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THE DÉFIBROSE MONT-SAINTE-ANNE

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CYSTIC FIBROSIS

Cystic fibrosis is the most common fatal genetic disease in Canadian children and young adults. It affects different organs, but especially the digestive system and lungs. In the lungs, where the effects are most devastating, the accumulation of thick mucus leads to the gradual loss of lung function. Mucus also accumulates in the digestive tract, making it difficult to digest and absorb nutrients. There is no cure.

CYSTIC FIBROSIS CANADA

Cystic Fibrosis Canada is a national, not-for-profit charity that is one of the leading charities committed to the search for a cure for cystic fibrosis worldwide. It is an internationally renowned leader in cystic fibrosis research, innovation, and clinical care. Cystic Fibrosis Canada invests more money in life-saving research and care for people with cystic fibrosis than any other non-governmental organization in Canada. Since 1960, Cystic Fibrosis Canada has invested more than $261 million in state-of-the-art research and clinical care and advocacy. The survival rates of Canadians with cystic fibrosis are among the highest in the world. For more information, visit cysticfibrosis.ca.