This is a cause that's close to my heart. Anyone with a special needs child understand what I go through daily. My son has Spina Bifida, club foot and hydrocephalus (water on the brain) for which he has a shunt in the head to relieve the pressure and leg braces. when I found out that the baby I was carrying had a neural tube defect I had no idea what the meant or what to expect. My worst nightmare came true, his clinical diagnosis is Spina Bifida with hydrocephalus. Which means his spine did not form correctly so his lower body does not work right either. His legs are twisted, plus needs medicine (which I have to pay out of pocket for) to release urine and bowels. Plus the hydrocephalus means water on the brain and one of his many surgeries put a shunt on his brain to help his body release the pressure of water on the brain. His eating habits are not that of a kid his age, he has a very strict diet, and it takes him way longer to finish his food.
or go here either one https://www.gofundme.com/funds-for-severely-disabled-child-equipment-needs&rcid=r01-154497818273-149c7751e89d414c&pc=ot_co_campmgmt_w
If you can only share this post it would be much appreciated.