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.

What unusual symptom did Eddie experience while listening to a bedtime story?

• He had a high fever.

• He was out of breath.

• He had a headache.

• He felt dizzy.

What did the chest X-ray reveal about Eddie's condition?

• An infection.

• Fluid in his lungs.

• A broken rib.

• A mass in his lung.

What was the family's immediate reaction upon learning about Eddie's diagnosis?

• They were angry.

• They felt like they were free falling.

• They were in disbelief.

• They felt relieved.

How did genome sequencing help in Eddie's case?

• It indicated a need for surgery.

• It predicted a short recovery time.

• It showed no complicating factors in treatment.

• It confirmed a rare genetic disorder.

What reassurance did the genome sequencing provide regarding Eddie's sibling?

• The sibling needed immediate testing.

• The sibling was at high risk.

• The sibling had a different condition.

• The sibling was no more likely to develop the condition than any other child.