NEWS
February 7, 2011 | By Thomas H. Maugh II
A Boston researcher will receive a $1-million prize from the Prize4Life foundation's ALS Biomarker Challenge, an effort to develop new ways to monitor the progression of amyotrophic lateral sclerosis to make it easier to test potential drugs for the disease. The prize is believed to be the biggest-ever challenge award related to a medical condition, but Prize4Life estimates it could halve the cost of clinical trials for new ALS drugs. Dr. Seward Rutkove of Beth Israel Deaconess Medical Center will receive the award formally in June.
NEWS
October 22, 2010
Matthew Ruchinski likely doesn’t completely understand what ALS means. The 4-year-old from Pennsylvania just knows that his dad is sick — and that he plans to walk two miles in an event Saturday that will benefit people who have the disease, reports the Allentown Morning Call . Matthew's dad, James, was just 35 and in the process of adopting the boy when he was diagnosed with the fatal neurogenerative disease. About 5,600 Americans each year are diagnosed with ALS, officially called amyotrophic lateral sclerosis, or Lou Gehrig's Disease, and life expectancy after diagnosis is just two to five years, according to the ALS Assn.
CALIFORNIA | LOCAL
August 28, 2010 | By Thomas Curwen, Los Angeles Times
If Elizabeth Uyehara were alive, she would be pleased. Everything was working out as she had hoped. The terrible banality of her illness had ended, and she was about to make her final journey. Two hours before she died, David Jones' pager went off. He canceled his lunch and made a few phone calls to sort out the details with the hospital and the family. He went to his lab and picked up the paperwork and, before heading over the Sepulveda Pass, stopped at a 7-Eleven for some ice that he tossed into a cooler.
NEWS
August 17, 2010 | Los Angeles Times Staff Writer
Repeated concussions may contribute to the development of symptoms that mimic amyotrophic lateral sclerosis , or Lou Gehrig's disease, a controversial group of researchers is suggesting in a provocative new study. The cause of most cases of ALS--a devastating degenerative disease named after the baseball great who was its most famous victim--is largely a mystery. Only 5% to 10% of those who are diagnosed with ALS carry the distinctive gene mutation known to give rise to the disease: Of the 30,000 Americans who have the disease at any given time, at least 27,000 have no clue as to its origins.
CALIFORNIA | LOCAL
August 8, 2010 | By Valerie J. Nelson, Los Angeles Times
Tony Judt, a leading historian of postwar Europe and outspoken political essayist who also wrote movingly about his struggle with Lou Gehrig's disease, has died. He was 62. Judt, who was a history professor at New York University, died Friday at his home in Manhattan of complications from the disease, the university announced. In 2005, his career reached its zenith with the publication of "Postwar: A History of Europe Since 1945," a hefty book that was a finalist for the Pulitzer Prize.
CALIFORNIA | LOCAL
June 5, 2010 | By Sam Farmer, Los Angeles Times
Charlie Wedemeyer, the inspirational high school football coach who battled Lou Gehrig's disease for more than 30 years, has died. He was 64. Wedemeyer died early Thursday in a San Jose hospital of pneumonia and was surrounded by family and friends, said his wife, Lucy. He had undergone five surgeries in the last two weeks because of intestinal blockages. "The last two weeks were actually a gift to me, kind of getting us ready," his wife said. "He was amazing right till the end."