How's Life? || Seven Years of Smith Magenis Syndrome

[@victoriabm4720]

Thank you for talking about this. There are not much videos about this. My daughter is 2 years old and has SMS. I would love to hear about the things that you notice of her growing up and how she is now. Sharing your experiences help me and my family. Thank you again so much and God bless you and your family 🙏🏽❤

[@nataliejackson87]

You both are amazing! With my own children's "disorders".. I love when Latoya says Design. 🙌🏼