The Hemifacial Spasm Association (HFSA) was formed to provide an international online support community for individuals, and their families, dealing with Hemifacial Spasms (HFS). We are a network of caring people, just like you. Current and former sufferers, who have also felt the embarrassment, frustration, depression, anger and other emotions, frequently experienced while trying to deal with Hemifacial Spasms. Through this network of dedicated individuals, the HFSA provides information, hope and reassurance based on individual personal experiences coping with and treating the symptoms of HFS.

We are not doctors, therapists, psychologists or in any way affiliated with the medical community. We do not offer medical advice or treatment of any kind. What we are is a group of individuals who offer support, understanding and friendship. We know what you've been through and where you are right now. If you would like to join us in our journey, then explore our site. We hope that you will come to call it home.

Disclaimer: The information you view on this page reflects the personal opinions/experiences of individual members and is not necessarily the view of the HFSA or group owner. This service is provided for information and educational purposes only. We do not endorse, advocate or warrant the accuracy or reliability of information provided, nor exert responsibility, editorial or other control over the contents. You, the user, assume all risks associated with the use of any information you obtain, directly or indirectly, from this website and your reliance upon it. You agree to hold harmless and not seek remedy in any court of law from the owners or any members because of your reliance upon anything derived from this website.

Always consult your own physician before proceeding with or deciding upon a course of treatment or in attempting to reach a diagnosis for treatment.

By joining the HFSA you agree to the above terms and conditions.