The last day of February marks a hopeful end to winter and a transition in the sporting world as well, but is also important in society as a day to recognize and raise awareness for rare diseases. Known as Rare Disease Day, the goal is this observance is to remind humanity that just because a disease is not prevalent or has as much research dedicated to it does not make it any less important, as certain individuals obviously suffer from these rare diseases and deserve accessibility to treatment and hopefully a cure. While it makes sense that more funding is funneled to cancer and neurology research since it affects so many more people, performing research in these comparatively uncommon maladies could offer insight into their diseases that get most of the research dollars.

Throughout the COVID-19 pandemic, I have been washing my hands with vigilance to prevent the spread of germs. As a result, the skin on my hands have become calloused on some parts and mostly dry, with cuts and slight bleeding on occasion. I thought this was inconvenient, but when I learned about children with a rare genetic skin disease, I stopped feeling sorry for myself and dug a bit deeper into their plight. After all, my skin issues are just due to excessive hand washing (which everyone should be doing anyway!); these poor kids have to live with this painful disease, known as dystrophic epidermolysis bullosa, for their entire lives.