Cystic Fibrosis Foundation Volunteer to Carry Torch for Vancouver 2010 Olympic Winter Games
Coca-Cola’s Liz Burns to Run in Honor of People With Cystic Fibrosis
January 18, 2010
(Bethesda, MD) – One of the Cystic Fibrosis Foundation’s most active volunteers will carry the Olympic Torch today in Calgary as it makes its way to Vancouver and the Opening Ceremony for the 2010 Olympic Winter Games. Liz Burns, incoming board president for the Foundation’s Georgia Chapter, has helped raise more than $600,000 for CF research, care and education programs. She is a senior national sales executive for Coca-Cola North America.
“Liz is a passionate and devoted volunteer, and we are thrilled she will carry the Olympic Flame in honor of people with cystic fibrosis and raise more awareness about this devastating disease,” said Robert J. Beall, Ph.D., president and CEO of the Cystic Fibrosis Foundation. “We thank Coca-Cola for selecting Liz for this honor and supporting her mission — and ours — to find a cure and change the lives of every person with CF.”
Cystic fibrosis is a fatal genetic disease that causes life-threatening lung infections and premature death, and affects about 70,000 people worldwide.
Burns is scheduled to carry the torch at 4:42 p.m. M.T. today, and is one of 20 U.S. Torchbearers selected by Coca-Cola for their commitment to create meaningful and enduring change in local and global communities. The Olympic Torch Relay lasts for 106 days, covers more than 27,000 miles and links more than 1,000 communities in Canada. The Olympics begin Feb. 12, 2010.
Burns was named “Volunteer of the Year” by the Foundation’s Georgia Chapter in 2008. She chairs one of the Foundation’s largest fundraising events, called Chocolate, an annual gala held in Atlanta.
The Foundation has fueled dramatic improvements in research and care that have significantly changed the prognosis for people with CF. The predicted median age of survival for people with CF has increased to more than 37 years — more than double what it was 25 years ago.
About the Cystic Fibrosis Foundation
The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis. The Foundation funds more CF research than any other organization and nearly every CF drug available today was made possible because of Foundation support. Based in Bethesda, Md., the Foundation also supports and accredits a national care center network that has been recognized by the National Institutes of Health as a model of care for a chronic disease.