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Dear Kristi,
Misunderstandings take place on this list all the time.  I feel bad that you
were attacked by two of our most influential writers.  Both have good reason
to be angry at this hideous disease.  Just remember it is the disease that
has provoked them.

Attacks from this list are the reason I rarely post any more.  It is
surprising
to me how phrases can be so misconstrued.

jjjane

----- Original Message -----
From: Kristi Fleming <[log in to unmask]>
To: <[log in to unmask]>
Sent: Monday, April 10, 2000 6:34 AM
Subject: Re: Kristi and her Question


> Hello all,
> I'm sorry to have caused such a commotion!   I do not take PD lightly.  I
had an
> uncle who was very dear to me become afflicted in his early forties.  If
you would
> like to see the full extent of my research go to:
> http://webpages.marshall.edu/~fleming11/
> you can find my homepage and at the bottom are the links to my research
paper's
> very rough draft.  My assignment was to make a presentation to my class
based on
> interesting facts, statistics, and such to prompt my peers who see the
> presentation to want to go and read my paper.  I'm sorry to have asked.  I
didn't
> think I would have been taken the wrong way.  THAT WAS NOT MY INTENTION in
joining
> this list or asking quesitons.  I wanted to further my knowlege.
> Kristi.
>
> Hilary Blue wrote:
>
> > Jon
> > you shane me and trivialize me. i am so sorry i have inadvertently given
this
> > young  lady the impression that it is fun not to be heard; cute to  have
your
> > children disrespect you, and fulfilling to be denied the right to parent
your
> > own  children.
> > my intentions were totally the opposite. in my struggle against the
social
> > work community,,, i used the phrase 'mask of Parkinsonism' many times as
a
> > defence against the accusation of nnon participation or lack of
interest. And
> > i hve begin to use ''muffled voice's in a similar fashion. vut your
words
> > struck  home, and i freely apologies for  giving tes wrong impression.
''and i
> > hand over to you the accolade i so recently was given --
> > aGIVING JOAN A MICROPHONE IS LIKES ARMING A GUIDED MISSILE
> >
> > Stan or Joan Snyder wrote:
> > >
> > > Dear Kristi: Hi sweetie and thanks for taking the time to research
your
> > > topic-you've certainly found the right place; but i think it's best to
> > > point out right at the start that there is nothing "cute" at all about
> > > our disease. i'm not trying to be a jerk hen you're obviously so well
> > > -intentioned and young and learning about awareness, but I'd like for
> > > you to think about ha being a mom w/ pd is really like...i have had "a
> > > muffled voice" for a long time now. My darling daughter who is 12
really
> > > need me to talk to, but she gets so discouraged by how long it takes
me
> > > to say what is in my heart, that she will stomp away in
frustration-not
> > > at me but at this disease that she hates so much. I don't know which
is
> > > worse, that kind of treatment or my 10 yr. old son crying because I
> > > never smile anymore although i am smiling inside!! They both don't
> > > understand the ramifications of this disase-they only know that mom
> > > can't drive for field trips anymore, can't make all of their games &
> > > concerts anymore and why we're always the first to leave any function.
> > > So please, while I know you heart is in the right place-try to put
> > > yourself in a situation where you have something so very important to
> > > say but have neither the energy nor the wherewithal to get it
out...and
> > > how hard it is to have people patronizingly smile and say yes, isn't
> > > that the truth (when you weren't even talking about anything like
that)
> > > and go merrily on their way...as if you we're even there.
> > > --
> > > Joan E. Snyder    48/10
> > > [log in to unmask]
> > > <http://members.tripod.lycos.nl/genugten/snyder.htm>
> > > "Hang tough.....no way through it but to do it."
> > >            Chris-in-the-Morning (Northern Exposure)