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The society is run by trustees, over half of whom have had children or grandchildren affected by neuroblastoma ; the remainder are all professional people, three of whom provide medical guidance and advice. There is also a Scientific Advisory Board (SAB), again volunteers who advise the trustees on which research should/shouldn't be funded.
Originator(s): Neuroblastoma Society
Resource added in:
30/10/2002
Available languages:
English
Objective:
This is the web site of The Neuroblastoma Society - a charity whose aim is to fund research into the illness and support parents whose children have been affected by the disease.
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