9401 Wilshire Blvd., Suite 650
Beverly Hills, CA 90212
Email: facialparalysisfound@gmail.com

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

Watch This Inspiring News Story!

From San Diego Support Group Leader Brian Apprille – click here to watch!

New Webinar Recording Available!

Our latest webinar, Beauty Tips to Improve Facial Symmetry with Carson Barenborg, is now available – click here to watch

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.

Upcoming Online Group Meetings

Join us for “Get Connected” – our series of online, interactive support group meetings!  This is a time when participants can share their personal experiences and support others dealing with facial paralysis. Here’s our upcoming schedule:

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.

Facebook Posts

If you are in the southern California area, then come meet others with facial paralysis at our first support group meeting of 2019 in San Diego this Saturday, January 12th, at 10:30 a.m.!

This group is led by Brian Apprille, a professional comedian who has experienced facial paralysis due to Ramsay Hunt syndrome. There will be plenty of time for networking and sharing with others who understand your concerns and experiences.

Please see our event post for all the details, and to RSVP.
All persons with facial paralysis and their families are welcome to attend!
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6 days ago

Facial Paralysis & Bell's Palsy Foundation
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Sending wishes for a wonderful 2019 to all of our facial paralysis warriors! ... See MoreSee Less

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