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FOUNDER

Sharon L. Monsky, 1953-2002


BOARD OF DIRECTORS

Luke Evnin, PhD, Chairman
Kristen Baker Bellamy
Dana Delany
Susan Feniger
Jeff Mace
Bob Saget
Deann Wright
Caryn Zucker

SCIENTIFIC ADVISORY BOARD

Bruce Alberts, PhD
National Academy of Sciences

David Botstein, PhD
Princeton University

Shaun R. Coughlin, MD, PhD
UC San Francisco

Susan Desmond-Hellmann, MD, MPH
UC San Francisco
Emeritus

Daniel Kastner, MD, PhD
National Institutes of Health

Regis B. Kelly, PhD
UC San Francisco

Henry Metzger, MD
National Institutes of Health

Antony Rosen, MD
Johns Hopkins University

William J. Rutter, PhD
Synergenics, LLC

Bruce U. Wintroub, MD
UC San Francisco

George Yancopoulos, MD, PhD
Regeneron Pharmaceuticals



 
 
 
 

   


SRF News & Events:

New York Cool Comedy - Hot Cuisine raises more than $525,000 for scleroderma research

Pictured left to right: Caryn Zucker, Seth Meyers, Colin Quinn, John Stamos, Ashley Olsen, Bob Saget,
Mary-Kate Olsen, Jeff Ross, Jeff Zucker

The Scleroderma Research Foundation thanks the sold out crowd of more than 350 guests who helped to make our
2009 New York Cool Comedy - Hot Cuisine event a tremendous success. More than $525,000 was raised to support medical
research.

The SRF gratefully acknowledges our presenting sponsor, Actelion Pharmaceuticals, for their ongoing commitment and
air partner Delta AirElite Business Jets for their participation.

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2008 Annual Report

The Scleroderma Research Foundation's 2008 Annual Report is now available for download. The Report outlines all research funding for the 2008-2009 fiscal year and includes donor and tribute lists. Also included are a description of the SRF research program, patient and volunteer profiles and a "year in review" letter by SRF Chairman Luke Evnin, PhD.

In addition to descriptions of all funded research, the 2008 Annual Report includes a "What this means for patients" paragraph about each project that explains how the research can benefit people living with scleroderma.

Please click here to view a PDF version of the Annual Report.
Please be patient. This is a very large file (19 MB) and may take several minutes to load depending on your connection speed.

SRF AR08 Cover

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Actress and Scleroderma Research Foundation Board Member Dana Delany speaks out about her "hero" on CNN's "Sharing the Spotlight: Celebrity Heroes." Her hero, SRF Chairman Luke Evnin, PhD, is a scleroderma patient and general partner at one of the world's largest investors in life sciences.

Delany calls his efforts and accomplishments on behalf of the thousands of scleroderma patients "nothing less than heroic."

In her own words, "If anybody's going to solve this problem, it's going to be Luke."

The staff and Board of Directors of the SRF congratulate both Dana Delany and Luke Evnin on their success. We thank them for helping to raise the profile of this life-threatening illness and for their dedication to improved therapies and a cure.

Please visit the CNN link here to view the print and video versions of this story.


Research Funding Levels

The Scleroderma Research Foundation (SRF) has become the nation’s largest nonprofit investor in scleroderma research, raising more than $26,000,000—with every dollar coming from charitable gifts from generous individuals, corporations and foundations. In 2009, the SRF has provided more than $1,101,000 in direct research grants. Unlike university and medical foundations restricted to one institution, the SRF actively searches out the most promising researchers and laboratories aimed at helping scleroderma patients around the world. We are now funding research at Boston University, Dartmouth, Johns Hopkins, Harvard, Northwestern University, Stanford, the University of Michigan, University of Washington and the Royal Free Centre for Rheumatology in London, England. To make a contribution, please click here.


 



There is currently no cure for scleroderma but,
in many cases, it can be managed.


About us:

The Scleroderma Research Foundation is a 501(c)(3) nonprofit organization whose mission is to find a cure for scleroderma by funding and facilitating the most promising, highest quality research and by placing the disease and the need for a cure in the public eye. Information provided by the SRF should not be considered medical advice, nor is it intended to replace consultation with a qualified physician. The SRF does not evaluate, endorse or recommend any particular medications, products, equipment or treatments. Scleroderma varies substantially from one patient to another, and treatment must be tailored by a physician for each individual case.
   
 
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