I NEED to know EXACTLY what you with Parkinson's and "Masking of the Face" NOT due to medication but due to the disease itself ----felt like when it started. I am trying to figure out if this is what is happening to me. Please be specific with every detail of how your face etc. felt and the progression and if the progression was slow or rapid and how it felt as it progressed.
Thank you. This will really help me to know from those of you who this has happened.
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