Hi all. I just joined this group. The statement says: ' Right now, we have a regular chat session every Friday night at 730PMEDT. Always check right here to...
Hello Nargis Thanks for your enquiry! There are several sites we use for carepartners chats, but we usually find now it is easier to meet in Yahoo Messenger,...
I hope that I am in the right chat room. I just recently signed on here. My mother has PD. She was diagnosed with it about 12 years ago. Since then she has...
Hi! My name is Shannon aka Laney. I am Toad's daughter, and I am a caregiver. My father was diagnosed with PD in '92. I am looking forward to giving and...
Hey! My name is Woody and I was diagnosed with PD in '98. My wife of 45 years has been my "care-giver" and I, quite frankly, couldn't funtion without...
Hello Woody! Toad says hello as well. I just want to say that I feel it is a privelege to be able to give back to the man who gave so much to me. I am a...
Hello to you all and Holiday Greetings. There has been some confusion about "OUR ROOM", and I finally figured it out! We have two Carepartner Rooms. Only...
Hello all. I am new to this group today. I suppose what I am looking for is support and information. I will try to be as concise as I can. My father-in-law...
Hello. first let me tell you that I don't have very much experience with PD meds etc. I take mirapex and stalevo and don't seem to have too much trouble but I...
Hi, all! My partner was diagnosed with a "Parkinsonism" nearly 3 years ago and I've been taking care of him ever since. He got WRETCHED healthcare where we...
Yo I am still here. It would appear we have all been "just poking along" Nice to hear from someone.. Cheers Bella Heather Mingo <heatherv@...> wrote: ...
Yepper...it's all there for anyone to read! It's tough going around here Heather at the moment. The old "3 steps backwards and later two steps forward" plan it...
There has been an upsurge of interest in us all getting together. That being the case, we have changed the times to 6.30pm EDST Friday nights for regular...
Yo there you two. How the heck are you? We thrilled you are getting inquiries about the chatroom. We will definitely put you back on the "radar screen."...
Cool Bananas The "Cavalry has arrived"!! Go you good things..Nan & Bren! We are still here! btucma2000 <no_reply@yahoogroups.com> wrote: Yo there you two. How...
Hi for all! I am new in this group. I have my father suffering from pd / MSA. He was diagnosed in 2002 and his condition is pretty bad already...He cant move...
Hello Aynor and welcome. We look forward to chatting to you. We have a meeting every week at 6.30pm-7.30pm Easten USA time on friday nights for them. I realize...
I sure hope I'm home this Friday evening and can remember to tune in. I've been trying for months now with no luck. I'm either away or totally forget. I'm a...
Dont' forget.. LOL We'll look forward to seeing some more of us..6.30pm (ish) friday!! Heather Mingo <heatherv@...> wrote: I sure hope I'm home this...
Hello, I hope this group message of mine finds the reader in good health and mood. I'm Anitha and this being my first post, I'll keep it short. You can find...
{{hugs to all}} I am Karen, a caregiver to my mother of 10 yrs dx pd. My father tends to her most of the time, but works f/t still to keep the medical...
I AM A DOCTOR AND UNFORTUNATELY SUFFERING FROM YOPD I CAN GIVE INFORMATIONS THAT EVEN RESEARCHERS HAVE NOT BEEN ABLE TO FIND OUT .MY INFORMATIONS ARE...
Of course we'd be interested in new information for PD. You have to keep track of treatments yourself in this day and age. The doctors on working on the...
ANYONE HERE WHO IS A PARKIE AND ALSO CAREGIVER FOR SPOUSE. I WAS DIAGNOSED IN 1999 AND WAS COPING FAIRLY WELL. SUDDENLY MY HUSBAND GOT ILL AND NOW I HAVE TO...
I hope this reaches you, Dee. I can't help you but there might be someone on the PLWP site who can. This is where you can find the home page and from there...
