Advocacy resources

Published in 2011, this is the first ever Charter setting out the fundamental rights of people living with diabetes. The document places the rights of people with diabetes, their parents and carers into three focus areas; the rights to care; information and education and social justice, whilst at the same time acknowledging the responsibilities held by people with diabetes.

This toolkit for IDF members provides information and tools to successfully engage with national policymakers to demand stronger action on diabetes on the road to the UN High Level Meeting on NCDs 2018.

This publication of the IDF Europe Region identifies the local and European-wide challenges of implementing diabetes evidence into practice and makes recommendations based on the findings.

In December 2016, IDF held a consultation with the Blue Circle Voices (BCV) network to establish the priorities of the network. The main issues identified by BCV members were access and affordability of medicines, devices and medical care; education; prevention and discrimination. This document presents the four priorities with an IDF call to action to governments to improve them.

On the occasion of the BRICS Leaders Summit in China, 3-5 September 2017, IDF worked with its Members and BCV members in Brazil, South Africa and Russia to develop policy recommendations to improve access to diabetes care in their countries.

Published in 2010, this guide builds on the 2003 NDP Toolbox and sets out considerations and source material for developing and implementing national diabetes programmes.