The Hudson Initiative
The Hudson Initiative was founded for a real life hero named Hudson.
He was diagnosed with Congenital Heart Defect soon after his birth and this was considered lucky as 1 in 3 CHD babies leave the hospital completely undiagnosed. There are many types of heart defects and his was Truncus Arteriosus. One of the rarest and most difficult to treat. After several surgeries Hudson’s little heart gave in; but out of that loss came a chance to make other parents aware that CHDs are real and can happen to anybody regardless of race or creed.
One in 100 babies are born with this defect and twice as many babies die from CHDs as those from all forms of childhood cancer combined and yet, barely a few cents of government spend on heart related research projects goes towards CHDs in infants.
Knowledge is power and this motto runs parallel to the initiatives two primary and fundamental aims:
To raise awareness: Awareness that this could happen to anybody, and all that you need to do is ask your doctor for the pulse ox test, which is a simple test to determine if there is a problem with a newborns heart, so that the necessary lifesaving precautions can be taken by doctors and parents.
To raise funds: People with medical aid or money who find their child has a CHD can most likely easily afford the surgeries but there are 250 000 babies on a waiting list for surgery across Africa. CHDs have no definitive, known cause but there has got to be a reason they happen – therefore, funds raised will be used to fund research organisations and, ultimately, surgeries (in the long run) with the latter being distributed to local clinics and government hospitals.
Sorry, no projects have been created yet.