Little Charlie Rocks
and Little Matthew Rolls
and Little Matthew Rolls
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Jorge Posada Foundation
Don't forget to visit our shop for charity page, to order Jorge Posada's shirts, sweatshirts, baby items, and even coffee cups!
The Foundation's Mission
The Jorge Posada Foundation is a non-profit organization established by the New York Yankees’ All-Star Catcher, Jorge Posada, and his wife, Laura. Their son, Jorge Jr., was diagnosed with Craniosynostosis when he was just ten days old and had to undergo five major surgeries to correct the condition.
The Jorge Posada Foundation is a non-profit organization established by the New York Yankees’ All-Star Catcher, Jorge Posada, and his wife, Laura. Their son, Jorge Jr., was diagnosed with Craniosynostosis when he was just ten days old and had to undergo five major surgeries to correct the condition.
Through the Foundation, the Posada Family is able to: reach out to those families in need, whose children are affected by Craniosynostosis, and provide them with emotional support through its family support network; provide financial assistance to underwrite a portion of the costs of initial surgeries in its partner medical centers; and encourage further research of this medical condition. The Foundation also strives to create awareness through events and through funding other educational outreach efforts.
Mentors Program
The Foundation receives a number of requests from families with children that have been diagnosed with Craniosynostosis, who just need to talk about their experience, or are looking for advice and emotional support. To serve this need, the foundation has developed a Mentors Program, where they recruit volunteers that have experienced Craniosynostosis in their family. These volunteers are then partnered up with those families looking for help.
We feel honored to have been choosen to be one of the foundation's mentors. You can see Charlie's photo on the program link.
The Foundation receives a number of requests from families with children that have been diagnosed with Craniosynostosis, who just need to talk about their experience, or are looking for advice and emotional support. To serve this need, the foundation has developed a Mentors Program, where they recruit volunteers that have experienced Craniosynostosis in their family. These volunteers are then partnered up with those families looking for help.
We feel honored to have been choosen to be one of the foundation's mentors. You can see Charlie's photo on the program link.
