Learn about what really matters to people living with diabetes around the world.

The #dedoc° blog features articles and opinion pieces written by our international network of diabetes advocates: the #dedoc° voices. From scientific conferences to the latest diabetes research and technology, from challenges faced by those living with diabetes to global disparities in healthcare — our #dedoc° voices cover it all.

Diabetes advocates wishing to contribute to the #dedoc° blog are welcome to submit a guest post using the link below. Don’t hesitate to get in touch — we love to hear from you, and so do thousands of others!

All opinions are those of the authors.

Contact: blog@dedoc.org

Michelle Law Michelle Law

Choosing Between Virtual and In-Person Diabetes Conferences 

Michelle Law has been to her fair share of diabetes conferences—both online and in person—and she’s here to spill the pros and cons of each. From the comfort of home in PJs to the buzz of real-life meetups, she shares what’s great (and not-so-great) about both formats. If you’re wondering which option might suit you best, Michelle’s got you covered with honest insights, a few laughs, and an important reminder to keep the language respectful and inclusive.

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Sebastián Haro Sebastián Haro

A light through the shadows: my personal odyssey with T1D

“Embarking on my journey with type 1 diabetes (T1D) over 31 years ago, I traversed through a landscape shadowed by secrecy and silence,” writes journalist, diabetes advocate and #dedoc° voice Sebastián Haro, “This voyage has been one of profound transformation, marked by challenges, revelations, and the eventual embrace of technology and community that illuminated my path to empowerment.

“This is not just a story of managing a chronic condition but a deeply personal narrative of finding my voice and place in a world that often misunderstands T1D.”

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Emma Doble Emma Doble

The next step in patient involvement in diabetes conferences

“Including people with lived experience in diabetes conferences is no longer just a ‘nice to have’,” writes patient advocate and #dedoc° voice Emma Doble.

But what is the Patients Included charter? How can a conference become ‘Patients Included’? And why is the inclusion of people with lived experience so important?

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