Contact: zebraandbear@rocofilms.com
Join our community of allies and advocates to make an impact on the lives of families who have children with rare diseases by hosting a screening of THE ZEBRA & THE BEAR.
spark meaningful change
Hosting an in-person or virtual screening with others is a powerful way to build & strengthen community, and create collective change in the lives of families with children navigating rare disease.
Advocates. Allies. Rare Disease Families. Educators. Organizational Leaders. Non-Profits. Students. Doctors. Researchers. Scientists. Changemakers.
YOU.
- Debbie, MSD Grandmother
Shares the real story of families with a child who has a rare disease
Inspires to move you from apathy to action
Celebrates the power of love in navigating the impossible
Reminds you of your capability to make change in the world, every small step you take
How could THE ZEBRA & THE BEAR serve as a tool to support your work and mission? How can we support the families dealing with rare disease, together?
Share your screening ideas with our film team & learn about pricing options using the form below (can’t see the form? use this link) or email our Impact Team at ROCO Films: zebraandbear@rocofilms.com. We offer custom rates for non-profits and the film is available to watch complementary for families. We can co-create an event for your audience:
✨ in-person, virtually, or a hybrid
✨ with Filmmaker Q&A
✨ with support tools to self-lead your screening
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
“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.