Team Jayme Foundation

Team Jayme Foundation is rated 3 out of 5 in the category nonprofit organization management. Read and write reviews about Team Jayme Foundation. 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.