Directory of Organizations Resources

Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > Williams Syndrome > Organizations

This category is for all associations or organizations that promote education, research, and advocacy for patients with Williams Syndrome, their families and caregivers.

Resources in This Category

• Autour des Williams

  http://www.autourdeswilliams.org/
  French Williams Syndrome Association, with limited information in English, Italian and Spanish, and French. Gives background of the organization, how to join, and clinical trials.

• Canadian Association For Williams Syndrome

  http://caws.sasktelwebhosting.com/
  Non-profit society dedicated to advancing research, education, and support. Includes about WS, resource centre, new parents, events and benefits, and how to help.

• New Zealand Williams Syndrome Association

  http://www.williams-syndrome.org.nz/
  Voluntary non-profit organization run by parents, offering help to families with a Williams Syndrome child dependent.

• The Williams Syndrome Foundation (UK)

  http://www.williams-syndrome.org.uk/
  Providing information about the condition, and support and help to UK-based WS families.

• Williams Syndrome Association

  http://www.williams-syndrome.org/
  Offers information and support to patients, their families and caregivers. Includes news and events, teacher and doctor information, regional services, WS listserve, and members area.

• Williams Syndrome Association in Romania

  http://www.williams-syndrome.ro/
  Supporting WS families in Romania.

Related Categories

• Home > Health > Conditions and Diseases > Genetic Disorders > Organizations

Other Languages

• French

 

Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > Williams Syndrome > Organizations

 

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