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

Donate

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 will hold an introductory meeting tomorrow night, Wednesday, June 16th, at 6:00 p.m. CST at the Jones Creek Library, 6222 Jones Creek Road in Baton Rouge, Louisiana!

A special guest at the meeting will be Dr. Kathleen Bogart, an Associate Professor of Psychology at Oregon State University. Kathleen has facial paralysis due to Moebius Syndrome, and is a facial paralysis advocate and researcher. In addition, she is a Baton Rouge native!

If you are interested in attending this meeting, please RSVP by email to: connect2fpsn@gmail.com. For more detailed information, you can also join the FPSN Facebook group at:
www.facebook.com/groups/262315318802357

Anyone dealing with facial paralysis is encouraged to attend, and family members are also welcome. This would be a great opportunity to meet Dr. Bogart, and to connect with others living with this condition!
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2 months ago

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Attention to those in the Baton Rouge, Louisiana area - a new facial paralysis support group is now forming!

The Facial Palsy Support Network of Baton Rouge will hold an introductory meeting on Wednesday, June 16th, at 6:00 p.m. CST at the Jones Creek Library, 6222 Jones Creek Road in Baton Rouge.

In attendance at this meeting will be Sara MacDowell, a facial physical therapist at Our Lady of the Lake Hearing and Balance Center.

And our special guest will be Dr. Kathleen Bogart, an Associate Professor of Psychology at Oregon State University. Kathleen has facial paralysis due to Moebius Syndrome, and is a facial paralysis advocate and researcher. In addition, she is a Baton Rouge native!

If you are interested in attending this meeting, you can RSVP by sending an email to: connect2fpsn@gmail.com. For more detailed information, you can also join the FPSN Facebook group at:
www.facebook.com/groups/262315318802357

Anyone dealing with facial paralysis is encouraged to attend, and family members are also welcome. Hope to see you there!
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