Eliza O'Neill has Sanfilippo Syndrome, a debilitating disease that will rob her of the ability to speak or walk.


Imagine if you were told your child would just fade away.  Wouldn’t you do everything in your power to change that?  Four-year-old Eliza O’Neill was diagnosed with a rare terminal genetic disease called Sanfillippo Syndrome-Type A.  Children with this rare disease are missing an essential enzyme for normal cellular function.  Over time a toxic material called heparin sulfate builds up in their brain and body leaving to severe disability and death before they even reach their teens.  THERE IS HOPE.  There is a gene therapy scheduled for late 2014 that is speicifically for children with Sanfilippo Syndrome.  This treatment could save Eliza. The only thing standing between Eliza and her miracle is money.  Watch a video on Eliza and then save a angel’s life: http://www.gofundme.com/ElizaONeill