Searching for Organizations That Support Angelman Syndrome information? Find all needed info by using official links provided below.
https://www.angelman.org/
The Angelman Syndrome Foundation raises awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties.
https://www.angelman.org/resources-education/support-resources/
The Angelman Syndrome Foundation is the largest non-governmental funder of Angelman syndrome-specific research. It is our hope that these funded researchers, and their collaborators and peers, will bring forth new discoveries that ultimately lead to treatments and a cure.
https://www.thinkgenetic.com/diseases/angelman-syndrome/organizations/5512
There are several support groups for families who have a loved one with a diagnosis of Angelman syndrome. As of June 1, 2016, support groups for Angelman syndrome include: Angelman Syndrome Foundation; Angelman Syndrome Support Education and Research Trust (ASSERT) in the UK; Canadian Angelman Syndrome Society
https://rarediseases.org/organizations/angelman-syndrome-support-education-and-research-trust/
Description The Angelman Syndrome Support and Research Trust (ASSERT) is an international non-profit organization dedicated to providing information and support to families and caregivers of individuals who have Angelman syndrome.
https://www.thinkgenetic.com/diseases/angelman-syndrome/organizations/5697
If you are interested in setting up a local support group, you can reach out to the national and international support organizations listed below to see about creating a support group for your area. If you do begin a local support group, consider reaching out to Angelman syndrome specialty clinics t
https://rarediseases.org/organizations/angelman-syndrome-foundation-inc/
Description The Angelman Syndrome Foundation, Inc., (ASF) is a non-profit organization. Its mission 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 …
https://www.angelman.org/resources-education/international-as-resources/
The Angelman Syndrome Foundation is the largest non-governmental funder of Angelman syndrome-specific research. It is our hope that these funded researchers, and their collaborators and peers, will bring forth new discoveries that ultimately lead to treatments and a cure.
https://www.angelman.org/author/webmaster/
The Angelman Syndrome Foundation is the largest non-governmental funder of Angelman syndrome-specific research. It is our hope that these funded researchers, and their collaborators and peers, will bring forth new discoveries that ultimately lead to treatments and a cure.
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