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▼
opener
 * Walk
 * Contact Registry
 * News
 * Blog

Search for:
DOnate
 * What is Angelman Syndrome
   * Symptoms and Causes
   * Testing and Diagnosis
   * Genetics of AS
   * Photo Gallery
 * For Parents
   * Newly Diagnosed
   * Accomplishments of Individuals
   * Participate in Research Studies
   * Angelman Therapeutics
 * Research
   * ASF Funded Research
   * Call for Proposals
   * Clinical Trials
   * Research Studies
   * LADDER
   * Research Funding Philosophy
 * Make an Impact
   * ASF Cure Club
   * Ways To Donate
   * Fundraise
   * Committees & Groups
   * Send Encouragement
   * Shop & Support ASF
   * Volunteer Opportunities
 * Clinics
   * Find a Clinic
   * Clinic Patient Survey
   * For Clinicians
   * Jacob Pritzker Fellowship Program
   * FAQs
 * Resources
   * Search by Topic
   * Adult Resources
   * ASF Family Resource Team
   * ASF Family Fund
   * ASF Family Champions
   * Angelman Syndrome A to Z
   * ASF Podcast
   * Behavior Resources
   * Communication Resources
   * Counseling Services
   * Educational Webinars
   * Federal Resources
   * IEP Resources
   * International AS Resources
   * Medical Resources
   * Medical & Social Referrals
   * Seizures
   * Sibling Programs
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 * Events
   * ASF Walk
   * Conferences and Symposia
   * Bank of America Chicago Marathon
   * All Events
 * About
   * Contact ASF
   * Contact Registry
   * Our Partners
   * Board of Directors
   * Communication Advisory Committee
   * Financial Transparency
   * History of ASF and Angelman Syndrome
   * Medical Advisory Board
   * Parent Advisory Committee
   * Scientific Advisory Committee
   * Receive Texts & Emails
   * Privacy


WITH YOU FOR THE JOURNEY


FAMILIES. RESEARCH. CLINICS. COMMUNITIES.

Support Resilience Now


ASF WALK

WE’RE CELEBRATING THE 25TH ANNIVERSARY OF THE ASF WALK

The ASF Walk has raised $19.5 million since 1999. Those funds have made an
enormous impact on the lives of those impacted by Angelman syndrome. Join us to
celebrate the trail blazers in the AS community who started a ripple of impact.
We will raise funds to support the ASF mission and have a great time doing it.


 * NEWLY DIAGNOSED
   
   Received a diagnosis and wondering, what now?
   
   WHAT TO DO


 * ASF CLINICS
   
   Specialized healthcare by experts who understand Angelman syndrome.
   
   FIND A CLINIC


 * ASF-FUNDED RESEARCH
   
   ASF funded research advance our understanding of AS and increase the
   potential for treatment & therapeutics.
   
   FIND OUT MORE


 * ANGELMAN RESOURCES
   
   The largest offering of help and resources for those impacted by AS.
   
   learn more


 * GOFUND WINGS
   
   Want to host a fundraiser? Looking for a current fundraiser to support?
   
   Find out more


 * JOIN THE CURE CLUB
   
   A special group of monthly donors dedicated to finding a cure.
   
   Learn more


WHAT IS ANGELMAN SYNDROME AND THE ANGELMAN SYNDROME FOUNDATION?

Watch


TESTIMONIALS

 * Since her diagnosis, we have relied on the Angelman Syndrome Foundation as a
   source of information and support.
   
   David and Jessica Garrick

 * The Angelman Syndrome Clinic at MGH is a blessing for my adult child. Now we
   have somebody who really understands our needs.
   
   Anonymous

 * Amazing things have happened because of the ASF-funded LGIT study from
   Boston’s MassGeneral Hospital. It was the beginning of a new era for
   treatments for our children with AS.
   
   
   Sybille Kraft Bellamy

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IN THE NEWS

Latest press releases, articles and announcements

March 7, 2024


FAMILY ADVOCATES URGE CONGRESS’ SUPPORT DURING INAUGURAL ANGELMAN SYNDROME (AS)
CONGRESSIONAL ADVOCACY DAY

Washington D.C., – The Angelman Syndrome Foundation (ASF) and the Foundation for
Angelman Syndrome Therapeutics (FAST) are hosting the inaugural Angelman
Syndrome (AS) Congressional Advocacy Day in Washington, D.C. Angelman syndrome
advocates from all corners of the country will head […]

Read more
January 13, 2024


ANGELMAN CLINIC OPENS AT CEDARS-SINAI GUERIN CHILDREN’S

The Angelman Syndrome Foundation is proud to announce a new collaboration with
Cedars-Sinai Guerin Children’s to launch a new clinic for patients with Angelman
syndrome, a rare neuro-genetic disorder. The clinic is led by Cesar
Ochoa-Lubinoff, MD, MPH, director of […]

Read more
October 13, 2023


ANGELMAN CLINIC OPENS AT CHILDREN’S HOSPITAL OF PHILADELPHIA (CHOP)

The Angelman Syndrome Foundation and the Dup15q Alliance are proud to announce
plans to launch a new clinic at Children’s Hospital of Philadelphia (CHOP) to
better serve the Angelman and Dup15q communities. “We are excited to join other
Angelman and […]

Read more
October 11, 2023


ASF AND .PROT PARTNER TO LAUNCH NEW ANGELMAN CENTER FOR FAMILIES IN POLAND

On September 23, The Angelman Center brought together around 50 Families at the
First National Gathering of families with Angelman syndrome (I Ogólnopolski Zlot
Aniołków). The meeting was organized by the families from the Angelman Syndrome
Project (Projekt Zespół Angelmana). […]

Read more


OUR ASF WALK SPONSORS!

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ALL SPONSORS


BROWSE

 * What is Angelman Syndrome
 * For Parents
 * ASF Funded Research
 * Make an Impact
 * Events
 * About
 * Angelman Resources & Education
 * Contact Registry
 * News

Address Angelman Syndrome Foundation
3015 E. New York Street
Suite A2 #285
Aurora, IL 60504 Phone800.432.6435 Emailinfo@angelman.org


CONNECT

 * facebook
 * twitter
 * linkedin
 * instagram
 * pinterest
 * rss
 * youtube


THE MISSION

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. We exist to give all of them a reason to smile, with the
ultimate goal of finding a cure.

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Copyright © 2024 Angelman Syndrome Foundation. ALL Rights Reserved. | Site
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