My Nonprofit Reviews

I cannot say enough about the Take a Breather Foundation. Matt and the team work hard every day to raise money and awareness in order to grant wishes with children living with Cystic Fibrosis. There isn't any bureaucracy - Take a Breather works directly with the CF Centers and the social workers to get in touch with families that could use a respite from this disease. Members of the Foundation meet with each and every wish recipient to welcome them into the Take a Breather family and let them know that there is support out there that understands what they are going through. Hopefully one day soon there will be a cure for CF, but in the meantime it is great that there is a foundation to help those that need something special to make the days brighter.