The Cervical Cancer Society advances social impact through a three-pillar strategy:

1. prevention education,
2. patient advocacy
3. systems improvement

We deliver evidence-informed HPV and cervical-cancer education through community partners (clinics, schools, faith groups), build patient navigation and peer-support pathways that reduce barriers to screening and care, and engage providers and health systems to strengthen early-detection practices and patient-rights protocols.

Our initiatives prioritize underserved populations and apply an equity lens across program design, outreach, and evaluation.

We formalize impact with hospitals and community organizations and use transparent metrics to guide iteration and scale.

Outcomes we track

1. Reach: # of individuals educated; # of partner sites activated

2. Advocacy: policy/practice changes adopted by partner institutions

3. Support: patients enrolled in navigation/support services and retention rates

4. Research/innovation: pilots initiated and completed; dissemination outputs