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Save the Date November 30, 2015
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Black Tie International:
Moving Forward Together to Fight Lupus Annual Gala
 

Moving Forward Together to Fight Lupus Annual Gala


 

MOVING FORWARD TOGETHER 
To Fight Lupus Annual Gala

WHEN:
Monday, November 30, 2015

6:30 pm Cocktail Reception
7:30 pm Dinner & Awards Presentation

WHERE: 
The Waldorf Astoria
301 Park Avenue, NYC

HONORING: 
Susan Golick and Jennie DeScherer
 with the Visionary Leadership Award 
Verizon Communications with the Corporate Leadership Award

CO-CHAIRS:
Richard K. DeScherer
, President, S.L.E. Lupus Foundation; Chief Legal and Compliance Officer, Bloomberg LP
Robert Wood Johnson IV, Chairman, Alliance for Lupus Research; Chairman and Chief Executive Officer, New York Jets
Robert W. Pittman, Chairman and CEO, iHeartMedia Inc.
Robert J. Ravitz, Chairman, Lupus Research Institute

Event DescriptionThe world's largest lupus gathering as the Alliance for Lupus Research, Lupus Research Institute and S.L.E. Lupus Foundation co-host our first joint Gala. Funds raised will advance the most innovative research to transform patients' lives. We are very excited to be 'Moving Forward Together' in the pursuit of better treatments and a cure for lupus.  

Event Agenda: Cocktails, Formal Program/Dinner, Entertainment

Table and Ticket Prices:

      Individual Tickets Start at: $1,500

      Table for 10 guests and program recognition at varying levels: Sponsor: $12,500; Patron: $15,000; Underwriter: $25,000

      Table for 20 guests and program recognition at varying levels: Benefactor: $50,000; Advocate $100,000+

 

About the Alliance for Lupus Research

The Alliance for Lupus Research (ALR) is a national voluntary health organization dedicated to finding better treatments and ultimately preventing and curing systemic lupus erythematosus (SLE, or lupus), a debilitating autoimmune disease. The organization is based in New York City and chaired by Robert Wood Johnson IV, a member of the founding family of Johnson & Johnson. Since its founding in 1999, the ALR has given more money to lupus research than any non-governmental agency in the world. The board of directors funds all administrative and fundraising costs, allowing one hundred percent of all donations from the public, and the proceeds of our signature grassroots fundraising program, Walk with Us to Cure Lupus, to go directly to support research programs. More information can be found at www.lupusresearch.org.

 

About the Lupus Research Institute 

The Lupus Research Institute (LRI), the world's leading private supporter of novel research in lupus, pioneers discovery and champions scientific creativity as it has successfully demonstrated the power of innovation to propel scientific solutions in this complex autoimmune disease. Founded by families and shaped by leading scientists, the Institute has generated more than $200 million for novel lupus research, delivering many of the decade's most pivotal breakthroughs, transforming treatment and advancing toward prevention and a cure. For more information, visit LupusResearchInstitute.org.

 

About S.L.E. Lupus Foundation

The S.L.E. Lupus Foundation is the country's preeminent organization supporting patient and professional education, advocacy and novel research at a national level. It was founded 45 years ago in New York City by lupus patients and their families as the first nonprofit to serve the lupus community. Learn more at LupusNY.org.

 

ContactKfitzpatrick@lupusny.org

 

Gerard Mc Keon and Joyce Brooks.  Photo by:  Rose Billings/Blacktiemagazine.com

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