For those that have followed some of my posts about my now almost 16-month old, got some great news today from Seattle Children's Hospital.
For those not following, check through previous posts and/or check the links to other social media where we are telling her story.
Anyway...her appointment today was with the ophthalmologist. Fairly routine, because children with spina bifida often have optic nerve damage either directly from the spina bifida (depending on where the defect is along the spinal cord) or because of related diagnoses, like hydrocephalus or chiari malformation.
My wife updated Evanna's Facebook Community Page with this:
That's my girl!
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Where Evanna's story is being told
Facebook Community Page: http://fb.com/EvannasJoy
Her website: http://evannasjoy.com
IG: mostly on mine, http://instagram.com/scotters2k1 though she has her own at http://instagram.com/evannasjoy
We'd love for you to join us on this journey!