The PNH Patient Travel Assistance Fund, based in White Hall, AR, is dedicated to supporting individuals affected by Paroxysmal Nocturnal Hemoglobinuria (PNH) by offering financial assistance for travel expenses. We understand the challenges of accessing specialized care, which is why we provide up to $800 per patient, annually, to help cover costs associated with visiting PNH specialists or obtaining second opinions. Our assistance can be applied towards various travel-related expenses, including airfare, ground transportation, lodging, meals, and necessary co-pays for medical visits and tests not covered by insurance. Patients are encouraged to bring a companion, ensuring they have the support they need during their journey. We are committed to facilitating better access to life-changing care for PNH patients across the United States.