This book brings the voices of people with serious illness, and those caring for them, into the debate about how far health and social care services can reflect the views of users when it comes to palliative care.

Chapter 1 Introduction; Chapter 2 User involvement; Chapter 3 Palliative and community care; Chapter 4 Multiple sclerosis; Chapter 5 Motor neurone disease; Chapter 6 Cystic Fibrosis; Chapter 7 Conclusions;