The main aim of the PCF is to engage with families who have children with SEND, whether diagnosed or not, and provide support and guidance around what is available as well as their rights. When engaging with families we aim to feedback their voices and opinions regarding services to professionals. This ensures services are relevant and accessible to families and meet the needs of our children and young people. By sitting at the table with professionals we aim to co-produce on as many services and workstreams as possible to ensure the views and needs of children and young people with SEND are valued and included.
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