Welcome to the Facial Paralysis and Bell’s Palsy Foundation

facial paralysis foundation webinars

The Facial Paralysis & Bell’s Palsy Foundation is a non-profit organization founded in 2009, with the goal to provide support, encouragement, and resources to individuals and families dealing with facial paralysis and Bell’s Palsy.

We are also dedicated to raising awareness of facial paralysis concerns within the medical community, and in society at large.

Thank you for visiting our website, and we hope that you will find resources and information to encourage you on your journey with facial paralysis.

Current Happenings

Upcoming Meetings!

Monday, January 13th  – Denver, Colorado Support Group Meeting –   For more information click here.

Saturday, January 25th – Pacific Northwest Facial Paralysis Group Meeting in Portland, Oregon –   For more information click here.

New Podcast Series

“Unique Smiles: The Facial Paralysis Podcast” with Brian Apprille – Click here to listen as Brian interviews a variety of guests who share their personal journey with facial paralysis.

Latest Posts


Please click on the button above to make a donation via PayPal.
You may also donate by check to:

Facial Paralysis & Bell’s Palsy Foundation

9401 Wilshire Blvd, Suite 650
Beverly Hills, California 90212

Contact us

To fill out our contact form, please click here.

REMINDER: The Facial Palsy Support Network of Baton Rouge, Louisiana will hold its next meeting on Tuesday, October 12, 2021, at 7:00 p.m.!This meeting will take place at the Main Library at Goodwood, 7711 Goodwood Blvd. in Baton Rouge. If you are interested in attending, then please RSVP by email to: connect2fpsn.com. If you have more questions, you can also call 225-445-3885.The group facilitators for this meeting are local residents Kasey Gary and Sara MacDowell, who is a facial physical therapist. This will be a chance to connect with others who are living with facial paralysis in a supportive and encouraging environment. If you live in the southern Louisiana area, we hope you can attend! ... See MoreSee Less
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If you have an interest in current research into the genetic causes of facial paralysis, then join in this zoom meeting today, hosted by the Moebius Syndrome Foundation!Join us on September 21 at 12 PM PDT as we talk to some of our Scientific Advisory Board about updates in the genetic research of Moebius syndrome. There will be time for a Q&A session as well, if anyone has questions. Please pre-register here zoom.us/webinar/register/WN_A0Nkh9WvQa6CYlplKt7YKA ... See MoreSee Less
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