For children with long-term or life-limiting illness, palliative care can transform their experience, helping them live with an enhanced quality of life, while also supporting their family and friends.

Paediatric palliative care is an active and total approach to care, from the point of diagnosis, throughout the child’s life, to death and beyond. It includes the management of distressing symptoms, care at the end of life and bereavement support.

Since 2018, we have been researching and building prototypes that help define the future of children’s hospice care, for a brand new children's hospice being developed by Fondazione Seràgnoli near Bologna in Italy. We believe hospice care that can use human-centred design and technology successfully and meaningfully can transform the way professionals deliver care, and significantly improve the care experience for patients and their families.

The majority of people who die every year, would prefer to die at home, yet only about half achieve this. This is often due to not being able to manage symptoms at the end of life. Laycarers care for their loved ones' physical and emotional needs and when faced with suffering, many want to do more, including clinical tasks, with the support of healthcare teams.

We believe there should be a choice for carers to be trained to give symptom control medications, should they wish and be suitable to do so.

Our solution - Palliate - seeks to improve the access and quality of training and support for carers to administer injectable (subcutaneous) medications in the home, to support patient preferences for a home death while also reducing pressure on community care teams. It does this by providing digital information and support via an app, to carers who have been trained to deliver medications. Palliate is being developed in collaboration with Central and North West London NHS Trust and hospice partners.

Research has shown that many patients near the end of life receive high-intensity services without clear evidence of benefits and often at odds with their preferences. For instance, while many people at the end of life would prefer to be cared for at home, around 90% of people spend some time in hospitals in their final year of life and over 50% of people die in hospital.

There is considerable evidence suggesting that excessive hospital-based care could be avoided if patients were offered high-quality care alternatives outside hospitals. This could reduce the overall cost of care which in the last year of life is, on average, five times higher than in other years.

Our study explores how carers and their loved ones make decisions about end-of-life care, which is necessary to effectively support carers and patients at the end of life to ensure there is high-quality care for all.

This study sits within a larger multi-year project with Edinburgh University, University of Lausanne and the Institute for Public Policy Research. The overall project is aiming to inform a more efficient allocation of health and social care resources in the provision of end-of-life care.

Suicide prevention is a vital health priority as suicide is the second leading cause of death in young people worldwide. Exposure to suicide in others increases the risk for young people to contemplate, attempt or die by suicide themselves. However, peer support may help reduce this risk and support those bereaved.

Our two-year project, supported by the Co-op Foundation, is framed around co-designing an innovative peer support solution for suicide bereaved 16-20-year-olds. We are co-producing the project with a diverse group of young people from North West London. We’re exploring the problem and generating a solution that we’ll train young people to deliver. We’ll also test, iterate and evaluate our process and product and disseminate this to the wider world.