NOSH – CYSTIC FIBROSIS FOUNDATION GALA 2020 THE IVORY … · 2019-12-12 · NOSH is the premiere...
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#NOSH2020 EVENTS.CFF.ORG/NOSH FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME. NOSH – CYSTIC FIBROSIS FOUNDATION GALA 2020 THE IVORY ROOM AT MIRANOVA SATURDAY, FEBRUARY 22, 2020 AT 5:30 PM
Transcript of NOSH – CYSTIC FIBROSIS FOUNDATION GALA 2020 THE IVORY … · 2019-12-12 · NOSH is the premiere...
#NOSH2020 EVENTS.CFF.ORG/NOSH FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
NOSH – CYSTIC FIBROSIS FOUNDATION GALA 2020
THE IVORY ROOM AT MIRANOVA SATURDAY, FEBRUARY 22, 2020 AT 5:30 PM
#NOSH2015 NOSH.EVENTSCFF.ORG
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
#NOSH2020 EVENTS.CFF.ORG/NOSH
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
CYSTIC FIBROSIS (CF) AFFECTS 30,000 PEOPLE ACROSS THE COUNTRY AND 70,000 WORLDWIDE.
WITH ROUGHLY 500 CHILDREN AND ADULTS WITH CYSTIC FIBROSIS LOCALLY, OHIO HAS THE 5TH HIGHEST PATIENT POPULATION ACROSS THE COUNTRY.
TOGETHER WE CAN WORK TOWARD A ONE-TIME CURE.
#NOSH2015 NOSH.EVENTSCFF.ORG
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
#NOSH2020 EVENTS.CFF.ORG/NOSH
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
#NOSH2015 NOSH.EVENTSCFF.ORG
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
#NOSH2020 EVENTS.CFF.ORG/NOSH
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
NOSH is the premiere event for the Central Ohio Chapter of the Cystic Fibrosis Foundation (CFF). Now in its 5th season, it has grown to be one of the most anticipated chapter events of the year. The evening will include by-the-bite tastings from six of Central Ohio’s top Executive Chefs employed by Cameron Mitchell. Each tasting will include at least one of three ingredients decided upon by CF dieticians. This year’s ingredients are: Butter, Gorgonzola Cheese and Dried Fruits. The chefs will then concoct their own creations based off this ingredient list to create a one-of-a-kind dish, not currently available on any Cameron Mitchell restaurant menu. Guests will enjoy their cocktail hour by tasting these unique dishes and placing bids on an exciting silent auction.
After guests have awakened their palates, they’ll be seated for dinner provided by Cameron Mitchell Premier Events and enjoy a presentation by a CF Fighter.
After the presentation, guests will then engage in a live auction and have an opportunity to be generous to the cause during our Bid-for-the Cure. To wrap up the night, guests will enjoy a live band, dancing, cocktails and dessert to celebrate the generosity of the evening! For more information please contact Ami DeAngelo at [email protected] or 614.890.6565.
WHEN Saturday, February 22, 2020 TIME 5:30 PM WHERE The Ivory Room at Miranova
2 Miranova Place, 6th Floor Columbus, OH 43215
PRICE $200 per person ($145 is tax-deductible)
$3,500 corporate table ($2,885 is tax-deductible) Purchase your tickets and tables quickly, event sells out at 250 guests (10 guests per table)
TICKETS events.cff.org/nosh or call 614.890.6565
NOSH GALA ABOUT THE EVENT
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS To reduce the risk of getting and spreading germs at Cystic Fibrosis 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 help further reduce the risk of cross-infection, the Foundation's attendance policy recommends inviting only one person with CF to an indoor Foundation-sponsored event at a specific time.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHAT IS CYSTIC FIBROSIS (CF)? Cystic fibrosis is a rare, genetic, life-shortening disease that affects every organ in the body and makes breathing difficult. Some people with the disease say it’s like breathing through a narrow straw. In people with CF, a defective gene causes a thick buildup of mucus in the lungs, pancreas, and other organs. In the lungs, the mucus clogs the airways and traps bacteria, leading to life-threatening lung infections. Sixty years ago, most children did not live long enough to attend elementary school, but thanks to Foundation-based research and care, the median survival age of people with CF is now into the 40s. Cystic fibrosis affects 30,000 people across the country and 70,000 worldwide. Ohio has the fifth highest patient population in the US with 1,550 patients. Roughly 500 of those children and adult patients live in the Central Ohio area. PROGRESS INFO Many people with CF are living long enough to realize their dreams of attending college, pursuing careers, getting married, and having children. This is due in large part to the work of the Foundation and the amazing CF community. We helped discover the gene that causes CF, created a state-of-the-art model for CF care, and have funded groundbreaking research. But we’re not done. We are working every day to build on this incredible momentum, and we won’t stop until there is a cure for all people living with CF.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
THE CYSTIC FIBROSIS FOUNDATION The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis, a life-threatening genetic disease that affects 30,000 children and adults in the United States and 70,000 people worldwide. The Foundation funds and accredits a nationwide network of 130 CF care centers, which provide vital resources and support to patients and families in your community. Dramatic improvements in the length and quality of life for people with CF are a direct result of the Foundation’s investments in quality care and research.
TRUSTING US WITH YOUR INVESTMENT The Foundation is an accredited charity of the Better Business Bureau’s Wise Giving Alliance, meeting all its Standards for Charitable Accountability. The Foundation has also been recognized by Forbes, Business Week, USA Today and The New York Times for its innovative approach to research. Learn more about the Foundation at www.cff.org
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WHY BE A PRESENTING SUPPORTER? With your support as a Presenting Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE $10,000 (tax-deductible $8,540) NUMBER OF SUPPORT PACKAGES 1 TABLES OF TEN 2 with premium seating EXTRAS Presenting rights to specific portion of event (ex. Tasting Reception Presented By COMPANY)
WHAT YOU GET • Inclusion in all pre-Gala publicity events as well as chapter
newsletter • 2 full-page acknowledgements in Event Program Book which may
be used to pay tribute to your company’s philanthropic activities • Opportunity to have two members sit on Event Planning Committee • Special recognition at the Event • Corporate signage throughout the Event • Special recognition at the Event • Right of first refusal for following years event • Lighted gobo featured in the Tasting Room • Four Tomorrow’s Leaders Enrollments and Name Recognition
during the event. Tomorrow’s Leaders is the Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A NOSH “PIT” SUPPORTER? With your support as a NOSH “PIT” Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE $7,500 (tax-deductible $6,770) NUMBER OF SUPPORT PACKAGES 1 TABLES OF TEN 1 table with premium seating EXTRAS • Corporate branding sections in NOSH “PIT” area featuring
desserts, coffee and water • Corporate signage at each section
WHAT YOU GET • Corporate signage at NOSH “PIT” Area • Corporate identity in all communications and event media • 1 full-page acknowledgement in Event Program Book which may
be used to pay tribute to your company’s philanthropic activities • Corporate signage at NOSH “PIT” Area • Inclusion in pre-Gala publicity • Special recognition at the Event • Two Tomorrow’s Leaders Enrollments and Name Recognition
during the event. Tomorrow’s Leaders is the Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
#NOSH2015 NOSH.EVENTSCFF.ORG
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A CHEF STATION SUPPORTER? With your support as a Chef Station Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE $5,000 (tax-deductible $4,320) NUMBER OF SUPPORT PACKAGES 6 TABLES OF TEN 1 with premium seating EXTRAS Logo featured at your supported Chef Station
WHAT YOU GET • Corporate identity in all communications and event media • 1 full-page acknowledgement in Event Program Book which may
be used to pay tribute to your company’s philanthropic activities • Corporate signage at Reception Area • Inclusion in pre-Gala publicity events • Special recognition at the Event • Two Tomorrow’s Leaders Enrollments. Tomorrow’s Leaders is the
Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
#NOSH2015 NOSH.EVENTSCFF.ORG
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WHY BE A SILENT AUCTION SUPPORTER? With your support as a Silent Auction Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE $5,000 (tax-deductible $4,320) NUMBER OF SUPPORT PACKAGES 1 TABLES OF TEN 1 with premium seating EXTRAS Company signage in Silent Auction area and on mobile bidding site
WHAT YOU GET • Logo recognition in program book as Silent Auction Supporter • Silent Auction signage (ex. Silent Auction presented by “Company”) • Recognition in each Silent Auction vendor thank you letter • Inclusion in all pre-Gala publicity • Corporate identity in all communications and event media • Two Tomorrow’s Leaders Enrollments. Tomorrow’s Leaders is the
Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
#NOSH2015 NOSH.EVENTSCFF.ORG
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
#NOSH2020 EVENTS.CFF.ORG/NOSH
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A LIVE AUCTION SUPPORTER? With your support as a Live Auction Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE $4,000 (tax-deductible $3,385) NUMBER OF SUPPORT PACKAGES 1 TABLES OF TEN 1 EXTRAS Logo on each Live Auction slide (4 slide min)
WHAT YOU GET • Logo recognition in program book as Live Auction Supporter • Live Auction signage (ex. Live Auction presented by “Company”) • Recognition in each Live Auction vendor thank you letter • Inclusion in all pre-Gala publicity • Corporate identity in all communications and event media • One Tomorrow’s Leaders Enrollment. Tomorrow’s Leaders is the
Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
#NOSH2015 NOSH.EVENTSCFF.ORG
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#NOSH2020 EVENTS.CFF.ORG/NOSH
FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A CORPORATE TABLE? With your support as a Corporate Table you’ll be helping families and children with CF through research, education and care centers. PRICE $3,500 (tax-deductible $2,885) NUMBER OF SUPPORT PACKAGES 25 TABLES OF TEN 1
WHAT YOU GET • Half- page recognition in Gala Program Book which may be
used to pay tribute to your company’s philanthropic activities • Corporate signage at Registration and your corporate table • One Tomorrow’s Leaders enrollment. Tomorrow’s Leaders is
the Cystic Fibrosis Foundation’s young professional program, designed to offer like-minded professionals leadership skills and networking opportunities while they make a difference in the lives of those with cystic fibrosis.
#NOSH2015 NOSH.EVENTSCFF.ORG
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A GUARDIAN ANGEL? With your support as a Guardian Angel you’ll be helping families and children with CF through research, education and care centers. PRICE $1,000 or $2,500 (100% tax-deductible) NUMBER OF SUPPORT PACKAGES Unlimited EXTRAS Name listed in NOSH event program
WHAT YOU GET • Be a guardian angel at a $1,000 or $2,500 level. • This is an outright donation that is 100% tax-deductible.
#NOSH2015 NOSH.EVENTSCFF.ORG
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
WHY BE A PROGRAM SUPPORTER? With your support as a Program Supporter you’ll be helping families and children with CF through research, education and care centers. PRICE (100% tax-deductible) Center Spread - $2,500 Outside Back Cover - $2,500 Inside Front Cover - $1,000 Inside Back Cover - $1,000 Full Page - $750 Half Page - $500 Quarter Page - $250 NUMBER OF SUPPORT PACKAGES There is only one Program Support Package available for each of the following: Center Spread, Outside Back Cover, Inside Front Cover and Inside Back Cover. Full, Half and Quarter Page Support Packages have unlimited availability.
WHAT YOU GET
• Opportunity to feature you, your company or organization in a premium location within the NOSH 2020 Gala program
• Custom designed acknowledgement template featuring your name, organization name or company name and logo
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FIGHTING CYSTIC FIBROSIS. ONE BITE AT A TIME.
For more information please contact the Cystic Fibrosis Foundation: Ami DeAngelo 575 Copeland Mill Rd #1A, Westerville, OH 43081, P:614.890.6565, [email protected]
The Cystic Fibrosis Foundation has unrestricted financial reserves of about 10 times its budgeted 2019 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, 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 [email protected] or call 1-800-FIGHT-CF.
Please choose a program acknowledgement option:
☐ CENTER SPREAD - $2,500
☐ OUTSIDE BACK COVER - $2,500
☐ INSIDE FRONT COVER- $1,000
☐ INSIDE BACK COVER- $1,000
☐ FULL PAGE - $750
☐ HALF PAGE - $500
☐ QUARTER PAGE - $250 Select what information you would like to appear in your company acknowledgement. Please send logo in eps, png or jpeg format to [email protected]
☐ COMPANY NAME ____________________________________________________
☐ ADDRESS __________________________________________________________
☐ PHONE _____________________________________________________________
☐ EMAIL _____________________________________________________________
☐ WEB ADDRESS _____________________________________________________
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This signature authorizes the Cystic Fibrosis Foundation to charge the credit card number above the stated and agreed upon amount. The credit card information on this form will be securely destroyed immediately after processing.
For more information please contact the Cystic Fibrosis Foundation: Ami DeAngelo 575 Copeland Mill Rd #1A, Westerville, OH 43081, P:614.890.6565, [email protected]
Please PRINT Company name as you would like it to appear for recognition purposes. Please send logo in eps or jpeg format to [email protected].
The Cystic Fibrosis Foundation has unrestricted financial reserves of about 10 times its budgeted 2019 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, 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 [email protected] or call 1-800-FIGHT-CF.
