|UPDATE: June, 2018
ERN-EuroBloodNet 1st annual report is already available
All the activities and results achieved during first year of ERN-EuroBloodNet implementation are gathered in its first annual report.
The report is going to be distributed during EHA Annual Congress in Stockholm.
The European Reference Network – EuroBloodNet covers all Rare Haematological Diseases (RHD) both non-oncological and oncological.
During its first year, important efforts from the coordination team have been focused on setting up the structure to ensure that all its 66 members become active participants.
Some of its initiatives have been the implementation of the ERN-EuroBloodNet website and the production of dissemination material to spread the word of ERN-EuroBloodNet, including powerpoint, poster, leaflets and flyers.
What are the European Reference Networks? Watch this video
Based on common unmet needs to all Rare Haematological Diseases identified during the 1st year of the network, the activities carried out were focused on mapping the existing expertise, services and facilities available across all its 66 ERN-EuroBloodNet Members as a starting point for further work in the future.
In addition, ERNEuroBloodNet has contributed to the pilot testing and promotion of the Clinical Patient Management System, the telemedicine platform for inter-professional consultation for the safe sharing of clinical data.
ERN-EuroBloodNet activities have been split into 5 Core Fields of Action with specific tasks linked to objectives:
1) Cross border health
2) Best practices
3) Continuing medical education
5) Clinical trials and research
Learn more in EuroBloodNet First Annual Report.
EuroBloodNet and the European Patient Advocacy Groups in Haematology
EuroBloodNet recognises the key role that patient organisations have in healthcare. They help patients and their carers to understand their condition, to find out about how and where to get access to the best treatment and care, to learn how to live with the disease, its symptoms and side effects, and help them to navigate their healthcare systems to achieve best possible outcomes.
Patient organisations serve as a key contact point for patients and carers through local support groups, websites and social media. In addition, patient advocacy organisations work with policy makers, healthcare institutions, clinicians, researchers and industry to make sure all health policy and research delivers to patients’ needs and priorities. To do all this, patient organisations operate on a regional, national and international level today.