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.

    Recently diagnosed? Start here.

    Reach out and our team will reply by email with educational resources and clear next steps. Every message is read by a person. We do not review medical records or advise on treatment.

    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

    How We Support Patients

    Patient Navigator Program

    Educational Navigation Support

    Active

    An educational program that explains how clinical trials and expanded access programs work, shares curated resources, and helps patients form better questions for their own doctors. We do not review cases, research individual situations, or contact manufacturers, trial sites, or physicians on anyone's behalf.

    Plain-language explanations of trials and expanded access
    Curated resources you can bring to your care team
    Questions to ask your own doctors

    Community Support

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

    Where Trials Actually Happen

    Clinical trials only run at certified sites, and they aren't evenly spread. This map shows 1,670 certified sites worldwide.

    It won't tell you which trial is right for you, that's a conversation for your doctor. But it will show you what exists near you, and knowing that is a useful thing to bring to that conversation.

    Built and licensed by Malar, LLC. How our technology works

    Playbooks You Can Print and Bring With You

    Free step-by-step guides written to be printed, filled in, and taken to an appointment. No sign-up, no email required.

    How to Search for a Clinical Trial

    Getting from a blank search box to a short list of real possibilities, plus a glossary and a worksheet to fill in.

    4 pages · PDF

    Getting a Drug That Isn't Approved Yet

    How expanded access and compassionate use actually work, why companies say no, and what to ask your doctor first.

    5 pages · PDF

    When You're Told There Are No More Options

    What that sentence usually means, the questions worth asking next, and what to do in the following two weeks.

    5 pages · PDF

    Getting a Second Opinion

    Whether it's worth it, how to ask your doctor without awkwardness, and exactly what to bring so the appointment counts.

    7 pages · PDF

    Care Resources

    A curated directory of trusted resources to help you explore clinical trials, understand expanded access programs, and find reliable health information.

    These external resources are provided for educational purposes. The Wondrlink Foundation does not provide medical advice or treatment plans.

    You Don't Have to Face This Alone

    Whether you're a patient seeking guidance or someone who wants to support others, we're here to help.