My Nonprofit Reviews

We are also located in Australia and have been on this journey three times now. So in total 5yrs of following this page for emotional support- in knowing that we are not alone. It can be a silent and isolating battle.. trying to feed a baby with an airway disorder. Ours has been Laryngomalacia. Both my boys had Supraglottalplasty surgery done. Our little 11 week daughter Millicent will be going in for surgery on the 9th June 2023. She will be our youngest child that goes in for surgery. The others were 9mo and 12mo. Feeding a child with airway malacia is a huge challenge.. we hope that things improve after the surgery as each feed is a real struggle and feeling of helplessness. We are praying that the surgery is straight forward and gives us the help that we need. Thank you for providing a page that supports these challenging times!!