06/02/2026
We often talk about cancer after diagnosis.
Not enough people are talking about what happens before it.
Before the diagnosis.
Before the treatment.
Before the emergency room visit.
Before the life-changing conversation.
A young Black mother being told cancer treatment may affect her ability to have children.
A patient learning they have cancer during an emergency visit instead of through routine screening.
A family left asking whether an earlier conversation could have changed everything.
These are not isolated stories.
They are reminders that prevention only works when people can access it, trust it, and act on it.
Colore**al cancer is increasingly affecting younger adults, particularly in underserved communities.
The challenge is not simply awareness.
The challenge is making prevention feel accessible, relevant, and worth acting on before symptoms force the issue.
When trust is missing, screenings get delayed.
When screenings get delayed, diagnoses often come later.
When diagnoses come later, outcomes become harder to change.
That is why culturally responsive care matters.
That is why trusted messengers matter.
That is why community engagement matters.
I recently spoke with Taneia Surles for BlackDoctor about these issues and what healthcare leaders, clinicians, researchers, and community advocates can do differently.
Read the interview here:
🔗 https://lnkd.in/e29fQsDi
What do you believe is the single most important thing we can do to improve trust and increase cancer screening in our communities?