Craniosynostosis Awareness Month & Bennett’s Continued Journey This month is Craniosynostosis Awareness Month. I find it fitting to, once again, pause to help spread the word and help other parents become informed. I also find it a bit ironic that we are currently dealing with the diagnosis of craniosynostosis that affected our lives four years ago, when our little one …
Five Things I Learned About Trusting My Momsense This month is Craniosynostosis Awareness Month. In last week’s blog, I shared about receiving the craniosynostosis diagnosis and what the journey was like from that point through surgery. But one thing I didn’t focus on too much in the last blog, is truly worth mentioning. So I thought this week we’d revisit …
Bennett’s Journey Birth defect. I remember the first time I heard the words, something inside me felt instantly nauseated. I felt both a rush of fear and anger. Don’t use that term for my baby! He is perfect! It has taken nearly three years for me to be able to utter those words and accept them with grace. So during …