It's the little things -- a smile or colorful flowers -- that are so delightful to Cindy Hood. At 54, she can see so much more than ever before.
"For the first time I could see my grandchildren. It was really overwhelming," said Hood, of rural Hastings. "It's neat to see somebody's smile."
Before her corneal lens transplants, Hood said her two granddaughters were shadowy shapes. She couldn't see well enough to walk alone safely. Now she can walk unassisted and see foods and signs in supermarkets.
"Food really looks different to me. It's so colorful." She no longer avoids buffet-style restaurants because "now I can go up and pick my own food."
Hood's surgery at the Mayo Clinic in Rochester treated a rare condition called aniridia, the congenital absence of the iris. The iris is the colored part of the eye which moderates incoming light.
Medicine and technology have come a long way since Hood had her first corneal transplant on her right eye at age 9 at the University of Minnesota hospital in 1966. "It didn't work. It was traumatizing," she recalled. A second attempt fared no better, and she lost much of the vision in her right eye, she said.
As a girl she was teased and picked last for kickball teams, she recalled. To avoid bright lights, she peered through slit eyes or shut them. At 16, she developed cataracts and glaucoma, which caused fluid buildup and painful pressure. She took many eye drops daily for decades to relieve the pain.
"It seemed like all I did was beg and pray and hope," she recalled. "I got angry at God and my parents." She drifted away from God, but "in my heart, I knew He was all I had to get me through it."