TY - JOUR
T1 - Beyond Adherence
T2 - Health Care Disparities and the Struggle to Get Screened for Colon Cancer
AU - Hunleth, Jean M.
AU - Steinmetz, Emily K.
AU - McQueen, Amy
AU - James, Aimee S.
N1 - Funding Information:
The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by a grant from the National Cancer Institute (R21 CA147794, Principal Investigator [PI]: James). Drs. Hunleth and James were supported by the Program for the Elimination of Cancer Disparities, a Community Networks Program Center (U54 CA153460 PI: Colditz). Funding also came from the Barnes Jewish Foundation and Siteman Cancer Center. Dr. McQueen was also supported by a Mentored Research Scholar Grant from the American Cancer Society MRSG-08-222-01-CPPB.
Publisher Copyright:
© SAGE Publications.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Dominant health care professional discourses on cancer take for granted high levels of individual responsibility in cancer prevention, especially in expectations about preventive screening. At the same time, adhering to screening guidelines can be difficult for lower income and under-insured individuals. Colorectal cancer (CRC) is a prime example. Since the advent of CRC screening, disparities in CRC mortality have widened along lines of income, insurance, and race in the United States. We used a community-engaged research method, Photovoice, to examine how people from medically under-served areas experienced and gave meaning to CRC screening. In our analysis, we first discuss ways in which participants recounted screening as a struggle. Second, we highlight a category that participants suggested was key to successful screening: social connections. Finally, we identify screening as an emotionally laden process that is underpinned by feelings of uncertainty, guilt, fear, and relief. We discuss the importance of these findings to research and practice.
AB - Dominant health care professional discourses on cancer take for granted high levels of individual responsibility in cancer prevention, especially in expectations about preventive screening. At the same time, adhering to screening guidelines can be difficult for lower income and under-insured individuals. Colorectal cancer (CRC) is a prime example. Since the advent of CRC screening, disparities in CRC mortality have widened along lines of income, insurance, and race in the United States. We used a community-engaged research method, Photovoice, to examine how people from medically under-served areas experienced and gave meaning to CRC screening. In our analysis, we first discuss ways in which participants recounted screening as a struggle. Second, we highlight a category that participants suggested was key to successful screening: social connections. Finally, we identify screening as an emotionally laden process that is underpinned by feelings of uncertainty, guilt, fear, and relief. We discuss the importance of these findings to research and practice.
KW - America, North
KW - adherence, compliance
KW - aging, older people
KW - cancer, screening, and prevention
KW - health care disparities
KW - health, lived experience
KW - photography/photovoice
KW - prevention, illness, and disease
UR - http://www.scopus.com/inward/record.url?scp=84951759689&partnerID=8YFLogxK
U2 - 10.1177/1049732315593549
DO - 10.1177/1049732315593549
M3 - Article
C2 - 26160775
AN - SCOPUS:84951759689
SN - 1049-7323
VL - 26
SP - 17
EP - 31
JO - Qualitative Health Research
JF - Qualitative Health Research
IS - 1
ER -