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Donor Recognition

Jean and Gary Wright

Counting on the promise of research
Advancing research into seizures, the Wright family funded the purchase of equipment to speed up DNA tests.
(From left) Tracy Glauser, MD, Gary Wright, Christine Wright, Jean Wright, Richard Wenstrup, MD

For more than three decades, Gary and Jean Wright have pursued every treatment option to help manage the seizures of their daughter Christine, now 32 years old. They even moved from Cincinnati to Florida to be closer to a program recommended by their physician at Cincinnati Children's Hospital Medical Center.

Breakthroughs in surgery, medications, diets and implants have helped others control their seizures, but not Christine, who continues to have 60-400 seizures each month. Yet the Wrights remain optimistic that research underway at Cincinnati Children's, led by neurologist Tracy Glauser, MD, and geneticist Richard Wenstrup, MD, will soon improve the lives of children with seizure disorders. To help advance that research, their family foundation, Children Helping Research Into Seizures (CHRIS), recently funded the purchase of equipment that automates DNA testing, speeding the processing of large numbers of DNA samples from people with seizure disorders.

"By using this data compiled from people nationwide, doctors eventually will be able to prescribe the most effective drug to control seizures based on a person's genetic makeup. Instead of being hit and miss with prescriptions, they'll be able to take a more systematic approach. The fact that Dr. Glauser was awarded the largest NIH research grant for pediatric epilepsy, totaling $17.3 million, shows that Cincinnati Children's is on the leading edge of this research," Gary says.

"It's very exciting research. I only wish it would go faster," Jean says.

Even after they moved to Florida in the 1980s, the Wrights remained in close contact with Christine's physician at Cincinnati Children's, Harold Fogelson, MD (now retired), and continued to make donations for his research. Today they live most of the year in Florida, but spend several months in Cincinnati. Their time is devoted to caring for Christine and helping to raise funds for research into seizure disorders at Cincinnati Children's.

Jean says, "We're doing this not only for Christine, but also for others who will find more successful treatment because of this research."