Located in Port Allen, LA, the PNH Patient Travel Assistance Fund is dedicated to supporting patients diagnosed with Paroxysmal Nocturnal Hemoglobinuria (PNH) by providing essential financial assistance for travel to specialized medical care. Each U.S.-based PNH patient can receive up to $800 annually to cover travel expenses, which may include airfare, train tickets, ground transportation, lodging, meals, and co-pays for doctor visits and medical tests not covered by insurance. Recognizing the importance of companionship during medical journeys, the fund also allows grantees to travel with one companion. Our mission is to ensure that PNH patients have the necessary resources to access the specialized care they need, fostering hope and health for those affected by this rare condition.