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...
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...
{{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...
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...
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...
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...
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...
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...
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...
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."...
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...
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...
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: ...
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...
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...
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 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 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...
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...
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...
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...
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,...
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...
I have a favor to ask of each of you ... and no, I'm not asking for money nor am I asking you to shed blood for PLWP! LOL (Though I really believe many of you...
There's so much confusion, so many questions...such an important time in the cure of neurological diseases. We have created a special forum for discussing...
Jane Stengel who is Co-Director of PLWP's Events Team is going to set up a PLWP Team with the Parkinson's Unity Walk. The walk is scheduled for April 26, 2003...
Hi all we shall once again try using the PLWP website for our Friday Evening Chat Fest. Anyone who would like to join in..just come to PLWP Communication ...
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