From Deseret News archives:
Generations of tears
"It seemed to me that a mission was a very good place for me to be for the next two years.
"This disease has really opened my eyes," he says today. "I remember my dad starting to get sick. I was 10 or 11, and financially it went downhill fast. I thought that happened to everybody. I would see some of my friends and think, 'Man, that's going to suck when it happens to them.' "
That it doesn't happen to everyone is driven home to him a lot. He played gene roulette unwillingly and seems to have lost. But he's determined not to let it ruin his life, as it has so many others who forget to live in the present while they're busy dreading the future.
"HD will and won't affect my future," he says. "I had to decide, if I have Huntington's, do I want to get married. I know that I need to be married and have a family. Because I have this doesn't necessarily mean I won't do those things. But I will do them differently."
He has a gift that John, Amy and Julie were denied, he says. Time to plan. And to save. "My dad's disease hurt my mom financially. I can do some planning for it. So it will affect me, but some of it will be in a good way."

It is possible now to do gene testing on a fertilized egg to see if it contains the mutation, according to Dr. Jay Jacobson, a bioethicist at the University and LDS hospitals. Eggs could be fertilized and tested, and one that was mutation-free could be implanted using in vitro fertilization. The technology exists, although no one seems sure if it has been used with Huntington's disease yet. It's very possible that sperm could be tested prior to fertilization, researchers say.
Recent comments
This is a truly horrible disease and my heart goes out to these girls...
Gale | Oct. 9, 2008 at 9:51 p.m.
I hope you are planning to make your story into a book. Not only...
Kathy | July 12, 2008 at 7:10 p.m.
This story of the Bishop's is incredible. Just browsing to look up...
Debbie RN | Sept. 23, 2007 at 2:43 a.m.
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