Thank you for providing a place for us too. I am very grateful to have found MGH and now we have PLWP. It has helped me to cope and will continue to help me...
Are there any other carepartners thinking of or going to start journaling? How do you write down your thoughts? The journaling chat meeting that's coming up...
My wife and I have helped many people with debilitating illnesses from CFS to Parkinson's. The products are 100% natural and offer a superior delivery system ...
I need some input from others living with someone that has Parkinsons. We are just going thru the stages, not really understanding what is happening. Does this...
Hi Becky;<br> I just join this chat area. My husband was just diagnosied with Parkinson's at the beginning of this year. His dad had Parkinson's and just died...
been sick and out of town so I have not checked in till now. I really appreciate both your inputs. It helps to know that someone else understands and can give...
Hi. One of the great frustrations that I have as the daughter of someone with PD, is how you deal when your loved one doesn't do something that is medically ...
Tough call Catluv....not one I have really had to cope with. Single minded Type A personality types apparently are a majority in PWP profiles.<br>I will only ...
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 ...
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...
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...
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...
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...
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