NSTA aims to support the needs and well being of affected individuals and families, promote awareness and education, and advance research. Information on available treatment options, resources, and support for individuals and families.
Support for individuals with ST and their families. Promotes research, public education, and establishment of spasmodic torticollis support groups throughout the US. Newsletter, list of neurologists, pen pals, phone network, and chapter development guidelines.
Meeting Info:
Please visit the website for current contact, support group, and/or resource information.
Fees:
Unknown