Cystic Fibrosis 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.

“As every person with cystic fibrosis knows, inspiration and motivation are essential when trying to get through the day. For me, there are only a handful of people that can provide this – Eva Markvoort is in that handful.” – Kim Wood

In February 2010, Eva was honoured with Cystic Fibrosis Canada’s Summerhayes Award, recognizing her exceptional commitment to the CF cause. Cystic Fibrosis Canada is pleased to be a part of continuing Eva’s legacy.

Cystic Fibrosis Canada

Cystic Fibrosis Canada is one of the world’s top three charitable organizations committed to finding a cure for cystic fibrosis. Cystic Fibrosis Canada is an internationally-recognized leader in CF research, innovation, and clinical care, and has invested more than $140 million in leading-edge research since 1960.

For more information, please visit www.cysticfibrosis.ca or connect with us on Facebook or Twitter.

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.