Phoenix's Life With Marshall Smith Syndrome

Hi, I'm Phoenix and when I was only 2 months old I was diagnosed with Marshall Smith Syndrome. Not a lot of information was out there about my syndrome, so my mom and dad relied on finding information from other parents of Marshall Smith Syndrome kids. My parents created this channel to provide a resource beyond medical jargon etc, to help other parents in search of hope. We are sharing our journey so that they can see there is a lot of living to do even with such an extremely rare and unpredictable syndrome. Thank you for stopping in, welcome to my story