Cystic Fibrosis Foundation - Click here for homepage
 | Stay Informed  |  Volunteer  |  Clinical Trials
ABOUT CYSTIC FIBROSIS ABOUT THE CYSTIC FIBROSIS FOUNDATION LIVING WITH CYSTIC FIBROSIS TREATMENTS RESEARCH OVERVIEW GET INVOLVED!
In This Section
Many Ways to Give
Raise CF Awareness
Volunteer
Become a Corporate Partner
Foundation Events
Fundraise for CF at College
CF Cycle for Life
CF Climb
Xtreme Hike
Give Us Your Ideas
Become an Advocate
Get Started
Sign Up
Take Action Now
Visit Your Member
Advocacy Toolkit
EXPERRT Act
EXPERRT Act FAQs
Current Issues
Action Materials
Tips to Tell Your Story
FAQs
Advocacy Achievements
News and Events
Briefings & Testimonies
Congressional CF Caucus
Make Every Breath Count
Participate In A Clinical Trial
Improve Your CF Care
Shop the Marketplace
Get CFF Limited Collectibles
Request Mailing Labels
65 Roses Donation Center
Quick Links
Find A Chapter
Great Strides
Become a Corporate Partner
Volunteer
Employment Opportunities
Become an Advocate
Find A Clinical Trial
Care Center Network
Drug Development Pipeline
CF Services Pharmacy
Make a Donation
Find a Chapter
Get Connected

 Watch Charlotte, whose son Trey has CF, talk about her dream for the future. 
 Watch Charlotte, whose son
 Trey has cystic fibrosis, talk
 about her dream for the future.
 

Join us on Facebook at www.facebook.com/CysticFibrosisFoundation Join us on Facebook





Follow us at twitter.com/CF_Foundation Follow us on Twitter





Join us on Google+. Join us on Google+





Join us on YouTube at http://www.youtube.com/CysticFibrosisUSA Join us on YouTube
Bookmark and Share Display a Printer Friendly Version This Page
Make Every Breath Count Logo 

 

 

 

 

 



Make a difference just by telling your story.

Be a part of Make Every Breath Count, the Cystic Fibrosis Foundation’s annual national advocacy campaign. In the summer and fall, U.S. representatives and senators return to their home states. You can inspire action in our fight against CF by meeting with your elected officials in your hometown.

Join Us!

We need your help to ensure we have the support in Congress to continue vital CF research, make sure new therapies are approved quickly and safely, and guarantee that all people with CF have access to lifesaving care.

Watch Rep. Ed Markey (D-MA), the Co-Chair of the Congressional CF Caucus, talk about how you can make a difference by visiting your Member of Congress.
How do I get involved? 

Step 1: Sign Up

Use the form below to establish your meeting goal.

Step 2: Schedule Your Meeting

After you set your goal, we’ll give you all the tools you’ll need to set up your meeting.

Step 3: Attend Your Meeting

It’s easy to meet with your elected officials! The most important thing is to tell your personal story. We’ll provide you with the materials you’ll need for your meeting and will help walk you through what to say.

Registration will reopen in July 2012.

Make a Donation - Click here to donate now.
Cystic Fibrosis Services Pharmacy
GoodSearch.com will make a donation to the CF Foundation for every search.
The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.