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Historic Time in Treatment of Rare Disease as Promising Drugs Reach Phase 3 Trials

This month, 15-year-old Molly Bonnell and her sister Emily, 13, who have cystic fibrosis, discovered how easy it is to make their voices heard in Congress -- without leaving their living room.

Legislation to Help Speed Research for Cystic Fibrosis and Other Rare Diseases

The Cystic Fibrosis Foundation has followed the health care reform discussion closely. While the Foundation has not taken a position on any particular health reform bill, we have consistently and aggressively encouraged officials to include specific reforms that are important for the treatment of cystic fibrosis.

Cystic Fibrosis Foundation Drug Development Model Spawns More Than 30 Promising Therapies

Foundation and Legislative Supporters Pushed for Bill