The Team Jayme Foundation was initially established to raise money for the treatment of Jayme Avery van Pelt, born 24-05-2019 and diagnosed with the neuromuscular disease SMA type 1. The goal of the Team Jayme Foundation is to support families in similar situations with both financial as social-emotional aspects of having a child with a rare neuromuscular disease. The Team Jayme Foundation also wants to generate more attention for rare neuromuscular diseases in general and SMA type 1 in particular, by providing information to specialists and other interested parties.