Danlos syndrome: Hamilton woman’s struggle shows hidden toll of rare condition
Kate Pudney, a 24-year-old from Hamilton, is sharing her experience living with hypermobile Ehlers-Danlos syndrome and vascular compression disorders. She highlights the daily challenges of managing an invisible disability and the difficulty of accessing specialized medical care in New Zealand.
Why it matters
The story sheds light on the systemic barriers faced by patients with rare, invisible conditions and the need for better healthcare accessibility.
Comet, Kate Pudney and Atlas. Photo / Supplied
The article is a human-interest feature focused on personal experience and healthcare advocacy without political or ideological bias.
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