The National Spasmodic Torticollis Association is a non-profit organization dedicated to:       Providing information and support to ST patients       Educating the public and medical community about ST       Advocating for the rights of those with ST       Promoting research on ST Over the years, NSTA has helped thousands of people in their search for relief from the pain and disability caused by ST. Our services are available to anyone, and in fact, the majority of people we help are not members of NSTA. We are, however, extremely grateful to our dues-paying members without whom we could not continue our work. We reward our dues-paying members with:           A quarterly news magazine       Deeply discounted prices to attend our symposiums, held at least annually       And many, many thanks for their support Member’s dues help pay for:        Our 1-800-HURTFUL support line       Our link to doctor referrals and medical advice from health care professionals on our          Medical Advisory Board       Our network of support groups around the country       And much, much more