On average, Black children with autism don’t receive a diagnosis until three years after their parents have voiced concerns about atypical behaviors to their pediatrician. There are several reasons why this might happen, including prejudice and inexperience with autism among healthcare providers. Additionally, parents may be reluctant to push for a diagnosis out of fear of the autism “label.” But a late diagnosis can cause children to miss out on early intervention services, which have proven to be critical for the development of important cognitive and language skills that will positively impact their future.

That’s why this week at childmind.org, we explore the barriers faced by Black parents when seeking an autism diagnosis for their child. And since having a solid support system is essential when navigating this process, we share tips on how to talk to family members and friends about autism and how they might offer a helping hand. We discuss what an autism evaluation should look like and explore other reasons why a child might receive a delayed diagnosis.

– Faith Wilkins, Staff Writer | ✉