A social network for families who have a loved one affected by a congenital heart defect. A place to share, learn and grow together.
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Hi!
I came across this site today. I have a 2 year old daughter, Cassidy, who was born with Tetralogy of Fallot w/ PA & MAPCA’s.
I think this is a great way to get the word about about CHD’s and I commend you for what you’re doing.
My wife and I are also on a mission to spread the word about CHD’s. We just started a jewelry company called Lucky 10. All of our products are handmade and pertain t
… ContinuePosted by Traci Lisa on March 1, 2010 at 5:05pm
Hey everyone =)
My Name is Sarah, and i was born with truncus arteriosus-type 2 (with the conduit and VSD), VSD, and 2 murmurs,
I have had 3 big heart operations, one of them being an aortic valve replacment, so this means i am on a anti-coagulant for the rest of my life =/ At the minute im on one called inoheparin tinzaparin or heprin for short =)
But previously i have been on warafrin and phenidione (I think thats how there spelt =P) but they hav
… ContinuePosted by Sarah Mckain on February 27, 2010 at 1:05pm
Posted by Veron Poh on December 16, 2009 at 10:26pm — 1 Comment
Posted by Veron Poh on December 3, 2009 at 4:15am
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