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| When Camp Awareness was founded in 1998, autism was not nearly as well-known as it is today. "When my son was diagnosed, 1 in 10,000 (births) were the numbers," according to Sue Hansen, camp founder and director. Earlier that year, Hansen spent a frustrating few days at Cub Scout camp with son Sean, then 9, whose behavior was a source of bewilderment to the other boys and parents. "I spent my whol | |
| Sweet and optimistic, Katie Mahar is a typical 10-year-old girl. The Craryville, N.Y., resident is the youngest of four children. She jumps on her trampoline, listens to the Backstreet Boys and plays with her kitten, Pumpkin. She also has a disease called xeroderma pigmentosum, a genetic disorder also known as XP. | |
| It all started 10 years ago. My dad set off to climb Mount Rainier, a 14,411-foot volcano an hour's drive from Seattle. He did not make it to the top. My dad tried again in 1999, with the same result. He made his final try in 2006, this time with me, his 16-year-old son. So here I was at 5 a.m., with five hours of climbing behind me. Having started our climb at midnight to avoid melting snow, I st | |
| When Andrew Kidd was 5, he fell from a piece of playground equipment and tore his lip and chin on a protruding bolt. His injuries were so bad that when he was taken to the hospital emergency room, the staff assumed he had been in a car accident. After 87 stitches and 15 plastic surgeries, Andrew, now 11, has recovered. But the incident was so severe that he and his mother, Judi Kidd, have joined t | |
| "If you can see these children's eyes when they hear their song -- they have tubes in their arms; they have oxygen to their face. They are small, they are hurting, and they hear their name and their song come out and such a smile comes to their face, a twinkle in their eye." Such are the reactions to Songs of Love, explained Steve Rudoff, whose youth group at Congregation Beth-El Zedeck is helping | |
| Children of different ages, shapes, colors and sizes huddle together in a warm cabin to pose for a picture on a cold winter's day. These children, although perfect strangers the week before, resemble a large family. Among this sea of smiles is former tennis pro Andrea Jaeger, whose Silver Lining Foundation is responsible for these smiles. A nonprofit organization, the Silver Lining Foundation help | |
| Everyone has quirks. You might pop your knuckles, bite your lip or twirl your hair. These habits might be hard to break, but it's not impossible. Unless you have Tourette syndrome. Although the condition is hard to diagnose, about one in 2,000 children have Tourette syndrome, a neurological disorder characterized by repeated involuntary movements and uncontrollable vocalizations known as tics. Tou | |
| "I'm not a genetic freak. I'm a genetic phenomenon,'' says Jennifer Oklak. Jennifer, 19, and her sister Heather, 13, are among about 18,000 Americans affected by albinism, a genetic condition in which a person has little to no pigment, or coloration. Jennifer graduated from the Indiana School for the Blind last spring and is studying graphic design at Ivy Tech State College. Heather is a seventh-g | |
| A few years ago, U.N. Secretary-General Kofi Annan said, "In too many countries, an official conspiracy of silence about AIDS has denied people information that could have saved their lives. We must empower young people to protect themselves through information and a supportive social environment that reduces their vulnerability to infection." No continent has been more devastated by AIDS than Afr |