Living With PXE: What Patients Face and What Orfenix Is Doing About It
PXE is a rare genetic disease where calcium builds up in soft tissues like the eyes, skin, and blood vessels. This can lead to serious problems such as vision loss, skin changes, and heart issues. Because symptoms often develop slowly and resemble other conditions, PXE is frequently misdiagnosed.
The article shares what daily life looks like for people with PXE and how it affects their well-being. It also highlights the work Orfenix is doing to develop a potential treatment, in collaboration with research partners.
Read the full story to understand PXE through the eyes of patients and learn what is being done to make a difference.