child, but the problem is there is no standardized screening so they turned their fate into a mission. so instead of asking why us, we decided to make sure that the tragedy of eden s story doesn t happen to another family. their work has grown into a new web-based education and screening program for 19 genetic diseases that are more common. it s allowing visitors to request an at-screen kit and a genetic counselor gives the results. and last year eden had another sister who is perfectly happy. i think she helped see the world in a different way that we
carriers of a disease they have a 25% of passing it on to their child, but the problem is there s no standardized screening, so they turned their fate into a mission. so, instead of asking why us, we decided to make sure that the tragedy of eden s story doesn t happen to another family. their work has grown into a new web-based education and screening program for 19 genetic diseases that are more common among a certain type of jews. established at emory university it is called j-screen and it allows visitors to request an at-home screening kit online and a genetic counselor delivers the results. last year eden became a big sister when the goulds added another daughter to their family. she is perfectly healthy. we believed in life again and that we had hope and we knew there would be joy and good times. i think she helped us see the world in a different way that we