Nov
23
2010
0

Make your voice count

Advances being made in CF research have the potential to make dreams come true for people with CF that were impossible just decades ago.

The CF Foundation asked some of the many extraordinary people affected by this disease, including Members of Congress and volunteers like you, to share their dreams for the future:

Watch Video

One of the most important reasons Members of Congress join our fight is that they?ve heard from someone touched by CF.

Join the hundreds of Advocates who speak out for CF by becoming a part of Make Every Breath Count — the CF Foundation?s national advocacy program that helps volunteers like you meet with their Members of Congress.

Speak out, get involved, and inspire action today by signing up for Make Every Breath Count!

Just like you, Senator James Inhofe (R-OK) was inspired to take action:

?Because I have a staffer with cystic fibrosis, the challenges faced by patients with CF hit particularly close to home. As a continued supporter for medical advancements in CF, I urge patients, their families, and friends to contact their state lawmakers to ensure your voice is heard in Congress. Together, we can make a dramatic difference in the lives of those affected by this debilitating disease and make CF a thing of the past.?

Make sure your lawmakers support our fight against CF by funding innovative CF research and quickly and safely moving promising new therapies into the hands of patients. If you don?t inspire them to act, who will?

Sign up for Make Every Breath Count!

Coming Soon: New Advocacy Website

Soon, it will be easier than ever to communicate with your elected officials about issues important to people with CF. The Cystic Fibrosis Foundation will unveil a new advocacy website later this month which will provide you with:

  • Faster, less complicated access to the contact information for your Members of Congress
  • The ability to easily track all of your communications with elected officials
  • A new tool to share your CF story with your elected officials
  • A reference guide showing where your elected officials stand on issues affecting people with CF

Thank you! Together, we are making a difference for people with CF.

Sincerely,

Cystic Fibrosis Foundation
800-FIGHT-CF
info@cff.org
www.cff.org

Written by Country Concert for Cystic Fibrosis in: Cystic Fibrosis |

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