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.

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Attention Australia! The Inaugural Facial Paralysis Awareness Day will take place in Sydney on Sunday, March 8, 2020, from 12:00 noon – 4:00 p.m.!

Sponsored by facial paralysis advocate Elizabeth Robinson, this will be an opportunity for those in Australia to meet and mix with other people who have facial paralysis, due to any cause.

The event will include a catered lunch, followed by speakers from the facial paralysis community, door prizes, a goodie bag, and ending with a walk of support!

The cost will be $30 per person, or $70 per family of four, and friends and supporters are welcome to attend. For more information, please contact organizer Elizabeth Robinson by email at: fpawarenessday2020@gmail.com.

You can also join Elizabeth’s Facebook group, Facial Paralysis Support Network Australia New Zealand Word, for the latest details!

If you live in Australia, please share this post, and come and support facial paralysis awareness!
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