The National Spasmodic Torticollis Association
Over the years, National Spasmodic Torticollis Association (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 if you or someone you know has symptoms that are similar of that of Spasmodic Torticollis, please contact our office for more information and find out what we can do in terms of support.
Support Through Email – NSTAmail@aol.com
Do you have questions about your symptoms, available treatments, or anything else concerning spasmodic torticollis? You can email us your questions at NSTAmail@aol.com. We will do our best to answer any inquires you have.
NSTA Support Line – 1 800 487-8385
Finding someone who understand what you are going through is difficult when it comes to Spasmodic Torticollis. Sometimes family members and friends, with their good intentions cannot provide provide the level of support you require because they cannot understand what you are going through. Please leave a detailed message on our voicemail and we will return your call as soon as possible. The NSTA is maned by two-part time staff members so we appreciate your patience and understanding.
The General Information Packet contains information about Spasmodic Torticollis, the treatments available and ways of coping. Contact our office to request a copy.
Support Through the ST Quarterly Magazine
The ST Quarterly magazine is a great source of information about research, treatments and ways of coping with this movement disorder.
Articles are submitted by neurologists, neurosurgeons, physical therapists and other physicians who specialize in movement disorders. The St Quarterly also contains articles submitted by people who have Spasmodic Torticollis. Four issues of the ST Quarterly magazine is included with a one year membership