Meet others with Facial Palsy or Bell's Palsy
Thanks to the internet, there is now quite a large network of people affected by facial paralysis who are
communicating with each other and supporting each other.
We know from our own experiences that one of the worst things about having facial palsy or Bell's palsy is the
feeling of being alone. Talking to others who live with facial paralysis or who parent a child with it,
really does help. Meeting someone else with facial paralysis helps you truly believe and understand that we
are not defined by our faces.
To be put in touch with our network of friends from all over the world, please complete the contact form
below. Please note that we do take online safety very seriously and our network of parents will monitor
introductions carefully to ensure that children are kept safe.