Emily Speaks and Is Honored at Global Genes RARE Patient Advocacy Summit
Catch the livestream on Friday, September 23rd at 4pm EST through Rare University’s platform. Today, there is nowhere that Emily would rather be than among other... Read More
GRANTS WE FUND
EE has awarded millions of dollars to multi-disciplinary teams around the world to advance research and drug development for the final 10% of people with CF.
CLINICAL TRIALS
Our cystic fibrosis clinical trial matchmaking program is direct-to-consumer, making trial recruitment faster, more targeted, and more efficient.
PATIENT DATABASE
Emily’s Entourage CF Clinical Trial Connect (CTC) is the only global patient database exclusively for people with CF who are unable to benefit from CFTR modulators. By joining, you can help accelerate the development of new, lifesaving CF therapies.
How EE Helped Land Me a Job
From time to time we invite guest bloggers who are part of the EE community to contribute their unique voices to our blog. Today’s guest... Read More
Through the Digital Screen: A Complicated Tale of Friendship in the CF Community
From time to time we invite guest bloggers who are part of the EE community to contribute their unique voices to our blog. Today’s guest... Read More
Jessica Bean’s “CF Superhero” Interview with Emily
We’re so honored that Australian health empowerment coach and blogger Jessica Bean chose to feature Emily on her “CF Superhero” blog series! We are reposting Jessica’s interview with Emily to give... Read More
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