Down Syndrome Association

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Children and adults with Down’s syndrome are all unique individuals with their own personalities, family backgrounds and preferences that make them who they are.
Here you will find answers to questions that we are often asked about Down’s syndrome. This information will help you to separate the facts from some common misconceptions. If you do not find what you are looking for ring our helpline and speak to one of our specialist advisors.

The Down’s Syndrome Association (DSA) is the only charity in the UK dealing with all aspects of Down’s syndrome. Its aim is to help people who have Down’s syndrome live full and rewarding lives.

Since 1970, we have grown from being a local parent support group into a national charity with over 20,000 members, a national office in Teddington, Middlesex and an office in Northern Ireland. Despite this, the organisation is run by a total staff of just over 40 (many of them part time). We also work closely with local support groups throughout the UK.

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