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For more information on Cystic Fibrosis please visit the Canadian Cystic Fibrosis Foundation at www.cysticfibrosis.ca

Each province in Canada has active Chapters. There are a total of 50 chapters located in Canada. Individual chapters are made up of volunteers who are deeply committed to finding a solution to CF. They organize and stage fund raising activates, raise awareness of CF in their local communities, and support family and friends who are coping with CF daily.

Click here to find a CCFF Chapter near you.

Contact Us

Canadian Cystic Fibrosis Foundation Vancouver and Lower Mainland

4050 Graveley Street
Burnaby
British Columbia
Canada
V5C 4A5

Telephone: (604)436-1158

Our chapter office is open
Monday-Friday from 9:30am-5:00pm

Latest News & Information!

Thank you to all of our Supporters

GearUp4CF 2010 raised $121,000

With your help we will find a cure!

Please visit our Flickr site to share some of our favorite memories http://www.flickr.com/photos/ccffvancouver/

GearUp4CF- June 19- 28, 2010

We've arrived in Banff on Sunday afternoon!

Everyone is fine, stories, photos, and donation update to come once everyone gets home!

Read about some of our riders experiences on this years ride!

Thanks for all your your support! Check back soon

2010 Ride Sponsors!

2010 Ride Sponsors

 June 24, 2010

The riders arrived in Creston on June 24, the Skimmerhorn Inn has been kind enough to donate a room to help with the fundraising effort!  Thank you Skimmerhorn Inn!

Please follow the riders on their journey at


http://gearup4cf2010.blogspot.com/

 

  
Donate Now!

We Need You!

A new adventure, a road to be cycled, a mountain to be climbed, a challenge to be embraced.

Our challenge is to find a cure for cystic fibrosis- a fatal genetic illness for which there is currently no cure. We are dedicated to meet this challenge, and are inviting you to support us in this effort during our 5th Annual GearUp4CF bike ride to the Rockies. Help inspire us as we Cycle from Vancouver to Banff, to raise funds to cure Cystic Fibrosis, and have the experience of a lifetime.

For Further Information please contact:

Sterling Aurel
Fundraising and Event Coordinator
Canadian Cystic Fibrosis Foundation
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
(604) 436-1158

www.cfvancouver.ca
www.gearup4cf.org

Participation in GearUp4CF is limited to 24 cyclists. Each participant is expected to fund raise a minimum of $5,000 in donations for the Canadian Cystic Fibrosis Foundation.

GearUp4CF 2010 has surpassed it's Fundraising Goal!

 

 

 

Is there a cure?

As yet, there is no known cure for CF, but there is real hope. Comprehensive treatment programs have dramatically extended the life expectancy of persons with CF and many are living into their 20s, 30s and beyond.

Recent years have seen remarkable progress in CF research. Since 1989 when Canadian researchers discovered the gene responsible for CF, global research to find a cure for the disease has brought us closer and closer to a solution.

The astonishing pace of CF science suggests that there is good reason to feel optimistic about the future.

How does CF affect daily life?

For persons with CF, life includes a daily routine of therapy and periodic visits to a CF clinic. Otherwise, most individuals with cystic fibrosis lead normal lives, for many years, in terms of education, physical activity, and social relationships. Eventually, however, lung disease places increasing limits on daily life.

Thanks to the advances in research and clinical care, growing numbers of children with CF are surviving into adulthood. In 1960, when the CCFF was founded, a child born with cystic fibrosis rarely lived four years. CCFF is one of the few organizations that maintains extensive records, tracking a CF patient from first diagnosis. This data base called, the Canadian Patient Data Registry, is proving that advances have been made with the recent announcement that the median age of survival of Canadians with CF has reached its highest point ever: 37 years of age. This means that Canadians with CF now have a 50% chance of living beyond the age of 37. While this is positive news, the need for a cure is crucial for the 50% who won't reach the age of 37.

Over 41% of all Canadians with CF are over the age of 18 years. These men and women are pursuing post-secondary education, careers and many are having families of their own; a tremendous accomplishment, but not enough.

More Info

What is Cystic Fibrosis?

Cystic Fibrosis (CF) is a fatal inherited disease. CF affects mainly the lungs and the digestive system. In the lungs, CF causes severe breathing problems. A build-up of thick mucus makes it difficult to clear bacteria and leads to cycles of infection and inflammation, which damage the delicate lung tissues.

In the digestive tract, CF makes it extremely difficult to digest and absorb adequate nutrients from food. Thick mucus also blocks the ducts of the pancreas, preventing enzymes from reaching the intestines to digest food. Therefore, persons with CF must consume a large number of artificial enzymes (up to 40 pills a day) with every meal and snack, to help them absorb adequate nutrition from their food. They must also follow a demanding daily routine of physical therapy to keep the lungs free of congestion and infection