Volume 5 Supplement 1

5th European Conference on Rare Diseases (ECRD 2010)

Open Access

Patient involvement and empowerment through the NPRD (Eastern Europe)

Orphanet Journal of Rare Diseases20105(Suppl 1):O32

https://doi.org/10.1186/1750-1172-5-S1-O32

Published: 19 October 2010

Patient involvement and empowerment through the National Plans for Rare Disorders (NPRD) (Eastern Europe)

We present the current situation of the NPRD from Bulgaria, Romania and Hungary: three different countries confronted with the same problems and limits, and most probably not so different realities.

Bulgaria: the NPRD was officially launched on 1 January 2009. The draft for rare diseases and orphan drugs programme was prepared by BAPES and proposed to the Bulgarian Ministry of Health (MoH) in November 2004. The national plan includes 9 priorities (total budget 11 294 515 Euro).

Romania: RPWA established RONARD – and organised the first working groups on a National Plan for RD on 9 August 2007. 1-2 November, RONARD organised the first National Conference on RD. 29 February 2008– signed a partnership agreement with MoH – NPRD with 6 priorities. The first national programme on RD started in June 2008. Still there is no NPRD in the National Strategy for Health.

Hungary: there are several improvements but still before designing the Plan. HUFERDIS and enthusiastic professionals pushed it, but they have four running national health plans, and there is no more money for a new one.

In all three countries, Patient Organisations and medical professionals are the main engine for drafting and lobbying for a national strategy on RD. They organised information campaigns with stronger and stronger impact, help lines, contribute in designing social and medical health care services, initiate therapies, respite care, involve in research and clinical trials, etc. They organised working groups with members of the national alliances, networks and advocates at national level.

The Plan should be promoted both to parliament members and Ministry of Health. More “actors” have to be involved because RD patients need varied social assistance as much as medical care.

EURORDIS offered specific tools for lobby and advocacy actions toPOs. Recommendations and Communications of the EC give the best tool to promote RD as a public health and research priority.

Authors’ Affiliations

(1)
Romanian National Alliance for Rare Diseases

Copyright

© Dan; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd.

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