For Immediate Release
Contact: info@stopsarcoidosis.org
THE FOUNDATION FOR SARCOIDOSIS
RESEARCH CELEBRATES 10TH ANNIVERSARY
AT K.I.S.S. CHICAGO 2010
Chicago,
IL (6 February 2010) On Saturday, February 6th, the Foundation for Sarcoidosis Research (FSR) launched the annual nationwide education and
awareness campaign, Kick In to Stop Sarcoidosis® (K.I.S.S.) at KISS
Chicago 2010. This event brought together supporters, patients and
local celebrities to raise funds and to raise awareness of this
devastating disease.
“This year's launch of the national
KISS Campaign is particularly special for FSR as we celebrate both
our anniversary and a decade of successful programs,” said Andrea Wilson,
President of FSR (pictured at right with 2010 event emcees Peggy
Kusinski and Karen Russell). She highlighted key
accomplishments over the last several years that include:
Accomplishments:
-
Support: The very nature
of sarcoidosis – a multisystem disease with varied symptoms and
no known cause – can foster anxiety and fear. Today, over 4500
members from all 50 states find daily information and support
online through the
Stop
Sarcoidosis Support Community. This life line has helped
many end their isolation.
-
Education & Awareness:
Innovative community based programs are key to improving the
lives of those currently living with sarcoidosis. Annual
education conferences bring patients, family members and
caregivers together with medical professionals to provide
cutting edge information about this disease. More than
15,000 patients have received free information from FSR in the
last five years.
-
Research: The causes of
sarcoidosis and ultimately a cure, will be uncovered through
rigorous and extensive scientific research. To date, FSR has
fostered over $750,000 in grants and remains the only private
organization funding sarcoidosis specific research.
Karen
Russell daughter of famed NBA player Bill Russell was joined in emcee
duties by NBC-5 sports anchor Peggy Kusinski in sharing personal experiences
with this disease. In 2002, NBC's Chicago Affiliate WMAQ lost well-known sports anchor
Darrian Chapman to undiagnosed cardiac sarcoidosis. "I
cannot think about this anniversary without thinking back to our own
loss at NBC. 10 years is an important milestone, especially in
these financially tumultuous times. We should all feel proud of the
work that has been made possible because of KISS," said Ms. Kusinski.
Both
emcees shared that FSR would not be where it is today without
Founder Andrea Wilson who when she was diagnosed
decided she would do everything she could to help herself and help
others who suffer. At the event, the Foundation premiered a
new video highlighting the path of the Foundation's progress over
the last decade.
"We look back on our first decade with pride
and look forward with hope for what the next years will bring," said
Mrs. Wilson whose story is featured in
the video.
Click on the photo
to view the video. Note this is a large file. Please be
patient while it downloads. You will need a video
player (Windows
Media Player, Real
Player, or
Quicktime) to view.
Sarcoidosis (pronounced SAR-COY-DO-SIS) is an inflammatory disease that
can affect almost any organ in the body. It causes heightened immunity which means
that a person's immune system, which normally protects the body from
infection and disease, overreacts, resulting in damage to the body's own
tissues. Sarcoidosis is often serious and can even be
life-threatening, especially if you do not know you have it. The cause remains unknown and there is no cure.
The Foundation for Sarcoidosis Research (FSR) is the nation’s leading
organization dedicated to improving care for patients and to finding a
cure for this disease. Since 2000, FSR has worked to position
sarcoidosis as a growing problem on the U.S. health care agenda and
established itself as the authoritative resource for patients, health
professionals and the public.
2010 Campaign Corporate Supporters include: Sloan Valve
Company, NBC-5 Chicago, Grey Goose Vodka, Burrell Communications Group
and @ World Properties.
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