My husband is 52 and has been dx with PD in Oct. We have 5 children, 2 still at home. a boy 10 and a girl 4. I am new to this site and am not sure how all...
I apologize, as this message will be long. My mother was diagnosed with young-onset PD ~8 years ago and the disease is now quite advanced. I am beside myself...
The CarePartners of PLWP would like to invite anyone who would be interested to join us for the 6th Christmas Carols Singalong in the PLWP2 Chat room. ...
Hello Friends, My Name is Baachandran. N, residing in Atlanta, georgia, Basically a Finance Pro, from India I have migrated close to 3 years be 4, here....
Dear Friends, Ii am new to PD. Someone told me that certain foods make the symptoms worse. Does anyone know if this is true? If so, can you please tell me...
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...
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...
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...
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...
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...
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...
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 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...
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...
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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