‘La Vida Normal’: Young people adapting to Type 1 diabetes in Bolivia

Author:

Souris Katherine J1ORCID,Caballero Gonzales Maria del Carmen2,Barrington Clare1,Klatman Emma L3,Anderson Barbara J4,Duarte Elizabeth2,Middlehurst Angela C3,Nostas Miriam C2,Ogle Graham D3

Affiliation:

1. Department of Health Behavior, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

2. Centro Vivir con Diabetes, Cochabamba, Bolivia

3. International Diabetes Federation Life for a Child Program, Diabetes NSW & ACT, Glebe, Sydney, Australia

4. Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA

Abstract

Objectives To identify challenges and coping strategies of young people with Type 1 diabetes (T1D) and their families in Bolivia through qualitative analysis of interviews with beneficiaries of Centro Vivir con Diabetes (CVCD), a diabetes health center supported by the International Diabetes Federation Life for a Child (LFAC) program. Methods Eighteen young people aged 14–33 and at least one caregiver participated in semi-structured interviews in five cities in Bolivia from May to June 2016. Interviews were recorded, transcribed, and analyzed using inductive thematic analysis. Results Participants described needing guidance at diagnosis and facing stigma in communities. Young people expressed that life with T1D was ‘la vida normal’ (a normal life), although interpretations of normalcy varied. For some, ‘la vida normal’ meant resistance to T1D; for others it indicated acceptance. Discussion Access to interdependent spheres of support allowed young people to form a new normal around T1D. Receiving supplies through the CVCD/LFAC partnership maintained family connection to clinical care, CVCD education helped families share in T1D management, and peer support mitigated stigma for young people. Programs like CVCD that combine supply-based aid with clinical education for whole families, create effective support for young people with T1D in low- and middle-income countries.

Funder

Leona M. and Harry B. Helmsley Charitable Trust

Scott and June Pearson Fund for Patient Advocacy in the Department of Health Behavior of the University of North Carolina Gillings School of Global Public Health

Publisher

SAGE Publications

Subject

Health Policy,General Medicine

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