Laura advocates at the Lansing Capitol. She testified before the Senate Health Policy Committee, asking Senators to pass the Rare Disease Advisory Council (RDAC). This will give all stakeholders (Insurance, Pharma, patients, parents, doctors, etc). Laura was in good company with the sponsor, Rep. Jason Morgan, Tara Britt, RDII and Carolyn Sheridan with the National Organization for Rare Disorders (NORD).
