LymeDisease.org represents you—the Lyme patient.

For more than 30 years, we’ve worked to empower those with Lyme disease and to bring about a medical system that will help patients reclaim their lives.

True power comes from having informed patients involved at all levels of decision making. As the largest communications hub in Lyme disease, LymeDisease.org keeps patients informed and provides them with the tools they need to advocate for science-based policy change.

Here’s some of what we have accomplished—in partnership with you.

Millions of patients have used our Symptom Checklist and our Physician Directory, to help them get properly diagnosed, tested, and treated.

We continue to provide accurate news and commentary through our website, blogs, social media postings, weekly newsletters, and our journal The Lyme Times—now in its 32^nd year.

Through these channels, we keep you abreast of the science, the politics, and the structural barriers that make it hard for Lyme patients to get the medical care they need. We provide inspiration, by telling you about who is getting better and how they did it. We update you about pending legislation and let you know about opportunities for you to get involved in advocacy.

Patients looking for community can join our online support and discussion forum: U.S. National Lyme Group.

Our patient-powered research project MyLymeData has enrolled more than 15,000 participants. They are making a key contribution towards future Lyme disease research.

Donations from people like you make it possible for all this–and more–to happen.

Whether you have Lyme disease or love someone who does, you understand our passion to improve the lives of patients. We won’t stop until every patient is promptly diagnosed and receives appropriate care. We can do this with your help.

There is strength in numbers, and we believe that with your support, we can change lives.

Click here to donate