We walk along life’s journey with those who have Down’s syndrome from birth to old age.

We are a national organisation, committed to improving quality of life for people who have Down’s syndrome, promoting their right to be included on a full and equal basis with others.

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A mum gives her toddler a hug. You can see both of their faces. They are both smiling. The little boy has Down's syndrome

"I am so grateful for the help and support for the Down’s Syndrome Association- ever since Edward was born, his childhood and education, you have helped every step of the way."

Parent

A young woman stands in a sunny garden. She is smiling. The young woman has Down's syndrome

"You have been tremendous over the past year, an ardent campaigner throughout the pandemic and Evie loves all of the DSengage activities."

Parent

a newborn baby who has Down's syndrome swaddled in a white cloth

"When my son was born I had no idea where to turn. I would say to parents, go to the DSA ask them the questions that you really want to know the answer to. It is a dynamic association, advocating, researching, improving the lives of people who have Down's syndrome on a personal level but also on a national one."

Parent

a young man eats a tortilla wrap that he's made himself. The young man has Down's syndrome

"I just wanted to say a huge thank you so much for inviting me into your incredible Our Voice group. I truly appreciate everything the DSA has done and providing for me so thanks for always being there Cheers to many great years ahead of the brilliant events and project work I’m so excited to be a part of - thank you."