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Ellen Lenox Smith’s recurring injuries and ailments were as baffling as they were disabling.
Some doctors thought they might even be psychological.
Why was she always in such pain? Why did she have difficulty swallowing? Why did she keep tearing cartilage and ligaments in her knees and shoulders?
And why at night did she sometimes struggle to draw a breath and wonder, “Will I be awake the next day?”
When she finally was given a diagnosis — Ehlers-Danlos Syndrome — Lenox Smith remembers being excited.
“I went home and thought, ‘Now I can get better,’ ” she recalls. “Then I read about it and saw it was incurable.”
The genetic connective-tissue disorder was taking an inexorable toll on her body, she was told, and while she might live a long life, eventually she would probably “die a Lou Gehrig’s-like death,” bedridden and choking on her own mucous.
Categorized in: Ehlers-Danlos in the News