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    • #20527
      Ally
      Keymaster

      Patients are an integral part of clinical trials and Parkinson’s research from a practical standpoint, but what about their ideas and voices in terms of influencing the future of PD research and healthcare?

      Have you ever heard of patient engagement or been involved in a patient engagement initiative through a healthcare provider, community group or research body? What was that like? If you haven’t been part of a patient engagement initiative, would you like to be?

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