Project Lyme

Project Lyme’s mission is to eradicate the epidemic of tick-borne diseases through awareness and education, support of cutting-edge science, and advocacy.

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3/3 More research is needed. Check out the science on @physorg_com https://t.co/ur2kZmEnMi

[Project Lyme @ProjectLyme]

🔬 1/3 NEW IN LYME SCIENCE: What if one of the keys to stopping tick-borne diseases is hidden inside tick saliva?

Researchers have identified a previously overlooked protein inside tiny particles called exosomes—microscopic "packages" in tick saliva that help cells communicate.

[Project Lyme @ProjectLyme]

2/3 This protein appears to play an important role in helping ticks feed and may also make it easier for pathogens to move between ticks and their hosts. If scientists can find ways to block this protein, they may be able to interfere with the disease transmission process.

[Project Lyme @ProjectLyme]

When Diana got a tick bite while 8 months pregnant, she was told not to worry. Over the next 3 years, she developed debilitating symptoms, saw more than 20 doctors, and was repeatedly dismissed before finally being diagnosed with Lyme disease.

Read more: https://t.co/HF0le0bCV3

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We would like to welcome everyone who has been affected by Lyme or tick-borne disease to our open Zoom support group on Wednesday (June 3rd) at 1 p.m. EST. Get some helpful tips and connect with others who are going through similar experiences. RSVP today: https://t.co/BTKHEgpo2r

[Project Lyme @ProjectLyme]

As Lyme Disease Awareness Month comes to a close, we want to recognize those who have helped advance our mission the past 10 years. Everyone who shares their story, supports research, advocates for change, and stands beside patients navigating tick-borne diseases — thank you 💚

[Project Lyme @ProjectLyme]

2/2 With the permission of the other group participants, we are posting a video to help spread awareness and valuable healing tips for those who are in need of them.

Watch it now: https://t.co/MTQUhnSp1E

[Project Lyme @ProjectLyme]

📢 1/2 Project Lyme had a special guest drop into a recent Men’s Support Group, hosted by Lyme advocate David Butler — Dr. Bill Rawls. Dr. Rawls shared his personal experience with tick-borne diseases and the treatments that have helped him and the patients he works with.

[Project Lyme @ProjectLyme]

🚨 ✨BIG NEWS FOR THE LYME COMMUNITY ✨

@HHSGov has just announced a series of major new initiatives aimed at tackling Lyme disease and other tick-borne illnesses. Check out some of the key changes in this encouraging announcement: https://t.co/sGkJsOIesu

[Project Lyme @ProjectLyme]

For 10 years, Project Lyme has worked to expand awareness, education, support, advocacy, and research.

This Fundraise Friday, we’re asking our community to give what they can —
$5, $10, or $20 can move this mission forward.

Donate today and help us build what comes next. 💚

[Project Lyme @ProjectLyme]

Project Lyme is hosting a webinar with Dr. Richard Horowitz, a leading clinician & researcher in tick-borne illness, on May 28th at 7 p.m. ET. @DrRHorowitz will explain the relationship between Lyme & Alzheimer's & what it means for testing & treatment: https://t.co/5C4YBDBFoS

[Project Lyme @ProjectLyme]

Many families have no idea that Lyme disease can be passed from mother to child during pregnancy. Isabel Rose, a member of our Board who runs free online support groups for moms affected by tick-borne illnesses, shares her story to raise awareness: https://t.co/JOVJWsopXx

[Project Lyme @ProjectLyme]

Here are 10 ways to support someone with Lyme disease.

✅ Share this to help educate friends and family.

✅Donate to fuel research, improve diagnosis and care, and ensure Lyme patients are seen, believed, and supported.

Visit https://t.co/SElQRZWBTq

[Project Lyme @ProjectLyme]

2/2 After 10 years, one thing is clear: when we come together, we’re stronger.

[Project Lyme @ProjectLyme]

🧵1/2 At Project Lyme, meetups are more than gatherings—they’re lifelines. Here are 10 ways these moments of connection have made a real impact.

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10 years later, we are still showing up, still speaking out, and still pushing for better.

Learn more about Project Lyme’s impact on our website: https://t.co/Upqz0eXPKn

#projectlyme10 #whywefight #lymeadvocate #lymediseaseawarenessmonth #tickbornediseases

[Project Lyme @ProjectLyme]

3/3 More studies are needed. These findings raise questions about whether some Lyme patients could also be experiencing undiagnosed AGS. Because symptoms can overlap, greater awareness could help more people get the answers & care they need. By @Lymenews https://t.co/XAJO3L27KO

[Project Lyme @ProjectLyme]

🧵1/3 Could there be a connection between Lyme disease & alpha-gal syndrome (AGS)?

Alpha-gal syndrome (AGS) is a tick-triggered allergy to a sugar found in red meat and other mammalian products that can cause hives, stomach problems, brain fog, joint pain, and even anaphylaxis.

[Project Lyme @ProjectLyme]

2/3 New study found alpha-gal antibodies were far more common in people who tested positive for Lyme than in healthy controls (17 vs. 2). The samples came from OH, where blacklegged ticks (which spread Lyme disease) are more common than the lone star ticks usually linked to AGS.

[Project Lyme @ProjectLyme]

Living with Lyme looks different for everyone, but shared experiences can make all the difference.

We want to hear from you. Share one thing that has made a difference in your journey. Your experience could help someone else feel less alone 💚