The website is for the 'Sunterra' Public Foundation, an organization founded by parents of children with Down syndrome in January 2016. The foundation aims to support and develop children with Down syndrome, provide psychological and methodological support to their families, raise public awareness about Down syndrome, and promote inclusion. They envision a future where individuals with Down syndrome are socially adapted, integrated into society, and receive adequate support from the community and the state.

VALID, or Victorian Advocacy League for Individuals with Disability, is an organization dedicated to advocating for people with disabilities in Victoria. Their main activities include individual and systemic advocacy, self-advocacy network support, community building projects, and hosting the 'Having a Say' conference. They also provide training programs and resources related to disability issues.

SH Jong is an organization for young people aged 12-30 who are hard of hearing. They organize events to help young people connect with each other and offer information and support to improve the situation for young people with hearing loss. The organization aims to empower young people with hearing loss to achieve their dreams.

The Corporación Síndrome de Down (CSD) is an organization focused on improving the lives of people with Down syndrome and their families. It generates services and programs that address the strengths and needs of individuals with Down syndrome, promoting skill development, social participation, and the exercise of their rights to improve their quality of life. The organization is based in Bogotá, Colombia.

Beyond Vitiligo is a South Africa-based support organization dedicated to creating awareness, providing education, and supporting individuals with vitiligo. They actively participate in research on vitiligo treatments and partner with pharmaceutical companies and other stakeholders to contribute to finding cures and improving treatments. The organization also focuses on anti-bullying campaigns for children living with vitiligo, known as BV Kids.

The website is for the New Zealand Down Syndrome Association (NZDSA). The organization's purpose is to support individuals with Down syndrome and their families in New Zealand.

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The South African Disability Alliance (SADA) is a voluntary consultative forum comprised of national disability organizations. SADA advocates for the rights and freedoms of individuals with disabilities in South Africa and aims to improve their quality of life. The organization represents various disability organizations and addresses shared concerns and interests.

The National Federation of the Disabled – Nepal advocates for the rights and inclusion of people with disabilities in Nepal, emphasizing the principle of 'Nothing about us, without us.' It is a national organization focused on disability rights.

The QuadPara Association of South Africa (QASA) is a leading agency representing people with spinal cord injury and physical disability in South Africa. QASA aims to develop programs and services that increase capacity among its members and create opportunities for social integration. The organization publishes the Rolling Inspiration magazine, a quarterly lifestyle publication for people with mobility impairments.

Akasa is a network of self-help groups primarily supporting persons with disabilities and their family members, with a focus on women. Based in Sri Lanka, the organization adopts a rights-based, bottom-up approach and strives to create a society with equal opportunities, especially in rural and poorer communities. They provide vocational training, educational programs, and employment opportunities.

Down Syndrome Education (DSE) International and DSE USA work to improve education for children with Down syndrome. They conduct research to understand developmental differences and provide evidence-based resources to families and professionals, focusing on effective teaching approaches and interventions. Their resources and training courses aim to help children achieve their full potential.

Down Syndrome Australia is the national voice for people with Down syndrome and their families. The organization provides advocacy, resources, services, and support to people with Down syndrome, their families, and professionals. They also focus on raising awareness, promoting inclusion, and ensuring the best possible start in life for individuals with Down syndrome.

YAI and its network of affiliate agencies provide a comprehensive range of services for children and adults with intellectual and developmental disabilities (I/DD). They are committed to seeing beyond disability, offering opportunities for people to live, love, work, and learn in their communities. YAI offers various services, including education, clinical services, and crisis & behavior supports.

The Down Syndrome Family Network aims to be a national advocate for people with Down syndrome by promoting their value, acceptance, and inclusion through research, information, and support. They provide families with the necessary tools to become strong advocates for children and adolescents with Down syndrome, offering consultations, information, and assistance in locating community services.

Down Syndrome Albania (DSA) is a foundation dedicated to supporting individuals with Down syndrome in Albania. It offers services through its PRO PAK center, including therapies, parental support, and various courses. The organization also advocates for the rights and inclusion of people with Down syndrome and raises awareness through campaigns and media engagement.

The European Disability Forum (EDF) is an independent non-governmental organization (NGO) that advocates for the rights and interests of over 100 million persons with disabilities in Europe. It brings together representative organizations of persons with disabilities from across Europe and is run by persons with disabilities and their families, serving as a united voice for this community.

Down Syndrome South Africa (DSSA) is a non-profit organization formed in 1986. It serves as a national umbrella body and advocacy group for the rights of individuals with Down syndrome and other intellectual disabilities. DSSA provides services to persons with Down syndrome, developmental delays, and their families through 12 regional associations and support groups across South Africa.

The Emirates Down Syndrome Association (EDSA) is dedicated to improving the lives of individuals with Down syndrome. It offers a range of services including educational rehabilitation, allied health services, early intervention, family support, and vocational training. The association also organizes events and advocates for the rights and inclusion of people with Down syndrome.

The National Association of the Deafblind People in Bulgaria, established in 1997, aims to support and represent individuals with deafblindness and multiple disabilities in Bulgaria. It focuses on their social inclusion, rehabilitation, and ensuring their rights and opportunities are met. The organization strives to provide a better quality of life for deafblind individuals and their families through various initiatives and programs.