Each year Universities across Canada raise money for the Canadian Cystic Fibrosis Foundation through our Shinerama Fundraiser

Cystic fibrosis (CF) is the most common, fatal genetic disease affecting Canadian children and young adults. There is no cure for cystic fibrosis. CF is a multi-organ disease, primarily affecting the lungs and digestive system. A build-up of thick mucus in the lungs causes severe breathing problems. It may be difficult to clear bacteria from the lungs, leading to cycles of infection and inflammation, which damage the delicate lung tissues.

Thick mucus also blocks the ducts of the pancreas, preventing enzymes from reaching the intestines to digest food. People with CF must consume a large amount of artificial enzymes (average 20 pills a day) with every meal and snack, to help digest and absorb adequate nutrition from food.

Shinerama is a campaign that stretches over the summer months through October. Although the annual “Shine Day” in September is our best known event where we take to the streets of Ottawa to busk for money, we also take part in various other fundraisers throughout the year such as sucker runs and pub nights.

Come to 101 Week with your fundraising ideas, and click HERE to see our team, or HERE to get more information on Shinerama and Cystic Fibrosis Canada.