Angelman Announcements February

DNA Test for Rare Disorders Becomes More Routine

New York Times –  The test found no sign of Angelman syndrome, the rare genetic disorder that had struck Jacob. But as months passed, Eli was not crawling or walking or babbling at ages when other babies were

Celebration highlights girl’s rare disorder
The Daily Post Jhyoti, 4, is believed to be the only person in Rotorua with neuro-genetic disorder Angelman syndrome, formerly known as “happy puppet syndrome” due to …

Feb 19

Inside Fair Lawn: Angelman Syndrome Awareness
– Polyi, who owns the River Road makeup studio, Glam Spot NJ, has a two-year-old daughter with Angelman Syndrome named Lyra. At nearly three years old, …

Summit Township girl with rare genetic disorder to be featured in …

The Jackson Citizen Patriot – MLive.com “She feels Angelman Syndrome is something that should be touched upon,” Brockie said … The study is being funded by the Foundation for Angelman Syndrome

Looking for Answers in DNA

New York Times –  The test found no sign of Angelman syndrome, the rare genetic disorder that had struck Jacob. But as months passed, Eli was not crawling or walking o

LETTER TO THE EDITOR: Angelman syndrome needs faster …

One in six children in the United States has a developmental disorder, according to the Centers for Disease Control and Prevention

FEB 18

Celebration highlights girl’s rare disorder
The Daily Post –  Jhyoti, 4, is believed to be the only person in Rotorua with neuro-genetic disorder Angelman syndrome, formerly known as “happy puppet syndrome” due to …

Getting help for children

Lompoc Record –  As the mother of an individual with Angelman syndrome, these statistics are … That is one of the traits of Angelman syndrome, as are life-threatening

Summit Township girl with rare genetic disorder to be featured in an Irish

The Jackson Citizen Patriot – MLive.com –  Seven-year-old Molly Brockie and her family have been chosen to be a part of a radio documentary about Angelman Syndrome, a disorder that affects the nervous system and can cause developmental delay, severe impairment and seizures.

PLOS Biology: Impairment of TrkB-PSD-95 Signaling in Angelman …

Angelman syndrome (AS) is a neurodevelopment disorder characterized by severe cognitive impairment and a high rate of autism. AS is caused by disrupted

Feb 17

Getting the care they need

Washington Post – Jason has Angelman syndrome, a rare and complex neuro-genetic disorder. He is extremely medically fragile and functions cognitively at about the level of a 6-month-old

Coping while hoping for a cure for Angelman Syndrome | Concord …

The First International Angelman Syndrome Awareness Day will be held Friday a

Mother Seeks Treatment, Awareness For Angelman Syndrome

Individuals often misdiagnosed; Melissa Winger wants education

Angelman Syndrome Day Brings Hope to Fair Lawn Mom – Topix

Angelman Syndrome Day Brings Hope to Fair Lawn Mom. Full story: Patch.com. Valentine’s Day may be all about Cupid, but starting this year, the day after will …

Feb 16

Scotty inspires parents to work to raise awareness of Angelman’s Syndrome

Buffalo News – Friday was International Angelman Day; Feb. 15 was chosen partly because the syndrome results from a problem with the mother’s chromosome 15. And the cause has an internationally known spokesman now, movie actor Colin Farrell, whose son James

Oakville Angelman Callum

Our beautiful baby boy was born on July 29th, 2004. Then came the doctor appointments, investigative tests and emergency hospital visits. My husband and I were finally told the devastating news about Callum’s condition in 2005. He had Angelman Syndrome. I remember sitting there in shock asking ‘wh…

Living with Angelman’s

Pilot Tribune – ‎Feb 15, 2013‎ – 23-year old Harli Kirkpatrick, Fonda, is raising awareness about Angelman Syndrome, a genetic neurological disorder she was born with. Researchers are optimistic a cure can soon be reached for the syndrome, which affects one in 15,000 births globally

KC girl participating in trials to cure Angelman Syndrome – KCTV5

Kacie has Angelman Syndrome, or AS. It’s a rare brain disorder only affecting about one in every 15,000 births. It’s caused when a certain gene doesn’t work properly, causing the brain to get backed up with information

Community Channel : Plea to help find Angelman ‘family’

More than 80% of people with a rare genetic condition could be missing out on vital support because of a lack of diagnosis, a charity has said. Assert – the Angelman Syndrome Support, Education and Research Trust – has launched a nationwide campaign to find the UK’s 2,500 “missing” members of its…

Feb 14

Compound could restore learning, memory in Angelman syndrome

Researchers at Brown University have concocted a compound that could restore neural functions in children with the rare genetic disorder Angelman syndrome

Bedford mother is spreading the world about Angelman syndrome, need for help

But the siblings both have Angelman syndrome, a rare genetic disease found in 1 in 15,000 births that is often misdiagnosed as cerebral palsy or autism. Characteristics of AS include developmental delay, speech difficulties and seizures. Their mother

Angelman Syndrome – Tomcat Trike Samuel’s …
Youtube  Our son, Samuel, 10, lives in Dorset and has Angelman Syndrome. Today he had his first go on …

Feb 13

First Annual International Angelman Syndrome Day

DOWNERS GROVE, Ill., Feb. 13, 2013 /PRNewswire-USNewswire/ — The Foundation for Angelman Syndrome Therapeutics (FAST) is proud to announce their participation in the 1st Annual International Day of Recognition for Angelman Syndrome. On the .

Mother Seeks Treatment, Awareness For Angelman Syndrome

“When Will wasn’t hitting the usual milestones, we didn’t stop visiting doctor after doctor until finally one knew about Angelman syndrome,” his mother, Melissa Winger, said. “But that process took too long, and my heart goes out to families across the

Feb 8

Day focuses on flaw with angelic touch

HAPPY FACE: Caleb Bradburn was diagnosed with a rare neuro-genetic disorder called Angelman syndrome a year ago.

Advertisements

About humphriesnz

Live in Christchurch New Zealand with my family, Catholic, interested in music historic Fiction, Angelman Syndrome Awareness
This entry was posted in Uncategorized. Bookmark the permalink.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s