Keegan Blair

Keegan was born with many medical complexities that I wasn’t aware of until birth. Some of them are: Arthrogryposis, microcephaly, hypotonia, brain abnormality, epilepsy, Club foot, and he has a feeding tube.

As most know I try to focus on the positive. Even though it is hard sometimes since Keegan will be 3 in August he is still not very mobile. He has made a lot of progress with his therapies, doing a little rolling, says a few words, and rocks at the eye gaze communication system. He also is such a happy boy and has the most beautiful smile. He is such a sweetheart and so very smart.

When Keegan had his last hospital stay 12/2021 (pneumonia and the beginning stage of sepsis) I found out about this site as it was hard to update people so many different ways. So I thought this would be a perfect place for everyone to go. I am using this for updates, appointments, and some journaling. With this journey it’s nice to get some of my feelings out there and just to share my beautiful boy.

Thank you everyone for following, prayers, thoughts, and love.