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Charlotte Mancuso wrote:

> Dear Senator Feinstein:
>
> I am forwarding the letter to the editor that I submitted to and that appeared today in the San Jose
> Mercury.  The undersigned were as follows; however the paper prints the principal author only:
>
> Charlotte Mancuso, and the Young Parkinson Support Group of Palo Alto;
> Diana Preice, Leader of the Los Altos Support Group;
> Early Onset Group of Walnut Creek, Dave Alexander, Leader;
> Kim Furlan, Seton, Support Groups in Daly City, Redwood City, and San Mateo.
> Sid Levin of Marin County
>
> I urge you once more to do everything in your power, along with other senators on both sides of the
> aisle, to support fully funding focused Parkinson's Disease research.  Senator Feinstein, please add
> Parkinson's Disease to your many health care achievements for the sake of California, the Nation,
> and for the millions who suffer from this devastating disease and their families.
> /////////////
>
>                        Fund more research
>
>                        CONGRESS will soon vote on appropriations for medical research
>                        under Health and Human Services. The Udall Act, enacted in 1997,
>                        authorizes $100 million on research focused on Parkinson's disease.
>                        To date, only 40 percent has been spent on Parkinson's disease. The
>                        rest has been spent on unrelated research. Some medical research
>                        funding is focused up to 99 percent. If fully funded, the Udall Act
>                        would correct these disparities.
>
>                        Parkinson's disease costs taxpayers $25 billion a year, not counting
>                        the huge loss of productivity and intense suffering that it inflicts. This
>                        annual calamity is far costlier than most natural disasters, and no less
>                        so than more publicized diseases.
>
>                        Over 1 million Americans suffer with Parkinson's disease, and over
>                        1,000 people a week are diagnosed with this cruel, fatal disease.
>                        Over a third are under 50, some as young as 10.
>
>                        My mother was 41, I was 49, and three others in my family were
>                        over 60 when diagnosed. Mom died of this progressive disease at 67
>                        because she could no longer swallow, move or speak. We were
>                        giving her 24-hour care before I was age 5.
>
>                        As a caretaker and now as a patient, I know that advanced
>                        Parkinson's is as devastating as Alzheimer's, and often worse.
>
>                        Californians should write or e-mail Sen. Dianne Feinstein, a member
>                        of the Health and Human Services subcommittee, to urge action.
>
>                                                            Charlotte Mancuso
>
>                                                  Young Parkinson Support Group
>                                                                    Palo Alto