We are not alone in this – by Yolande & Monty

“Our neurologist suggested we contact PAA for support and information after confirming Monty’s diagnosis just over a year ago. We also joined a monthly support group, which we both attend, and I joined a caregiver group.

These care groups reinforce the feeling that we are not alone in dealing with PD.

They also offer us a tremendous opportunity to share information that might not be readily available”

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