I am an embryologist, but I’m first and foremost the father of two young adults. Like all of us, my daughter and son are shaped by the 3 billion base pairs of DNA they carry in every cell in their body, but this does not define them. Rather, their strengths and weaknesses are formed by their instincts, their interests, and the community that surrounds them. I wouldn’t change a single thing about them.
While some might see gene editing as a chance to make “better” babies, I see it as using new genetic tools to correct mutations, or errors in genes, that cause human suffering.
Where I work, health care professionals treat people from across the Pacific Northwest who come to us with devastating diseases caused by a single mutation coded in their DNA. Many of these patients worry about passing these conditions on to their children.
There are thousands of such heritable diseases affecting hundreds of millions of people around the world. These include Huntington’s, an incurable brain disease, certain breast cancers, and a chronic heart condition—hypertrophic cardiomyopathy—that affects an estimated 1 in 500 people and can lead to sudden death.