Parkinsn's Email List Message

Posting to the Parkinsn List is a benefit of Subscription


[Message Prev][Message Next][Thread Prev][Thread Next][Message Index][Thread Index]

Fw: hello


Re: hello

I tried to answer you off list Deborah, but it was not accepted twice. I
decided to send this through the list because I can tell how overwhelmed you
feel. It has to be tough to be far from your home, job and most of all your
partner. I do know how it feels to be far away from home and to be isloated
in a place that I heartedly disliked. I believe that from your posting that
you have been given the care of your father without too much idea of what it
involved day to day?  I am a friend of a pwp who lives 10000 miles away from
me in Australia and I knew nothing about PD when I met him 16 months ago. I
found out all I could about what the disease was, and yet I knew so little
about how it affected the lives of so many until I found the list. John * my
friend* has had it most likely 10 years, dx 6 years ago ( he rarely
discusses it ) and should be retired at 48 but is still working daily. Your
father is the age my mother is who has essential tremors which is similar
but far different in the outcome. I see you feel that many on the list have
helped you . They helped me too when I felt I had so little in common with
those who were family, care takers, or the pwp. I do not know if this is
being pushy or not, but when you said you hated to sound * victimy* it
sounded so familar. If you have time and want to mail me I am here most of
the time and I am a good listener Deborah.

Audrey *seattle*   friend of  pwp aussie  John  48/42/38??




----- Original Message -----
From: Eugene Hughes <ehughes@xxxxxxxxxx>
To: <PARKINSN@xxxxxxxxxxxxxxxxxxxx>
Sent: Thursday, April 06, 2000 8:25 PM
Subject: hello


> I just read a "greeting" that suggested I post basic information about
> myself and my Dad, the person with PD.  My father is 79, will be 80 in
June,
> he has been diagnosed about 10 years, we are not sure.  My mother was the
> "keeper" of that kind of information, and she passed away 4 years ago.  I
am
> the sole caregiver of my dad,   the next thing I want to describe is going
> to sound "victimy" and I don't want it to but here goes..... I left my
life,
> my partner, my home, my work, etc. you get the picture, to come here and
> take care of my Dad.  He had an accident October 24...... I have no
friends
> in this town, have never liked this part of the country, and am isolated
> beyond belief.  I am doing the b est I can every day.  He has ups and
downs
> as you all describe on this site.  I am grateful for this resource.
Thanks
> for your generosity....with information, time, etc.  Hope that is a proper
> introduction.     Deborah caregiver for Eugene 79/10
>


Parkinsn's List Subject Index

Parkinsn's List Thread Index

Parkinsn's Archive Treasures Doctors, students, patients and caregivers find current Parkinson's information such as the Algorithm, Caregivers Handbook, and talks by respected Movement Disorder Specialists.

Mail converted by MHonArc 2.6.10
Site Hosting donated by He.net
&
Grant from The Parkinson Alliance