What happens when you move over 1,000 miles away… and suddenly realize rebuilding your medical team means more than finding new doctors—it means confronting the reality that many parts of the healthcare system still lack basic education around what it means to care for a previvor.

In this episode of BRCA & Beyond, Marisa shares the emotional and practical realities of starting over medically after relocating—leaving behind trusted specialists, navigating new insurance, rebuilding care from scratch, and coming face-to-face with a difficult truth: many primary care providers are not adequately equipped with even foundational knowledge about hereditary cancer syndromes, BRCA, or the long-term needs of previvors.

This conversation dives into the grief of losing a carefully built medical team, the exhaustion of retelling your story, and the larger systemic gaps that often leave patients with genetic mutations doing far too much of the educating themselves.

Inside this episode:

• The emotional toll of leaving behind specialists who knew your history

• Why moving with BRCA or hereditary cancer risk can feel medically overwhelming

• The healthcare system gaps previvors often face

• Why many primary care doctors lack basic education on hereditary cancer syndromes

• The burden of self-advocacy when providers don’t fully understand your risk

• How genetic counselors can help bridge critical gaps in care

• Building a strategic medical roadmap after relocation

This episode is not about blaming individual doctors—it’s about exposing a bigger issue: patients with BRCA, hereditary cancer syndromes, and complex medical histories deserve broader awareness, better physician education, and more informed care pathways.

Because previvors should not have to be the ones teaching the healthcare system how to protect them.

If you’ve ever felt like your medical complexity was bigger than the system designed to support it… this conversation is for you.

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