Angelman Announcements – February 2014

BISD parent: Special education teacher struck my daughter

Thibodeaux’s daughter has Angelman Syndrome and does not talk, but, Thibodeaux said, she understands everything someone says to her.

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Parents lobby for son’s rare disease

Richard Newton holds his 20-month-old son, Garrett, as he and his wife, Alyssa, talk about the boy’s diagnosis with Angelman syndrome during a fundraiser Monday at Chili’s Grill & Bar. Glenn Moore/Tracy Press. slideshow. Twenty-month-old Garrett Newton _________________________________

ASF Educational Webinar Series

Stay up-to-date with important topics related to Angelman syndrome with these interactive webinars.

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Angels’ fight to find cure for rare genetic disorder

Monroe Courier – 20 January 2014

Two-year-old Monroe resident Joey Moretti is fighting Angelman Syndrome, a rare genetic disorder that experts believe there may be a cure for.

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Support shown for youngster with Angelman syndrome

The Chronicle Journal

Leia Portfors, mother of Kandem Trewin, 7, who has Angelman syndrome, spoke about the school fundraising on Tuesday. “Gorham and Ware did the ..

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Living with Sean and Angelman syndrome

Gibraltar Chronicle

The permanent smiles on the faces of most individuals with Angelman syndrome (AS), Sean included, belie a life marked by daily challenges 

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Calling all angels 

The Rivard family pose in front of their Medicine Hat home. Alan holds son Jacob while Sarah holds daughter Hannah, who has Angelman’s

 

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Devizes Opportunity Centre ‘fantastic for us’

The Wiltshire Gazette and Herald

Ollie, two, of Cromwell Road, Devizes, suffers from Angelman syndrome. He made a dramatic appearance into the world when he was born at home 

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Glenwood Springs mom runs to raise funds for son’s rare medical 

Glenwood Springs Post Independent – COM Candy Granger-Underhill of Glenwood Springs with her son Sam Underhill, who was born with Angelman Syndrome, a rare neuro-genetic 
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Salisbury family hope for a cure for their son Timmy, 2, with Angelman Syndrome ahead of 

The Queensland Angelman Association Picnic is on February 15 from 11am at Broadwater Park, Mansfield. For more information on the syndrome 

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About humphriesnz

Live in Christchurch New Zealand with my family, Catholic, interested in music historic Fiction, Angelman Syndrome Awareness
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