Friday, May 15, 2015 Tier3MD President Mike Cherico, and Director of Operations Adam Holtman played in the Annual Cystic Fibrosis Golf Tournament hosted by the Georgia Cystic Fibrosis Chapter. “Great fun for a great cause” says Cherico. “Everyone had a blast, and the weather held out for us!” Tier3MD is happy to donate to this great cause. Of course the biggest secret is how did Mike and Adam shoot?

Mission

The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.

Adding Tomorrows

Adding tomorrows expresses the mission — and results — of the Cystic Fibrosis Foundation’s steadfast efforts to extend the length and quality of life for people with cystic fibrosis (CF). CF presents daily challenges for approximately 30,000 Americans. But life with the disease is far different today than it was 50, 30, or even 10 years ago. 

Perhaps the best evidence that many people with cystic fibrosis are living longer is the fact that nearly half of the CF patient population is now age 18 or older. 

Recently developed therapies and specialized care have enabled people with CF to gain greater control over their disease. So, children and adults are not only living longer, but also living a better quality of life.

 

More about the Cystic Fibrosis Foundation

The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis. We fund more CF research than any other organization, and nearly every CF drug available today was made possible because of Foundation support. We are a nonprofit donor-supported organization dedicated to attacking cystic fibrosis from every angle. Our focus is to support the development of new drugs to fight the disease, improve the quality of life for those with CF, and ultimately to find a cure. The Foundation’s drug development success has been recognized by Harvard Business School and by publications such as Forbes and The Wall Street Journal. Based in Bethesda, Md., the Foundation funds 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. The Cystic Fibrosis Foundation is one of the most efficient organizations of its kind and is an accredited charity of the Better Business Bureau’s Wise Giving Alliance.