6th Student Conference on Rare Diseases
Simultaneously with the observance of International Rare Disease Day at Cvjetni Square, the 6th Student Symposium on Rare Diseases was opened at the University of Zagreb's School of Medicine. The event was organized by the Students' Section for Rare Diseases in collaboration with the Croatian Alliance for Rare Diseases.
Hugs For Rare - Rare Disease Day Campaign
Join us for the special campaign 'Hug for Rare' that we are organizing for International Rare Disease Day on February 28! This campaign aims to raise public awareness about the challenges that people living with rare diseases and their families face every day. Rare diseases are often invisible ...
Program of the 6th Student Conference on Rare Diseases
The Students' Section for Rare Diseases at the Faculty of Medicine in Zagreb, in collaboration with the Croatian Alliance for Rare Diseases, invites all interested students to the 6th Student Conference on Rare Diseases, titled "ZEBRA 2025." This year's conference will focus on rare metabolic diseases, and the preliminary program of the event is provided below.
Development of the Student Helpline – "Meet the Rare"
In 2025, our Section for Rare Diseases at the University of Zagreb School of Medicine continues its lecture series aimed at educating medical students about rare diagnoses and the specific needs of those affected. Each lecture in the series includes a presentation by a medical expert on a particular rare disease, followed by a patient’s personal…
Development of the Rare Disease Helpline – Educational Brochure "Rare Infotheque for Healthcare Professionals"
Radio Student recognized the importance of the educational brochure “Rare Infotheque for Healthcare Professionals,” created by students from the Student Line for Rare Diseases. The news about the brochure’s distribution and its availability on the website was featured in the “Hodalica” program, broadcast on January 30, 2025.
Development of the Rare Disease Helpline – Volunteer Activities
The Student Helpline, operated by our dedicated volunteers from the Student Section for Rare Diseases at the University of Zagreb School of Medicine, welcomes new volunteers each academic year. Volunteering involves a wide range of activities. Throughout our collaboration, in addition to answering countless medical inquiries, our volunteers have also prepared numerous expert articles…
Rare Disease Counseling Center – A Comprehensive Support System – Association Counseling
The Alliance for Rare Diseases is dedicated to creating better conditions for individuals facing rare diseases and actively supports its member associations in various aspects of their activities. Through different initiatives, the Alliance focuses on providing support in areas that are crucial for improving quality of life...
Development of the Student Helpline – Student Conference on Rare Diseases "ZEBRA 2025"
On the occasion of the 2025 International Rare Disease Day, the Student Section for Rare Diseases of the University of Zagreb School of Medicine, in collaboration with the Croatian Alliance for Rare Diseases, is organizing the 6th Student Conference on Rare Diseases titled "ZEBRA 2025." The theme of this year’s conference is rare metabolic diseases, and numerous...
Rare Disease Counseling Center – A Comprehensive Support System – Rare Diagnosis Calendar
According to the reference portal for rare diseases, Orphanet, there are currently more than 6,400 rare diagnoses. These diseases, often unrecognized and insufficiently researched, require special attention and support in order to improve the quality of life of those affected and to enable better diagnosis and treatment. Rare diseases are...
Development of the Student Helpline – Brochure for Healthcare Professionals
In collaboration with the Student Section for Rare Diseases of the University of Zagreb School of Medicine, an educational and informational brochure titled "Rare Info Library for Healthcare Professionals" has been developed. The brochure contains information about rare diseases that is important for primary healthcare physicians, details about reference centers for rare diseases,...
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