Boy whose cancer was half the size of a lung takes part in new trial

The transcript details a family's journey through the diagnosis and treatment of their child, Eddie, who was found to have a mass in his lung. Initial symptoms included recurring fevers and breathlessness. A chest X-ray revealed the mass, prompting immediate medical action. The family sought genome sequencing to understand the prognosis and potential genetic implications for their other child. The results showed no genetic predisposition, providing reassurance. The narrative highlights the emotional and practical challenges faced by the family during this period.

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