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AJ is the light of our life. He was diagnosed at 6 months and since then it has been a roller coaster that regardless of how stressful it is, we are having a blast through it. I would not have it any other way. PKS is stressful on families but one thing I have learned is that it is a special honor to be chosen by our kids to be their parents. He has multiple needs but as a family we are providing them the best we can in partnership with his awesome medical team. He has therapy sessions 3 -4 times every week which gives this mama a lot of bonding time and I love it. He is our special boy and we Iove him so much. He might not be vocal but he sure knows how to show that he is happy to be with us. Sorry, there is just so much to say that I tend to be all over the place. We are very grateful to always receive this gift every Xmas because AJ loves it. Thank you so much for all you do for our special kids.
