Angelman Syndrome Support Services

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


Support Resources - Angelman Syndrome Foundation

    https://www.angelman.org/resources-education/support-resources/
    Advancing the awareness and treatment of Angelman syndrome through research, education and support for individuals with Angelman syndrome and their families, with the ultimate goal of finding a cure.

Shop and Support ASF - Angelman Syndrome Foundation

    https://www.angelman.org/make-an-impact/shop-and-support-asf/
    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.

Information About Angelman Syndrome Support Groups ...

    https://angelmansyndromenews.com/2019/11/01/information-about-angelman-syndrome-support-groups/
    Nov 01, 2019 · Support groups can offer a sense of community and be a great information resource for caregivers of patients with rare diseases such as Angelman syndrome. Caring for a child or relative with a rare disorder such as Angelman syndrome can be challenging, with information hard to find about the disease or doctors who specialize in treating it.

FAQs - Angelman Syndrome - Angelman Syndrome

    https://www.angelmanuk.org/what-is-angelman-syndrome/faqs/
    With Angelman Syndrome, there are two professionals who most typify the role of case manager – the GP who determines that certain specialists are needed then refers the patient on to them. They then provide the follow up support on an ongoing basis typical of a case manager.

Angelman syndrome - NHS

    https://www.nhs.uk/conditions/angelman-syndrome/
    Angelman syndrome is a genetic condition that affects the nervous system and causes severe physical and learning disabilities. A person with Angelman syndrome will have a near-normal life expectancy, but they will need support throughout their life.

The Carolina Institute - Angelman Syndrome - Clinic Services

    https://www.cidd.unc.edu/Angelman-Syndrome/clinic-services.aspx
    Overview of Clinical Services Angelman syndrome is a genetic disorder characterized by developmental delay, speech impairment, severe intellectual disability, microcephaly, seizures, movement disorder and a happy demeanor with frequent laughter.

Angelman syndrome - Genetics Home Reference - NIH

    https://ghr.nlm.nih.gov/condition/angelman-syndrome
    Oct 15, 2019 · Angelman syndrome is a complex genetic disorder that primarily affects the nervous system. Characteristic features of this condition include delayed development, intellectual disability, severe speech impairment, and problems with movement and balance (ataxia).

Home The Angelman Network

    https://www.angelman.org.nz/
    CONNECTION & SUPPORT: We connect and support NZ families by encouraging and assisting with regional gatherings and fundraising activities across the country. [For free and confidential support services, s ee Parent to Parent.] ADVOCACY: The Angelman Network advocates on behalf of families and those with Angelman Syndrome in NZ.



Need to find Angelman Syndrome Support Services information?

To find needed information please read the text beloow. If you need to know more you can click on the links to visit sites with more detailed data.

Related Support Info