Age, Biography and Wiki

Lorenzo Odone was born on 29 May, 1978 in Washington, D.C., United States, is an Economist. Discover Lorenzo Odone's Biography, Age, Height, Physical Stats, Dating/Affairs, Family and career updates. Learn How rich is He in this year and how He spends money? Also learn how He earned most of networth at the age of 30 years old?

Popular As N/A
Occupation Economist
Age 30 years old
Zodiac Sign Gemini
Born 29 May, 1978
Birthday 29 May
Birthplace Rome, Italy
Date of death 30 May 2008,
Died Place Acqui Terme, Piedmont, Italy
Nationality United States

We recommend you to check the complete list of Famous People born on 29 May. He is a member of famous Economist with the age 30 years old group.

Lorenzo Odone Height, Weight & Measurements

At 30 years old, Lorenzo Odone height not available right now. We will update Lorenzo Odone's Height, weight, Body Measurements, Eye Color, Hair Color, Shoe & Dress size soon as possible.

Physical Status
Height Not Available
Weight Not Available
Body Measurements Not Available
Eye Color Not Available
Hair Color Not Available

Dating & Relationship status

He is currently single. He is not dating anyone. We don't have much information about He's past relationship and any previous engaged. According to our Database, He has no children.

Family
Parents Not Available
Wife Not Available
Sibling Not Available
Children Not Available

Lorenzo Odone Net Worth

His net worth has been growing significantly in 2022-2023. So, how much is Lorenzo Odone worth at the age of 30 years old? Lorenzo Odone’s income source is mostly from being a successful Economist. He is from United States. We have estimated Lorenzo Odone's net worth , money, salary, income, and assets.

Net Worth in 2023 $1 Million - $5 Million
Salary in 2023 Under Review
Net Worth in 2022 Pending
Salary in 2022 Under Review
House Not Available
Cars Not Available
Source of Income Economist

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Timeline

2013

In mid-2010, two years after Lorenzo's death, Augusto Odone sold his home in Virginia and moved to Acqui Terme in his native Italy, near his father's village of Gamalero where he lived when he was young. He died there on 24 October 2013, at the age of 80, and was survived by the son and daughter from his first marriage, as well as a grandchild by his daughter Cristina Odone.

2000

In recognition of the parents' work, Augusto Odone received an honorary doctorate from the University of Stirling. He continued to raise funds and drive the scientific task force known as The Myelin Project until his death. Michaela Odone battled lung cancer for some time and died on June 10, 2000, at the age of 61.

1996

A poem Michaela wrote about Lorenzo was set to music by Phil Collins. Titled "Lorenzo", it was featured on his 1996 album Dance into the Light.

1994

The 1994 episode of The Critic entitled "Dr. Jay", in which the main character Jay Sherman works to discover a cure for his boss' terminal disease was a send-up of the story.

1990

The Odones' story was first depicted in the 1990 Italian television film Voglia di vivere, starring Tomas Milian and Dominique Sanda. It was later made into the 1992 film Lorenzo's Oil, in which Augusto was played by Nick Nolte and Michaela by Susan Sarandon, who through her involvement with the movie became the spokesperson of The Myelin Project.

1933

Augusto Daniel Odone (March 6, 1933 – October 24, 2013) and Michaela Teresa Murphy Odone (January 10, 1939 – June 10, 2000) were the parents of Lorenzo Michael Murphy Odone (May 29, 1978 – May 30, 2008), a child with the illness adrenoleukodystrophy (ALD). They became famous for developing a controversial treatment using Lorenzo's oil, for their son's incurable illness, and this quest was recounted in the film Lorenzo's Oil (1992). Augusto had previously been an economist for the World Bank.

1923

This severe form of adrenoleukodystrophy was first described by Ernst Siemerling and Hans Gerhard Creutzfeldt in 1923. Lorenzo was diagnosed in April 1984, using a new blood test that had been recently developed. At the time, people diagnosed with the disease were usually young boys between 5 and 10 years old, who would gradually become mute, deaf, blind and paralysed before dying, which typically happened within two years due to aspiration or neurological causes.