Last updated 4 Jan 2020, 09:47 PM
Rare disease advocates across the country, including patients, caregivers, patient advocates and advocacy organizations, are connecting with congressional members and the National Institutes of Health at Rare Disease Week on Capitol Hill, February 25-28. Attendees can learn about how government policy impacts rare diseases and interact with other advocacy group representatives. The event is free for registered advocates. For more information visit http://www.rareadvocates.org/rdw.