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...
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...
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....
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. ...
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...
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...
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...
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...
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...
