Advocacy Agenda

The Advocacy Agenda of People Living with NCDs will be used as an NCD advocacy compass to mobilise the movement, from local communities to the global collective.

The Advocacy Agenda will build on the knowledge and first hand experiences of people living with NCDs. It is being produced by means of broad consultation and aims to articulate the advocacy issues of most importance to those affected by NCDs.

To promote the views of people living with NCDs, we are consulting with individuals from different world regions, disease and risk factor communities to better understand their priority asks.

Two means of consultation, community conversations and an online survey, will feed into the Advocacy Agenda, which will be launched in December, 2017. You can read more about these below, including information about how you can get involved!

Community Conversations

In-person community conversations are being conducted in the different world regions to identify common issues faced by people living with NCDs, main recommendations, and how people living with NCDs would like to be meaningfully involved in the NCD response.

Find out more


Have Your Say: Online Consultation of People Living with NCDs

If you have or have had an NCD, or if you are a care partner or close to someone who has or has had an NCD, make your mark on the Advocacy Agenda of People Living with NCDs by responding to our online consultation! 

Find out more and respond to the survey