Nico’s Journey with Sagittal craniosynostosis

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31 donors
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$2,355 raised of $2K

Nico’s Journey with Sagittal craniosynostosis

As many of you may know, Aimee’s entire world came crashing down on October 1, 2021 when she learned that her smart, handsome, perfect baby boy Nico was diagnosed with Sagittal craniosynostosis. In simple terms, Nico’s skull fused together entirely way to early, causing his skull to be deformed, leaving little room for his brain to grow and develop. Nico is experiencing some (mild) developmental delays, but we are thankful that Aimee was able to catch this diagnosis before things took a turn for the worst. Without Aimee catching this when she did, he would begin suffering from seizures, blindness, permanent damage to the brain, and even death. Nico will be having a major surgery on February 14, 2022 at the Children’s Hospital of Philadelphia with the most knowledgeable and skilled surgeons that handle his condition. Nico will spend several days in the hospital while he begins his recovery, until he is able to be at home with his family. This will be a VERY difficult time for Aimee; not only mentally, but financially as well. While we know God is going to cover Nico, the Doctors, and the family during this time, we are asking for PRAYERS and any donations to help alleviate stress from Aimee during this time. We will continue to update everyone, and cannot thank you enough for being the support that Aimee and Nico need in the coming days, weeks, and months.

Co-organizers3

Amanda Kline
Organizer
Pottstown, PA
Aimee Campbell
Beneficiary
Tina Campbell
Co-organizer
Alisha Nesmith
Co-organizer
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