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Canadian patient experiences of lupus nephritis: a qualitative analysis.

Francesca S CardwellSusan J ElliottMegan R W BarberKim CheemaSydney GeorgeAdrian BoucherAnn Elaine Clarke
Published in: Lupus science & medicine (2023)
The unpredictability of living with LN, the heavy treatment burden and a lack of patient/societal awareness substantially affect the lived experience of LN. These findings will inform the development of LN-specific patient resources to increase understanding of LN and improve well-being for patients.
Keyphrases
  • case report
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • mental health
  • risk factors
  • peritoneal dialysis
  • replacement therapy
  • patient reported