Brain & Nervous System More Neurological Diseases Lorenzo Odone's Life and Disease By Mary Kugler, RN Mary Kugler, RN Mary Kugler, RN, is a pediatric nurse whose specialty is caring for children with long-term or severe medical problems. Learn about our editorial process Updated on November 11, 2022 Medically reviewed by Smita Patel, MD Medically reviewed by Smita Patel, MD LinkedIn Twitter Smita Patel, MD is triple board-certified in neurology, sleep medicine, and integrative medicine. Learn about our Medical Expert Board Fact checked by Angela Underwood Fact checked by Angela Underwood LinkedIn Angela Underwood's extensive local, state, and federal healthcare and environmental news coverage includes 911 first-responder compensation policy to the Ciba-Geigy water contamination case in Toms River, NJ. Her additional health-related coverage includes death and dying, skin care, and autism spectrum disorder. Learn about our editorial process Print Lorenzo Odone was born on May 29, 1978, to Michaela and Augusto Odone. By the time he reached school age, he began to show symptoms of problems with his nervous system. At age 6, in 1984, he was diagnosed with the childhood cerebral form of adrenoleukodystrophy (ALD), a progressive degenerative myelin disorder, meaning that myelin, the "insulation" around nerves, breaks down over time. In Lorenzo's case, the nerves in the brain were gradually being destroyed. In the cerebral form of ALD, symptoms typically begin to appear in mid-childhood (four to eight years old); the rate of progression is variable, but the disease leads to death within one to 10 years. Corbis via Getty Images / Getty Images Search For a Cure Michaela and Augusto, devastated by Lorenzo's diagnosis, decided to research ALD even though neither had a scientific or medical background. They eventually learned that ALD leaves the body unable to break down big fat molecules, either molecules the body makes itself or ones that enter the body through food. After much hard work, they helped develop an oil made from olive and rapeseed, which they named "Lorenzo's Oil." The oil, if started early in boys with ALD but no symptoms, is now known to have some benefit in preventing the form of ALD that Lorenzo had. Film Based on the Odones In 1992 director George Miller turned the story of the Odones and their struggle to find a cure for ALD into the movie, "Lorenzo's Oil" starring Susan Sarandon and Nick NolteSarandon received an Oscar nomination for Best Actress for her role as Michaela Odone. Lorenzo's Life and Disease Unfortunately, Lorenzo became bedridden and unable to communicate by the time he was 7 years old. Nurses and his parents cared for him 24 hours a day. He was treated with Lorenzo's Oil even though his disease had already progressed. He far outlived his prognosis, surviving to age 30. He died on May 30, 2008, one day after his 30th birthday. Both his father Augusto and his life-long friend Oumouri Hassane were at his side when he passed away. His mother died of lung cancer in 2002. 4 Sources Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy. National Institute of Neurological Disorders and Stroke. Adrenoleukodystrophy Information Page. U.S. National Library of Medicine Clinicaltrials.gov. Expanded Access for Lorenzo's Oil (GTO/GTE) in Andrenoleukodystrophy. IMDb. Lorenzo's Oil. Los Angeles Times. Michaela Odone: Focus of 1992 Movie. Additional Reading "Lorenzo Odone." The Myelin Project. 04 Mar 2009 By Mary Kugler, RN Mary Kugler, RN, is a pediatric nurse whose specialty is caring for children with long-term or severe medical problems. See Our Editorial Process Meet Our Medical Expert Board Share Feedback Was this page helpful? Thanks for your feedback! What is your feedback? Other Helpful Report an Error Submit