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Copyright © 2006 Person et al; licensee BioMed Central Ltd. Health-seeking behaviors and self-care practices of Dominican women with lymphoedema of the leg: implications for lymphoedema management programs Bobbie Person,1 David G Addiss,2 L Kay Bartholomew,3 Cecilia Meijer,1 Victor Pou,4 and Bart van den Borne5 1Centers for Disease Control and Prevention, National Center for Infectious Diseases, Office of Health Communication, Atlanta, Georgia, USA 2Centers for Disease Control and Prevention, National Center for Infectious Diseases, Division of Parasitic Diseases, Atlanta, Georgia, USA 3Center for Health Promotion and Prevention Research, School of Public Health, University of Texas Health Science Center at Houston, USA 4Instituto Dermatológico de Cirugia y Piel (IDCP), Santo Domingo, the Dominican Republic 5University of Maastricht, School of Health Promotion, Maastricht, the Netherlands Corresponding author. Bobbie Person: bep2/at/cdc.gov; David G Addiss: dga1/at/cdc.gov; L Kay Bartholomew: Leona.K.Bartholomew/at/uth.tmc.edu; Cecilia Meijer: aoe5/at/cdc.gov; Victor Pou: dvep001/at/yahoo.com; Bart van den Borne: b.vdborne/at/gvo.unimaas.nl Received July 10, 2006; Accepted December 22, 2006. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This article has been cited by other articles in PMC. Abstract Background In the Dominican Republic, a Latin American country with filariasis-endemic areas, more than 63,000 people have lymphatic filariasis and more than 400,000 people are at risk of future infection. In this paper, we explore the health beliefs, health-seeking behaviors and self-care practices of women with lymphoedema in filariasis-endemic areas to better understand the needs of women when developing lymphoedema morbidity control programs. Methods Qualitative data were collected through semi-structured interviews of 28 women, 3 focus group discussions with 28 women, field notes and photographs. Results Women described exhaustive and expensive attempts at seeking a cure for their lymphoedema. Family members were influential in providing women with initial care seeking referrals to indigenous healers credited with influence over physical, mental, spiritual and supernatural properties of illness. When indigenous treatments proved to be ineffectual, the women sought care from trained healthcare providers. Most healthcare providers incorrectly diagnosed the edema, failed to adequately treat and meet the needs of women and were viewed as expensive. Most women resorted to self-prescribing injectable, oral, or topical antibiotics along with oral analgesics as a standard practice of self-care. Conclusion Healthcare providers must understand a woman's cultural perspectives of illness, her natural networks of support and referral, her behavioural practices of care-seeking and self-care and the financial burden of seeking care. In the culture of the Dominican Republic family members and traditional healthcare providers are influential advisors on initial health-seeking behaviors and self-care practices. For this reason family-oriented interventions, support groups for women and their families, community education and training on simple, low cost lymphoedema management techniques for indigenous healers are viable ways to influence the early detection, diagnosis and treatment of women with lymphoedema. The extensive use of injectable, oral and topical antibiotics by indigenous healers and women without medical supervision suggests a need for health education messages related to the risks of such practices. Background The global prevalence of lymphatic filariasis, a mosquito-transmitted parasitic disease, is vast [
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