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On Valentine’s Day 2020, Peter Fodera’s heart broke. It stopped working. He collapsed in the middle of teaching a dance class. Someone performed CPR, someone called an ambulance. EMT’s showed up and he lay motionless. Many people in the class thought they had just witnessed the death of their favorite teacher. But later at the hospital, Peter’s heart started beating again. On the anniversary of Peter’s brush with death, he sat down with his daughter Juliana who has Noonan Syndrome, a rare genetic disorder. While Peter’s experience may seem miraculous to some of us, it doesn’t to Juliana. By her count, she’s died 21 times.
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4.6
12181,218 ratings
On Valentine’s Day 2020, Peter Fodera’s heart broke. It stopped working. He collapsed in the middle of teaching a dance class. Someone performed CPR, someone called an ambulance. EMT’s showed up and he lay motionless. Many people in the class thought they had just witnessed the death of their favorite teacher. But later at the hospital, Peter’s heart started beating again. On the anniversary of Peter’s brush with death, he sat down with his daughter Juliana who has Noonan Syndrome, a rare genetic disorder. While Peter’s experience may seem miraculous to some of us, it doesn’t to Juliana. By her count, she’s died 21 times.
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