Please join Michigan Rare Action Network and Amyloidosis Foundation Thursday, February 20, 2020 10:30am-12:00pm Michigan State Capitol, Speaker's Library, 100 N Capitol Ave, Lansing, MI Join patients, families, caregivers and other rare disease stakeholders at this important event to learn about the challenges rare disease patients face. You'll also learn how you can make a difference in the lives of rare disease patients and their families here in Michigan. Lunch will be provided and there is no cost to participate in this event. CLICK HERE TO REGISTER