Show simple item record

dc.contributor.authorNational Clinical Programme for Rare Diseases
dc.date.accessioned2019-11-18T16:37:20Z
dc.date.available2019-11-18T16:37:20Z
dc.date.issued2018-09
dc.identifier.urihttp://hdl.handle.net/10147/626925
dc.descriptionThis document has been developed to assist healthcare professionals who provide care for young adults with rare diseases. It focuses specifically on guiding principles to support the successful transition of young adults who are living with a rare disease from paediatric to adult healthcare providers. This document is a summary of the key recommendations from the Model of Care for Transition from Paediatric to Adult Healthcare Providers in Rare Diseases which was published by the National Clinical Programme for Rare Diseases in July 2018.en_US
dc.language.isoenen_US
dc.publisherHealth Service Executive (HSE)en_US
dc.subjectMODELS OF CAREen_US
dc.subjectRARE DISEASEen_US
dc.subjectYOUNG PEOPLEen_US
dc.titleSummary: Model of Care for Transition from Paediatric to Adult Healthcare Providers in Rare Diseasesen_US
dc.typeGuidelineen_US
refterms.dateFOA2019-11-18T16:37:21Z


Files in this item

Thumbnail
Name:
Summary. Model of Care for ...
Size:
536.7Kb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record