The PNH Patient Travel Assistance Fund is dedicated to supporting individuals diagnosed with Paroxysmal Nocturnal Hemoglobinuria (PNH) by offering crucial financial assistance for travel needs. Based in De Queen, AR, we provide up to $800 per year to help patients reach specialized care or obtain a second opinion from PNH experts. Our funds can be applied towards essential travel expenses including airfare or train tickets, ground transportation, lodging, meals, and co-pays for medical visits or necessary tests not covered by insurance. We believe that every patient deserves convenient access to specialized care, and we allow grantees to travel with one companion, ensuring that no one faces their journey alone. We are committed to making a meaningful difference in the lives of PNH patients by removing travel barriers and promoting better health outcomes.