7 years
1000 scholarships
400 voices
100 countries

who are the #dedocº voices?

Since its creation in 2019, #dedoc° has been promoting and supporting access to some of the world’s most renowned scientific conferences for people living with or affected by diabetes.

The #dedoc° voices Scholarship Program offers a unique opportunity for diabetes advocates, to learn about the latest developments in diabetes treatments, technologies, and scientific research. It’s also a chance to network and connect with healthcare professionals, industry leaders, and the global diabetes research community. Most importantly, it allows diabetes advocates to join a strong, supportive network of like-minded peers who mentor one another and collaborate on advocacy efforts—ensuring the voices of people living with or affected by diabetes is present at scientific conferences, in line with our core principle: #NothingAboutUsWithoutUs.

#dedoc° voices, receive full conference registration, including access to all sessions and the exhibition hall, as well as their travel and accommodation costs covered. They also receive a digital badge to share their participation on social media and be featured in the #voicebook°, a special publication highlighting scholarship awardees that’s shared with both attendees and fellow voices at the event.

Participation will also connect advocates to key parts of the #dedoc° presence at conferences—such as the #dedoc° symposium, the #dedoc° exhibitor booth, and #dedoc° workshop sessions. Through these platforms, your voice won’t just be heard—it will help shape the conversation.

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why DO WE DO THIS?

Diabetes scientific conferences, created for knowledge exchange between medical professionals and diabetes industry partners, are not usually accessible to people with or impacted by diabetes.

Having lived experience present at scientific conferences provides:

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Insightful Perspectives: Unique insights help make care more practical, compassionate, and effective

Stronger Advocacy and Communication: We play a key role in translating scientific information for and to the wider diabetes community and in advocating for meaningful change.

Including people with lived experience at scientific conferences is important because we ensure that research and healthcare stay grounded in real-life needs and values.

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Shared Decision-Making and Empowerment: Being part of these events also empowers us with knowledge to have a voice in decisions about our health.

Person-Centred Research and Care: Our involvement holds researchers and healthcare professionals accountable to ethical, real-world standards.

  • The #dedoc° voices program has helped me find my voice as a diabetes advocate. I have learned to speak up and pay it forward to my community. So if you are an advocate, I encourage you to apply!

    Thapi Semenya, T1D

    #dedoc° voice from South Africa

  • The #dedoc° voices program has given me the opportunity to speak to a wider audience about diabetes, especially about type 2 diabetes – without the fear of stigmatisation.

    Ken Tait, T2D
    #dedoc° voice from the UK