What the Cancer Survivorship Checklist on Cancer Nation Is For
Updated
The Cancer Survivorship Checklist is a practical resource on canceradvocacy.org (the site of Cancer Nation, formerly NCCS) that helps people affected by cancer organize the care and life tasks that follow diagnosis and treatment. It is aimed at cancer patients and survivors, and it works best as a personal planning tool rather than a clinical document. The site presents it alongside its advocacy, research, and storytelling resources, so treat it as a starting point for organizing your own survivorship needs and conversations with your care team.
What the checklist is
Cancer Nation describes itself as representing Americans living with, through, and beyond a cancer diagnosis. Its site groups resources under headings such as Cancer Survivorship Checklist, Cancer Nation Advocates, Survivorship Champions, and Survivor Stories. The checklist sits in that survivorship section: it is a survivor-facing tool, not a policy paper or a research instrument.
That distinction matters. The site's research offering is the annual Survivorship Survey, which collects perspectives on how patients and survivors live with and beyond cancer. The checklist is different in kind — it is something an individual uses to get organized, while the survey is something an individual responds to so the organization can understand a population.
Who it is for
- People recently finished with active treatment who need to track follow-up appointments, records, and open questions.
- Long-term survivors managing ongoing monitoring, late effects, or practical matters like insurance and work.
- Caregivers and family members helping someone keep track of survivorship tasks.
- Anyone preparing for a survivorship care conversation who wants a written list of what to raise.
It is less useful for someone still in the middle of an acute treatment decision, where a care team's own protocol should lead.
How to use it
- Open the checklist from the Cancer Nation site and read through the categories before filling anything in.
- Mark what already applies to you — follow-up scans, prescriptions, records requests, support needs.
- Add your own items for anything the list does not cover, such as workplace accommodations or financial questions.
- Bring it to an appointment and use it to structure questions with your oncology or primary care team.
- Revisit it periodically, since survivorship needs shift over months and years.
The expected result is a single working document you can update, rather than a one-time read.
What it does not do
The checklist is not a medical protocol and does not replace advice from your care team. The site does not present it as a clinical guideline, and nothing in the available material suggests it is personalized to a specific diagnosis. Use it to organize, not to decide treatment.
Where it fits in the wider site
If your interest is broader than the checklist, Cancer Nation offers three adjacent paths:
| Resource | What it is for | Best if you want to |
|---|---|---|
| Cancer Survivorship Checklist | Organizing personal survivorship tasks | Get your own follow-up care in order |
| Cancer Nation Advocates | A program teaching how policy shapes cancer care | Learn to advocate for system-level change |
| Survivorship Survey | Annual research capturing survivor perspectives | Contribute data on the survivor experience |
| Survivor Stories | A place to share personal experience | Add your voice to the survivorship movement |
The site also invites visitors to subscribe to Cancer Nation updates, which is the simplest way to hear when resources like the checklist are revised.
Common sticking points
- Expecting a downloadable clinical form. The checklist is a planning aid; your hospital's own survivorship care plan is the clinical counterpart.
- Filling it out alone. Its value increases when you review it with a clinician or navigator.
- Treating it as one-and-done. Survivorship is long; the list should change as your needs do.
Start with the checklist if your goal is personal organization, and move to the Advocates program or the survey if your goal is broader engagement with cancer care policy or research.