Find all needed information about Organizations That Support Angelman Syndrome. Below you can see links where you can find everything you want to know about Organizations That Support Angelman Syndrome.
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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