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In 2005, the Lynne Cohen Foundation expanded its mission with the establishment of the Lynne Cohen Consortium.
This Consortium allows researchers and scientists at our five preventive care programs to pool the data from
the high-risk communities served by each program and link these at-risk women with the science of screening and prevention.
While each preventive care program addresses state-of-the-art patient care, the Lynne Cohen Consortium emphasizes
the importance of data collection, highly-focussed research, and cross-institutional collaboration. To facilitate
this collaboration, the Lynne Cohen Consortium meets annually to assess progress, discuss advances in women's cancer
research and to identify cross-institutional research projects.
The specific objectives of the Lynne Cohen Registry are to:
- Collect and store demographic, cancer risk, and breast and ovarian disease history, as well as family history of breast
and ovarian cancer on patients who are at risk of breast or ovarian cancer or who have had a diagnosis of either cancer
- Make available summary information regarding patients in the registry to Lynne Cohen Consortium members, and other
investigators, who can use the data to plan research projects and evaluate the feasibility of such projects
- Make available summary information to the Lynne Cohen Foundation and it's donors in order to show the number of women and
families who are directly impacted by the Lynne Cohen Prevention Clinics.
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