After a Parkinson's diagnosis, something strange happens. Suddenly, your social media feeds, YouTube recommendations, news articles, podcasts, and Facebook groups are filled with Parkinson's. Some of it is incredibly helpful. Some of it is inspiring. And some of it can leave you feeling more overwhelmed than informed.In this episode, we have an honest conversation about navigating the flood of Parkinson's information in today's digital world. We discuss how social media has transformed the Parkinson's community, the benefits and pitfalls of having endless information at our fingertips, and why it's okay to step back when the noise becomes too much.Whether you're newly diagnosed or have been living with Parkinson's for years, this episode is a reminder that you don't have to consume everything. Finding a few trusted resources, building real connections, and focusing on what helps you can make all the difference.Chapters:00:00 Suddenly, All You See Is Parkinson's01:20 What We Did After Our Diagnosis02:18 How the Parkinson's Community Has Changed03:44 The Problem with Misinformation05:12 Who (and What) Should You Trust?07:40 Information Overload Is Real09:09 Why We Create Content the Way We Do10:35 The Emotional Journey After Diagnosis12:24 Advice for Anyone Newly Diagnosed13:51 Finding Balance in a World of Constant Information15:12 Final Thoughts & Helpful Resources

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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