For the last few months our office has been working with children and young people on revising the Charter of Rights for Children and Young People in Care, and now we want your feedback.
Every five years we are required to review the charter to make sure it is still relevant and reflects what young people in care want and need today. As part of this year’s review nearly 100 children and young people who are in care or who have a care experience told us what is important to them and what they thought their rights should be while in care. They shared their voices through participating in workshops, online surveys, worksheets and activity books.
With the voices of these young people at the centre, the Charter of Rights working group (which included two care leavers) set about collating the responses and drafting a set of rights that reflected what the young cohort said. Based on their feedback, the revised charter has a strong emphasis on being safe, the right to be heard, being respected as an individual, and of connecting to and being part of culture.
The next step in the review process is to get feedback from you – the adults, carers and workers who care for this young cohort. We want to know if you think these new rights reflect the needs and concerns of the children and young people that you work with and care for every day. Remember these rights are for the young people themselves so they should reflect their voices and what they consider to be important.
How to share your feedback
Once we have your feedback, we will be sharing the final version of the revised charter to a group of children and young people for endorsement during the October school holidays. The updated charter is expected to be legislated in Parliament early next year, with the roll out to begin soon after.
On behalf of our office and the working group we would like to send a big heartfelt thanks to the people who helped facilitate the activities that enabled children and young people to have their say, and to the young people themselves who were willing to share their thoughts and feelings openly about their rights in care.