a cure and to provide various therapy programs.
About
We're in this together.
Team Hunt was created in January 2011 by Ellen and Michael Hollis to honor their son Hunt. Hunt Michael Hollis has mitochondrial disease which is a chronic, genetic disorder that occurs when the mitochondria of the cell fails to product enough energy for cell or organ function. This is associated with slow growth and developmental delays. Hunt receives many therapies including feeding, speech, occupational, and physical therapy. He is a happy, lovable, curly headed ten-year old and full of life. Inspired by Hunt, we work to improve the quality of life for children who have special needs by supporting therapy programs.
We want to spread the message of hope and create awareness of what’s possible regardless of circumstance through a combination of fundraising to support therapy programs and providing resources to families to make exposure to the outdoors more accessible. Hunt’s doctors said he wouldn’t walk, and now he’s not just walking, but thriving through a combination of traditional therapies and exposure to the therapeutic benefits of exploration and adventure. We invite you to join us in celebrating the everyday victories, compiling resources for families whose lives are affected by disease and disability, and helping to show that adventure is accessible no matter the limitations.
Our Impact
Since 2011, Team Hunt has raised over $500,000 to support life changing initiatives locally and nationally. From donating supplies and building new treatment rooms to funding electronic medical record systems and partnering with the Make-A-Wish Foundation, our goal is to support children and families with special needs however we can.
500,000
Raised
4
Therapy Clinics & Programs Funded
50
Walks, Runs and Triathlons
1
Wish Granted
Video
Not A Statistic
In 2013, Filmmaker Shelby Hadden spent some time with our family to document our daily life and struggle with mitochondrial disease, our fight to find a cure, and our passion to make a difference in the lives of others fighting disease and disability.
Important Note Regarding Funding
Team Hunt and Team Hunt Adventure are the driving force and fundraising efforts behind The Hunt Michael Hollis Fund of The Community Foundation of Middle TN. The Hunt Michael Hollis Fund supports families who have loved ones with mitochondrial disease, developmental delays, and special needs through raising awareness and money to help find a cure and to provide various therapy programs. We are a 401c3 non-profit and none of the money we raise goes towards Hunt’s therapies, medical needs, or our travel.
