The Registry is an ongoing research project enrolling participants who are 18 years of age or older and have a diagnosis of MS. The goal of this registry is to estimate the number of people living with MS in the Northwest and to develop a database for MS research. Participation in the registry is voluntary. If you participate, you will be asked to answer a few questions about yourself and your diagnosis when you sign up, and one to two surveys per year about your MS, the MS treatment you receive, and the impact of MS you experience.
To learn more about the registry, please visit www.pacificNWms.org or call 503-216-1022 for information.
Principal investigator: Stanley Cohan, MD, PhD
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