In this conversation, Curtis interviews Cara, a mother whose son Cameron was diagnosed with a rare form of
brain cancer. They discuss the challenges and misconceptions surrounding pediatric cancer, including the resilience of children, the ongoing fear of
relapse, and the lack of funding and research for pediatric cancers. They also highlight the importance of finding the right medical team and advocating for the best care for their children. The conversation emphasizes the need for
greater awareness and support for childhood cancer. Parents need to be their child's best advocate when it comes to pediatric cancer. They should ask
questions, demand answers, and seek second opinions. It is important to have the right care team and not settle for subpar treatment. The medical community needs to stop using the word 'rare' when referring to childhood cancer and start taking action to improve outcomes. The government should pass legislation that allows access to experimental treatments and increase funding for
pediatric cancer research. The public needs to be educated about the realities of childhood cancer and the long-term effects it has on survivors. In this final part of the conversation, Cara and Curtis discuss the importance of sharing stories about the negative effects of cancer treatments and the need for more transparency in the medical community. They emphasize the need for
research and awareness about the long-term effects of treatments and the importance of supporting organizations that prioritize supporting families.
They also discuss the importance of normalizing conversations about childhood cancer and treating families in the community with empathy and understanding. They encourage listeners to join the fight against childhood cancer and be part of a supportive community.
