2020 SPONSORSHIP OPPORTUNITIES MARCH 21, 2020 6:30 PM - Ameris Bank Amphitheatre Alpharetta
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SH A MROCKIN '
FOR A CURE
2020 SPONSORSHIP
OPPORTUNITIES
MARCH 21, 2020
6:30 PM
Ameris Bank Amphitheatre
Alpharetta
ShamRockin’ for a Cure 2019 Committee
An event which began in 2009 with 150 people, beer, and wings, has now grown into North
Atlanta’s premier St. Paddy’s Day themed celebration. On March 21, 2020, more than 1,500 guests
will enjoy 30+ food and drink vendors, participate in live and silent auctions, dance the night away
with live entertainment, and support the ShamRockin’ Army in the fight against cystic fibrosis at
Ameris Bank Amphitheatre in Alpharetta. See how you can become a part of the cure... and the fun!
About ShamRockin’ Join the ShamRockin’ Army
In 2002, our only son was diagnosed with ShamRockin’ for a Cure provides a unique
cystic fibrosis. Soon after that, our second unborn experience to give back to the community and
son was also diagnosed with CF. The world stopped have a great time while doing it. When you
turning. Hopes of first football games, girlfriends, become a ShamRockin’ sponsor, you become
graduations and grandchildren turned to a future part of a tireless family committed to curing CF.
full of hospitals, mounting bills and a parent’s We work hard to deliver a positive,
worst nightmare. We have been fighting that dark collaborative experience to each sponsor.
cloud ever since.
Many people with CF are living long enough
In 2009, ShamRockin’ was born out of love and
to realize their dreams of attending college,
friendship. The idea of throwing a “Party with a
pursuing careers, getting married, and having
Purpose” took off and has grown due to the blood,
children. This is due in large part to the work of
sweat and tears of hundreds of volunteers,
the Foundation and the amazing CF community.
committee members, donors, and supporters
We helped discover the gene that causes CF,
sharing the passion for a cure.
created a state-of-the-art model for CF care,
Since inception, we have raised over $2.9 million and have funded groundbreaking research.
and inspired countless guests who have
attended the event. It’s hard to describe what But we’re not done. We are working every
happens when you look out on to the sea of day to build on this incredible momentum,
people who make ShamRockin’ come alive. and we won’t stop until there is a cure for
all people living with CF.
ShamRockin’ is more than a party. It is more than
raising money or awareness. ShamRockin’ is Hope.
-Jon Baker, CF Dad
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.
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.
THE CYSTIC FIBROSIS FOUNDATION,
leading the way
ABOUT THE CYSTIC FIBROSIS FOUNDATION ABOUT CYSTIC FIBROSIS
Founded in 1955, the Cystic Fibrosis Foundation Cystic fibrosis is a rare, genetic, life-shortening
is the world's leader in the search for a cure for disease that affects every organ in the body and
cystic fibrosis. The Foundation was started by makes breathing difficult. Some people with the
parents desperate to save their children’s lives. disease say it’s like breathing through a narrow
Their relentless and impassioned determination straw. In people with CF, a defective gene
to prolong life has resulted in tremendous strides causes a thick buildup of mucus in the lungs,
over the past 60 years in accelerating innovative pancreas and other organs. In the lungs, the
research and drug development, as well as mucus clogs the airways and traps bacteria,
advancing care and advocacy. Virtually every leading to life-threatening lung infections. Sixty
approved cystic fibrosis drug therapy available years ago, most children did not live long
now was made possible because of the enough to attend elementary school, but
Foundation and its supporters. Still, we believe thanks to Foundation-based research and
no one should have to die at a young age. We care, the median survival age of people with
will not rest until we have a cure for all CF is now into the 40’s.
people living with CF.
POT O’ GOLD PRESENTING SHAMROCK EMERALD LEPRECHAUN CLOVER
SPONSORSHIP BENEFITS (One available) (One available) $10,000 $5,000 $3,500 $2,500
$50,000 $25,000
NIGHT OF BENEFITS
Opportunity to speak onstage*
Overnight guest room at Hilton Garden Inn
2 rooms 1 room
Alpharetta for night of event
Verbal recognition from event stage
VIP Tickets to ShamRockin’ 2020 60 50 26 16 12 8
VIP Lounge VIP Lounge VIP Lounge Premier Suite in pit Reserved Box
Suite Details on stage on stage on stage or on stage
Premier Box Seating
Seating
Early event admission 6:00 PM 6:00 PM 6:00 PM 6:30 PM 6:30 PM 6:30 PM
Access to VIP Sponsor Bar
Recognition on Sponsor Banner**
Logo included in
Recognition on-screen at event 4 Slides 3 Slides 2 Slides 1 Slide Half Slide Clover Slide
Special ShamRockin’ SWAG
PRE-EVENT BENEFITS
Inclusion in 2020 ShamRockin’ for a Cure press Joint press release
announcement with Name listed Name listed Name listed
releases optional quote*
Company
Recognition on ShamRockin’ for a Cure Social Company profile & Company profile & Logo included in Name included in
profile* + CEO/Exec Logo and shoutout
Media (Facebook & Instagram) Spotlight
optional quote* optional quote* Leprechaun posting Clover posting
Invitations to Sponsor Appreciation and
Momentum Events
Company profile*
Company profile* +
Inclusion in Event e-newsletter + premier logo
featured logo
Logo Logo Name listed Name listed
placement
Company branded name/logo/link on
ShamRockin’ website through 2020
Tax Deductible Amount $46,495 $22,145 $8,551 $4,091 $2,807 $2,023
*Guidelines provided **If received by print deadline
CONFIRM YOUR
2020 ShamRockin’ for a Cure Sponsorship
POT O’ GOLD SPONSOR $50,000 EMERALD SPONSOR $5,000
$46,495 Tax Deductible $4,091 Tax Deductible
PRESENTING SPONSOR $25,000 LEPRECHAUN SPONSOR $3,500
$22,145 Tax Deductible $2,807 Tax Deductible
SHAMROCK SPONSOR $10,000 CLOVER SPONSOR $2,500
$8,551 Tax Deductible $2,023 Tax Deductible
Contact Information
____________________________________________________________________________
Contact Us
Person or Organization (as it should appear in printed material) with any questions or comments.
____________________________________________________________________________
Address CFF Georgia Chapter
57 Executive Park South, Ste. 380
____________________________________________________________________________ Atlanta, GA 30329
City State Zip 404.325.6973
____________________________________________________________________________
Telephone Email Ginny Conrad
vconrad@cff.org
____________________________________________________________________________
Authorized signature Date
Payment Information
Check Enclosed (Made payable to CFF) Please Invoice Me Credit Card Pay online
events.cff.org/shamrockinforacure
Visa Mastercard AMEX Discover AMOUNT TO CHARGE $
NAME ON CARD
SIGNATURE
This signature authorizes the Cystic Fibrosis Foundation to charge the credit card number below the stated and agreed upon amount.
/
CREDIT CARD NUMBER EXPIRATION
The credit card information at the bottom of this form will be securely destroyed immediately after processing.
The Cystic Fibrosis Foundation has unrestricted financial reserves of about 10 times its 2019 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 lifelong 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 800 FIGHT-CF.You can also read
