Hello, our son Greyson is 4 and he is special needs. He's been through 13 surgeries, 2 were brain surgeries. He has hydrocephalus (water on the brain) he has a gene mutation tuba1a, a kink in his brainstem and part of his brain is smooth and other parts are like cobblestone. He has epilepsy and a very complex airway. On 7-25-23 Greyson was brought 3.5 hours from home to Cincinnati children's hospital where he has been in the PICU (pediatric intensive care unit) due to Greyson's conditions and complex airway doctors have decided a Tracheostomy is the best option for him. He is also having both his hip sockets and femur heads reconstructed on August 21st. We aren't sure how long we'll be in the hospital and I'm unable to work (I have a job just can't work due to being here with my baby boy) and we still have bills coming in back home. If you could please find it in your heart to spare even $1 it would help and be greatly appreciated. If you can't spare anything we will also accept prayers, as without prayers our baby boy wouldn't have made it this far. Thank you for taking the time to read, God bless 💙
Greyson has been admitted again since September 15th. He had surgery today and unfortunately we didn't get the news we wanted. He will be inpatient for a while and bills are piling up. Monday we should be starting the discussion of moving forward with the Tracheostomy
