Rachelle’s daughter was originally diagnosed with Wilms at 16 months old, and then relapsed at 3 years old in a new city without the family and support system they’d had for her daughter’s initial treatment.

Rachelle candidly and honestly talks about the need to “claw” together a community of cancer parents to help them survive her daughter’s treatment. We talk about connections, finding comfort in other oncology parents, and how it feels when a bereaved parent supports families of NED kids, and the complicated emotions that come up of comparative suffering and survivors guilt.

This conversation spans different topics that will all sound familiar to oncology parents, not necessarily because you’ve had them out loud before, but because you’ve thought and felt every single word - and that’s what makes Rachelle and her deep insights and take away’s so valuable and important to hear.

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