MISSION: TO CONTINUOUSLY IMPROVE THE QUALITY, SAFETY, EFFECTIVENESS AND COSTS OF CARE OF CF PATIENTS AND THEIR FAMILIES.

***SPECIAL NOTICE***
Virtual Events for Adults With CF CF MiniCon: Transplant & Young Adult Transitions
This year the Cystic Fibrosis Foundation will be supporting three virtual events created by and for adults with CF to connect and share their experiences. In addition to BreatheCon, we are also introducing CF MiniCons, which are single-day, topic-specific virtual events. All virtual events will include presentations, group chats, and small group video breakouts on topics specific to life with CF. On Sunday, May 21 from 6 9:30 p.m. ET, members of the CF community will be hosting CF MiniCon: Transplant, where adults with CF can have an open and honest dialogue about the transplant process. Discussion will focus on lifestyle, not on medical topics.

Registration is open now through May 18 at www.cf.org/minicon

Please check back this summer for additional details about the other virtual events, CF MiniCon: Young Adult Transition (July 22) and BreatheCon 2017 (September 8-9).
For questions or more information, email breathecon@cff.org.




<> <>