ACCESS TO CFRI’S 34TH NATIONAL CF EDUCATION CONFERENCE THIS WEEKEND!
If you registered for our upcoming virtual conference, you should have received an email from email@example.com with your log-in information.
If you haven’t received the email, please check your clutter and junk mail inboxes for an email from firstname.lastname@example.org. If you cannot locate this, or if you have any technical difficulties, please go to https://events.vizzi.live/cfri-techsupport/ or contact email@example.com.
We are excited to share presentations by renowned speakers addressing phage, mRNA and gene therapies, mental health, exacerbations, and much more. We hope you can join us! https://www.cfri.org/education-support/national-cf-conference/
ABOUT CYSTIC FIBROSIS RESEARCH INSTITUTE
To be a global resource for the cystic fibrosis community while pursuing a cure through research, education, advocacy, and support.
CFRI is a nonprofit organization that funds innovative CF research and offers education, advocacy and psychosocial support programs to those affected by CF.
To find a cure for cystic fibrosis while enhancing quality of life for the CF community.
WHAT IS CYSTIC FIBROSIS?
Cystic fibrosis (CF) is a rare genetic, chronic, progressive disease that affects over 30,000 people in the United States, and over 70,000 people worldwide. While most people associate cystic fibrosis with progressive lung disease, CF impacts the respiratory, digestive, reproductive, and endocrine systems. Once considered a childhood disease, over half of those living with CF in the United States are over the age of 18. While life expectancy for those recently diagnosed has reached the mid-forties, the median age of death remains only thirty years. Progress in research has led to new therapies that can extend and enhance the lives of those with CF, but there is still no cure.