'I'd rather be dead than disabled."
I remember feeling that way several months before I became severely disabled. In 1980, I had taken a group of teenage girls to see a young quadriplegic named Joni Eareckson Tada, who painted beautifully by holding a paintbrush in her mouth. Though inspired by her talent, I remember telling the girls, "I could never live like that."
A few months later my neck was broken in a car accident, and I became a quadriplegic, paralyzed below my shoulders. I would spend the next year and a half in various hospitals and rehabilitation centers, dealing with medical problems and learning to live with a spinal cord injury.
Reality hit after four months, when the hospital let me go home for a few days. I saw the piano and realized I'd never play it again. The kitchen reminded me I could no longer fry an egg for myself. Simple tasks like taking a shower were now major productions requiring lots of time and lots of help. My independent days were over.
I fell into a depression. I'd lie in bed crying, becoming more frustrated when I couldn't wipe my tears and nose. At times I really thought my life was over, that I was a burden. I definitely felt I'd rather be dead than disabled.
But, thank God, those around me provided me with what I really needed — good medical care, prayers and loving support. Other quadriplegics assured me that life can go on and renewed my hope. I slowly came out of this depression, and I began to see that my life was far from over.
Fast-forward 36 years. Although my life has not been easy and I occasionally deal with serious medical conditions, I can honestly say I'm grateful to be alive.
But I might not be if assisted suicide had been legal in Minnesota at the time of my accident. If it had been, I might have given in to my depression and the false belief that the value of my life had diminished. I might have chosen to end my life, depriving myself and my loved ones of the opportunities to learn and grow and enjoy living.