This category is for all associations or organizations that promote education, research, and advocacy for patients with Williams Syndrome, their families and caregivers.
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Sites 4
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.
Voluntary non-profit organization run by parents, offering help to families with a Williams Syndrome child dependent.
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.
Providing information about the condition, and support and help to UK-based WS families.
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.
Voluntary non-profit organization run by parents, offering help to families with a Williams Syndrome child dependent.
Providing information about the condition, and support and help to UK-based WS families.
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.
Other languages 1
