**rescheduled to Wednesday, September 19**

— a celebration of —

Charleston's Finest:

brews, food, -&- difference makers

wednesday, September 19, 2018 | 7:00 -10:00 PM
Founders Hall @ Charles Towne Landing


Tickets: $85*

(includes unlimited drink & food)


*48 tax deductible


The Brewer’s Ball

A Celebration of Charleston’s Finest

Join Charleston’s Finest business and community leaders, young professional guests, and more for an evening of beer, food, music and networking in support of a great cause.

The Brewer's Ball invites guests to enjoy hand crafted beers from the best local brewers and food samplings from the hottest local restaurants, listen to music, bid on fabulous prizes in live and silent auctions, and mix and mingle with Charleston’s best and brightest - while honoring the 2018 class of Charleston’s Finest.

The Brewer's Ball celebrates this year's class of Charleston’s Finest Honorees – over 20 outstanding Lowcountry professionals who are nominated for their exemplary leadership, active involvement in the community, and business excellence – and invited to participate in a four-month fundraising and awareness building campaign to help support innovative research towards a cure for cystic fibrosis. Join us in celebrating these remarkable community leaders while learning about CF through a brief program highlighting new developments in the search for a cure, and indulging in the city's best beer, food, music, and more.

CFF Brewer's Ball - CHS Logo.png

Additional Details

Cocktail Attire | 21+ event
VIP Honoree and Sponsors Reception at 6:00 p.m.
Free parking available onsite


Please don't drink and drive. Use LYFT code CFFBREWCHS for 20% off rides to and from Brewer's Ball.

Sponsors –&– Brewers


our sponsors

participating brewers –&– restaurants

Interested in becoming a sponsor?


in-kind sponsors



1500 Old Towne Rd, Charleston, SC






About Cystic fibrosis

Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. In people with CF, a defective gene causes a thick, sticky buildup of mucus in the lungs, pancreas, and other organs. In the lungs, the mucus clogs the airways and traps bacteria leading to infections, extensive lung damage, and eventually, respiratory failure. In the pancreas, the mucus prevents the release of digestive enzymes that allow the body to break down food and absorb vital nutrients.

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. Breakthrough treatments have added years to the lives of people with cystic fibrosis. Today, the median predicted survival age is close to 40. This is a dramatic improvement from the 1950s, when a child with CF rarely lived long enough to attend elementary school.

Because of tremendous advancements in research and care, many people with CF are living long enough to realize their dreams of attending college, pursuing careers, getting married, and having kids.

While there has been significant progress in treating this disease, there is still no cure and too many lives are cut far too short.


To learn more about cystic fibrosis and the work of the Cystic Fibrosis Foundation, please visit, https://www.cff.org/About-Us/ .




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