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Lyme Disease Resources: 60+ Trusted Websites

A directory of 78 reputable Lyme and tickborne disease websites, from CDC and university labs to patient advocacy groups, each with a short note on what you will find there.

By the Beat Lyme editorial teamChecked against each site visited October 2026Updated October 11, 2026Not medical advice

Quick answer

The most reliable Lyme disease information comes from government health agencies (such as CDC, NIH and your state health department), medical societies and university research centers. Patient advocacy groups add support and lived experience, and some disagree with official guidance. Below are 78 active websites we checked in October 2026, grouped by type.

Listing is not an endorsement. Beat Lyme has no financial relationship with these organizations. Suggest a site: /contact/.

How to judge a Lyme website

Lyme disease is a topic where you will find strong opinions, so it helps to check a few things before you trust a page:

  • Who runs it? Look for an About page. A government agency, university, medical society or registered nonprofit should say who it is and how to contact it.
  • Where does the information come from? Good pages cite studies or guidelines you can look up, and explain how content is reviewed.
  • Is it selling something? Be cautious if the same site sells tests, supplements or treatments, or promises a cure that sounds too good to be true.
  • Is it dated? Check when the page was written or last updated. Guidance on testing and treatment changes over time.
  • Does it fit a perspective? On contested topics such as chronic Lyme, compare the CDC/IDSA view with the patient-advocate/ILADS view. Our guide to IDSA vs ILADS explains the differences.
What trusted sources say

The National Library of Medicine (MedlinePlus) suggests asking who operates and pays for a health website, whether ads are clearly labeled, whether sources and dates are shown, and how content is reviewed. It warns against sites that push products or promise cures.

What the tags mean: Government a public health agency or official program Mainstream follows CDC/IDSA-style medical guidance Research a university, lab or research program Advocacy a patient-advocacy or ILADS-aligned view, which may differ from CDC/IDSA on chronic Lyme, testing or treatment length

US government health agencies 15

Federal agencies publish the official US guidance on Lyme disease and fund most of the research. Start here if you want the standard medical view.

  • GovernmentCDC: Lyme Disease

    The main federal hub on Lyme disease, with plain-language pages on how it spreads, symptoms, testing, treatment and prevention.

    cdc.gov
  • GovernmentCDC: Ticks

    CDC home page for ticks and the illnesses they spread, including where ticks live, how to avoid bites and what to do after one.

    cdc.gov
  • GovernmentCDC: Lyme Disease Surveillance and Data

    Explains how Lyme cases are counted in the US and links to national case maps, charts and data tables.

    cdc.gov
  • GovernmentCDC: Clinical Care of Lyme Disease

    Guidance written for clinicians on treating Lyme disease and managing symptoms that last after treatment; useful to bring to appointments.

    cdc.gov
  • GovernmentCDC: Tick Bite Data Tracker

    An interactive dashboard showing emergency department visits for tick bites by week, region, age and sex.

    cdc.gov
  • GovernmentCDC: Alpha-gal Syndrome

    CDC information on alpha-gal syndrome, a tick-linked allergy to red meat and other mammal products.

    cdc.gov
  • GovernmentCDC/NIOSH: Tickborne Diseases in Workers

    Prevention steps for people who work outdoors and for their employers, plus signs that mean it is time to see a doctor.

    cdc.gov
  • GovernmentCDC Yellow Book: Mosquitoes, Ticks and Other Arthropods

    Travel-health guidance on avoiding tick and insect bites abroad, including repellents and protective clothing.

    cdc.gov
  • GovernmentNIAID: Lyme Disease

    The NIH institute that funds most federal Lyme research describes the disease and its research priorities on diagnosis, treatment and prevention.

    niaid.nih.gov
  • GovernmentMedlinePlus: Lyme Disease

    The National Library of Medicine’s patient page, gathering trusted links on Lyme symptoms, tests, treatment and current research.

    medlineplus.gov
  • GovernmentMedlinePlus: Tick Bites

    A plain-language overview of tick bites, how to remove a tick and when to call a health care provider.

    medlineplus.gov
  • GovernmentFDA: New Indications for Lyme Disease Tests (2019)

    An FDA announcement explaining its 2019 clearance of a blood-testing approach that uses two antibody tests instead of a Western blot as the second step.

    fda.gov
  • GovernmentEPA: Find the Repellent That Is Right for You

    A search tool for EPA-registered skin repellents that lets you filter by ticks, active ingredient and hours of protection.

    epa.gov
  • GovernmentClinicalTrials.gov: Lyme Disease Studies

    The official US registry of clinical studies; this search lists Lyme disease trials that are recruiting, active or completed.

    clinicaltrials.gov
  • GovernmentDoD Tick-Borne Disease Research Program

    A congressionally directed program that funds research on preventing, diagnosing and treating Lyme and other tickborne diseases.

    cdmrp.health.mil

State health departments 8

Your state health department tracks local cases and often has its own tick and Lyme pages. We list high-incidence states below. For every state, see Lyme disease by state.

International health agencies and groups 10

Lyme disease is also common in Canada, the UK and much of Europe. Guidance in these countries is similar in most ways but not identical to US guidance.

Medical societies and guidelines 6

Doctors rely on clinical guidelines. In the US, the 2020 IDSA/AAN/ACR guideline is the mainstream U.S. guideline, and CDC says its treatment regimens are consistent with it; the 2014 ILADS guideline is an alternative used by some clinicians. Read our plain-language IDSA vs ILADS comparison.

Academic research centers and university tick labs 9

University centers run studies on persistent symptoms, better tests and tick ecology. Many list clinical trials you may be able to join. See also our Lyme disease research overview.

Patient and advocacy organizations 12

These nonprofits offer community, education and research funding. Several take a patient-advocacy view that differs from CDC/IDSA on chronic Lyme and long-term treatment. For local groups, see Lyme disease support groups.

  • AdvocacyLymeDisease.org

    A long-running patient advocacy nonprofit with education, news, advocacy updates and links to online support.

    lymedisease.org
  • AdvocacyLymeDisease.org: “I found a tick. Now what?”

    A 2026 article comparing how the IDSA and ILADS guidelines approach a tick bite, written from a patient-advocacy point of view.

    lymedisease.org
  • AdvocacyMyLymeData

    LymeDisease.org’s patient registry, where people with Lyme can share their health data for research.

    mylymedata.org
  • AdvocacyGlobal Lyme Alliance

    A nonprofit that funds research, runs awareness and physician-education programs and lists patient resources.

    globallymealliance.org
  • AdvocacyBay Area Lyme Foundation

    A nonprofit that funds Lyme research, shares prevention resources and runs a free tick-testing citizen-science program.

    bayarealyme.org
  • ResearchLyme Disease Biobank

    A Bay Area Lyme Foundation program that collects samples from volunteers and shares them with researchers developing better tests.

    bayarealyme.org
  • AdvocacyProject Lyme

    A nonprofit with patient education, webinars, a provider search and support resources.

    projectlyme.org
  • AdvocacyLymeLight Foundation

    A California nonprofit that gives treatment grants to eligible children and young adults with Lyme disease.

    lymelightfoundation.org
  • AdvocacyNational Capital Lyme Disease Association

    A Washington, DC–area nonprofit offering local support groups, education and tickborne disease advocacy.

    natcaplyme.org
  • AdvocacyLyme Connection

    An all-volunteer Connecticut group focused on tick-bite prevention and support for local patients.

    lymeconnection.org
  • MainstreamAmerican Lyme Disease Foundation

    A nonprofit sharing education on Lyme and other tickborne illnesses that generally follows mainstream medical guidance.

    aldf.com
  • AdvocacyAlpha-gal Information

    A patient-led project summarizing research and practical tips on alpha-gal syndrome, the tick-linked meat allergy.

    alphagalinformation.org

Note: The Lyme Disease Association, a long-running national group, announced on its website that it closed in December 2024, so we no longer list it.

Tick identification and testing 5

Knowing what kind of tick bit you can help you and your provider decide what to watch for. Testing a tick for germs is different: CDC generally does not recommend it for treatment decisions, because a positive tick does not mean you were infected and a negative result does not rule it out. Read our guide to tick testing before you pay for a test, and see what to do after a tick bite.

Pets and animals 5

Dogs and horses can get Lyme disease too. These veterinary resources follow mainstream veterinary guidance. Always check with your own veterinarian. Start with our guide to Lyme disease in dogs.

Books and media

We keep a separate, balanced list of memoirs, science books and investigative reporting on Lyme disease, with notes on each book’s perspective.

See Lyme disease books

Support and mental health 8

Living with Lyme, especially when symptoms linger, can affect mood, work and money. These services can help. See also Lyme disease and mental health and financial help.

If you need help now

If you are thinking about suicide or are in crisis, call or text 988 (Suicide & Crisis Lifeline) or chat at 988lifeline.org. If you are in immediate danger, call 911.

  • Mainstream988 Suicide & Crisis Lifeline

    Free, confidential support 24/7 by calling or texting 988 or chatting online.

    988lifeline.org
  • MainstreamCrisis Text Line

    Free, 24/7 text support with a trained volunteer when you text HOME to 741741.

    crisistextline.org
  • MainstreamNAMI (National Alliance on Mental Illness)

    A national grassroots organization offering education, support groups and advocacy for people affected by mental health conditions.

    nami.org
  • MainstreamNAMI HelpLine

    A free peer-support line for information and referrals on weekdays; it is not a crisis line.

    nami.org
  • GovernmentNIMH: Chronic Illness and Mental Health

    A National Institute of Mental Health guide to how long-term illness and depression affect each other and how to find help.

    nimh.nih.gov
  • GovernmentFindTreatment.gov

    A confidential federal locator for state-licensed mental health and substance use treatment.

    findtreatment.gov
  • GovernmentJob Accommodation Network (JAN)

    A free, Department of Labor–funded service with guidance on workplace accommodations for health conditions.

    askjan.org
  • GovernmentSocial Security: Disability Benefits

    The official starting point for learning about Social Security disability benefits and how to apply.

    ssa.gov
What patients tell us

We are collecting real experiences about the websites and organizations that helped you most from people who have lived it, shared with their permission. As stories come in, they will appear here, clearly marked as personal experience rather than medical advice.

Share your experience

Frequently asked questions

What is the most reliable website for Lyme disease information?

For the official US medical view, start with CDC’s Lyme disease pages, NIH’s MedlinePlus and NIAID, and your state health department. University research centers such as Johns Hopkins and Columbia are also strong sources. Patient advocacy groups can add support and lived experience.

Why do some Lyme websites disagree with each other?

Doctors and patient groups disagree about some topics, especially chronic Lyme, testing and how long to treat. Mainstream sites follow the IDSA/CDC view; some advocacy groups and ILADS take a different view. Our IDSA vs ILADS page explains both.

Are Lyme disease websites a substitute for seeing a doctor?

No. Websites can help you prepare and ask better questions, but only a clinician who knows your history can diagnose or treat you. See preparing for your Lyme doctor visit.

How did you choose these sites?

We opened every site in October 2026 and only listed ones that loaded and showed recent activity. We aimed to include both mainstream and patient-advocacy perspectives. Listing is not an endorsement, and we have no financial relationship with any of them.

Can I suggest a Lyme disease website?

Yes. Send it through our contact page. We review suggestions using the checklist on this page.

Part of Step 7: Learn and connect

This directory is one part of our step-by-step plan. See every step in How to beat Lyme, or browse all Beat Lyme guides.