Not medical advice. StopMyCancer is an educational resource. It does not diagnose, predict outcomes, or replace your care team. If you experience severe symptoms — sudden pain, difficulty breathing, high fever, or bleeding — seek emergency medical care immediately.

Why This Matters

Cancer doesn't affect everyone equally. Systemic barriers, cultural factors, geography, and identity all shape who gets diagnosed early, who gets quality treatment, and who falls through the cracks. A Black woman with breast cancer in the United States faces higher mortality than a white woman with the same diagnosis. A trans man may avoid screening entirely because the system wasn't built to include him. A rural patient may drive four hours each way for radiation. These are not edge cases — they are patterns.

StopMyCancer addresses these realities directly — not as politics, but as documented facts that affect survival. When we ignore disparities, we fail the people who need information the most. When we name them clearly and respectfully, we create space for advocacy, better care, and better outcomes.

This section provides advocacy tools, resource directories, and clinician conversation guides for patients and families navigating cancer care from marginalized positions. Each guide follows a consistent structure: name the gap, explain what drives it, and give you something concrete to do about it.

Access Guides

Each guide names the gap, explains the system, provides advocacy scripts, and links to resources. Select a topic to begin.

Black Women & Breast Cancer

Higher mortality rates despite similar incidence. Understanding the gap, advocating for care, finding culturally competent providers.

Read guide

Indigenous Screening Barriers

Geographic isolation, cultural factors, and systemic gaps in screening programs. Resources and advocacy for Indigenous communities.

Read guide

Trans & Nonbinary Oncology

Navigating cancer care when the system wasn't built for you. Hormone considerations, provider communication, finding affirming care.

Read guide

Rural vs. Urban Access

Distance to treatment centers, telemedicine options, transportation resources, and clinical trial access for rural patients.

Read guide

Migrant Language Barriers

Right to interpreter services, finding multilingual providers, and navigating foreign health systems as a migrant patient.

Read guide

Disability & Cancer Care

Accessible screening, adaptive equipment, communication accommodations, and advocacy scripts for disabled patients.

Read guide

Neurodiversity & Medical Trauma

Sensory accommodations, communication preferences, managing medical anxiety, and advocate scripts for neurodivergent patients.

Read guide

Cultural Norms & Consent

Modesty considerations, family decision-making, culturally safe communication, and patient rights across cultural contexts.

Read guide

Poverty & Financial Barriers

Assistance programs, insurance navigation, medication costs, and employer rights for patients facing financial hardship.

Read guide

Age-Related Disparities

Young adults dismissed, elderly under-treated. Advocating for appropriate care across age groups and life stages.

Read guide

How to Use These Guides

Every access guide follows the same template so you always know what to expect and where to find what you need.

What the gap is — clearly and respectfully named, with data where available
What contributes to it — the systems, policies, and realities that create and sustain the disparity
How to advocate — copy-paste scripts, conversation starters, and step-by-step checklists you can use immediately
Resource links — country-specific where possible, including organizations, hotlines, and support networks
Clinician conversation guide — a section designed to help providers understand the patient perspective and improve care
Sources and last reviewed date — every claim cited, every guide dated, so you know the information is current and evidence-based

My oncologist had never treated a trans patient before. I had to educate my own doctor about my body while also processing a cancer diagnosis. No one should have to do that alone.

— The reality that drives this work

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