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Rare doesn t mean rare, this affects thousands of people

Everything became painful: Eugene woman raises money for proper wheelchair

Everything became painful: Eugene woman raises money for proper wheelchair
kezi.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from kezi.com Daily Mail and Mail on Sunday newspapers.

Long Covid cash branded too little too late as children struggle on without specialist help

Long Covid cash branded too little too late as children struggle on without specialist help
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Former Rocky student shares 10-year journey to diagnosis

Premium Content Subscriber only Stacey Schmidt, a former Rockhampton Girls Grammar School student, wears silver ring-like devices on her fingers which, at first glance, look like some form of punk jewellery. They are, in fact, finger splints which reduce the hyperextension and pain associated with her rare, genetic and chronic condition. Ahead of Hypermobile Ehlers-Danlos Awareness Month in May, Ms Schmidt told the story of her diagnosis to The Morning Bulletin. What followed were three years of what she described as a “traumatic” journey. The initial diagnosis of an iron deficiency did little to explain Ms Schmidt’s multitude of symptoms which impacted virtually every system and organ in her body.

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