“My body is a prison,” Steve Gleason writes. “I face insurmountable adversity every day, yet my family and I are able to survive and live within this miraculous, wonderful life.” A LIFE IMPOSSIBLE: Living With ALS: Finding Peace and Wisdom Within a Fragile Existence, by Steve Gleason with Jeff Duncan After you turn 70, as I will this year, any celebration will be muted by an ever-increasing awareness of mortality. I fear death, but what I fear even more is the way in which I’ll die. I hope it’s a heart attack in the dark of night — quick and painless, here today, gone tomorrow. I’m terrified that the cause will be amyotrophic lateral sclerosis, also known as A.L.S. or Lou Gehrig’s disease. It fundamentally destroys the nervous system, not all at once but in excruciating steps, leading to loss of muscle and the inability to speak, swallow or breathe on your own, constipation, drooling: You name it, A.L.S. will destroy it. The one area not affected is your brain. You understand what’s happening; you’re conscious of every indignity and humiliation until you die, usually within two to five years of diagnosis. Which leads us to Steve Gleason’s memoir, “A Life Impossible,” written with Jeff Duncan. More than a decade after learning he had A.L.S. at the age of 33, Gleason has survived with the help of faith, resilience and the support of his wife, Michel, who has endured her own share of suffering. I greatly admire “A Life Impossible” — its unflinching honesty and candor — but I’m not sure I am better off for reading it. Sometimes, ignorance is a mercy. Gleason was a football player from Spokane, Wash., one of those athletes who supplemented his talent with a relentless work ethic, measuring himself by how much pain he could withstand, the more the better. He went to Washington State University, where he was a star linebacker on a team that went to the Rose Bowl. He wasn’t drafted but several teams expressed interest in signing him. For eight years, until his retirement in 2008, Gleason played […]
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