2/5/10 Ryan & Riley Dempster update
Nice article in NY Times about Ryan Dempster and how he’s dealing with 10-month-old daughter Riley, who has a rare disease that makes it difficult to swallow.
Dempster and his wife have created the Ryan and Jenny Dempster Family Foundation dedicated to raising awareness of DiGeorge Syndrome, which Riley has, and reach out to families with children who have this, and help them deal with difficult situations they face. Go to his website for more info:
– Carrie Muskat