Learn how to partner with "The Zebra & The Bear" Film Team to spark meaningful change in the perceptions around rare disease, how rare disease therapies are developed, and most importantly, how we might ease pain for the families dealing with rare diseases.
In addition to the opportunities to partner below, download the full Partnership Kit to learn more about our:
⭐️ Impact Campaign Goals
⭐️ Partnership Goals
⭐️ Share what you are working on with us
⭐️ Schedule a one-on-one chat with our team
By hosting a screening you are joining a network of rare disease advocates who are using the film to strengthen their work in the rare disease world. We’ll share exclusive updates with you when the film is ready so you can either host a screening or join us for a screening of The Zebra & The Bear.
Fill out a screening request form here or write us at zebraandbear@rocofilms.com. Pricing for screenings varies and customizable options are available.
Let's make a difference, together.
If you know someone who might want to join our efforts, you can share this Partnership Inquiry Form, or direct them to ROCO Films at zebraandbear@rocofilms.com.
The more people we reach, the more impact we have.
Follow and/or tag us:
Facebook: https://www.facebook.com/zebrabearfilm
Instagram: https://www.instagram.com/zebrabearfilm
"The Zebra & The Bear"
“That line gave me chills twice: "turns out, she might just change the world."
“I find that so tender – even knowing from day 1 that it may not help her own daughter from day 1, that she was willing to fight for other children diagnosed in the future. So so tender.”
“This is a really honest conversation that our parents need to hear.”
“ This is hard, but I'm glad you're including this. No one ever talks about the strains on the family. I've known so many rare disease couples that divorce.”
UT Southwestern Medical Center
“I’m in tears… a powerful witness to a mother’s commitment to finding a cure as a part of her daughter’s legacy.”
“A story about love, commitment, family and compassion.”
For updates on the film & ways to spark positive change in the lives of families dealing with rare disease.