Access to Critical Oncological Support Systems For Newly Diagnosed Breast Cancer Patients

Presenter: Julie Reid, Planning, Public Policy and Management

Panel: Strategies for Support & Recovery

Mentor: Jessica Greene, Planning, Public Policy and Management

Time: 1:15pm – 2:15pm

Location: Century A

A woman newly diagnosed with breast cancer is required to have a team of doctors who work together to carry out the various phases of treatment. It is important to new patients that they trust their doctor, yet women rarely are given the choice about who that doctor will be. Women lack knowledge about local support groups and patient advocates, are confused about who may attend support groups, and unclear about where to go to find answers to basic questions. This is a qualitative study of thirteen breast cancer patients diagnosed within the last seven years in Eugene, Oregon. The study examines the knowledge and accessibility of critical support systems, such as a good doctor-patient relationship, a support group, and a patient advocate. Results suggest that doctor trust and support is more likely to develop when the patient receives a referral from a familiar source. Results also suggest that support groups are important sources of information and comfort for patients that medical professionals could utilize. The role of a patient advocate needs to be further defined and expanded to provide resources for patients seeking ways to fill the gaps of a fragmented medical system in Eugene, Oregon.

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