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Leta Anderson 53/53/38 Lakewood, CO [log in to unmask]



---David Moreland <[log in to unmask]> wrote:
>
> At 01:31 AM 11/29/98 -0500, you wrote:
> >Dear friends on the World Parkinson's Exchange List,
> >
> >  I have been following the discussion on our World List about
Michael J.
> >Fox. His courage  is an enormous opportunity in the battle for both
> >publicity and research funds about Parkinson's, whether "young
onset" or
> >not. For a moment, allow me to shift the focus to the rest of us
who live
> >daily with this dreadful disease.
> >
> >   I suggest that each Listmember immediately decide whether, if
called,
> >he or she could  appear on live TV, or be taped for broadcast on TV.
> >BOLD LEADERSHIP is needed from the ranks of PWP's and their CG's
(Persons
> >with Parkinson's and their CareGivers) to increase our visibility.
> >
> >   If you are available, PLEASE SIGN ON to the list BELOW.     PLEASE
> >post your reply..
> >
> >   I would emphasize that the $100,000,000.00 annual research
spending
> >authorized by the 1997 Udall Act remains UNFUNDED.  Projected
spending at
> >the NIH, despite all of our work, only rose from $34.4 million to
$37.4
> >million between  fiscal year 1997 and the current fiscal year 1999,
> >according to the Parkinson's Action Reporter, vol. ix, no.4,
November,
> >1998, p.1, "Udall Spending Gap Continues." This is TERRIBLE news.
> >
> >   I am "sponsoring" this listing, below, of TV-available PWP's and
CG's
> >.  Please add your name, i.d., and address, if you are willing to
either
> >be seen live or be taped for broadcast on TV..  WE MUST BE
VISIBLE,and
> >join with Mr. Fox.  Our stories  must be heard.
> >
> >   It follows that Susan Reese's appearance in New York City, on the
> >Today Show, on Monday, November 30, at 8:00 AM, would be enhanced
if it
> >were to include  one or more PWP's or CG's. OUR faces must be
televised.
> >Let's get the leading organizations and the general public talking
about
> >our  own appearances on TV.
> >
> >  WE are the most knowledgeable people  to explain the horrors and
the
> >hopes of living with Parkinson's Disease. WE can provide so much
> >information and education as advocates for the research to cure PD.
> >
> >PLEASE sign on to the list below:
> >
> >     LIST OF PWP'S AND CG'S WILLING TO APPEAR ON TV/ BE TAPED FOR
> >BROADCAST
> >
> >          NAME               I.D.          Address
Country
> >  PWP or CG    e-mail address
> >
> >       1. Ivan Suzman     49/39/36   Portland, Maine    USA
> >pwp           [log in to unmask]
> >       2. David Moreland  55/11            Salem,  Oregon   USA  PWP
> [log in to unmask]
> >       3.
> >       4.
> >       5.
> >       6.
> >       7.
> >       8.
> >       9.
> >     10.
> >     11.
> >     12.
> >     13.
> >     14.
> >     15.
> >     16.
> >     17.
> >     18.
> >     19.
> >     20.
> >^^^^^^  WARM GREETINGS  FROM  ^^^^^^^^^^^^  :-)
> > Ivan Suzman        49/39/36       [log in to unmask]   :-)
> > Portland, Maine   land of lighthouses    38  deg. F   :-)
> >********************************************************************
> >
> >
> >>We also spoke a little about the issues arising from MJF going
public,
> >>especial how they affect YOPDs, and how the MJF publicity is
painting
> >>too rosy
> >>a picture - but we agreed that increased public awareness can only
> >>stimulate
> >>more interest in finding a cure. And she said that she could not say
> >>in
> >>advance exactly what she would say on Monday but would have to be
> >>guided by
> >>what questions she was asked - but that she would always have our
> >>interests at
> >>heart. And that she would try and get as much into her 4 minutes as
> >>possible.
> >>Lets hope that she is successful.
> >>Good Luck, Susan!!
> >>
> >>Hilary Blue (49,25,16)
> >
> >>Hilary Blue wrote:
> >>>>> [log in to unmask] wrote:
> >
> >>> > Susan Reese, RN, LCSW-- Director of the American Parkinson's
> >>Disease
> >>> > Association's Young PD Information & Referral Center will be
> >>interviewed on
> >>> > the Today Show, Monday, November 30 about young-onset PD and the
> >>APDA Center
> >>> > created specifically to address the needs of the young person
with
> >>PD.
> >
> >
>

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