Support groups will of people with Down’s syndrome will meet
2-3 times yearly to advance research of the condition. The group was created in late September. They will be collaborating with the National Institute
of Health. (NIH)
The group will also analyze the status of Down’s syndrome. The primary focus they will have will be
to execute the Institute’s research agenda for the condition as well as create
goals to continue their research. These
principals brought together will help minimize the repeating of Down’s syndrome
research and will allow support systems to share knowledge and ideas regarding
the condition.
“The consortium will allow NIH to inform the Down syndrome
community of advances in the field, ongoing studies and potential avenues for
future research,” said Yvonne Maddox, deputy director of the NIH’s Eunice
Kennedy Shriver National Institute of Child Health and Human Development, which
is heading up the new cooperative. “In turn, those who work in Down syndrome
research and patient care can share their experiences and ideas for potential
research opportunities with NIH.”
People with Down’s syndrome will participate in the
group. It will also include members of
Down’s syndrome pediatric groups and representatives of NIH’s Down’s syndrome
Working Group. The organization is
similar to Interagency Autism Coordinating Committee, but won’t have as much influence as the autism committee in Congress.
Activism for Down’s: http://www.disabilityscoop.com/2011/10/03/down-syndrome-research-hub/14156/
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