08/07/2024
I’m so glad this article was published because it’s so true. Our medical system and support transitioning from pediatrics to adults is very scary because our kiddo’s still need help, yet the support and services tend to drop off as they become an adult. It’s important to get a team in place prior to your kiddo becoming an adult. Lifelong disabilities don’t end when your kid becomes an adult. I can tell you that families get burnt out and need help. When your child is non-verbal and they can’t speak for themselves as an adult they are stuck in this loop hole between pediatrics and adults and finding a doctor who is willing to take this on is few and far between. Most kiddo’s with intellectual disabilities are developmentally delayed meaning they may be 9 years old but developmentally are really on 5 years old. This life can be hard to navigate but I appreciate this family sharing their story so families don’t have to navigate this alone.
Colin Farrell is launching a foundation in honor of his 20-year-old son who has Angelman syndrome. The actor opens up to PEOPLE about their life together, saying he thinks his son James is "magic."