The Educated Patient: The Facial Pain Association

December 28, 2009

The Facial Pain Association's Learning Center provides numerous patient-focused guides, one of which aid individuals fighting insurance coverage denials and another that helps neuropathic facial pain sufferers better understand their rights as disabled individuals under various state and federal laws.

The Facial Pain Association’s (FPA) Learning Center provides numerous patient-focused guides, one of which aid individuals fighting insurance coverage denials and another that helps neuropathic facial pain sufferers better understand their rights as disabled individuals under various state and federal laws. Formerly the Trigeminal Neuralgia Association, the FPA connects individuals as care-seekers and caregivers through numerous support group listings under the “Patient Support” tab. Under the same tab is a resource for children, teens, and young adults suffering from facial pain.

Click here to view this third party resource.