During the first genetic counseling visit, we collect a personal and family medical history (please see the enclosed questionnaire).  If a family member has cancer, we ask about the primary diagnosis, the age of onset, and how the cancer was treated.  Additional medical records may need to be obtained.  The average visit lasts one hour.

We use this information to create a personalized risk assessment for 1) developing certain cancers, and, 2) for hereditary cancer syndromes.  If the risk assessment indicates a possible hereditary cancer syndrome, we review options for genetic testing.  The risks, benefits, and limitations of genetic testing are discussed.  Testing is often performed at a later date, after insurance authorization has been obtained (if appropriate).  A summary letter is sent to the individual and the referring physician (unless we are instructed otherwise).

Individuals who have chosen to have genetic testing return to discuss their test results in person (most results are available in approximately four weeks).  This follow-up appointment includes interpretation of test results, a discussion of how this information affects medical management, and the impact on extended family members.

PLEASE NOTE, IF YOU HAVE AN APPOINTMENT AT THE HELEN AND HARRY GRAY CANCER CENTER AT HARTFORD HOSPITAL: You will receive an automated telephone reminder of your appointment, but at the West Hartford location (our administrative office). 
PLEASE DISREGARD THE TELEPHONE REMINDER AND COME TO THE HARTFORD HOSPTIAL LOCATION.