The PNH Patient Travel Assistance Fund, located in Jacksonville, AR, is dedicated to supporting U.S.-based patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) by providing financial assistance for travel expenses. Each patient can receive up to $800 per year to visit a PNH specialist or obtain a second opinion. Our program covers essential travel costs such as airfare, train tickets, ground transportation, lodging, meals, and medical co-pays that may not be covered by insurance. We understand the importance of connecting with specialized care, which is why we allow grantees to bring one companion, ensuring that patients have the support they need during their journey toward better health.