Zoo Atlanta has received a prestigious grant from the federal Institute of Museum and Library Services (IMLS) to lead a multi-institutional effort to examine heart disease in great apes. The $92,000 grant represents an historic show of support for an area of ape health care that has until now been poorly understood by veterinarians.
Identified as a leading cause of death in great apes living in zoological settings, cardiovascular disease (CVD) requires advanced understanding of diagnosing, treating and monitoring affected individuals, as well as adapting techniques already in use for treatment of heart disease in humans and domestic animals. Under the leadership of Hayley Murphy, DVM, Director of Veterinary Services, the Zoo Atlanta Veterinary Team will use the one-year grant to design an innovative national program for investigating ape CVD and establishing state-of-the-art diagnostics, treatment and prevention. Additional partners are The University of Georgia (including Rita McManamon, DVM, one of the project’s principal investigators and former head veterinarian at Zoo Atlanta); Cleveland Metroparks Zoo; and more than 15 other zoos, universities and scientists.
“We are pleased and proud that IMLS saw the merit in a project that will have a positive impact on great apes in zoological collections throughout the world,” said Raymond King, President and CEO. “This is an important step forward that will allow experts from around the country to share knowledge and build on their individual strengths.”
Zoo Atlanta is a likely candidate for leadership in a great ape heart health initiative. The organization houses the nation’s largest collection of western lowland gorillas, with 23 individuals, as well as the largest zoological collection of orangutans in the U.S., currently with 11 individuals. Four of the Zoo’s great apes are over the age of 45.
“National Leadership Collaborative Planning Grants provide opportunities to conduct research and develop the framework to support future projects that have the potential to generate new tools, research, models, services, practices, or alliances that will positively impact museums, libraries, and the communities they serve. These projects encourage partnerships that address national issues of importance impacting education, scholarship, and public service and encourage the broad application of standards and models to improve professional practice,” said IMLS Acting Director Marsha L. Semmel.
The Institute of Museum and Library Services is the primary source of federal support for the nation’s 123,000 libraries and 17,500 museums. The Institute’s mission is to create strong libraries and museums that connect people to information and ideas. The Institute works at the national level and in coordination with state and local organizations to sustain heritage, culture, and knowledge; enhance learning and innovation; and support professional development. To learn more about the Institute, visit www.imls.gov.
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Showing posts with label disease. Show all posts
Showing posts with label disease. Show all posts
Tuesday, September 7, 2010
Tuesday, February 3, 2009
Teenager Spearheads Fundraiser for Emory ALS Center
After being inspired by two athletes who lost their lives in their prime from a devastating disease, teenager Brian Duffy and his family have raised more than $17,000 for research and programs at Emory University's ALS Center.
Also known as Lou Gehrig's disease, amyotrophic lateral sclerosis (ALS) kills the motor neuron cells in the brain and spinal cord, which causes the brain to lose the ability to control the muscles in the body, leading to paralysis and problems swallowing, eating and breathing. The person's mental capacity remains completely intact, making the disease a cruel sentence for patients who are often otherwise healthy and active before being diagnosed.
Brian Duffy, 15, first learned about ALS in 2005 after watching the Ironman Triathlon from Kona, Hawaii. That year racer Jon Blais became the first person with ALS to ever complete the race. Having said he would finish even if he had to be rolled over the finish line, Blais symbolically laid down at the finish line and "log-rolled" across under his own power. A year later, Blais was in a wheelchair. Less than two years after his diagnosis, he succumbed to the disease.
At the end of a news story on Blais, Brian told his parents, Karen and Mike Duffy, that he wanted to do something to help. With his parents' support, Brian began a letter-writing campaign in January 2006 to family and friends and raised more than $2,200 that year. His parents ran triathlons to raise money, and his younger brother, Kevin, a golfer, sold golf balls as an ALS fundraiser. That was good, but for Brian, it wasn't enough.
At Brian's urging, the family held its first annual "Run for Life 5K - A Race to End Lou Gehrig's Disease" race in 2006, and to date has raised more than $17,000 for ALS research, donating the proceeds to the Emory ALS Center. The third annual race is set for May 2, 2009 - coincidentally the 70th anniversary of the day in 1939 when Lou Gehrig took himself out of the New York Yankees lineup because of the disease.
Proceeds will continue to support the Emory ALS Center where medical professionals partner with the Muscular Dystrophy Association of Georgia and the ALS Association of Georgia, searching for new understanding of the illness and seeking to minimize its toll on families. Research at the Emory ALS Center focuses on basic mechanisms of motor neuron degeneration, genetics of ALS, and new experimental treatments. The Emory ALS Center also provides multidisciplinary care to ALS patients and their families, focusing on independence and quality of life through state-of-the-art intervention. Together, Emory neurologists, nurses, a speech-language pathologist, occupational, physical, and respiratory therapists, dieticians, and a social worker address all aspects and stages of this debilitating disease.
"This disease is a horrific one," says Jonathan Glass, MD, director of the Emory ALS Center and professor of neurology, Emory School of Medicine. "It hits people smack in the middle of their productive lives, and it affects not only the individual, but the whole family. We have created a patient-centered approach at Emory that has been very successful. The family comes to us, and we bring all of the providers they need to them. The support that we receive from donors drives the research we are doing."
Demand for care at the Emory ALS Center has increased dramatically since the center was named an MDA regional network clinical research center, one of only five in the country and the only center in the Southeast. Glass says volunteers, such as Karen Duffy, are vital to the Center's ability to provide emotional and social support for ALS patients and their families who come to the Center.
"These volunteers provide a link to the community and let people know how important this Center is and that what we have here is special and is not happening anywhere else," Glass says. "Brian's efforts are what really started this, and he and his brother are amazing kids. They are examples of what people really can do to make an impact. With public understanding of how important this is we will get the support we need to continue."
Now a freshman at South Forsyth High School, Brian, 15, runs cross-country and is on the swim team. He often has to explain to classmates what ALS is when they see the "Cure for ALS" bumper sticker on the family car.
"My goal is to have ALS become as well-known as other diseases, so people will become more aware of it and do more to help find a cure," Brian says.
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Also known as Lou Gehrig's disease, amyotrophic lateral sclerosis (ALS) kills the motor neuron cells in the brain and spinal cord, which causes the brain to lose the ability to control the muscles in the body, leading to paralysis and problems swallowing, eating and breathing. The person's mental capacity remains completely intact, making the disease a cruel sentence for patients who are often otherwise healthy and active before being diagnosed.
Brian Duffy, 15, first learned about ALS in 2005 after watching the Ironman Triathlon from Kona, Hawaii. That year racer Jon Blais became the first person with ALS to ever complete the race. Having said he would finish even if he had to be rolled over the finish line, Blais symbolically laid down at the finish line and "log-rolled" across under his own power. A year later, Blais was in a wheelchair. Less than two years after his diagnosis, he succumbed to the disease.
At the end of a news story on Blais, Brian told his parents, Karen and Mike Duffy, that he wanted to do something to help. With his parents' support, Brian began a letter-writing campaign in January 2006 to family and friends and raised more than $2,200 that year. His parents ran triathlons to raise money, and his younger brother, Kevin, a golfer, sold golf balls as an ALS fundraiser. That was good, but for Brian, it wasn't enough.
At Brian's urging, the family held its first annual "Run for Life 5K - A Race to End Lou Gehrig's Disease" race in 2006, and to date has raised more than $17,000 for ALS research, donating the proceeds to the Emory ALS Center. The third annual race is set for May 2, 2009 - coincidentally the 70th anniversary of the day in 1939 when Lou Gehrig took himself out of the New York Yankees lineup because of the disease.
Proceeds will continue to support the Emory ALS Center where medical professionals partner with the Muscular Dystrophy Association of Georgia and the ALS Association of Georgia, searching for new understanding of the illness and seeking to minimize its toll on families. Research at the Emory ALS Center focuses on basic mechanisms of motor neuron degeneration, genetics of ALS, and new experimental treatments. The Emory ALS Center also provides multidisciplinary care to ALS patients and their families, focusing on independence and quality of life through state-of-the-art intervention. Together, Emory neurologists, nurses, a speech-language pathologist, occupational, physical, and respiratory therapists, dieticians, and a social worker address all aspects and stages of this debilitating disease.
"This disease is a horrific one," says Jonathan Glass, MD, director of the Emory ALS Center and professor of neurology, Emory School of Medicine. "It hits people smack in the middle of their productive lives, and it affects not only the individual, but the whole family. We have created a patient-centered approach at Emory that has been very successful. The family comes to us, and we bring all of the providers they need to them. The support that we receive from donors drives the research we are doing."
Demand for care at the Emory ALS Center has increased dramatically since the center was named an MDA regional network clinical research center, one of only five in the country and the only center in the Southeast. Glass says volunteers, such as Karen Duffy, are vital to the Center's ability to provide emotional and social support for ALS patients and their families who come to the Center.
"These volunteers provide a link to the community and let people know how important this Center is and that what we have here is special and is not happening anywhere else," Glass says. "Brian's efforts are what really started this, and he and his brother are amazing kids. They are examples of what people really can do to make an impact. With public understanding of how important this is we will get the support we need to continue."
Now a freshman at South Forsyth High School, Brian, 15, runs cross-country and is on the swim team. He often has to explain to classmates what ALS is when they see the "Cure for ALS" bumper sticker on the family car.
"My goal is to have ALS become as well-known as other diseases, so people will become more aware of it and do more to help find a cure," Brian says.
-----
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