Advocacy in rare disease: Closing the funding gap

Advocacy in rare disease: Crafting the public narrative

Advocacy in rare disease: Surveying the landscape

Humanizing the support of patients living with a Rare Disease

The urgent need to internationalize databases for rare disease patients

Doing better where it counts: Bringing rare disease care to underserved populations

Where hope knocks: Personalized therapies in rare disease

Combating the fragmentation of data and disciplines: Innovation hubs to address rare diseases

Reimagining rare disease detection: Who needs to be at the table?

Uniquely singular: Exploring what it means to be rare

What’s the plan? From detection to diagnosis to treatment of rare diseases

The psychological cost of rare disease

Finding rare diseases in common places

Intelligent detection and diagnosis of rare diseases

Neonatal testing for rare diseases: The power of knowing

Detecting rare disease- Revealing the methods, motivations, and implications

Fiscal fitness for scientists- The price you pay for ignorance

The poor diagnosis of rare diseases

The science of incarceration- A realistic look at the cost of imprisonment

From grassroots to 30,000 feet- A discussion on the fate of graduate education