The PNH Patient Travel Assistance Fund, located in Mansfield, LA, is dedicated to supporting individuals diagnosed with Paroxysmal Nocturnal Hemoglobinuria (PNH) by alleviating the financial burden of travel to specialists. Our mission is to ensure that patients can access critical care and second opinions without the added stress of travel costs. Each eligible patient can receive up to $800 per year to cover essential expenses, including airfare, ground transportation, lodging, meals, and co-pays for medical visits and tests not covered by insurance. We understand the importance of having support during these travels, which is why we allow grantees to bring one companion along. Our commitment is to provide practical assistance that directly enhances the wellbeing and treatment journey of PNH patients across the U.S.