Caelyn Nicolette Osbourn was born still June 27, 2007. We found out during a routine ultrasound at 21 weeks that something was terribly wrong with our precious baby. The doctor told us our baby was very small, had a heart defect, and had very little amniotic fluid. Due to the lack of fluid, her lungs could not develop and therefore was not expected to live long after birth. Our world was turned upside down...all of our dreams were crushed. We later found out that Caelyn had a rare genetic syndrome called Smith-Lemli-Opitz Type II. We were able to hold and love on Caelyn for as long as we desired. She had so many people waiting for her arrival, so many people to love her. We will treasure these beautiful pictures forever. We are so thankful to the NILMDTS foundation and to Jessica Lamb for her time and for this wonderful gift she was able to give us. Caelyn Nicolette, we love you and miss you and can't wait to hold you one more time in heaven. Love your Mommy and Daddy.