In a new @reflectornews opinion, RDII founder and pres. Tara Britt urges @SenTedBuddNC, @SenThomTillis & Congress to reform the role that #PBMs play in driving up health care costs for North Carolina patients. Read more: https://t.co/Dvt7TDKWgj
We don't want to let the month of May end without recognizing National Foster Care Month. Thank you to all of the foster families who take in children with rare diseases and love them like their own. We appreciate you!
We're excited to be participating in the Seattle Rare Disease Fair!
Payer Forum: May 30
Seattle Rare Disease Fair: May 31 to June 1
RSVP today for FREE. These events will have a lots of great speakers, discussions and advocacy opportunities!
https://t.co/NDMmWWgi2Z
80% of rare diseases are genetic in origin, and thus are present throughout a person's life - even if symptoms do not immediately appear. #rarediseaseawareness