Sleeping is one of life's greatest pleasures. In the case of young Erin Bousquet, just 19 years old, not so much. It's basically a prison sentence! The American has been suffering from a illness rare that makes her sleep 20 hours a day since 2017. She also has to deal with constant irritability, difficulty following orders, and ravenous hunger. See how this lady ended up having to sleep for so long throughout the day.
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Discover the story of Erin Bousquet and her illness
After two and a half years of searching for answers, Erin was diagnosed with Kleine-Levin Syndrome, also known as “Sleeping Beauty Syndrome”. This is a very rare and rarely seen sleep disorder.
Because of this problem, Erin ended up missing several important moments in life, such as birthdays and even family trips. According to her, this is precisely what bothers her the most in this whole story.
Kleine-Levin Syndrome
The disease triggers "sudden blackouts" when the body is in the process of inflammation or menstruation. The uncertainty of when these blackouts will arrive is what frightens young Bousquet and her family the most.
The first manifestation of the rare disease occurred when Erin was 14 years old, in 2017. It was when the girl was suffering from strep throat. At that time, the young woman took antibiotics for three days, but as she did not notice any responses from the body, she had to change the medications, which resulted in her improvement.
According to Kristen Bousquet, Erin's mother, after her pharyngitis, the girl began to show mental confusion, excessive fatigue, irritation, dilated pupils and also started to sleep for 20 hours straight. At first, Kristen thought it was her daughter's game, but it was soon possible to realize that it wasn't her game.
The situation got scary.
What is most curious about this case is that when the blackout season ends, Erin goes on with her life as usual and does not remember what happened. For two and a half years, the girl underwent various psychiatric and neurological tests. The doctors' initial suspicion was that it was infectious mononucleosis, but this possibility was ruled out.
Found diagnosis
In the year 2020, the family sought out physician Robert Sundell, a specialist in neurology. Upon hearing all the reports, he diagnosed Erin with Kleine-Levin Syndrome. Although the disease has no effective treatment, it can disappear over time. Usually after ten years since the first episode.
