Bio
I am a mom of 3 amazing children, 2 diagnosed with Classical HCU. My first born, Benjamin, was picked up by Newborn Screening in MA and Gabrielle, my youngest, was the first baby diagnosed through Amnio. Although siblings, they have very different stories. I, as well as, a couple of PKU moms, was one of the founding members to start the non-profit NECPAD hoping to make a difference in our children's lives. Today Ben is 34 and Gabbi is 24. They have gone through a lot in those years, but are strong, smart, successful and compassionate people and I am so honored to be their mom.
"Amniocentesis: Family Planning"
Building a family is a journey of hope, but when a rare disease is part of the story, that journey often includes a complex landscape of uncertainty and difficult decisions. In this session, Karen, Krista, Valerie, and Brittany share their deeply personal and professional perspectives on navigating the challenges of family building when a genetic or rare condition is involved. This panel will explore the "diagnostic odyssey" many families face and the emotional, financial and relational strains it places on parents and siblings alike. Drawing from their own experiences and expertise.
