About the Foundation
What We Do
The Brachial Plexus Care Foundation supports people with brachial plexus injuries and their families, financially, educationally, and emotionally. Many families come to us after a diagnosis with more questions than answers, and often without knowing which questions to ask. We're here to help with that, at any age and any stage.
Connecting families
We host virtual meet-and-greets where families, teens, and adults living with brachial plexus injuries can meet others who understand what they're going through. Whether you're a new parent or an adult navigating life with a BPI, you don't have to figure it out alone.
Answering your questions
Have a question about treatment, therapy, school, or what to expect as your child grows? Reach out anytime. We'll share what we know, point you toward trusted resources, and help you prepare for conversations with your care team.
Making camp possible
Through fundraisers like Art for Palsies, we've raised $13,500 to send children and families, including families from outside the U.S., to Camp UBPN, where kids with brachial plexus injuries can build confidence and friendships with peers who share their experience.
Raising awareness
We take part in community efforts to bring visibility to brachial plexus injuries and the people who live with them.
