The Sunshine Dreamer Horizontal Poster

Our Why

Our Goals

With the release of The Sunshine Dreamer, we hope the audience gains insight into what it’s like to live with or be affected by a rare disease and why accessible and equitable stem cell therapy is so necessary.


In The Sunshine Dreamer, viewers are invited to witness the inspiring story of Ryan’s life with Duchenne Muscular Dystrophy (DMD) and the groundbreaking potential of stem cell therapy. In this film, you will hear from Ryan, The Benton Family, doctors, researchers, other families affected by rare diseases, and more.

This film illuminates a path forward in advocating for stem cell therapy as the standard of care for those with DMD and other rare diseases. With a compelling blend of personal anecdotes and expert insights, The Sunshine Dreamer exposes the harsh reality of all the red tape that hinders widespread access to this life-changing treatment. Through poignant storytelling, it sheds light on the urgent need for pharmaceutical reform and increased awareness to make stem cell therapy the standard of care for DMD and other rare diseases.

Ultimately, The Sunshine Dreamer is a call to action, urging the audience to join the movement in advocating for accessible, equitable stem cell therapy. By amplifying the voices of those touched by DMD and showcasing the profound difference stem cell therapy can make, the documentary sparks dialogue, ignites passion, and inspires change on a global scale.

Behind The Scenes

Check Out Our Sizzle Reel For The Sunshine Dreamer

This is the Sizzle Reel for The Sunshine Dreamer. This is a concept piece to assist with our initial funding and film production.