Friendship, inclusion and opportunities were the topics under discussion with young people with Down Syndrome on what they want to do to combat loneliness. The discussion was held as part of the activities linked to World Down Syndrome Day.

Minister for Inclusion and the Voluntary Sector Julia Farrugia welcomed a group of young people who are members of the Down Syndrome Association Malta for an informal meeting at the Jake Vella NGO Hub.

This activity was held as part of the activities linked to World Down Syndrome Day, which is commemorated annually on 21 March, to raise awareness about Down Syndrome and to promote a more inclusive society.

The meeting aimed to create a safe and open space where young people can share their experiences and ideas, particularly on friendships, inclusion and the challenges that sometimes lead to feelings of loneliness.

During the discussion, young people were encouraged to express their opinions and share suggestions on how the community can further strengthen their participation in society.

This initiative is also a continuation of the work of the Down Syndrome Association Malta to promote self-advocacy among young people with Down Syndrome. Through various programs and activities, the organisation helps its members develop confidence, communication skills and the ability to speak up about their own rights and experiences.

Over the years, the association said it has carried out several important initiatives, including empowerment and self-advocacy programmes for young people, social activities that strengthen friendships and independence, as well as awareness campaigns to change perceptions in society about the potential of people with Down Syndrome.

During the meeting, Minister Julia Farrugia explained that, “at the heart of our policy is the principle that every person should live with dignity, a voice and equal opportunities. This informal meeting with young people with Down Syndrome was an important opportunity to hear directly from them about their experiences, their friendships and the challenges they sometimes face. They have much to offer our society, and it is our duty to continue to build an environment where everyone feels included and appreciated.”

She added that ”as we approach World Down Syndrome Day, we must continue to work together with organisations and families to strengthen self-advocacy and ensure that the voice of these young people continues to be heard clearly in our society.”

Joeanna Xerri, President of the Down Syndrome Association Malta said, “this meeting was a wonderful opportunity for our young people to meet in an informal setting and share their experiences with each other and with the Minister. For us as the Down Syndrome Association Malta it is very important that we continue to create spaces where young people with Down Syndrome can speak with confidence about friendships, inclusion and what they would like to see change in society. Activities such as these, especially in the context of World Down Syndrome Day, help to make their voices heard more and to continue to build a more inclusive community for all.”

Essien Mifsud, a young man, 20 years old member of the same organisation, explained how for him, “World Down Syndrome Day is a very important day because it gives us the chance to show who we really are and what we can do. It is not only about talking about Down Syndrome, but to show society that we too have dreams, talents and much to contribute.”

The organisation, which was founded in 1981 by parents of people with Down Syndrome, remains one of the most important voices in Malta that protects the interests of these people and their families, while working to ensure that everyone has the opportunity to live a fulfilling and inclusive life in the community.

Photos: DOI

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