READ MORE STEVENS JOHNSON SYNDROME (SJS) LEGAL NEWS
Kaitlyn Fletcher, the 14 year old afflicted by the syndrome, suffered so badly from the disorder that blisters on her mouth prevented her from eating even via a feeding tube, resulting in her being fed intravenously. She is now recovering, although she still suffers from side effects of the condition like headaches and having her fingernails break off.
"The only medicine she took was Pepto-Bismol. I don't think we'll ever pinpoint what triggered it," Laurie Fletcher, Kaitlyn's mother, told the news source.
Due to their lack of insurance, the family is applying for a disability program that could help offset the cost of the medical bills accrued during the course of Kaitlyn's illness.