Resource was added by: Bec Hanley
This grid outlines what CRIG members have on offer in terms of training for Patient and Public Involvement (PPI) representatives/members. The grid does not list training for researchers. It is broken down into different categories and has sections for people who are new to PPI and those who are more experienced. It is a resource for CRIG members who may be looking to develop training for the PPI representatives involved in their work and who want to see if there are any existing resources that can be adapted, or for those looking to provide training and want to see if there is anything that already exists that would be suitable. If you would like to use one of the training resources below, please ensure that you let the relevant contact know before doing so.
For this to be a useful resource, we ask that all CRIG members add training that their organisations have available to this grid.
MS Society Research Network distance learning pack
Resource was added by: Bec Hanley
This pack is sent to people affected by MS who join the MS Society's Research Network. Thanks to Jenny Robertson for sharing it.
Groups, networks, panels – what are the key ingredients for success?
Resource was added by: Bec Hanley
This paper looks at groups, networks and panels, and what helps people to stay involved in a group (of any size) that exists over a period of time. It summarises discussion and presentations at a Shared Learning Group on Involvement meeting in October 2017.
Getting connected using the web – involving people with personal experience
Resource was added by: Bec Hanley
This guide was developed by Jo Black at the National Council for Palliative Care, and gives advice on using the web to involve people with personal experience of palliative care. This is quite old, and some of the links don't work any more, but it's still felt to be useful.