A Waterloo family is using their difficult experiences to help others in similar situations. 

The Magee family is doing that through speaking and serving with two national organizations for hemophilia, The National Hemophilia Foundation and the  Hemophilia Federation Association.

“I have felt very privileged to help represent the rare bleeding disorder community at such a high level,” said Carlisa “Carly” Magee, the mother of the family. “It is awesome to be able to advocate for my children and help forge a platform for the rare bleeding disorders for the future.”

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