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can make that difference
LymeDisease.org seeks to make the patient voice stronger, to support patient-centered research, and to create a future where Lyme patients can receive the treatments they need to get well. Its focus is on large scale science-based advocacy, communications and big data research.
Founded in 1989, it is one of the oldest, largest, and most trusted sources of patient information on Lyme disease, drawing millions of unique website visitors a year. Its MyLymeData patient registry and research platform has enrolled over 16,000 patients and is among the top 5% of patient-led registries in the nation. Its communications network distributes resources and educates the public about the science of tick-borne diseases via website content, blogs, social media, and an online journal, the Lyme Times.
You can also donate through the mail. Please make checks payable to LymeDisease.org and mail them to LymeDisease.org, PO Box 716, San Ramon, CA 94583.
If you have any questions, please call Carolyn Degnan, COO at 510-807-0133 or Barbara Barsocchini at 310-456-9931 (PST daytime only).
LDO achieved Gold level:
Committment To Transparency