Engaging People With ME As Partners In The CRCS

 

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From #MEAction.

 

A view from the US.

 

The National Institute of Health’s RFA for ME/CFS Collaborative Research Centers breaks new ground. For the first time, the funding agency is strongly encouraging researchers “to establish partnerships with patients groups and solicit their input” as part of their research plan.

#MEAction assembled a team of volunteers to assist researchers in thinking about this, and today we release the first version of “Engaging People with ME as Partners in the Collaborative Research Centers.” This document shares best practices identified by the volunteers, along with resources for more information.

“Engaging patients and caregivers in research is not a new concept,” says Jennie Spotila. “Patient-centered approaches to research have been developed and applied in many areas, but this is the first time NIH has encouraged it in ME research.” Spotila led the volunteers, drawing on her training as an Ambassador for the Patient Centered Outcomes Research Institute. “We are fortunate that our team could rely on what PCORI and others have already learned,” she added.

 

To read the rest of this story, click on the link below:

 

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