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    • #20290
      Ally
      Keymaster

      How has having Parkinson’s disease affected your social life? Have you made new friends through online or in-person support groups for people with PD and/or caregivers? Have you enjoyed connecting with people in this forum?

      Do you prefer to connect with people in-person or online? For me, it’s a bit of both but everyone is different. What works for you?

      For anyone who might be new to the PD community and looking for friends, where would you recommend they start?

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