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Lorenzo's Oil is a 1992 drama film directed and co-written by George Miller. It is based on the true story of Augusto and Michaela Odone, parents who search for a cure for their son Lorenzo's adrenoleukodystrophy (ALD), leading to the development of Lorenzo's oil.
Jan 29, 1993 · Lorenzo Odone, a Virginia 5-year-old, develops a degenerative nerve disease so rare that nobody is working on a cure, so his parents decide to immerse themselves in research and tackle the problem themselves.
Lorenzo's oil is used to treat an inherited disorder that affects the nervous system and adrenal glands (adrenoleukodystrophy or ALD), and an inherited condition that affects the spinal cord...
Dec 22, 2021 · Lorenzo's oil is touted to slow the progression of a neurological disease called adrenoleukodystrophy (ALD). This article explores whether it works.
Nov 17, 2023 · Lorenzo's oil is a liquid used to treat a rare and typically fatal degenerative myelin disorder called adrenoleukodystrophy (ALD). Here's what you need to know.
You may have heard that "Lorenzo's Oil" is a harrowing movie experience. It is, but in the best way. It takes a heartbreaking story and pushes it to the limit, showing us the lengths of courage and imagination that people can summon when they must.
True-life drama of a father and mother who battled against the odds to save their son's life. Augusto and Michaela Odone are dealt a cruel blow by fate: five-year-old Lorenzo is diagnosed with a...
- (40)
- Drama
- PG-13
Jul 21, 2004 · Their astonishing story was told in the Hollywood movie, Lorenzo's Oil. The movie painted a fairytale picture of a miracle cure, and gave hope to thousands of young children suffering the same...
Dec 30, 1992 · Augusto and Michaela Odone are dealt a cruel blow by fate when their five-year-old son Lorenzo is diagnosed with a rare and incurable disease. But the Odones' persistence and faith leads to an unorthodox cure which saves their boy and re-writes medical history.
Lorenzo Odone, a Virginia 5-year-old, develops a degenerative nerve disease so rare that nobody is working on a cure, so his parents decide to immerse themselves in research and tackle the problem themselves.
