Isabella Rose was born December 7th, 2020. As a lot of you are aware she was born with Craniofrontalnasal Dysplasia. When she was born she was in the NICU for about a week receiving tests and being monitored very closely. This disorder varies in severity. Because of this she has craniosynastosis  (prematurely fused skull), a missing corpus callosum, and facial abnormalities. We are seeing 7 different specialist who are worried about the possibilities of seizures, vision problems, and developmental delays. She will need physical therapy and occupational therapy throughout her childhood to ensure that she meets all of her developmental milestones.
At 3 months of age Isabella will endure an extensive surgery that will help fix her skull, but then at 6 months will have surgery to take out her hardware.  The medical bills that have been received thus far are just continuing to grow.  Any donation that can help towards current and future medical bills would be greatly appreciated! 

Thank you to all of our support we have received from family and friends! We are so grateful

Megan, Salvador, and Baby Isabella