A disease registry is a database of information on patients with a particular disease and their biological relatives. The registry can be accessed and used by researchers, clinicians, and physicians interested in studying the disease. Registries are absolutely essential in diseases like FSHD where access to patients and materials is limited. Participation by unaffected family members is especially important in FSHD, as these individuals provide genetically similar controls and, especially, because some turn out to have FSHD at the genetic level. Such individuals can shed light on the mechanism of FSHD and point the way to treatments. Many more research projects and avenues of investigation will result from FSHD patients and their families signing up and becoming involved!
TREAT-NMD maintains a list of international registries here.
There are several patient registries available for FSHD in the United States:
National Registry of Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy
Leann Lewis, MS Health Project Coordinator at the University of Rochester Medical Center/Fields Center/Neuromuscular Disease Center Phone: 585-275-7680 Email: email@example.com
The National Registry of Myotonic Dystrophy and FSHD, 601 Elmwood Avenue, Box 673, Rochester, NY 14642-8673; USA Toll free: (888) 925-4302 (9 a.m. to 4 p.m. weekdays, EST); Local (Rochester, NY): (585) 276-0004 Fax: (585) 273-1255; Email: firstname.lastname@example.org; Web: http://www.dystrophyregistry.org
UC Davis Research Volunteer Registry
Stanford volunteer registry
The FSH Society maintains an FSHD registry of patients and families wishing to become involved in research. To join, simply fill out this contact form: