The EURORDIS Policy Fact Sheets empower patient advocates to participate in key rare disease policy development processes
EURORDIS has added three new Policy Fact Sheets to its growing repertoire: one on Newborn Screening and two others on the Specialised Social Services, particularly Adapted Housing Services and Resource Centres. Other Policy Fact Sheets have recently been revised and updated, including those on Rare Disease Patient Registries, Orphanet, Centres of Expertise, National Rare Disease Help Lines, European Network of Rare Disease Help Lines, Respite Care Services and Therapeutic Recreation Programmes.
Each of the EURORDIS Policy Fact Sheets describes why the topic is important and necessary to people living with a rare disease, how to address the issue, related matters, and useful references. The information contained in the Fact Sheets is complemented by related articles, documents and reference materials available on the EURORDIS website. Many of the issues are further explored during the annual EURORDIS Membership Meetings, where targeted workshops provide a venue for the exchange of knowledge and ideas.
Consult the full list of the freely downloadable and printable Policy Fact Sheets and other related materials.
Louise Taylor, Communications and Development Writer, EURORDIS
Page created: 29/05/2013
Page last updated: 29/05/2013
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