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CF On The Daily: Dreams And Realities

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Shamrockin’ for a Cure 2016

  • October 21, 2015

Here We Go Again… ShamRockin’ 8.0 is in MOTION!

We’re baaaaack! Did you miss us?? We certainly missed YOU and our entire army of ShamRockers. Oh, did you think ShamRockin’ for a Cure was just a one-night party that only comes once a year? Well we’re about to ShamROCK your world…
Planning the BIGGEST and BEST St. Patrick’s Day celebration in town begins months before you enter the gate, plan your green get-up or even buy your ticket. We’ve been thinking about the 8th Annual ShamRockin’ for a Cure, ShamRockin’ 8.0 as it has been dubbed, since last call of ShamRockin’ 2015.
This week, we had our first OFFICIAL full committee meeting to introduce the new year of ShamRockin’ and get down to business. It takes an army to put it all together and maybe it’s the “luck of the Irish” but we’ve lucked out with the best committee of soldiers who are devoted and determined to throw you a party you’ll never forget!

Here are some of the things you can look forward to this year:

  • More food than ever before! All of your faves will be back and we’ll be bringing a few new restaurants to join the mix!
  • Mobile bidding! You asked and we heard – this year, we’ll be unveiling a new way to bid on the INSANE silent auction you’ve come to love all through your smart phone!
  • Jams to get jiggy with! The stage is set for our live band to get the groove going – your feet won’t be able to resist the dancefloor!
  • Once-in-a-lifetime live auction! Our track record runs deeps with dream vacations, exclusive tours, and more that you can ONLY get at ShamRockin’!
  • Chance to make a difference! Our mission is always the same: “Eat, Drink and CURE CF” and YOU are a part of this fight!

We can’t wait to see you on March 12! Save the date!

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ShamRockin' for a Cure
Cystic Fibrosis Foundation
57 Executive Park S, Suite 380
Atlanta, GA 30329
Phone: 404.325.6973 Email: georgia@cff.org

    The Cystic Fibrosis Foundation has unrestricted financial reserves of about 13 times its 2018 budgeted expenses following a one-time royalty sale in 2014. These funds, along with the public’s continuing support, are needed to help accelerate our efforts to pursue a cure for this fatal disease, fund development of new therapies, and help all people with CF live full, productive lives. To obtain a copy of our latest Annual Report, visit https://www.cff.org/About-Us/Reports-and-Financials/, email info@cff.org or call 1-800-FIGHT-CF.

    Important Note on Attendance at Foundation Events: To reduce the risk of getting and spreading germs at CF Foundation-sponsored events, we ask that everyone follow basic best practices by regularly cleaning your hands with soap and water or with an alcohol-based hand gel, covering your cough or sneeze with a tissue or your inner elbow and maintaining a safe 6-foot distance from anyone with a cold or infection. Medical evidence shows that germs may spread among people with CF through direct and indirect contact as well as through droplets that travel short distances when a person coughs or sneezes. These germs can lead to worsening symptoms and speed decline in lung function. To further help reduce the risk of cross-infection, the Foundation’s attendance policy recommends that all people with CF maintain a safe 6-foot distance from each other at all times while attending an outdoor Foundation-sponsored event.

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