The CF Wind Sprint video series offers quick tips for living with CF. Topics include traveling, nutrition,exercise and treatments.
Every day, researchers around the world come one step closer to discovering a cure for cystic fibrosis. In the meantime, the CF drug “pipeline” ensures therapies are moving from the laboratory to the marketplace. We keep an eye on medical news sources from around the world and report on these developments as they occur.
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CF Foundation Kicks Off 'Make Every Breath Count' Campaign

08/01/2011

Volunteers from all over the country will meet with their elected officials in their hometowns this summer as part of Make Every Breath Count, the Cystic Fibrosis Foundation’s annual national advocacy campaign.

By participating in Make Every Breath Count, volunteers hope to build support in Congress for vital cystic fibrosis research and care.

"You have to stand up. You have to visit your congressman," says Rep. Edward Markey (D-MA), co-chair of the Congressional CF Caucus, emphasizing the importance of advocacy in the fight against CF.

Between now and Labor Day, Foundation volunteers plan to hold at least 75 meetings with representatives — one or more meeting in every state.

Go to the CFF website to find out more about Make Every Breath Count and to schedule a meeting with your representative in your hometown.

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