I'm a 26 yr old with Classical PKU. PKU is a rare genetic mutation to where I am lacking the liver enzyme that breaks down an amino acid in protein called, phenylalanine. Therefore if I eat more than my recommended 6 gm of protein daily, it will eventually cause mental retardation since its very toxic to my brain. I have been so sick for years and unable to work. I need funding for my much needed medical food and cant afford it. Since its a rare disease, theres not a whole lot of funding out there for help with this. When I get on the right track, I can begin work again which I have bee hired as a HHA but cannot start working till I get some of my health back. Please if you can help at all it would be soooo appreciated. Thanks!