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FW: [DownSyndromeInfoExchange] US Rep. Cathy McMorris Rodgers   Topic List   < Prev Topic  |  Next Topic >
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Thought this was interesting and thought you would enjoy it as well. I especially agree with the part of the focus needed on research beyond prenatal diagnosis.




US   Rep. Cathy McMorris Rodgers (part 2)
Sunday,   March 22, 2009 - Daniel J Vance
Rocklin & Roseville Today  http://www.rocklint oday.com/ 
Recently,   I featured in this column 39-year-old Congresswoman Cathy McMorris Rodgers   (R-WA), who in 2007 gave birth to a son with Down syndrome. Now age two, Cole   is an inquisitive and happy toddler making his presence felt.
McMorris   Rodgers is in her third term, Vice Chair of the House Republican Conference,   and one of the House's highest-ranking Republicans. Having Cole has opened up   new avenues for her to represent families affected by disability all over the   nation.
"I want to tell Cole's story," she said in a telephone interview   from her Capitol Hill office. "Cole has given me a whole new reason and   passion for life right now in Congress."
Last year,   along with others, McMorris Rodgers helped launch the Congressional Down Syndrome   Caucus, which claims 50 members. The other three founding members were Pete   Sessions (R-TX), Eleanor Holmes Norton (D-DC), and Patrick Kennedy (D-RI).   Sessions and Norton also have children with Down syndrome.
She said,   "Cole has opened doors for me to work across the aisle and even in the   Senate in ways I could never have done on my own. People are aware of Cole   and they often ask me about him and are very supportive. I've become   acquainted with members of Congress because of Cole."
She has   talked over the telephone with Gov. Sarah Palin, who also has a child with   Down syndrome. In their conversation, Palin mentioned having seen McMorris   Rodgers' YouTube video that helped launch the Congressional Down Syndrome   Caucus.
Overall,   nonprofit groups representing people with Down syndrome haven't been nearly   as politically active as groups for people with other disabilities.   Historically, Down syndrome groups have focused more on interpersonal   support, she said.
"But   I think it's important the Down syndrome community get involved in the   national debate over funding for research and educational opportunities,"   she said. "A lot of the research with Down syndrome has been focused on   prenatal diagnosis. But we believe there is potential for other research. Down   syndrome is simply a duplicate No. 21 chromosome. The Alzheimer's gene is   also in the No. 21 chromosome. We believe if we were to study what is   happening in that chromosome, the effort could also help adults with   Alzheimer's disease."
Children   with special needs often help families clarify life's priorities, she added.   She wants to do all she can to help Cole maximize his potential.

Rocklin   & Roseville Today  http://www.rocklint oday.com/ 
 
 


Mon Mar 23, 2009 10:20 pm

mom2gh
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Thought this was interesting and thought you would enjoy it as well. I especially agree with the part of the focus needed on research beyond prenatal...
Julie Tutwiler
mom2gh
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Mar 23, 2009
10:27 pm
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