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

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: