Austin's Story: Living with L-CMD

Guest Hannah Lowe Corman joins Linda today share her journey with her son, Austin, and rare diseases – with hope. Through random de novo occurrence, neither Hannah or her husband, Mark, carry the genetic mutation that causes the very rare disease or LMNA-related congenital muscular dystrophy. Their second son, Austin is neurologically typical, but has weakened musculature and will not be able walk or sit independently. Learn about adapting to shock, life, and parenting with grace. More at www.LCMDResearch.org. Also on iTunes. Helping Women Thrive!