Lainey Moseley
Introduction (2-3 lines)
I am a former television producer that segued into making my first documentary film about rare disease because my daughter was born with an ultra rare disease and I felt the hero journey of rare disease parents needed to be told.
Lainey Moseley is an Emmy® award winning journalist who has worked for CBS and NBC News for the past 30 years. She is also the founder of CHOPS Syndrome Global; an organization raising awareness for her daughter Leta’s rare disease CHOPS Syndrome. She is married with 5 grown children and splits her time between Portland, Maine and Philadelphia.
