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Correcting others about PD assumptions
Do you ever run into people who think they know or understand more about Parkinson’s disease than you do? Have you ever had the experience of someone explaining your life experience to you, or telling you you’re wrong about your own experience?
I’ve run into this many times in my life, and sometimes I just don’t feel like correcting them. Sometimes it’s just not worth my time or energy. Can you relate, or do you always try to correct people’s misconceptions about PD?
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