Health Psychology / Behavioral Medicine - Adult
Cancer-Peer Connection in the Young Adult Cancer Context: Relocating Cancer Support to Community Settings
Maiya Hotchkiss, B.A.
Project Coordinator
Hunter College, City University of New York
Brooklyn, New York
Alyssa M. Ciniglio, None
Research Assistant
Hunter College, City University of New York
Glendale, New York
Zobaida Maria, None
Research Assistant
Hunter College, City University of New York
Brooklyn, New York
Zeba N. Ahmad, M.A., Other
Post-Doctoral Collaborator
Hunter College, City University of New York & The Graduate Center, City University of New York
New York, New York
Megan R. Wirtz, B.A.
Doctoral Student
The Graduate Center, City University of New York
Brooklyn, New York
Jennifer Ford, Ph.D.
Professor
Hunter College, City University of New York
New York, New York
Social support is insufficient for young adults (YAs) during and after cancer. Cancer-peer patient/survivor interaction offers the opportunity for individuals to provide, receive, or engage in mutual support based upon shared illness experience. Despite past research demonstrating that peer-to-peer connection can be an effective source of social support among healthy YAs and older patients and survivors, cancer-peer support has not yet been explored in the YA cancer context. This study aimed to explore YA cancer-peer connection by examining reported experiences, needs, preferences, and concerns among YA survivors. YA survivors (N = 129), aged 20-40 years (M = 31.3 years; SD = 5.25 years) diagnosed with cancer between the ages of 12 and 37 (M = 27.7 years; SD = 5.87 years) completed an online survey as part of a larger study on YA survivors perceptions of their futures. Data were analyzed to examine experiences, needs, preferences, and concerns related to cancer-peer support between patients and/or survivors during and following cancer treatment. Preliminary findings indicate that a majority of participants felt it is important to meet other patients/survivors during treatment and survivorship. A majority of participants had the opportunity to meet a cancer-peer during treatment (81.4%) and in survivorship (80.6%). Nearly all participants (85.3%) expressed interest in participating in cancer-peer volunteering and/or support, with highest levels of interest in mentoring a cancer patient one-on-one, exchanging support with survivors in a group, and giving speeches/sharing their story. Regardless of when (during treatment/survivorship) and cancer-peer type (patient/survivor), findings demonstrate preferences for cancer-peer interaction between one and eight times/month, located on social media, the hospital/clinic, or outdoors, and having age and diagnosis in common. Reported experiences were often in line with these preferences. Participants most often reported cancer-peer connection as making them feel understood in treatment/survivorship, and reciprocal support and community building in survivorship. Common barriers to cancer-peer connection included logistical barriers (time, distance), exposure to sickness/death, fear it would be awkward/forced, desire to return to normal, and feeling sufficiently supported. Study findings demonstrate the importance of cancer-peer connection, both during treatment and survivorship. Findings also demonstrate a high level of opportunities, engagement, interest and perceived benefits in cancer-peer connection among YA survivors. Future research should explore the ways in which formal and informal cancer-peer support can be tailored to best serve the YA patient/survivor population, and to mitigate related concerns. Results can inform facilitation and structuring of YA cancer-peer connection and support the relocation of dependency from healthcare to community contexts among this underserved and often isolated survivor population.