My first brother was born early and the doctors didn't know what to do for him. He passed away after several days I the NICU. Because of him, I live. Genetic testing prepared the physicians for what to expect when my mom started once again to have polyamniohydrosis. I am one year old and get tube feed only at night now. Mom still administer medication throughout the day. I am below the 10th percentile in growth and weight. I can sit up for awhile but not pull myself up to a sitting position and it will be a long time until I walk.