A Whole New World

Welcome to my blog about our family's journey through congenital urology defects. We entered this world last December, and now a year later 2 of our 3 children have been diagnosed with related conditions. When our daughter was first diagnosed, I went to the Web to find information and hopefully hear other families' stories. There is plenty of clinical research and information out there, but I came up short when searching for stories of other children. Now, with a second child entering into similar territory, I have decided to start this for others looking for information (take note: I am not a physician!), and our friends and family who are wanting to check in on the kids' progress and/or better understand what we are going through.