If you cannot contribute to this monetarily, please give this a share! 

My daughter was born with a genetic metabolic disorder called Glutaric Acidemia type 1, which prohibits her body from breaking down protein. 

Your body naturally breaks down proteins when you’re ill, dehydrated, or fasting, and that leaves her high risk for illness and medically fragile.

My sweet girl was awarded a Make-A-Wish trip to Give Kids The World (and Disney World) in Orlando in October, and we are trying so hard to get Bryce there too! 

Make A Wish only funds the biological parents, and having him there in addition to both of us biological parents for extra hands to help take care of and keep an eye on our girl would benefit us all greatly. He is an integral part of our family, and maintaining a united front for Lilah throughout the highs and lows of her illness is sooo important to her wellbeing. 

We genuinely appreciate any and all support we have!