Advocating for awareness, access and equality in diabetes careStarting with this newsletter edition, we are excited to open our editorials to special guests from the IDF Europe community. For this issue, we are pleased to feature Konstantina Taki, a Medical Doctor and Diabetes Advocate from Greece and a member of our YOURAH network, who shares her perspective on improving the lives of people living with diabetes (PwD) across Europe. I have been living with diabetes for almost 20 years. It has shaped my identity and influenced my life in countless ways. I could speak endlessly about diabetes – sharing my experiences, challenges and insights – something I actively do through my advocacy work. However, if I had to identify the root cause of the barriers PwD face, it would be the widespread lack of awareness. Today, diabetes remains widely misunderstood. There is a blurred perception of what diabetes really is, particularly Type 1 diabetes (T1D), and how those of us living with it manage the condition daily. As a result, many of us hide their condition to “fit in,” avoiding the risk of being treated differently. But there is an essential distinction that needs to be made: being respected and having our needs met is not the same as being treated as an individual with "special needs." For example, it would make a significant difference globally if PwD were granted additional health-related leave days at work – without having to reach the point of diabetes burnout to justify them. Managing an often-invisible disease can make us question our own rights, even though we are continuously battling a serious health condition. As a healthcare professional (HCP), a diabetes advocate and someone with lived experience, I approach diabetes from a holistic perspective. My advocacy journey has made me realise how often I, too, have been dismissive of my own condition, struggling to find the courage to claim my rights. I fight hard to reverse this internalised behaviour, but it is a challenge. The first time I felt completely free with my diabetes was during the IDF Youth Leadership Lab in Ub, Serbia. The power of visibility and access We live in an era where information is consumed at an unprecedented pace. Raising awareness about diabetes is easier than ever before, yet representation and visibility remain crucial. PwD must have a voice – one that reflects their lived reality. However, awareness alone is not enough. Access to healthcare and essential medicines and devices remains a fundamental issue. The disparities in diabetes care worldwide are staggering. While some have seamless access to insulin and advanced technologies, others struggle with unaffordable insulin prices or hospitals that are hours away. How can we speak of equality in diabetes care when 50% of PwD globally lack access to insulin – the very substance that keeps them alive? Living with diabetes follows a hierarchy of needs, much like Maslow’s. The foundation is access to life-saving medication and healthcare. Beyond this, education and awareness improve quality of life. But true freedom comes when our health rights are universally secured. While I feel privileged to speak from a position of relative safety regarding my own access to care, that does not mean we should stop striving for better. There is still so much more to be done. A call for action Prevention is always more effective – and more cost-efficient – than treatment. Ensuring access to medicines, technologies and education for PwD not only improves their quality of life but also helps prevent complications which place a significant financial burden on healthcare systems. Investing in new technologies such as insulin pumps and continuous glucose monitors (CGMs) is far more sustainable than treating preventable complications. Diabetes is not a punishment. It is a condition that millions across the globe live with every day. It is time to open our eyes – and our empathy – to their struggles. If every policymaker could experience just one day in the life of a person living with diabetes, I have no doubt that our rights and needs would be secured the very next day. Until that day comes, advocacy remains essential. I hope to look back on this piece in the future and see that meaningful progress has been made.
![]() YOUTH PLATFORMApplications are open for the IDF Europe Youth Leadership Lab 2025! Are you between 18 and 30 years old and would like to become part of a dynamic community of young diabetes advocates? Join the IDF Europe Youth Leadership Lab (YLL) 2025! The YLL was launched in 2011 and it is aimed at creating a strong pan-European network of young diabetes advocates. Each year, around 24 young advocates (aged 18-30) from IDF Europe’s member associations are invited to take part in this transformative experience. This year, the YLL 2025 will take place in Parma, Italy, from July 6-12, hosted by AGD Parma in collaboration with the Italian Association of Athletes Living with Diabetes (ANIAD). Do not miss out on a week filled with hands-on workshops, community events, training sessions, networking opportunities and much more! We wish to thank AGD Parma and ANIAD for their dedication in making this event a success. ![]() The application deadline is March 21! Apply now and be part of this life-changing experience! MEMBER NEWSCelebrating the 50th anniversary of the Hellenic Diabetes Association ![]() APDP President, Dr. Boavida, discusses “Diabetes as a consequence of society’s evolution” in a recent interview ![]() The Bulgarian Diabetes Association to host the 2025 European Futsal Championship for Diabetes (DiaEuro) ![]() READINGS ON DIABETESWe deal with the management of diabetes on a daily basis as people with lived experience or healthcare professionals; we deal with politics, policies, research and many other aspects of diabetes, but rarely do we find the time to frame diabetes in a historical context. Readings on Diabetes, presented to IDF Europe by Angelo Argenteri, MD, Maria Stella de Sabata, MA, and Andrea Ascoli Marchetti, MD, is a journey through the major milestones in diabetes, one of the oldest and still most widespread diseases, with anecdotes, stories, historical facts and a very rich iconography. You may be familiar with some, less with others. We invite you to discover more about diabetes than your daily experience of it and trust you will be enriched and inspired by these stories. The IDF Europe Newsletter will present each month a chapter from Readings on Diabetes, which can be downloaded in full here. 1.BEGINNINGS: FROM PHARAOS TO PARACELSUS The story of diabetes is a journey from mystical affliction to medical curiosity, with each era contributing fragments to our understanding of the disease. It begins in ancient Egypt, with references found in the Ebers Papyrus (1534 BC) where symptoms such as excessive thirst, hunger and urination were linked to divine interventions. In the sixth century BC, the physician Sushruta calls diabetes "honey urine", after noticing ants drawn to its sweetness. Greek and Roman physicians expand the understanding of the condition, with Hippocrates (460-370 BC), Aristotle (384-322 BC) and Galen (129-216) connecting diabetes symptoms to fluid imbalances in the body. The term "diabetes" itself is coined by Apollonius of Memphis (3rd century BC) to describe fluids "passing through" the body. In the first century AC, Aretaeus of Cappadocia (1st century AD) fully justifies the name of the disease by linking diabetes to a siphon draining the body's strength. In the Middle Ages, Avicenna (980-1037) advances the conversation, introducing the idea of sweet urine linked to a liver dysfunction. Finally, in the Renaissance, Paracelsus (1493-1541) proposes diabetes as a systemic disease caused by altered blood chemistry. Are you curious to learn how the long quest to understand diabetes began? Explore this fascinating story in Chapter One of Readings on Diabetes. ![]() IDF EUROPE NEWS, ACTIVITIES AND EVENTS
News from the IDF Europe Team We are delighted to announce that T1D Advocate, Joana Amorim, has joined our team as Youth Programme Coordinator Intern. With a background in Marketing Management, Joana combines communication and innovation to drive meaningful change. As IDF Europe Youth Programme Coordinator, she is committed to fostering a global network of young leaders, empowering them in diabetes advocacy and leadership while ensuring a sense of belonging and achievement. ![]() We would also like to take this opportunity to thank Adam Gyurcsik, former Youth Programme Coordinator, who left our team to pursue other educational opportunities. We are thankful for his precious contribution to the work of IDF Europe and the diabetes community, and we wish him the best of luck in his new endeavours! ![]() IDF EUROPE ADVOCACY AND COMMUNICATION WORK
Rare Disease Day On February 28 we celebrated Rare Disease Day by raising awareness of rare genetic disorders linked to diabetes. While diabetes is the most common hormonal and endocrine disorder, some of its subtypes fall under the category of rare diseases, including mitochondrial diabetes, neonatal diabetes and MODY. Due to the rarity of these conditions, people often face long diagnostic journeys, with symptoms frequently misunderstood or misdiagnosed. Many also require lifelong management and highly specialised treatments that may not be widely accessible. ![]() More research is needed to improve diagnosis and treatment. Engaging more people living with these rare forms of diabetes in research is crucial to address their unmet needs and improve care for all. NEWS FROM EUROPE
EU-FUNDED PROJECTSASSESS-DHT: new publication on safe AI-enabled digital health technologies IDF Europe is part of the Horizon 2020 ASSESS-DHT project, which aims to boost the adoption of trustworthy and effective Digital Health Technologies (DHT) across Europe. ASSESS-DHT consortium members recently published a new article in Nature Medicine on the importance of integrating transparent and mandatory feedback-collection mechanisms into AI-enabled digital health technology interfaces for holistic development and user safety. According to the publication, these mechanisms could:
![]() MMD NEWS
MEP Metz’s white paper on access to quality healthcare On January 27, MMD Member MEP Tilly Metz hosted an event at the European Parliament to launch her policy white paper, "Making access to quality healthcare a top priority for the EU." The paper calls for a fundamental shift in healthcare policy, recognising health as a public good and addressing key challenges such as workforce shortages and rising medicine costs. MEP Metz advocates for a One Health approach, stronger EU-driven research and policies that prioritise public health needs. The MMD Group welcomed the white paper and congratulated MEP Metz on the successful launch event. ![]() UPCOMING EVENTS ACROSS EUROPEAdvanced Technologies and Treatments of Diabetes (ATTD) 18th International Conference EU4Health Civil Society Alliance event: "Unlocking Europe's future: prioritising health under the next Multiannual Financial Framework" International Diabetes Federation (IDF) World Diabetes Congress 2025 International Conference on Integrated Care Seventy-eight World Health Assembly European Health Management Conference European Association for the Study of Diabetes (EASD) 60th Annual Meeting ![]() Do you want to know more about IDF Europe's news and events? Please confirm that you are still happy to hear from us! |