In a heartwarming Instagram post, Tallulah Willis, youngest daughter of Hollywood stars Bruce Willis and Demi Moore, shared a touching childhood memory of her father carrying her on the red carpet. However, the post carried a deeper meaning, hinting at Tallulah’s recent autism diagnosis. Let’s delve into her story and learn more about her condition!
Tallulah’s Instagram video clip showed her as a young child playfully interacting with her father’s head while he spoke to the media at a film premiere. She captioned the clip with the phrase “tell me your autistic without telling me your autistic [sic],” inviting her followers to engage in a conversation about autism.
The response from Tallulah’s 408,000 followers was overwhelmingly supportive and loving. Many shared their own knowledge and experiences with autism, discussing Tallulah’s symptoms and the loving reaction of her father. One user even praised Bruce for his exceptional care, saying, “Your dad is one-of-a-kind honey, and so are you.”
When questioned by a psychologist specializing in neurodivergent conditions, Tallulah revealed that this was the first time she had publicly shared her diagnosis. She discovered her autism diagnosis during the summer, and it has had a significant impact on her life.
Autism spectrum disorder (ASD) is a developmental disability that affects social communication, interaction, and behavior. According to the Centers for Disease Control and Prevention (CDC), individuals with ASD often display restricted or repetitive behaviors and interests. Tallulah’s sister, Scout LaRue Willis, provided further insight by explaining that Tallulah’s actions in the video, such as folding her father’s ear, are a form of stimming. Stimming helps individuals regulate sensory input.
Tallulah’s revelation comes at a challenging time for the Willis family, as they continue to support their father, Bruce Willis, in his battle with aphasia and frontotemporal dementia (FTD). Bruce was diagnosed with FTD, a degenerative condition primarily affecting communication and behavior, in 2023. One of the early symptoms he experienced was aphasia, which affects language skills.
For now, Tallulah has chosen not to disclose further details about her diagnosis. The outpouring of love and support for her speaks volumes about the resilience of the Willis family. Let’s send our best wishes to Tallulah and her family as they navigate this new chapter in their lives.
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In 1993, This Boy Was Born With Enough Skin For A Five-Year-Old. But Wait Till You See Him Today
Tomm Tennent was born in 1993 with an extremely rare condition that baffled doctors—he had excess skin, making him a medical enigma. His parents, Geoff and Debbie, were unsure whether to continue with the pregnancy when they first learned something was wrong. Geoff recalled, “We decided what’s meant to be is meant to be.”
Despite extensive testing, doctors couldn’t diagnose Tomm’s condition or offer treatment. At birth, Debbie was shocked, saying, “It was nice to pick him up and hug him, but my heart was racing.” Doctors eventually discovered Tomm had 100 times the normal amount of hyaluronic acid, similar to Shar Pei puppies. They hoped his skin would normalize as he grew.
As Tomm grew older, he faced challenges, especially at school where some kids teased him. However, Tomm stayed positive, saying, “They don’t really care how I look.” By 2003, he embraced his uniqueness, adding, “I see a kind, loving person when I look in the mirror.”
Now 28, Tomm is happily married and lives a content life in Australia. His outlook remains simple: “You make choices, and you don’t look back.” His story serves as an inspiration of resilience and self-acceptance.
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