Hi, my name is Chrissy Burniche. My son Logan is 7 with CPKU and I also have a 12 year old daughter Alexis, NON PKU. I am new to this site. I wanted to let everyone know that we are having an upcoming PKU benefit in Albany, NY on 10/09/11. If you are interested please email me at firstname.lastname@example.org or get me on here. I am excited to meet new people who have children and/or are PKU patients. My son is at an age that he is questioning his diet and why he is different. How do you handle this??