Frank Stephens, a young man living with Down Syndrome, gives a powerful speech on his life experience and the importance of people living with Down Syndrome in science and research.
FRANK STEPHENS: Mr. Chairman and members of the committee,
Just so there is no confusion let me say that I am not a research scientist. However, no one knows more about life with Down Syndrome than I do. Whatever you learn today, please remember this: I am a man with Down Syndrome and my life is worth living.
Sadly, across the world, a notion is being sold that maybe we don't need research concerning Down Syndrome. Some people say prenatal screens will identify Down Syndrome in the womb and those pregnancies will just be terminated.
It's hard for me to sit here and say those words.
I completely understand that the people pushing this particular â€śfinal solutionâ€ť are saying that people like me should not exist. That view is deeply prejudice by an outdated idea of life with Down Syndrome.
Seriously, I have a great life!
I have lectured at universities, acted in an award-winning film and an Emmy-winning TV show, and spoken to thousands of young people about the value of inclusion in making America great. I have been to the White House twiceâ€“â€“and I didn't have to jump the fence either time.
Seriously, I don't feel I should have to justify my existence, but to those who question the value of people with Down Syndrome, I would make three points.
First, we are a medical gift to society, a blueprint for medical research into cancer, Alzheimers, and immune system diroders. Second, we are an unusually powerful source of happiness: a Harvard-based study has discovered that people with Down Syndrome, as well as their parents and siblings, are happier than society at large. Surely happiness is worth something? Finally, we are the canary in the eugenics coal mine. We are giving the world a chance to think about the ethics of choosing which humans get a chance at life. So we are helping to defeat cancer and Alzheimers and we make the world a happier place. Is there really no place for us in the world?
Is there really no place for us in the NIH budget?
On a deeply personal note, I cannot tell you how much it means to me that my extra chromosome might lead to the answer to Alzheimers. It's likely that this thief will one day steal my memories, my very life, from me. This is very hard for me to say, but it has already begun to steal my mom from me. Please, think about all those people you love the way I love my mom. Help us make this difference, if not for me and my mom then for you and the ones you love. Fund this research. Let's be America, not Iceland or Denmark. Let's pursue answers, not "final solutions." Let's make our goal to be Alzheimer's free, not Down Syndrome free. Thank you.