You are receiving this email because you had previously met with a genetic counselor at UT Southwestern or an affiliated site (Moncrief Cancer Institute, Parkland Hospital, John Peter Smith Hospital, Texas Health Resources, or the Center for Cancer and Blood Disorders) and have a genetic change (mutation) in the BRCA1 or BRCA2 genes; this mutation causes a condition known as Hereditary Breast and Ovarian Cancer Syndrome (HBOC).
The purpose of this confidential medical follow-up survey is to measure if families are receiving appropriate care. This information is also used to improve our understanding of BRCA1 and BRCA2.
The survey will take less than 5 minutes to complete.
If you need assistance completing this survey, please contact the Genetic Patient Navigator, Kathy Pratt, at or 214-645-7302.

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To save your responses and end the survey, click the 'End Survey' button below. If you have selected the wrong option by accident and/or wish to return to the survey, click the 'Return and Edit Response' button.