Ophelia’s Cranio Journey

Our sweet Ophelia was born with Craniosynostosis. It's a condition in which the skull's sutures (openings) close too early causing pressure & if not taken care of could cause brain damage, blindness, seizures & neurological issues. After many doctors appointments and travels to and from UofM (162.8 miles one way), surgery for Bicoronal Craniosynostosis is VERY important for her future brain growth. 12 days after her 1st birthday, Ophelia will be having her surgery with an outstanding team of doctors at UofM Mott Children's Hospital on January 26th. She is expected to be in ICU for 24-48 hours and in recovery for about a week. Ophelia's surgery is being covered by Health insurance, however we have humbly come to ask you to help her parents (Mirsad-Dad & Lachen-Mom) with overwhelming expenses. On top of traveling back & forth from Ann Arbor, both parents have had to miss many days of work that will continue & has made it difficult to make ends meet. We are asking for financial help so they can focus on Ophelia's health and not stress over on-going expenses. Please consider helping in any way you can...either financially or in diligent prayer. Thank you in advance! We are so grateful for your help in a time like this.