Doug Lindsay was 21 years old and starting his senior year at Rockhurst University, a Jesuit college in Kansas City, Missouri, when his world imploded.
After his first day of classes, the biology main collapsed at the house on the eating room table, the room spinning around him.
It was 1999. The signs quickly turned intense and untreatable. His heart would race, he felt weak, and he often got dizzy. Lindsay may walk only about 50 feet at a time and couldn’t stand for quite a lot of minutes.
“Even lying on the floor didn’t really feel like it was low enough,” he mentioned.
The previous high school track athlete had dreamed of turning into a biochemistry professor or perhaps an author for “The Simpsons.”
As a substitute, he would spend the following 11 years mostly confined to a hospital bed in his living room in St. Louis, hamstrung by a mysterious ailment.
Doctors have been baffled. Therapies didn’t help. And Lindsay ultimately realized that if he needed his life back, he must do it himself.
His journey since has amazed medical professionals.
“He did one thing extraordinary,” mentioned John Novack, spokesman for Inspire, a healthcare social community for uncommon and chronic-illness patients. When folks hear Lindsay’s story, Novack mentioned, they typically say, “I can do one thing similar for my child.”
No matter was wrong with him ran in the family.
By the point Lindsay was 18 months old, his mom was so weak she might not pick him up.