1 in 1500 children are born with cranio-facial abnormalities. Our daughter was one of them.
Kate was born with with Saggital Synostosis in 2002. She underwent surgery to re-shape her skull when she was six months old. Today she is eight years old and doing great.
Three years ago we started the "Kate Singer Endowment for Cranio-Facial Surgery and Research" at Dell Children's Hospital of Central Texas. We donate 5% of the speaking fees I receive as a professional speaker to this cause.
In February, to celebrate Kate's birthday, we ask the readers of this blog to join us in raising money for this cause. Any amount helps the doctors discover new ways to treat children born with issues similar to what Kate faced.
So far this year we have raised $1015.oo in donations ranging from $5 to $100.
Would you please join us in trying to meet our February goal of $2000.00? DONATE NOW!!