Experiences of patients identifying with chronic Lyme disease in the healthcare system: a qualitative study

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Summary

Four major themes emerged from participants’ descriptions of their experiences and perceptions: changes in health status and the social impact of chronic Lyme disease, doubts about recovery and the future, contrasting doctor-patient relationships, and the use of unconventional therapies to treat Chronic Lyme disease.

Type
book
Published
2014-05-01
Cited by
80
References
42
Access
Open access

Keywords

Political science

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