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Jacob's Story: Angelman Syndrome | Studio 10


Jacob's Story: Angelman Syndrome | Studio 10


Young Jacob suffers from a rare disease that affects 1 in 20000 children. Studio 10 | 8:30am on TEN.
 


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More Angelman Syndrome videos

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What does Angelman Syndrome look like?


Angelman Syndrome (AS) is a rare condition with different genotypes and varying degrees of severity affecting approximately 1:15000 births. Around 490000 individuals worldwide. There is...
 

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Prader-Willi vs. Angelman Syndrome (Imprinting)


Please DONATE to DirtyUSMLE: https://goo.gl/rK1CjC.
 

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4 siblings with Angelman Syndrome


 

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Colin Farrell Talks about Angelman Syndrome on Ellen


April 2, 2012 - Colin Farrell talks with Ellen about his new movie, Total Recall, and then talks about his true passion, his two sons, James and Henry. Colin shares a personal moment with...
 

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A Friend with Angelman Syndrome


Conor is diagnosed with Angelman Syndrome and communicates mostly through physical gestures. Brendan, his brother, worried that his peers may not understand Conor's unique language. Brendan...
 

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Behaviour in Angelman Syndrome - ASSERT


This film gives an insight into what behaviours are commonly seen in people with Angelman Syndrome. You get to hear from family's who have adapted their lives to suit Angelman Syndrome and...
 

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Living with Angelman's- Gracie's Story


 

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A Story about Angelman Syndrome


Angelman Syndrome is a rare genetic condition. You can read the clinical characteristics and what individuals and their families may go through, however it is impossible to picture what that...
 

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finds a user from Hungary on Feb 18, 2018
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Colin Farrell Talks About His Son's Condition, Angelman Syndrome


Angelman Syndrome, or AS, is an unusual disease to diagnose. It's also very rare, striking only one in 30000 children, according to Colin Farrell on 'Late Show' (Weeknights, 11:35PM ET on...
 

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Angelman Syndrome - What is it? - ASSERT


What is Angelman Syndrome? The question everyone wants to know. This short film gives you an insight into what somebody with Angelman Syndrome is like and how it effects the individuals and...
 

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Family shares story of son with rare Angelman Syndrome


Governor Malloy has declared Saturday, April 25 as \
 

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Life with Angelman syndrome is...


There is no better way to tell the world about Angelman syndrome than through YOU, the faces and voices of Angelman families. YOU are the very reason the Angelman Syndrome Foundation exists...
 

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Angelman Syndrome Visual Presentation


Communication Disorders graduate program.
 

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Bio project on Angelman Syndrome!
 

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Angelman Syndrome interview with Tanya O'Rourke


Angelman Syndrome Walk on May 17.
 

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Maisie Angelman Syndrome 2018


This video is to inform you about Angelman Syndrome and how it impacts Maisie. Help us find a cure! #angelmansyndrome.
 

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3-year-old boy battles Angelman Syndrome


A relatively little known disorder known as Angelman Syndrome is drawing focus in the medical world.
 

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My angel with Angelman syndrome 💙


 

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Angelman syndrome : Boy who never stops SMILING with rare genetic disorder


A toddler suffers from a rare genetic condition which means he cannot stop smiling. Ollie Petherick, two, from Devizes, Wiltshire, was born with Angelman syndrome - a chromosome disorder which...
 

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Angelman's Syndrome - CRASH! Medical Review Series


Disclaimer: The medical information contained herein is intended for physician medical licensing exam review purposes only, and are not intended for diagnosis of any illness. If you think...
 

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The struggle of night time (Angelman syndrome)


Just a typical night with multiple kids and one who struggles with Angelman syndrome. We are trying to teach AJ to go to bed on her own (like she used to), and that she doesn't need mom to...
 

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Angelman Syndrome - ABA - Verbal Prompt and UNPROMPTED Response from Payden


A small task for someone who has Angelman Syndrome is such a HUGE accomplishment! We are so proud of how far Payden has come over the years. For many parents/guardians, seeing an 8 year old...
 

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ALEX HAS ANGELMAN SYNDROME


My grandson Alex was diagnosed with Angelman Syndrome in 1992. He is non-verbal but makes his needs known. He is very social and I thought it would be important to know him as quite ordinary...
 

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Epigenetics, Prader-Willi Sydrome, Angelman Syndrome, Methylation, Imprinting, Heterochromatin


http://www.stomponstep1.com/epigenetics-prader-willi-sydrome-angelman-syndrome/ While genetics is the study of DNA sequence, Epigenetics is the study of heritable changes that do not affect...
 

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Christopher Angelman Syndrome


Bits and pieces of Christopher's life.
 

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Angelman Syndrome: Lily's Healing Progress April 2013- May 2014


Music: Sunrise Day 6 Shirley Cason We started using natural therapies for Lily, April 2013, a week after being diagnosed with Angelman syndrome. Lily was aged 16 months at the time. We were...
 

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Managing Angelman Syndrome


At the Angelman Syndrome Foundation Scientific Symposium in Rockville, Md., Dr. Ron Thibert of Massachusetts General Hospital in Boston discussed the presentation and management of patients...
 

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My sibling has Angelman Syndrome - ASSERT


'My sibling has Angelman Syndrome' is a film about young carers. It offers an insight into the emotions and experiences of children with physically & mentally disabled siblings. The film is...
 

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Angelman Syndrome


Angelman Syndrome Awareness.
 

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Ava's journey with Angelman Syndrome


 




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