Erythropoietic Protoporphyria (EPP)
Erythropoietic Protoporphyria (EPP) is a rare inherited metabolic disorder caused by a deficiency of the enzyme ferrochelatase (FECH), which results from changes (mutations) in the FECH gene. This isn’t a widely known disease, because all over the world, there are only about 10,000 people who go through EPP. But even the torment these selected people go through is enough to send shivers down one’s spine. It’s impossible for one to even imagine what the EPP patients undergo. Recently, the Covid-19 hit the planet and it affected almost every place on the earth. Almost every country was locked down completely for at least some time. All of us were locked inside our houses, and barely got to go out. This was temporary. But for the patients of EPP, it’s nearly permanent. EPP causes skin pain on exposure to sunlight, most often on the tops of the hands and feet, face and ears. Pain can be severe and last days after sun exposure. There may not be anything to see at the...