Many of the symptoms of Parkinson’s are physical (i.e., tremors, loss of mobility) and/or cognitive, and both types can really slow you down and sometimes even make it impossible for you to do the things you’re used to doing with ease. This can be a frustrating and isolating experience. How do you cope with having to slow down or change how you do things? Do you find you need to rely more on others for help? How does that feel?
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