The Our Views, Our Voices initiative promotes the meaningful involvement of people living with noncommunicable diseases in the NCD response by supporting and enabling individuals to share their views in order to take action and drive change.

An initiative of the NCD Alliance and people living with NCDs, it seeks to advance the rights of people living with NCDs and combat stigma and discrimination.


The Advocacy Agenda of People Living with NCDs is a living document that highlights the priorities of people living with NCDs to guide and inform efforts to improve NCD prevention and control.

The Advocacy Agenda of People Living with NCDs was built with the generous contributions of 1,893 people living with NCDs who took part in the Our Views, Our Voices consultation efforts. It serves as a compass for the NCD community to advocate for improvements in NCD prevention and control globally.

NCDs do not discriminate – they can affect anyone, anywhere – and account for 70% of all deaths globally. No measure of technical knowledge can replace the insight of the lived experience.

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Are you living with an NCD yourself? Are you a care partner for someone who is living with or has had an NCD? Get in touch to stay informed about opportunities to get involved in Our Views, Our Voices activities!

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Why is it taking you so long to act? We've all had enough of late diagnoses that leave patients helpless & hopeless. You absolutely need to make access to NCD healthcare possible & affordable for all.

Lived experience of sickle cell disease, Kenya

The Our Views, Our Voices digital platform has been made possible thanks to NCD Alliance’s partnership with Access Accelerated.