Exploring the lived experiences of individuals living with Charcot neuro‐osteoarthropathy in Australia: A qualitative research study
The burden of CNO extends beyond the physical limitations of living with a significant foot deformity and the associated increased risk for further limb threatening complications. Individuals with CNO report feelings of increased anxiety, a loss of independence and feel they are a burden to their family impacting on their individual roles at home, including the ability to provide financially. This should be considered when managing individuals with CNO, with more holistic approaches to care required. This research highlights that increased engagement with mental health support services, social work and peer-group support along with greater access to evidence-based information on the management of CNO may better support the psycho-social needs of this population.
Authors
- Peta Ellen Tehan (ORCID: https://orcid.org/0000-0002-0014-3023)
- Nancy Chapman (ORCID: https://orcid.org/0009-0006-5354-6017)
Institutions
- Hunter New England Local Health District (AU)
- Monash University (AU)
Publication Details
- Journal
- Journal of Foot and Ankle Research
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1002/jfa2.70037
- Citations
- 4
- Primary Topic
- Diabetic Foot Ulcer Assessment and Management
- Type
- article
- Field-Weighted Citation Impact
- 5.18
Funders
- Monash University