education, advocacy and research for Lyme disease
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About represents the patient population on all levels—through engagement with legislators, educating advocates, training physicians, funding research that matters to patients, and generating patient-oriented healthcare policy information through the MyLymeData patient registry which surveyed thousands of patients. We tell our story in The Lyme Times, our blogs, at congressional hearings, in editorials, and in medical publications and through our nationwide network of state groups, our website, weekly newsletter, Facebook,Twitter, Instagram and Pinterest.

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You can also donate through the mail. Please make checks payable to and mail them to, PO Box 716, San Ramon, CA 94583. Fax credit card information to: (530) 899-9841.
If you have any questions, please call Barbara Barsocchini at 310-456-9931 (PST daytime only).