As the revamped
21st Century Cures Act winds its way through the lame duck Congress, I�m reminded of a spellbinding dinner on Sunday night, October 16. It was the eve of the annual "breakthrough summit" for the
National Organization for Rare Disorders
, and I�d introduced a group of new friends to share their stories of life with a child who has had, or will have, gene therapy.
Published on December 01, 2016 21:00