Diagnosing rare diseases and mental well-being: a family's story
- PMID: 36879253
- PMCID: PMC9990187
- DOI: 10.1186/s13023-023-02648-y
Diagnosing rare diseases and mental well-being: a family's story
Abstract
When we experience symptoms, most of us walk into the clinic or hospital expecting immediate answers. For individuals with a rare condition, the path to diagnosis can be tortuous, involving months to years of waiting and a seemingly interminable search for answers. All this while, physical and psychological stress can negatively impact mental health. Each diagnostic journey is unique, but they epitomise common themes and inadequacies of the medical system. This article presents the stories of two sisters whose diagnostic journeys diverged then converged, reflecting on the impact of these experiences on mental well-being and what we can learn going forward. Hopefully, with more research and knowledge, we can catch these conditions earlier and provide better recommendations for treatment, management and prevention.
Keywords: Diagnosis; Mental well-being; Patient perspective; Rare disease; Vascular Ehlers-Danlos syndrome.
© 2023. The Author(s).
Conflict of interest statement
The author declares that they have no competing interests.
References
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