Cystic Fibrosis London

The 3 on 3 Face Off Against CF Road Hockey Tournament

chapter admin — Thu, 06 May 2010 04:24:17 +0000

Held annually in September, the 3 on 3 Face Off Against CF Road Hockey Tournament has raised over $60,000 for Cystic Fibrosis Research. Every year teams from all over Ontario meet to compete in either Competitive or Recreational Divisions for fun, bragging rights and to raise money for Cystic Fibrosis research and care. Teams and players return year after year – this is a great tournament for a great cause…

We look forward to seeing you in September 2010!

http://www.roadhockeylondon.ca/

40th Canadian Cystic Fibrosis Annual Charity Golf Tournament and Auction

chapter admin — Thu, 06 May 2010 04:17:24 +0000

Date: Friday, August 27, 2010 Time: Brunch: 11:00 a.m. – Noon | Golf: 12:30 p.m. (Shot gun start)
Start the day with Brunch and Live Entertainment with Live Auction, Dinner & prizes to follow.

Auction and Reception ~ New! Live Entertainment
Join us on Thursday, August 26, 6:30 p.m. for an evening filled with great friends, culinary delights and fabulous silent auction items. Located conveniently in the Grand Highland Hall at the Highland COuntry Club.

Flagswipe Paintball charity game

chapter admin — Thu, 06 May 2010 03:49:49 +0000

Cruizin for CF

chapter admin — Thu, 06 May 2010 03:44:26 +0000

Cruizin’ for CF 2010 RACE DAY!
Join the Drive for a Cure

This years’ event could be the best ever! Slated for June 20, 2010, the event will include many of the most popular activities that have attracted a loyal following of ‘CF Cruisers’! Additionally, there are plans for new and exciting activities and attractions that will be of interest to auto enthusiasts and CF supporters alike!

While complete details will be released in the near future, some of the highlights include:

• Full Pancake Breakfast
• Watch, ride along or drive your own vehicle in the W.O.S.C.A. timed slalom course.
• Win prizes on a leisurely Road Cruize Scavenger Hunt to several iconic destinations in and around London
• Test your driving skills with hot laps at Delaware Speedway!
• Full lunch for all participants
• Live entertainment at the prestigious Plunkett Estate
• Silent and live auctions of highly desirable products and services
• Sponsor demonstrations, exhibitions and giveaways
• Door prizes
• Valuable Cruizin’ Navigator packages for each registered driver
• Much more!

Registration
• Pre-registration begins April 1, 2009. check out www.cruzinforcf.com or call 519-661-0308 for further details
• NEW!! Bring a friend program. Referral program – all registered returning drivers will receive a special gift for each confirmed new driver. (details to follow)

Event details are developing weekly so check back often for the latest news!

http://www.cruizinforcf.com/

Carstar Soaps It Up!

chapter admin — Thu, 06 May 2010 03:42:57 +0000

Carstar Soaps It Up!
On June 12, 2010, CARSTAR will host its annual Soaps It Up National Car Wash Fundraiser in support of the Canadian Cystic Fibrosis Foundation and other local charities. To find a location nearest you and to purchase tickets, visit: www.carstar.ca

Advisory Committee

chapter admin — Thu, 06 May 2010 03:41:26 +0000

Advisory Committee

Top-ranking researchers, physicians and stakeholder representatives belong to the Medical/Scientific Advisory Committee (M/SAC). The Committee makes recommendations on how Foundation funds should be directed. Members volunteer hundreds of hours each year to ensure fund allocation is balanced, cost-efficient and highly effective.

M/SAC Member List

Knowledgeable members of the CCFF community can serve as Advisory Committee stakeholders. These volunteers play a vital role in M/SAC policy decisions and recommendations. They take part in the review process which allocates funds to outstanding cystic fibrosis research projects, lung transplantation and clinical care. Learn more

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about the stakeholder membership role, requirements, responsibilities and selection process.
Reviewed/updated: 2010-02-19

Research

chapter admin — Thu, 06 May 2010 03:38:07 +0000

Research

Research gives people with CF and their families real hope.

Progress in CF research is making a positive difference; Canadians with CF are living longer and healthier lives. In the 1960s, when the Foundation started serving the CF community, most children with cystic fibrosis did not live long enough to attend kindergarten.

Today, 50% of Canadians with CF are expected to live into their late 30s and beyond. This is a tremendous accomplishment, but it’s not nearly enough.

Our mission is to help people with cystic fibrosis, principally by funding research. In fact, the Foundation is one of the world’s largest non-governmental granting agencies in the field of cystic fibrosis research. In 2009-2010, we are investing nearly $6 million in programs that are investigating many aspects of the CF puzzle. With more funds, we could do even more!

With your support and the dedication of our researchers, we will find a cure or control for this devastating disease!

Reviewed/updated: 2009-07-30