DAI Survey on Advocacy & Involvement in Dementia Research & Policy

DAI wants to hear ALL of the voices of dementia, and invites YOU to have YOUR say. This includes, but is not limited to:

  • People with dementia
  • Care partners
  • Families
  • Researchers
  • Policy makers
  • Advocacy organisation staff
  • Health Care Professionals

Dementia Alliance International (DAI) wants to hear from you about your experience being involved in advocacy, research or policy.  If you are a person with dementia, a supporter or family member, a researcher, or dementia policy maker- please consider completing our short survey and help shape the future of dementia advocacy.

You can complete the survey here: https://www.surveymonkey.com/r/SurveyDAI

In many countries, policy makers, researchers and service planners are increasingly valuing the inclusion of lived experience advocates with dementia and care partners in projects. At the same time, there continues to be challenges in understanding what involvement should mean, who should be involved and how their involvement will be supported.

This research will help to identify the next steps in ensuring meaningful and valued participation and involvement of people with a lived experience of dementia. DAI will be releasing a publication mid-next year which will include recommendations about next steps.

Don’t miss your opportunity to have a say and be part of this important work.

Any questions about the Survey can be sent to [email protected].
Or complete the survey here: https://www.surveymonkey.com/r/SurveyDAI

The deadline to complete this survey has been extended to  February 7, 2020.