Scleroderma Education Days
The Scleroderma Foundation hosts various educational events for individuals who have scleroderma, and their family members and caregivers throughout the year. Many of these events are run by our chapters and support groups. To find an event near you, contact your local chapter or support group.
National Scleroderma Conference
The 2021 virtual National Scleroderma Conference, Connect & Thrive Together, will take place July 17 & 18. Although the COVID-19 pandemic appears to be on the decline, a virtual conference is the best option to protect vulnerable members of the scleroderma community. A virtual conference still provides access to vital scleroderma information and experts, and to others affected by the disease. Details about registration and programming are available on the conference web page. Register today before rates increase July 9. You may also submit your email here to receive conference aAlerts form time to time.
The Scleroderma Foundation's National Scleroderma Conference brings together leading scleroderma experts from around the world to educate and connect with individuals affected by scleroderma. Typically held in a different city in the United States each year, the National Conference is one of the largest gatherings for the scleroderma community. It includes panel discussions, workshops, and other activities to help answer your questions about the disease. Sample workshops and discussion topics include:
Conference attendees also can meet with vendors in our exhibit hall, attend a welcome networking dessert reception, and meet with high-profile scleroderma physicians, researchers and other health care professionals in a one-on-one environment. The conference is an excellent opportunity to meet new friends and discuss ways to cope with the disease the a supportive, positive environment.
**Please note that these titles are examples only. If you attend the conference, the program book will contain the actual listing of topics and workshops.
The Foundation also offers the Kids Get Scleroderma, Too! (KGS2) conference for youth, ages 5 to 17, who have scleroderma, and for their parents or guardians and siblings. The 2021 KGS2 conference takes place later in the year. Enter your email address here to receive updates when programming information is available.
The Scleroderma Foundation "Virtual University" Patient Education Series was a series of exciting webinars, live meetings, workshops, and Scleroderma-related education videos during 2020 in place of the in-person National Scleroderma Conference. Follow these links to watch video recordings of the 2020 summer series and the fall series.
Juvenile Scleroderma Education
African-American Scleroderma Education Day
In 2014, the Scleroderma Foundation hosted its second educational event dedicated solely to the African-American community. The Foundation partnered with scleroderma experts from Johns Hopkins University Medical Center and Georgetown University Medical Center to host this important event.Find out more about the African-American Scleroderma Education Day
Physician and Continuing Education Courses
The following continuing medical education (CME) and continuing education (CE) courses are available for health care professionals about scleroderma and related diseases:
- Patients & Newly Diagnosed
- Healthcare Professionals