Meet Carter

Tomorrow is national MPS Awareness Day and I just wanted you all to take the time, if you haven’t already to visit www.mpssociety.org and learn more about this terrible disease. What a lot of people don’t realize is that MPS is so rare in some cases that some children go undiagnosed and with no cure, it will take funding and knowledge to overcome. We learn somthing new each day and we meet more and more parents that are going through or have gone through similar situation as Carter’s and it breaks our heart, to see these very special kids who have the ability to light up the world with thier smiles, laughter and courage and know that with out our help they and many children in the future won’t stand a chance, because in a way that’s all they want is a chance at a normal life.  We love you guys and Carter says hi.   Here are some photos of him from the past couple of weeks.