The Angelman Syndrome Foundation (ASF) is a non-profit organization dedicated to advancing the awareness and treatment of Angelman syndrome. Their mission encompasses funding research, providing education and information, and offering comprehensive support to individuals with Angelman syndrome, their families, and caregivers. ASF strives to bring hope and practical assistance to the Angelman community worldwide, working towards a future where individuals with Angelman syndrome can thrive.
Serves as the main administrative and operational center for the foundation, coordinating research funding, family support services, educational programs, and awareness campaigns.
Standard professional office space designed for administrative and outreach functions.
A mission-driven, compassionate, and collaborative environment focused on supporting the Angelman syndrome community and advancing research. Staff are dedicated and passionate about making a difference.
The headquarters is pivotal for coordinating the foundation's nationwide and international efforts, managing resources, and serving as a primary contact point for families, researchers, and donors.
The Angelman Syndrome Foundation supports and funds research initiatives globally, collaborates with international Angelman syndrome organizations, and provides resources to families and professionals around the world. Their efforts aim to build a global community united in the fight against Angelman syndrome.
3015 E. New York Street, Suite A2 #285
Aurora
IL
USA
Address: N/A
Focus on centralized management for efficiency and broad impact, with localized support delivered through programs rather than physical branch offices.
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As of April 2025, Angelman Syndrome Foundation' leadership includes:
Angelman Syndrome Foundation has been backed by several prominent investors over the years, including:
No major C-suite level executive hires or exits have been publicly announced by the Angelman Syndrome Foundation in the last 12 months. The foundation may announce new board members or program directors periodically.
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The Angelman Syndrome Foundation primarily uses an email format that combines the first initial and last name of the employee.
[first_initial][last_name]@angelman.org
Format
amoore@angelman.org
Example
90%
Success rate
angelman.org • December 7, 2023
The Angelman Syndrome Foundation announced it has awarded $1.2 million in research grants to six researchers. These grants aim to advance understanding and treatment of Angelman syndrome, focusing on areas like gene therapy, novel drug targets, and improved diagnostic methods....more
angelman.org • May 15, 2024
The ASF National Walk, a key annual fundraising and awareness event, is ongoing in various locations and virtually. It unites families, researchers, and supporters to raise critical funds for research, education, and family support programs managed by the foundation....more
angelman.org • February 15, 2024
The Angelman Syndrome Foundation actively participated in International Angelman Day on February 15th, promoting awareness globally through various campaigns, sharing family stories, and highlighting research advancements to educate the public and support the AS community....more
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