元NFLプレーヤーのティムグリーンがALSとの生活についてブライアンキルミードに門戸を開く

“声が使えなくなった, そして私のすべての手足, でも、本を書いたり、法律事務所で働いたり、今のようにあなたとコミュニケーションをとることができるテクノロジーにはとても感謝しています。,” グリーンは言った “狐 & 友達” host Brian Kilmeade, alongside his son Troy.

Green’s son explained that his father has a tablet tracking his eyes, so when he looks at the screen, it functions as a keyboard, and when he leaves his eyes idle on a letter for a certain amount of time, it’ll select that letter. Green has a button he can click to speak.

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Green attended Syracuse University where he was an All-American football player. Green was drafted in the first round of the 1986 NFL Draft by the Atlanta Falcons and played as a linebacker and defensive end for eight years.

While playing in the NFL, Green also studied law and began his writing career. By the time he retired from football in 1994, Green had already published his first book and became a lawyer. While working those two jobs, he began working as a television broadcaster forFOX NFL Sunday,” “グッドモーニングアメリカ,” “A Current Affair,” その他.

Green’s new bookThe Final Seasondetails his 12-year-old son’s point of view of chasing anelusive championship trophyduring the final season of football and coping with his father’s physical deterioration and near-death caused by ALS.

緑, who was diagnosed with ALS in 2018, said the book is amiddle-grade novel” あれは “pretty close to what really happened to him, his three boys and, and his youngest son’s final season of football.

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Troy and his other brother were coaching on the sideline with his father. Troy said that he was coaching the offense and his brother coached the defense.

It was a different experience for sure,” Troy recalled, noting that it was his father’s last season before his condition worsened.

To join the fight against ALS, Green urged people to buy the book, since all proceeds will be donated to Tackle ALS.

ALS is a rare disease that causes progressive degeneration and death of the nerve cells that control voluntary muscle movements, such as chewing, 歩く, talking and breathing, による NINDS. Most people with ALS develop symptoms between ages 55 そして 75, and the disease usually progresses rapidly, with death occurring in three to five years after diagnosis.

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