 So I met both Mrs. Hansen and Cody in August of 1979 when I had just moved to Utah. I joined the faculty in the first week in August and I met these guys three weeks later. And I was immediately inspired to see if we could figure out and understand the condition that Cody and his sister Tanya had. We loved him and the baby and knew that he was going to require a lot of care day and night persistent for many years because of his muscle weaknesses, getting problems, the extreme flim that he would get and have to be such and every 10 or 15 minutes day and night. The essence of the condition is the overall muscle condition that affects the movement of the facial muscles, the eye muscles, the jaw muscles, and even the muscles of the chest and the limbs. So it's an overall underdeveloped muscle condition. I personally want to let people know that they're not alone and it's just so conscious about them. You know, right now it's me and my mom and Dr. Terry and I want to help people understand when they're alone, if they can get through that for a couple of years, they have a whole life ahead of them, they can do anything they want to do and help and hope. It's not a sad thing, it's just that. Well, I always thought we would eventually figure out this gene and two years ago when the new technology came out, it took us a year to be able to get our institutional review board to let us study Tanya and Cody's DNA because we had collected it in the mid-1990s. I'm excited about what's happening. Dr. Terry has done such a great job with trying to get this gene and all of this medical expertise. It's just wonderful. We're excited and we're hoping that it will help other people in the future.