Because everyone needs to breathe!

Imagine spending hours every day doing physical therapy, taking antibiotics, and using aerosol solutions.
Imagine having thick mucus build up in your lungs that clogs your airways.
Imagine being 1 of the almost 3,600 Canadians living with Cystic Fibrosis.

Come join NAITSA’s SHINERAMA campaign September 11, 2010. We will shine anything and everything, to help raise over a million dollars across Canada for Shinerama.

Cystic Fibrosis (CF) is a fatal, inherited disorder that affects mainly the lungs and digestive system. Sticky mucus clogs the small bronchial tubes in the lungs, making it difficult to breathe. A bacterium collects in the clogged tubes, leading to infections. Mucus also plugs the tiny ducts of the pancreas, an organ that supplies enzymes to aid digestion. As a result, food is not properly digested and nutritional value is lost.

Most people with Cystic Fibrosis die of lung disease.

Want to help out?

E-Mail us at naitsavolunteers@nait.ca

Get your V.I.P Card!

Get some awesome deals at local clubs and businesses. Check it out!

Thanks to our Sponsors!