More about D.C. Brewer's Ball and the CFF

 Be part of the best nonprofit craft beer event in DC!

WHAT:  The 10th Annual matchboxfoodgroup Brewer’s Ball  offers close to 1,500 of the area's business and community leaders the opportunity to sample a variety of hand crafted beers from more than 30 of the region's best craft breweries, while also enjoying the cuisine of over 20 popular area restaurants. The evening will feature live entertainment and one of the region’s most memorable silent auctions. Invite your clients, colleagues, family and friends to enjoy hand-crafted brews, delicious restaurant samplings and to mingle with supporters and elite young professionals. Brewer’s Ball is the craft brew gala of the season!

WHEN:  Saturday, March, 7, 2015  - 7pm - Midnight

WHERE: National Building Museum, 401 F St NW, Washington D.C., 20001


DRESS CODE: Cocktail Attire

DONATE: Unable to attend but would like to make a donation? 
Please visit:

WHY:    Imagine struggling for every breath you take – something most people don’t have to think twice  about. For most, breathing is a voluntary act, the simple process of inhaling and exhaling to produce  oxygen in the brain. For those with cystic fibrosis (CF), this simple act is a daily battle.

The CF Foundation is the world’s leader in the  search for a cure for cystic fibrosis. We take great  pride in being one of the most efficient and effective organizations of our kind, and are careful stewards of  every dollar raised in support of our mission. Through  our venture philanthropy model, we are able to invest in promising CF research to develop a robust pipeline of  potential therapies that target the disease from every angle.

The most recent example of the success of the CF  Foundation’s model is Kalydeco, the first drug to treat the  genetic defect causing CF. While Kalydeco is a breakthrough in  CF research and development, this drug works for only 4% of our CF population. Real progress toward a cure has been made, but the lives  of young people with CF are still cut far too short. We  urgently need the public’s continued support to fulfill our mission and help extend the lives of those with the disease.

Our work is not yet done. Help us to assure that all people with CF live a long and healthy life.

CONTACT:  For more information contact Erin Leahey at the Cystic Fibrosis Foundation Metropolitan Washington, D.C. Chapter at (301) 657-8444 x 201 or via email at