Whatch the film. Join the movment. #4Eva
 

Support Cystic Fibrosis

At 23 Eva Markvoort  started an online journal, sharing her story of living with the fatal genetic illness cystic fibrosis, while on the wait list for a life-saving double lung transplant.

Eva’s online name was 65_redroses – from “65 Roses” – a term coined by child CF sufferers who couldn’t pronounce cystic fibrosis. Eva added ‘red’ because it was her favourite colour.

When  Eva agreed to open up her life and that of her family’s for the documentary 65_RedRoses she gave a gift to the world. Eva believed that after seeing her film and witnessing her struggle with cystic fibrosis, people would finally understand the importance of supporting CF research and awareness, as well as be inspired to become an organ donor.

Eva knew that a transplant would never cure her CF, but wanted what was most important to her – more time to spend with her loving friends and family.The film records her excruciating wait, the contrasting emotions of excitement and fear as her pager goes off, her transplant and road to recovery.

Eva experienced two years living life to the fullest before her body rejected her lungs and she was listed for a second transplant. During those two jam-packed years she was an inspiration for all those living with CF, and throughout it all she kept her blog going. Even when she knew the end was near. In her own words: “this is the end of my life, but it is not the end of my love. It is not the end of the story.”

Eva’s breath finally ran out on March 27th, 2010. Her legacy lives on. In the documentary, in her site and through the love that is being shared around the world as her campaign for CF awareness and organ donation grows. Please support her movement. #4Eva. Buy the DVD and help us spread the campaign. Contact us  at outreach@65RedRoses.com for bulk orders of the DVD and other campaign materials at a discount.

Cystic Fibrosis

Cystic fibrosis is a multi-system disease that affects mainly the lungs and the digestive system. In the lungs, where the effects are most devastating, a build-up of thick mucus causes severe respiratory problems. Mucus and protein also build up in the digestive tract, making it difficult to digest and absorb nutrients from food. As improved therapies have helped to address the malnutrition issues, ultimately most cystic fibrosis-related deaths are due to lung disease.

Thank you to our supporters in CF Awareness! 

USA

The Boomer Esiason Foundation is a dynamic partnership of leaders in the medical and business communities joining with a committed core of volunteers to heighten awareness, education and the quality of life for those affected by cystic fibrosis, while providing financial support to research aimed at finding a cure. Thank you for co-promoting our campaign!

Cystic Fibrosis Research, Inc. exists to fund research, to provide educational and personal support, and to spread awareness of cystic fibrosis, a life-threatening genetic disease. As we work to find a cure for cystic fibrosis, CFRI envisions informing, engaging, and empowering the CF community to help all who have this challenging disease attain the highest possible quality of life. Thank you for co-promoting our campaign!

CANADA

Cystic Fibrosis Canada is a proud partner of 65_RedRoses. Eva Markvoort was an inspiration to people worldwide. Her undeniable strength, courage, and spirit have moved many people in the CF community and beyond. Visit CF Canada’s partner page.

 

Whatch the film. Join the movment. #4Eva