ALS Patient Story: Judy Lochridge

ALS Patient Story: Judy Lochridge


Judy Lochridge, a nurse for 14 years, suddenly noticed that her arms weren't working like they used to. Her arms had become so weak that she began to have trouble putting in IVs or giving shots. Then one day, she had a fall, hit her face, and broke her nose. After a series of tests, Lochridge was diagnosed with ALS. Read the accompanying magazine article, "On Borrowed Time," published in Emory Health magazine, Fall 2009: About This 6-Part Video Series ALS, also known as Lou Gehrigs Disease, affects the motor neurons, the cells that initiate and control movement of muscles. Listen to these Emory patients talk about their diagnosis with ALS and how they and their families are coping with the devastating disease. About ALS Commonly called Lou Gehrig's disease for the popular New York Yankees baseball player who died of it in 1941, ALS is a devastating disease that kills the motor neuron cells in the brain and spinal cord, causing the brain to lose ability to control muscles in the body. It inevitably leads to paralysis and problems with swallowing, eating, and breathing. The persons mental capacity remains intact, making the disease a cruel sentence for patients who are often otherwise healthy and active before being diagnosed. Related Links On borrowed time Emory ALS Center

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