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The Human-Computer Interaction Institute at Carnegie Mellon University is conducting a study of how individuals with chronic Lyme disease, and their caregivers, use online resources to support themselves. Such resources include sites offering medical information as well as research and experience blogs, forums, and so on.
We seek participants for interviews about their experiences as patients or caregivers. All information from the interviews is confidential. Interviews can be done by phone, IM, or in person, and participants are compensated $10 for each hour they are interviewed.
In order to participate, you must be (1) Between 18 and 90 years of age, and (2) Either have chronic Lyme disease or provide close support to someone with chronic Lyme disease.
The results of our study will be used to drive the design and development of tools to help individuals with chronic illness and their caregivers find, use, and share online information.
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/