Former Hollywood actor Bruce Willis is currently living under full-time care as he continues his battle with frontotemporal dementia, his wife Emma Heming revealed during her appearance on Emma and Bruce Willis: The Unexpected Journey – A Diane Sawyer Special.
She explained that the actor now resides in a nearby home with professional aides, while she lives with their daughters, Mabel, 13, and Evelyn, 11. “It was one of the hardest decisions that I’ve had to make so far,” Emma admitted. She went on to add, “But I knew, first and foremost, Bruce would want that for our daughters. You know, he would want them to be in a home that was more tailored to their needs, not his.”
Though the arrangement may sound unusual, the family remains closely knit, joining Willis for breakfast and dinner. For Emma, the decision came after noticing early changes in her husband. She explained, “He was quieter, distant, and stopped doing things he loved, like school runs. That wasn’t like him.”
Bruce’s family had publicly revealed his diagnosis with frontotemporal dementia (FTD) in 2023, a condition that affects behaviour, language, and personality. Emma shared that his greatest struggle has been the loss of language, which has forced them to find new ways to connect. She also recalled the early days of his illness, saying she would often stay up through the night for his safety and began limiting his exposure to social situations to prioritise peace and comfort.
So, how can families balance the care needs of a loved one with dementia while also ensuring a sense of normalcy and stability for children in the household?
Dr Bhaskar Shukla, consultant neurology at PSRI Hospital, tells indianexpress.com, “Balancing dementia care with children’s needs can be challenging, but it is possible with thoughtful planning. Families should establish a routine that gives children consistency while also addressing the care needs of the person with dementia. Involving children in simple caregiving activities, such as reading aloud or helping with small tasks, can create positive connections and reduce feelings of disruption.”
At the same time, he adds that it is important to ensure children have their own space, activities, and emotional support. Staying together as a family is not always necessary; what matters most is ensuring the person with dementia receives safe, compassionate care, while children continue to feel secure and supported.
Effective ways to maintain communication and emotional connection
Dr Shukla states, “When language becomes limited, communication can still be nurtured through non-verbal means. Eye contact, gentle touch, facial expressions, and body language can convey love and reassurance. Using visual cues, music, or photographs can spark memories and encourage interaction. Speaking slowly, using short sentences, and maintaining a calm tone also help the person feel understood. Even when words are lost, the emotional connection remains strong, and caregivers should focus on presence, patience, and empathy to maintain closeness.”
Practical strategies or support systems that can ease the burden and prevent burnout
Caregiving is demanding, and feelings of overwhelm are common. “Practical strategies include setting realistic expectations, sharing responsibilities with other family members, and making use of respite care services to allow for rest. Support groups, whether in person or online, can provide emotional comfort and practical advice. Seeking guidance from healthcare professionals, such as geriatricians or social workers, can also help in planning long-term care. Most importantly, caregivers should prioritise their own health by maintaining sleep, nutrition, and time for personal activities. By caring for themselves, caregivers are better able to provide sustained and compassionate care for their loved one,” asserts Dr Shukla.