Hypothetical Family Situation Excited to be pregnant, my husband and I knew there was a 1 in 4 chance our baby would be born with Merosin Negative Congenital Muscular Dystrophy. This particular type of developmental disability is autosomal recessive which means, “Both parents are carriers of the conditions, although clinically unaffected” (MDC, 2008, p. 1). Prior to becoming pregnant, my husband and I were tested and our results revealed, we both carried the pathogenic variant (Quijano-Roy, 2012, para. 5). Even though we knew it was a possibility, we never actually believed it would become our reality until the results from the, “Chorionic villus sampling (CVS), is a prenatal test in which a sample of chorionic villi is removed from the placenta” (Chorionic, 2015) came back positive. As the doctor began describing what Merosin Negative Congenital Muscular Dystrophy was, my body quickly became paralyzed by fear, denial, and an overwh...