Our daughter was diagnosed with Food Protein Induced Enterocolitis Syndrome (FPIES) in February 2015. She was 6 months old at the time. I decided to write this blog mostly as an outlet for myself, as well as to keep documentation that we can look back on as things progress. It seems it will be an ongoing journey, and we’ll need good notes to remind us where we’ve already been. If it can also help other FPIES parents, or educate people about it, or keep our family and friends up to date, that’s an added bonus.
As with most blogs about real people, I won’t be using real names. The internet is a big, vast world that I don’t understand, so we’ll just keep it somewhat anonymous. At least as anonymous as you can get on here. There’s mom (me), Dad, and Acorn. She is our little acorn, because she has the strength of an oak tree inside of her.
As with most blogs about real people, I won’t be using real names. The internet is a big, vast world that I don’t understand, so we’ll just keep it somewhat anonymous. At least as anonymous as you can get on here. There’s mom (me), Dad, and Acorn. She is our little acorn, because she has the strength of an oak tree inside of her.