WELCOME! Come on in and chat with people who are on the same journey you are! We have fun as well as talk about things that are important to all of us.
This chatroom is not restricted to just CarePartners...ALL ARE WELCOME!
Right now, we have a regular chat session every Friday night at 730PMEDT. Always check right here to see if that's changed or if we've added other times.
We are an extension of PLWP People Living With Parkinson's. The main chatroom is at http://www.groups.yahoo.com/group/plwp2 ... the PLWP website is http://www.plwp.org. You are invited to all of these sites as well as this one.
I am the care giver for my husband who has Parkinsons. I need some advice. We currently have a Mountaineer with a nice large flat
step, but my husband's legs
Thanks for your response. I did get a hold of the Washington State Parkinsons Association. They sent me a DVD on Parkinsons. I can't get my husband to watch
hi there, well it me began with me i have had pd for going on 13 years now. i must have had it for a couple of years with not knowing the pd symtoms, but that