Layna Lou

Hi, my name is Sydney and this is Layna Lou. Layna was born with an extremely rare genetic disorder called PBX1 Genetic Mutation. She has many diagnosis’s such; left lung hypoplasia, chronic kidney disease (horeshoe kidneys), pulmonary hypertension, hydrocephalus, low muscle tone. She is GTube and Oxygen dependent. Layna has spent over 430 days. Mainly at Jim Pattison Children’s hospital in Saskatoon, Sk but we also spent time at the Stollery Children’s hospital in Edmonton,AB. During this time Layna required a few ambulance trips to and from the airport and we did not know those weren’t covered, so therefore now have a hefty bill of $975 through MD Ambulance that also took us to collections because we did not know about it. We can’t get it paid through Jordan’s Principle as it was denied. We can’t pay it all out of pocket, so we need your help. Any amount helps us and it would def take a load off of us. We try really hard to do what we can but it’s hard when we get curveballs like this. Please and thank you in advance if you’re able to help us. We appreciate it so much.