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Your answers to LymeDisease.org's survey will help develop a research agenda for the Lyme community. It will be used as an advocacy tool to ensure the funding of research that matters most to patients.
If you are a Lyme patient, caregiver, family member, advocate, researcher, or healthcare professional, we want to hear from you.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/