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CFRI exists to fund CF research, provide personal support,
						 and advocate for the CF community. We're connecting CF
						 resources with community needs.

CFRI Research

cystic fibrosis research

Since 1975, CFRI has supported cystic fibrosis research at well-established medical facilities through the funding of grants. Our investment in new ideas has enabled researchers to bring new perspectives to the study of this disease.

CFRI research is funded through two programs: the Elizabeth Nash Memorial Fellowship and the New Horizons Campaign.

To learn more, click here.

CFRI Community

CFRI Community - spring issue

We are pleased to introduce the first issue of our newly redesigned and renamed newsletter: CFRI Community! CFRI publishes CFRI Community three times a year to provide you with cystic fibrosis updates and resources. We hope you will enjoy reading the many important articles including, The Time is Now: The Critical Need for Increased Research Funding by Paul Quinton, Ph.D., A Transplant's Journey, Inflammation and CF, and CF Research Challenge Match. Click here for 'Lessons Learned' by Dave Cartnal.

CF Discovery Series

Carolyn Givens, M.D.

Sherri Sager, Chief Government and Community Relations Officer at Lucile Children's Hospital, recently spoke about the Affordable Care Act and its potential impact on families with cystic fibrosis nationwide. She also discussed potential changes to California Children’s Services (CCS) and the Genetically Handicapped Persons Program (GHPP).

To watch a recording of this presentation, click here. Stay tuned to hear about our next presentation in May.

Save the Dates!


CFRI's 27th National Family
Cystic Fibrosis Education Conference

August 1 - August 3, 2014
Sofitel San Francisco Bay

CFRI's Teen and Adult Retreat
July 27 - August 1, 2014
Vallombrosa Center

CF Golf Tournament at Pasatiempo
Monday, August 4, 2014
Pasatiempo Golf Club

To read CFRI's Infection Control Policy,
click here

CF in the Classroom

CF in the Classroom Front Cover

Help distribute CF in the Classroom booklets to teachers, school nurses and others so they can understand the needs of your child living with cystic fibrosis.

This publication also contains essential information to help prepare your child for higher education.

For electronic or hard copies, click here. Your help today means increased help in the classroom for your child and others with CF.

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