What we do for you: the value of your membership in the Scleroderma Foundation

Here are some of the programs and services your membership helps support:

  • RESEARCH. Thanks to you, we are funding around $1 million of original research this year.

  • EDUCATION. We maintain a full line of updated literature, written by leading experts, on a wide range of medical conditions related to scleroderma.
  • SUPPORT. We manage a nationwide network of Chapters and Support Groups.
  • INFO LINE. We have a full-time Education Manager who staffs our Info Line (1-800-722-HOPE), provides doctor referrals, and mails out information to people who inquire by phone or our website.
  • ADVOCACY. We are building alliances with similar health organizations and making our case on Capitol Hill.
  • NATIONAL CONFERENCE. Each year, we bring together medical experts to present you with the latest information about scleroderma and personally answer your questions, and members receive $50 off the registration fee!

Become a member and receive our quarterly magazine!It's easy to support our mission!

For only $25 a year, you can support our mission ... and receive our quarterly magazine, packed with 

  • Updates on the latest scleroderma research and treatments.
  • Articles by leading doctors and other health professionals.
  • Answers to your medical questions by health professionals.
  • Practical tips on coping with scleroderma.
  • Heartwarming stories about people with scleroderma, describing how they have met and overcome their challenges.
  • And not least, articles about what the Scleroderma Foundation is doing for you—such as funding over $1 million in new research in 2007; advocating for more federal research funding on Capitol Hill; and working nationwide, year-round to raise public awareness of scleroderma and its impact on individuals and their families.

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