Parent Voices Count is a group of parents who in recent years have been told that their child has a life threatening or life shortening illness. We are working in partnership with the North West Children’s Palliative Care Network, which is committed to involving parents and carers in meaningful engagement. We are keen to work with other parents and carers to encourage involvement and participation in the design, implementation and evaluation of children’s palliative care services. In addition, we have currently identified a list of projects that seek to improve current palliative care for children and would like to work with more parents and carers as well as professionals in the North West to make a difference!
You can find out more information on what we are trying to achieve by visiting our website at: