Medical Fund For Baby Allie Kavanagh

We are reaching out to you today on behalf of Kevin and Jessica, the loving parents of their eighteen-month-old daughter, Leah, and their newest daughter, Allie.

Allie was born with a rare condition called Bosma Arhinia Microphthalmia Syndrome (BAMS). BAMS is an extremely rare condition (fewer than 100 cases to date) in which a baby is born without a nose. This syndrome presents immediate challenges, including increased difficulty with breathing and eating. Allie’s condition requires immediate medical attention upon birth, several months in the NICU, and potentially multiple surgeries - all critical to improving her ability to thrive and live a healthy life.

Kevin and Jessica, as parents, are facing an immense emotional and financial burden. They are seeking out the best available medical care for Allie and consulting with specialists familiar with Allie's rare syndrome. The costs associated with surgeries, hospital/hotel stays, medications, and ongoing therapies are overwhelming. At the same time, they are also dedicated to providing care and support for their oldest daughter, Leah.

Please join us in our support for Kevin, Jessica, Leah and Allie during this challenging time by donating and sharing. Every contribution, no matter how small, can help alleviate the financial strain and allow them to focus on what matters most – giving baby Allie the best possible chance at a healthy, happy life.

Thank you for your kindness, compassion, and generosity.