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PD Friends, Have Any Of You Been Surprised By How Difficult It Can Be To Find Local (non Medical) Resources For PD?
Things like support groups, exercise classes, etc? I feel like it should be easier than it currently is to find such resources by Googling "Parkinson's resources near me" with up to date contact info, location, timing, and cost. I have an idea about how to make this easier, but wanted to first see if others with PD feel the same way.
I agree. Information should be much easier to access.
🌈TheaD
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Looking For A Recommendation For Medications To Treat Anxiety And Hallucinations In An Older Adult With Moderately Progressed PD.
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