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...
46
Laura Navoy
thpyke11
Nov 10, 2004 11:00 pm
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...
47
Randy
mrbentley2
Jan 23, 2005 3:53 pm
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...
48
Heather Mingo
heatherveld
Apr 7, 2005 9:23 pm
I haven't been checking this web site lately but it seems there has been no activity at all for several months. Anyone there? Heather...
49
Virginia Fay
aussiebella
Apr 9, 2005 12:27 am
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: ...
50
Heather
heatherveld
Apr 9, 2005 10:55 pm
If you reply to this email rather than go to the web site, is this message posted? Hi Bella. How is your battle going? Heather ... From:...
51
Virginia Fay
aussiebella
Apr 10, 2005 1:51 am
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...
52
bella
aussiebella
May 6, 2005 11:21 pm
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...
53
btucma2000
May 9, 2005 12:49 am
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."...
54
Virginia Fay
aussiebella
May 9, 2005 12:18 pm
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...
55
aynor35
May 10, 2005 10:54 pm
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...
56
Virginia Fay
aussiebella
May 10, 2005 11:00 pm
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...
57
Heather Mingo
heatherveld
May 11, 2005 5:37 pm
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...
58
Virginia Fay
aussiebella
May 12, 2005 1:40 am
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...
59
geetha_post1
May 17, 2005 5:58 pm
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...
62
Karen
pcsg2005
Aug 8, 2005 12:27 pm
{{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...
64
MAJ GANI JAWAID BANK
majganibank
Aug 24, 2005 5:59 pm
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...
65
paule607
Aug 24, 2005 7:31 pm
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...
67
bella
aussiebella
Aug 30, 2005 12:39 pm
Be not alarmed! It would appear that we have inadvertantly got the use of two completely different Carepartners Chat and Message areas, this one, ...
69
kulpa9
Oct 2, 2005 1:27 pm
dr.banks- i would enjoy talking to youabout pd. i also have yopd. please contact me at wingnuts2@... fran...
74
dee_136
Oct 30, 2005 7:29 pm
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...
75
Heather
heatherveld
Nov 1, 2005 12:51 am
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...
80
Jim
jrolen8247
Nov 28, 2005 9:06 pm
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...
81
BALACHANDRAN NATARAJAN
bala_n05
Dec 3, 2005 11:35 am
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....
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bella
aussiebella
Dec 18, 2005 12:26 am
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. ...
85
nsb042005
Jan 12, 2006 2:19 pm
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...
114
tammismith30
Dec 21, 2007 7:45 am
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...
115
s.ZELTSERMAN@...
chmaximumrum...
Dec 21, 2007 2:15 pm
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...
116
tammismith30
Dec 28, 2007 6:22 am
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...
125
girlaoiblog
Jun 6, 2008 4:16 am
I created this cool friends network and added you to my friends network. Hit-up now: http://daisukeh.zoomshare.com/files/newmessage.htm...
