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When a parent is diagnosed with debilitating disease, life doesn’t just change — it redefines everything.

In Part 1 of this deeply personal conversation, I sit down with my sister, Terrie Slaughter — our mom’s primary caregiver — to talk about what happens after the diagnosis. From the moment everything shifted, to the quiet realization that she would become “the one” responsible for our mother’s care, we unpack the emotional, physical, and the mental weight of caregiving.

We talk about:

The shock of diagnosis vs. the reality of progression
What caregiving really looks like day-to-day
The invisible responsibilities no one prepares you for
How family roles shift — sometimes unevenly
The beginning of grief… long before loss

This is an honest look at what it means to show up when it’s hard, when it’s exhausting, and when there’s no roadmap. If you’ve ever found yourself stepping into a role you didn’t ask for — but couldn’t walk away from — this conversation will meet you there.