Cystic Fibrosis Foundation Board Chair KC White Advocates for CF Awareness and Progress in Nationwide Media Tour
Cystic Fibrosis Foundation Board Chair KC White Advocates for CF Awareness and Progress in Nationwide Media Tour

Key Takeaways (TLDR)
The Cystic Fibrosis Foundation's research and treatments give an advantage to 90% of the CF population, including KC White, leading to transformative health improvements.
The Cystic Fibrosis Foundation funds research, drug development, and specialized care to improve the lives of people with CF.
The Cystic Fibrosis Foundation is dedicated to finding a cure and providing all people with CF the opportunity to lead long, fulfilling lives.
KC White, the first person with CF to serve as board chair, shares her inspiring personal journey and advocates for the CF community.
Why it Matters
The news sheds light on the challenges faced by those living with cystic fibrosis and the Foundation's relentless pursuit of a cure. It emphasizes the importance of raising awareness about the disease and the need for continued support for research and high-quality care. The impact statement highlights the personal journey of KC White and the transformative advancements in treatments, inspiring hope for the CF community.
Summary
The Cystic Fibrosis Foundation's Board Chair, KC White, recently participated in a nationwide media tour to shed light on the rare disease, her personal journey, and the Foundation's efforts to progress care and treatment options. CF is a life-shortening disease that affects about 40,000 people in the United States, and White, diagnosed at age 3, is the first person with CF to serve as board chair. The Foundation is dedicated to finding a cure and providing all people with CF the opportunity to lead long, fulfilling lives through funding research, drug development, and support programs.

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