As part of the National Institute for Health Research, we use the skills, knowledge and expertise of researchers, health and social care professionals, managers, commissioners and patients to conduct high quality research projects to find new ways of improving healthcare. Our aim is to ensure the results of the research are translated quickly and effectively into benefits for patients, the wider NHS and social care.
Sickle Cell Patient Survey
Posted 24 Mar 2015, 09:26 by Derryn LovettThe Picker Institute along with CLAHRC NWL and Sickle Cell Society have launched a new feedback tool which allows healthcare services to obtain feedback from Sickle Cell Disorder (SCD) patients of all ages, and channel these insights into long-term care improvements.The survey is now live and available for completion from now (March 2015) until late summer.For further information look to the Sickle Cell Societies blog on this survey.
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