FAIRHOPE, Alabama -- A sense of doom enveloped Jayne Godfrey when doctors diagnosed her in 2007 with early onset Parkinsons disease at 39. "It was depressing," said the Spanish Fort mother of two, paralegal and recreational runner. "Doctors told me, You have a progressive neurological disease for which there is no cure. I kept thinking, Could this be a wrong diagnosis? Where was the hope?" A persistent tremor and increasingly frequent falls while jogging brought Godfrey to neurologists in Fairhope and in Jacksonville, Fla. at the Mayo Clinic. "My life was unraveling and I had to do something about it," Godfrey said. The diagnosis confirmed her worst fears. "It was so absolutely devastating for both of us," Godfreys mother, Mary Robbins of Daphne, said. "You are told there is no hope. It is a death sentence." But during an Internet search for information about the chronic, progressive movement disorder, Godfrey happened upon to The Michael J. Fox Foundation for Parkinsons Research. It was a beacon in an otherwise bleak landscape, connecting Godfrey to others in the Parkinsons community and illuminating her with knowledge and hope. Established in 2001 by actor Michael J. Fox, who has Parkinsons, the foundations mission is … Continue reading
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