Megan DeJarnett was diagnosed at the age of 2 with Spinal Muscular Atrophy (SMA). SMA is a genetic neuromuscular disorder that affects motor neurons in the spinal cord causing progressive muscle degeneration and weakness. The life challenges that Megan has faced with a neuromuscular disease are more difficult than more people. With a tremendous faith in God and the love and support of her family, Megan lives life determined to experience life to the fullest and choose joy over despair.
Megan’s passion is motivating others to approach life with an ‘I can do this’ attitude. Her ability to share her story and encourage others to look at life through a new lens is only one of her tremendous gifts.
Megan’s proudest personal accomplishments are as a wife and a mother. Megan, along with her husband Jake, are raising two sons in Nashville, TN. Jake is a professional musician and when either of them travel, the entire family goes alone. Their sons, Brox and Shai, are always in tow and part of everything they do.
For Megan, life is providing amazing family, friends, and an inspiring story about overcoming improbabilities. Let her story be an inspiration for you and your organization. Please contact her by filling out the form on this website.
We are so thrilled for your interest in contacting Megan DeJarnett. Whether it be a fundraiser, business conference or church event, Megan has a passion for sharing her story to inspire others to live life without limits!
"NO SUCH THING"
Megan DeJarnett is the organizational founder of No Such Thing, a company with a mission to help others redefine purpose by removing defining labels. As an author, she is currently producing a series of children’s books.