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Angelman Today is an online resource featuring information, research and inspiration for all things related to Angelman Syndrome. This website is created for families by families. Our articles feature information that we hope will revolutionize the current care and standard of practice for the treatment and education of those affected by AS.
Angelman Today offers every Angelman Syndrome Foundation across the globe the opportunity to submit articles so that everyone can benefit from the brilliant minds involved in the care, research and treatment of those affected by AS.
Feb 7, 2020 · The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties.
“What is Angelman Syndrome?” That is usually the first question we ask the doctor as soon as our child is diagnosed with this rare disease. The following questions may be of the kind: What can we do? Is there a treatment? What is their life expectancy?
Jan 22, 2018 · Angelman Syndrome: Communication, Educational, and Related Considerations is a unique, exhaustive compilation of existing material related to understanding the nature of AS and how individuals’ communication and related skills can be fostered most effectively.
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- 2017
- Stephen N. Calculator, Eileen Braun, Robert Didden, Amy Girouard, Vanessa Green, Teresa Iacono, Hila...
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Searching for a foundation for Angelman syndrome? FAST is here to advance groundbreaking efforts in Angelman syndrome cure research.
It is important to find a study that is right for your individual with AS and your family. See the list of active research studies below. Click to find out details about each and how to participate. Clinical Trials If you are interested in Clinical Trials in Angelman syndrome, see the Clinical Trials page. ×.
