Alliance Documentation

About the Alliance

Croatian Alliance for Rare Diseases (HSRB) is a social-humanitarian, non-partisan, and non-profit association that brings together organizations with members affected by rare diseases, individuals suffering from rare diseases, and persons with disabilities resulting from rare diseases. This unites them into a single community within the Republic of Croatia to achieve, harmonize, and protect their individual and collective rights and interests.

The Alliance represents its members in promoting humanitarian efforts, social inclusion, advancements in treatment, research, rehabilitation, and the protection of people affected by rare diseases in Croatia and worldwide.

Through daily activities, the Alliance provides necessary support to its patient-members—directly via phone or email—and advocates for their rights to accurate information, access to treatment, and social services. It serves as an umbrella organization which brings together existing associations of rare disease patients, as well as individuals who, due to their small numbers, could not form their own organizations to address their issues collectively.

By working together, we aim to ensure quality medical and psychosocial care for people with rare diseases through the adoption of a National Program for Rare Diseases.
Furthermore, we strive to improve access to existing treatments, develop centers of excellence for specific diseases and/or groups of diseases, enable Croatian patients to participate in international medical research, provide psychological support for families, and reduce the social exclusion of rare disease patients.

 

Statute

Personal Data Protection Policy


Annual Reports

Activity Reports

Annual Activity Report – 2022

Annual Activity Report – 2023 

Annual Activity Report – 2021

Annual Activity Report – 2020

Annual Activity Report – 2019

Annual Activity Report – 2018

Annual Activity Report – 2017

Annual Activity Report – 2016


Financial Reports

Financial Report - 2023Download

Financial Report – 2021 

Financial Report – 2022

Financial Report – 2020


Operational Plans

Operational Plan - 2023

Operational Plan - 2024

Operational Plan - 2022

Operational Plan - 2021

Operational Plan - 2020

Operational Plan - 2019

Operational Plan - 2018

Operational Plan - 2017

Operational Plan - 2016


Financial Plans

Financial Plan - 2023

Financial Plan - 2024

Financial Plan - 2022

Financial Plan - 2021

Financial Plan - 2020

Financial Plan - 2019

Financial Plan - 2018

Financial Plan - 2017

Financial Plan - 2016

The Croatian Alliance for Rare Diseases is a recipient of institutional support from the National Foundation for Civil Society Development for the stabilization and/or development of the association.
The content of the website is the sole responsibility of the Croatian Alliance for Rare Diseases
The creation of the website was co-financed by the European Union from the European Social Fund
European Union

Together for EU Funds

About us

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