iPhone's, iPad's, non-Flash users - Nightwire Magazine
iPhone's, iPad's, non-Flash users - Nightwire Magazine
iPhone's, iPad's, non-Flash users - Nightwire Magazine
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Cystic Fibrosis Brewers Ball<br />
Do you like beer? Do you enjoy food? Then the<br />
Brewer’s Ball is the place for you! The Fat Head's<br />
Saloon Brewer’s Ball is a local beer tasting event to<br />
benefit the Cystic Fibrosis Foundation. The 3rd Annual Fat<br />
Head's Saloon Brewer’s Ball will be held on Friday, April 23,<br />
2009 from 6-9 pm at the Soldier's & Sailors Memorial Hall<br />
Ballroom. The event will be a fun and casual evening you<br />
won’t want to miss.<br />
The 2010 Brewer’s Ball will offer guests the opportunity to<br />
sample a variety of handcrafted ales and lagers from the<br />
region’s best microbreweries and brew pubs along with<br />
samples of cuisine from several popular restaurants. Last<br />
year’s event featured food and beer from Fat Head’s Saloon,<br />
Rock Bottom Restaurant and Brewery, Great Lakes Brewing<br />
company and select beers from Magic Hat Brewing Company.<br />
The night will be highlighted by entertainment and the chance<br />
to bid on some of the regions most unique auction items.<br />
This event is the perfect opportunity for guests to network<br />
amongst the city’s most successful young professionals.<br />
Approximately 30,000 people nationwide have this fatal<br />
disease. In addition, more than 10 million Americans are<br />
genetic carriers. Carriers each have one copy of the defective<br />
CF gene, but do not have the disease and its symptoms. It<br />
takes two copies of the gene for a child to be born with cystic<br />
fibrosis. For people with CF, the defective gene causes the<br />
body to produce a faulty protein that leads to abnormally<br />
thick, sticky mucus that clogs the lungs and can result in fatal<br />
lung infections. The mucus also obstructs the pancreas,<br />
making it difficult to absorb nutrients in food.<br />
With the support of the CF Foundation, there has been<br />
tremendous progress in cystic fibrosis research and care. The<br />
median age of survival has increased from early childhood in<br />
the 1950s to more than 37 today. However, CF continues to be<br />
a critical health matter, as most individuals with cystic fibrosis<br />
must battle lung disease for their entire lives. At least one<br />
person dies each day from this disease.<br />
Please join us in supporting the Foundation by attending<br />
The Fat Head’s Saloon Brewer’s Ball on April 23 2010. For<br />
more information on this DON’T WANT TO MISS EVENING<br />
visit www.cff.org/Chapters/wpa or call 412.321.4422<br />
About the Cystic Fibrosis Foundation<br />
The Cystic Fibrosis Foundation, headquartered in Bethesda, Md., is a donorsupported,<br />
<strong>non</strong>profit organization committed to finding therapies and<br />
ultimately a cure for cystic fibrosis, and to improving the lives of those with the<br />
disease. For more information, visit www.cff.org.