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    • #18963
      Ally
      Keymaster

      There is a lot of bad and misleading information on the Internet about a lot of topics, and Parkinson’s alternative treatments is one of them.

      How do you evaluate if something you read online is trustworthy? What are some red flags you look for when reading about alternative treatments for PD?

      Have you come across any health scams recently that you would like to warn others in this community about?

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