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patient registry ( G.)

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I recently submitted my name to the Registry. After 5yrs. I have a probable dx of PLS. I am curious to know how you are doing with the Registry and how many people have PLS. I really think that there are more people with PLS than the doctors know of. One of the reasons is that it is so hard to diagnose and the doctors don't want to commit themselves for fear of being wrong and possible wrong treatment!!!

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