We are Williams Syndrome Strong!

Our journey began July 2016 when our precious Wonder baby Delilah was hospitalized with hypercalcimia and no answers as to why her levels were so deadly! As I sat in the hospital with her for 9 days, witnessing things happening to her clinically I could never begin to express.. poked and prodded constantly until finally they decided to do genetic testing on a disorder we had heard nothing about.. terrified and insulted my husband and I just couldn't wrap our heads around how these Drs could say something like that about our perfectly healthy beauty baby.. how dare they was the vibe we gave off.. and yet we decided to go ahead allow the analysis to be preformed and were finally discharge with a new diet and low calcium formula and several different specialist as a follow up.. I began researching.. Williams Syndrome.. and what I found was an amazing support group that has became my family and back bone through the diagnosis and up until this day... I realised what a beautiful thing Williams Syndrome really is rather than looking at it as a missing piece of their chromosome, I look at it now as a unique journey we are apart of and how blessed I am to have been given the privilege to be her mommy. She is the sweetest little girl you could ever meet and I have met many other families that are now family to us... as we embark on this new chapter I will make it my duty to make Williams Syndrome a well known genetic disorder and educate others so that we can normalize it for our kids and those around us! We will celebrate every single milestone and share this journey through my daughter's beautiful starburst eyes! Smile Brighter, We are Williams Syndrome Strong!