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The Scleroderma Foundation is the leading non-profit supporter
of scleroderma research in the United States, allotting more
than $1 million annually to find the cause of and cure for
scleroderma. Since 1989, nearly $12 million in research funds
has been allotted. To promote education of the disease, the
foundation facilitates health and professional seminars, produces
and distributes literature and conducts publicity campaigns.
To help support the 300,000 people living with scleroderma,
the foundation offers peer counseling, mutual support programs,
and physician referrals.
In this section, members of the media can access information
about scleroderma through press releases, disease overviews,
fact sheets, public service announcements, and advertisements.
Both current and archived news releases on scleroderma are
included, as is information on key individuals with the foundation.
To access key individuals affiliated with scleroderma, including
physicians, patients, and management, please contact Liz Dorsett
so she can facilitate your request. |
