Baby Ariel (Goldenhar Syndrome)

Ariel had her surgery on Monday 8/20 and it’s such a relief to see her breath with easy.  It’s never a moms plan to see her child with needles and tubes in them but the choice of a trachea and a feeding tube was made with Ariel’s well being in mind.  The same way as I sit and learn from the nurses and doctors at the NICU I have come to the realization that Iwon’t be able to go back to work.  With a one year old at home (Jubilee) and Ariel coming home with a treachea and feeding tube. The amount of care Ariel will need is the care only her mother will  be able to provide. 


I thank all those who have donated it has been a big help but unfortunately we have a long road ahead of therapy, doctors visits, and special cares that Ariel will need.  


Please continue to share her valient story and thank you for all the support. 


❤️ From a great full mommy.