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CYSTIC FIBROSIS FOUNDATION GEORGIA CHAPTER RESTAURANT PROPOSAL SHAMROCKIN’ FOR A CURE SATURDAY, MARCH 25, 2017 VERIZON AMPHITHEATRE JAKE & GAVIN SOLDIERS IN THE FIGHT

CYSTIC FIBROSIS FOUNDATION GEORGIA …...cystic fibrosis in approximately eight percent of the CF population. Orkambi, approved in July 2015, could eventually benefit nearly 50 percent

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Page 1: CYSTIC FIBROSIS FOUNDATION GEORGIA …...cystic fibrosis in approximately eight percent of the CF population. Orkambi, approved in July 2015, could eventually benefit nearly 50 percent

CYSTIC FIBROSIS FOUNDATIONGEORGIA CHAPTER

RESTAURANT PROPOSAL

SHAMROCKIN’ FOR A CURESATURDAY, MARCH 25, 2017VERIZON AMPHITHEATRE

JAKE & GAVINSOLDIERS IN THE FIGHT

Page 2: CYSTIC FIBROSIS FOUNDATION GEORGIA …...cystic fibrosis in approximately eight percent of the CF population. Orkambi, approved in July 2015, could eventually benefit nearly 50 percent

ShamRockin’ for A Cure

Restaurant In-Kind SponsorshipTODAY. TOMORROW. AND EVERY BREATH THERAFTER.Your company will have an area allocated in the event space to showcase your craft to guests through tasting experiences.

Restaurant Tasting Donation Request• Provide heavy hors d’oeuvres to showcase a signature sampling of your craft (sugested 500 servings)• Provide at least one chef and/or representative to serve, educate and mingle with our guests. Up to 3 total

company representatives may attend to serve.

Pre-event Sponsorship Recognition• Company logo in Georgia Chapter CF Foundation e-newsletter that includes company name, tagline and

link to your website• Company logo and link to your website on ShamRockin’ for a Cure webpage• Recognition of company as in-kind supporter on Georgia Chapter Facebook

Night of event Sponsorship Recognition• Prestige of being recognized as one of ShamRockin’ for a Cure’s honored restaurants• Interaction with ShamRockin’ for a Cure guests, networking with Metro Atlanta’s best chefs and local

business leaders• Prominent signage at the event• Verbal recognition from the stage• Company and logo recognition on the looping sponsor PowerPoint• Two (2) tickets to ShamRockin’ for a Cure (in addition to servers representing your company) Additional tickets to the event may be purchased for $95 each.

Post event Sponsorship Recognition• Restaurant mention in post-event email blast

Unquestionably the definitive St. Paddy’s Day Celebration in town, the 8th Annual ShamRockin’ for a Cure is a premier party with a purpose where over 1,500 attendees gather at Verizon Wireless Amphitheatre to “eat, drink, and cure cystic fibrosis.” With over 25 local restaurant and drink vendors, an incredible silent and live auction, and the best band in town; ShamRockin’ for a Cure packs more entertainment in one night than you can imagine!

Over the past seven years, ShamRockin’ for a Cure has raised over $1.9 million to help forward the mission of the Cystic Fibrosis Foundation 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. Each year, the ShamRockin’ committee enlists the support of corporate and individual donors to help the Cystic Fibrosis Foundation “add tomorrows” for the over 33,000 individuals living with cystic fibrosis in the United States.

Let’s join together to save lives... even if it takes all night!

MARCH 25, 2017 • VERIZON AMPHITHEATRE

Page 3: CYSTIC FIBROSIS FOUNDATION GEORGIA …...cystic fibrosis in approximately eight percent of the CF population. Orkambi, approved in July 2015, could eventually benefit nearly 50 percent

33,000: CF is a chronic, progressive and life-threatening genetic disease that affects the lungs and digestive systems of approximately 30,000 children and young adults in the United States.

10 MILLION: Approximately 10 million Americans are symptomless carriers of the defective gene responsible for the disease.

1,000: CF occurs in one of every 3,500 births of all Americans and about 1,000 new cases of CF are diagnosed each year.

1: One mission...to help develop new drugs, improve the quality of life, and to ultimately cure cystic fibrosis.

About the Cystic Fibrosis FoundationThe Foundation’s innovative approach to research has yielded a pipeline of more than 30 potential CF therapies. The CF Foundation is proud to have played an important role in the research and development of two game-changing drugs - Kalydeco and Orkambi - the latest examples of the Foundation’s innovative venture philanthropy drug development model.

Kalydeco, which came to market in 2012, is a breakthrough drug and the first to address the underlying cause of cystic fibrosis in approximately eight percent of the CF population.

Orkambi, approved in July 2015, could eventually benefit nearly 50 percent of people with CF and the science behind the drug advances our understanding of the disease in ways that could benefit all people with the disease.

The Cystic Fibrosis Foundation is the world’s leader in the search for a cure, funding promising research and working to provide access to quality, specialized care and treatments for people with CF. Nearly every CF drug available today was made possible because of the Foundation’s support.

Contributions to the Foundation are used wisely. The Foundation is an accredited charity of the Better Business Bureau’s Wise Giving Alliance.

Reason to Support

The science behind Kalydeco and Orkambi has opened exciting new doors to research and development that may eventually lead to a cure for all people living with CF. Real progress has been made, but the lives of young people with CF are still cut far too short and we will not rest until we reach our goal to find a cure for all people with cystic fibrosis.

THANK YOU!

Page 4: CYSTIC FIBROSIS FOUNDATION GEORGIA …...cystic fibrosis in approximately eight percent of the CF population. Orkambi, approved in July 2015, could eventually benefit nearly 50 percent

Restaurant Name: ____________________________________________________________________

Contact Name: ____________________________________________________________________

Address: ____________________________________________________________________

City, State Zip: ____________________________________________________________________ Phone & Fax: ____________________________________________________________________

Contact E-mail: ____________________________________________________________________

Restaurant Web Site: ____________________________________________________________________

Chef Name: ____________________________________________________________________

Insurance Policy Contact Name: ____________________________________________________________

Insurance Policy Contact Email: ____________________________________________________________

Insurance Policy Contact Phone: ____________________________________________________________ I agree to participate as a Restaurant Tasting In-Kind Sponsor for ShamRockin’ for a Cure on March 25, 2017. I will have staff for my booth to serve the samples and will provide collateral promoting my restaurant.

* Food must be pre-prepared - open flames and/or oils are not permitted on-site. Sternos are allowed.

Signature: ___________________________________________ Date: ______________

* Please provide a description of what you are intending to serve. This helps us ensure a variety of tastings and an opportunity to highlight your item in promotional materials.

Item Description: _________________________________________________________________________________________________________________________________________________________________

Please return completed form to the Cystic Fibrosis Foundation2302 Parklake Drive NE, Suite 210, Atlanta, GA 30345 | [email protected] | 404-325-6973 (t) | 404-325-7921 (f)

RESTAURANT PARTCIPATION FORM

I need access to electricity at the event for my tasting (please check if needed)

I would like to include items in the event swag bag (600 items needed by 3/10/2017)

I will have a banner ready for pick-up by 3/20/2017. (Banner size not to exceed 8’ wide x 3’ high)

The Cystic Fibrosis Foundation has unrestricted financial reserves of about 12 times its budgeted annual 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 lifelong cure for this fatal disease, develop lifesaving new therapies and help all people with CF live full, productive lives. To request a copy of our Strategic Plan, email [email protected] or call 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.