Patient receiving compassionate care Patient receiving compassionate care

Every Patient Deserves
to Know Their Options

We believe every patient deserves to know their options. We provide education, resources, and real human support to help them find answers.

Make a Quick Donation

What We Actually Do

We explain things in plain language.

Clinical trials, expanded access, compassionate use: how they work, who qualifies, what to ask.

We point you to sources you can check yourself.

Curated, current, and always someone else's data rather than our opinion.

We answer every message.

A person reads it and replies by email. We are not a chatbot and not a call center.

We are independent.

No pharmaceutical company or institution funds us or directs what we publish.

Our Programs

Three programs, one idea. Every patient deserves to know their options, before a diagnosis, after one, and all the way through.

Other areas are still in development, and we say so plainly.

Before a diagnosis

WondrPath

A short, confidential health survey. Find out where your health stands and which screenings are recommended for someone your age, because a cancer found early is often a far more treatable disease than one found late. Organizations can also run it for their community.

After a diagnosis

Patient Support & Education

Education, curated resources, and encouragement. We help patients learn how clinical trials and expanded access programs work so they can ask better questions of their own care team.

All the way through

Community Support

Encouragement from real people. Through WondrVoices we collect and deliver handwritten cards, drawings, and messages to patients so no one feels forgotten.

Our active, patient-facing work is WondrPath, Patient Support & Education, and Community Support. The two areas below are in development. We describe what we actually do in each today, and what we do not do yet.

We are educators and advocates, not a concierge service. Every resource, guide, and program we create is available to all patients equally. Because when it comes to hope, no one should be left behind.

What We Do and What We Don't

So you know what to expect before you reach out.

What we do

  • Explain how clinical trials and expanded access programs work, in plain language
  • Point you to trusted, curated resources you can bring to your care team
  • Read every message a person sends us and reply by email
  • Send encouragement through WondrVoices cards and messages

What we don't do

  • Give medical advice, diagnoses, or treatment recommendations
  • Review medical records or build a case-by-case treatment plan
  • Find, match, or enroll you in a specific clinical trial
  • Contact your doctors, insurer, or trial sites on your behalf
~7%

of adult cancer patients enroll in a treatment trial

40M+

Americans face life-threatening illness yearly

Most

patients are never told a trial is an option

You Can Help Change This

Right now, someone is trying to understand options nobody has explained to them. Your gift funds the guides, resources, and community that make those options understandable.

Wondrlink Foundation Inc is a registered 501(c)(3) nonprofit. Tax ID: 33-4493221