I have told my family about my PD diagnosis and told them to look at the MJF website. Very good info organized and explained in a way that everyone could understand what's going on with me and why I don't have answers to questions like "how will you be in a year?" I just do not know, that seems to be the scariest part for them and for me too. I have learned this week to live a day at a time. If I'm having a bad day and need to just rest all day I am allowed to, and should, do that. Tomorrow will be different and I'll deal with that then.

APDA and Brian Grant Foundation are good too🙂

Parkinson's connect is another good one

PD Conversations through ParkinsonsFoundation.org
https://www.pdconversations.org/s/

The conversation forum