Sweet Baby Hudson’s Medical Bill

When Sweet Hudson was 1 day old he started having extreme hypoglycemia (low blood sugar) and uncontrolled seizures. He has now spent his first 3 weeks of life in the NICU (Neonatal Intensive Care Unit). 

Yesterday the doctors found that Baby Hudson has a rare genetic disorder called Agenesis of the Corpus Callosum (ACC), meaning part of his brain, that connects the left and right hemispheres, never developed. This disorder caused the many seizures but can also cause physical and mental delays. Worse yet, the seizures at one day old damaged the part of his brain controlling his vision (occipital lobe), meaning he could have poor eye sight or may be blind. 

His parents are 25 years old, this is their first child, and they found out their little boy has a rare genetic disorder. OVERWHELMING is an understatement.  Baby Hudson’s condition requires many speciality doctors and he is still in the NICU indefinitely. We want to make sure medical bills are not a reason this baby is unable to get the medical care and therapy he needs, as this disorder will be a life long condition. 

Sweet Hudson is the first child to his mom and dad, he’s the first grandchild on BOTH sides, and the first GREAT grandchild! This family is a rock of support and has had constant faith trusting the Lord. This baby is very loved and this family knows Hudson is fearfully and wonderfully made!

They have a great deal of love, but we want to help this family pay for the NICU bills, and the many medical bills to come. If you feel called to, please help this sweet family, ANY amount you’re able to donate will be helpful and appreciated!
 
If you’re not able to donate, we ask that you PRAY and pray fervently for this little boy to stop having seizures FOREVER, to have good eye sight one day, and to overcome any developmental delays he may experience due to his condition. ❤️

The family’s remarks: "Mostly we covet your prayers. But if you feel called to help in more than prayers a donation for Hudson will be a blessing.”


For more information on agenesis of corpus callosum please visit:  https://rarediseases.org/rare-diseases/agenesis-of-corpus-callosum/