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The Trigeminal Neuralgia Association provides information, mutual aid, support, and encouragement, promotes increased awareness and understanding of the condition, and serves as a resource and information center. They also facilitate and promote research on trigeminal neuralgia. They have local support groups with a directory available. They will provide assistance to persons who wish to start a support group in their locality. TNA provides parent-to-parent matching through direct telephone contact.
The Association publishes a quarterly newsletter TNAlert. There is no charge for the first copy, but donations are requested for further copies. The Association has a brochure that explains the condition and the organization and videotapes of various presentations at support group meetings.
TNA collects information on physicians and researchers who treat/study the condition and disseminates this information through articles in the quarterly newsletter. Additionally they will provide referrals to other resources.
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