Living with CACNA1E
She is the super girl who pushes me to be a better mother. She has a Mona Lisa smile that melts my heart every single time. And even though she cannot speak or hold my hand I know that she knows who I am. She is the biggest blessing God has ever given me. ... Continue Reading →
The past few months have been extremely hard for Diyanna. I will post a blog about the last few months soon but first I want to share some wonderful news we received on Friday afternoon. Diyanna has officially been diagnosed as having a variant of the gene CACNA1E mutation. This is the 1st step in... Continue Reading →
The joy I felt this morning cannot be described. We got through another year! She is three! A milestone which we were told might never come to pass. But here we are celebrating an amazing achievement. She is a fighter. And we will fight with her all the way and one day we will say... Continue Reading →
Diyanna's Gene 