Friends With FOP

Posted by Karen Of course, the purpose of this blog is to discuss all manner of stuff connected to my daughter Miranda and her Fibrodysplasia Ossificans Progressiva.  As such, I usually only mention my son, Owen, in passing.  I think it's time I rectify that a bit and tell you about Owen, and how FOP affects his world. Owen was born on January 28, 2002, which means he just turned 8 years old.  Owen is tall for his age, blond like both his mom and dad at that age, and his worst health issue is a lazy eye inherited from his dad ...