There are a few articles aimed at caregivers, but most of them are general info on Parkinson's and Parkinsonism. There are a lot of caregivers here on the forum. I am one. If you have specific questions and concerns, just ask. You' ll get answers from other caregivers but also from people with PD who can speak from their experience as well. I think it's helpful to see both sides. And for PWP, I think it can be useful to see what caregivers sometimes have to deal with. Understanding goes both ways.

Thank you I agree we need to know both sides. However, it is nice to sometimes be able to reach out for more specific answers as needed. Thank you for reaching out to me.