Who Are We? We are men and women who happen to have scleroderma and live in New York, New Jersey, or Connecticut. Thousands of people live with scleroderma. Most of us, perhaps just like you, have found the world of scleroderma to be strange, and at times, scary. We have a vast array of medical problems due to scleroderma, and varying degrees of life experience dealing with those problems. Some of us are new to this world; others have been living with scleroderma in one form or another for 5, 10, 20, 30, 40, and yes, even 50 years or more. We are here for each other and for you. Our Mission The mission of the Scleroderma Foundation Tri-State Chapter is threefold: To provide educational and emotional support to people with scleroderma and their families; To stimulate and support research designed to identify the cause and cure of scleroderma as well as improve methods of treatment and; To enhance the public’s awareness of this disease.
Raffle Prize: Yes
Interactive Element: We will give out information on Scleroderma, a rare disease. Interactive discussions
Brings Printed Materials: Yes
Brings Giveaways & Freebies: Yes
Zeba Hyder
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