Global nonprofit Foundation for Sarcoidosis Research announced today that it will be attending the upcoming Rare Disease Week on Capitol Hill from February 23 -27. They will be joining the Rare Disease Legislative Advocates to learn about how they can advocate for sarcoidosis.
The foundation will be attending events such as the legislative conference to learn about lobbying rights and its impact. FSR will also be joining RDLA for Rare Disease Lobby Day.
By attending Rare Disease Week we will hope to learn about the impact lobbyist have and what they can do to raise awareness for sarcoidosis and create a voice on Capitol Hill. Follow them on Twitter as they will be tweeting throughout the week @FdnSarcResearch.