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About CDSC |
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The Connecticut Down Syndrome Congress was formed in May 1986 as a special interest group to advocate for persons with Down syndrome in the state of Connecticut. Today we are a welcoming and supportive network of over 350 parents, numerous professionals and over 20 advocacy groups statewide.
Our mission is:
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 To advocate for the realization and enhancement of the full spectrum of human and civil rights for persons with Down syndrome
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To address social policy issues and conditions that affect the growth and the potential of persons with Down syndrome
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To gather and disseminate accurate information regarding Down syndrome
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To promote public awareness and a better understanding of Down syndrome
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To encourage partnerships between parents and medical and educational professionals concerned with Down syndrome
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To provide support to families of children with Down syndrome
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To encourage quality services for persons with Down syndrome
We implement our mission with these activities:
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Annual convention, featuring nationally known speakers, workshops on best practices in education, medicine and social issues, and the largest state-wide gathering of families and professionals concerned with Down syndrome.
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In addition to the annual convention, we co-sponsor parent/professional conferences with nationally known speakers, on such topics as Speech and language, medical issues, inclusive education and sexuality.
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Extensive Internet based communication: email notification of federal and state legislative initiatives which affect our families, member group message board to facilitate discussion, support and information among members.
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Providing cash grants to schools and organizations that promote best practices.
- Scholarships awarded annually to persons with Down syndrome pursuing post-secondary education and to an educator pursuing a master degree in Special Education.
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Membership benefits include:
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Network of support in the largest state-wide organization dedicated to improving the lives of those affected by Down syndrome