Let's help Leo with his PKU Formula

Hi, my name is Daniela, I’m Leo’s mom, he is a sweet little boy diagnosed with phenylketonuria, a genetic disease that doesn’t have a cure but follows a lifelong treatment that consist in a low protein diet. I’m trying to help my son to stay healthy but it’s very hard. We are from Bolivia, a small country in South America where we don’t have any access to any of the things he needs for his treatment. The most important is his formula that’s named Phenyl Free 2, a formula that is sell in the USA and for me is very hard to get because it’s very expensive.

if you would like to help us and donate we would appreciate a lot.

Thank you