Tracing the Path of Breast Cancer
The war on breast cancer is particularly important
to the women of Vermont because our state has a
disproportionately high percentage
of women who die from breast cancer. These alarmingly high mortality
rates present throughout the Northeastern and Mid-Atlantic region led
to our introduction of legislation calling for the
Northeast/Mid-Atlantic Breast Cancer Program.
In July 2000, the U.S. Department of Health and Human Services published
for Congress "The Northeast and Mid-Atlantic Breast Cancer Study (NE/MA),"
the final report for the Program's findings on breast cancer incidence
and mortality rates in these regions.
The
Northeast/Mid-Atlantic Breast Cancer Program became part of a larger piece of
legislation that Congressman Sanders and I introduced, the Cancer
Registries Amendment Act of 1992
(S 3312),
which created a nationwide cancer surveillance system. Data collected by the
registries keep us informed on regional cancer differences based on lifestyle,
access to health care, and the carcinogenic effects of environmental
contaminants.
The Vermont Cancer Registry
began collecting information in November 1993. In February 2000, the Vermont
Department of Health released Cancer in Vermont
(requires an Adobe Reader),
a report based on data collected by the Vermont Cancer Registry, which
provides encouraging news for those concerned about breast cancer. The Report
maintains that Vermont's breast cancer incidence rate is not higher than the
rest of the country and the state's breast cancer death rate is
declining. This good news reinforces the importance of continuing
efforts to make mammograms and clinical breast exams available to all women.
Source: Report to the U.S. Congress: The Northeast
and Mid-Atlantic Breast Cancer Study (NE/MA), July 2000

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