Print

Print


Marjorie Moorefield and other PIEN members:

I am forwarding a copy of the e-mail I've sent to all those senators
Marjorie listed addresses of on the senate hearing committee for stem cell
research.  I also will forward my post along with personalized comments to
my two state senators and my state representative who will eventually be
asked to vote and lobby for this type of research funding.

Feel free to use this post to model your own post to the senators,
personalizing with your own story and to your own senators and reps.  Your
sen/rep is elected to represent YOU and needs to know what YOU NEED.  Tell
them.

Jeanette Fuhr 49/47/44?

----------
From: Leo Fuhr <[log in to unmask]>
To: [log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask];
[log in to unmask]; [log in to unmask]
Cc: [log in to unmask]
Subject: MJFox testimony on stem cell research to senate hearing-216
Date: Wednesday, September 13, 2000 2:03 PM

Dear Senators and Members of the Subcommitte on Labor, Health & Human
Services, Education on stem cell research appropriations:

I am unable to attend on Thursday, 9/24/00, the hearing when Michael J. Fox
is scheduled to speak to you on the reasons he and I want you to understand
why stem cell research is so important to us and to the thousands of
persons with Parkinson's(pwp) in the USA.  Many pwp would like to attend
the hearing and speak loudly, clearly and with emotion as to our need for
this research to be funded and to search for the cure for this incurable
disease we live with daily.

Not all of us are able to speak as eloquently and as forcibly as Michael.
Some of us tremble, drool, whisper and with our faces looking frozen or
masklike due to the Parkinson's symptoms you might think we didn't care
where you spend research funds. In truth, we care passionately and we would
shout and pound the podium, if we just had the strength to do so.

I, myself, a teacher of Public Speaking, who has been diagnosed with
Parkinson's since November 1997, find that I am not always able to speak as
long, or as forcibly at the lecturn as I once could.  Even the challenge of
standing in front of a class of students for the entire 85 min., twice
weekly class isn't always met.  I must have a desk to lean on or a
chair/stool to sit on when my energy level drops.   I'm 49 years young,
still in the early stages of Parkinson's, with the promise of continuing
decline in the future, especially if that future doesn't include stem cell
research.

I feel strongly that not only Parkinson's but other neurological disorders
like Alzheimer's, Multiple Sclerosis, Lou Gehrig's and spinal cord injuries
and diabetes may benefit from stem cell research.  When Michael Fox speaks
to you on Thursday, listen carefully and note that he speaks for all of the
chronically ill constituents, many who are from your state.

Sincerely,

Jeanette R. Fuhr
1802 Crestview Terrace
Trenton, MO  64683
660/359-3100
e-mail <[log in to unmask]>