In honor of a young woman named Eva and thousands of those who suffer from a fatal genetic disease called Cystic Fibrosis, I am sending this message to you.
Because many had never heard of Cystic Fibrosis, Eva made it her duty to change that.
May is Cystic Fibrosis Awareness Month, and in honor of Eva I wanted to continue her wish......a film to launch an international movement for organ donation and Cystic Fibrosis awareness.
The US Television Premier (65_RedRoses) will air on the Oprah Winfrey Network, OWN Documentary Thursday May 3rd 9/8c.
Watch the preview below.
|65_RedRoses - Trailer - OWN Documentary Club - Oprah Winfrey Network|
Because the Cystic Fibrosis Foundation receives no government funding, it must rely soley on individuals and corporations to help advance the cause. To learn more about Cystic Fibrosis and how you can help please visit: http://www.cff.org/