(Credit-brucewillisbw)
Dementia has claimed many lives over the year, and like many other chronic diseases and watching your loved one’s lives deteriorate takes a heavy toll on the people around them as well. In March 2022 Bruce Willis, the media legend who dominated Hollywood in his prime, was diagnosed with dementia and since then his family has been sharing their struggle with his diagnosis, and how slowly it has been taking a toll on his health. The following year his diagnosis was confirmed as frontotemporal dementia, which is a degenerative disease, that slowly chips your motor skills, communication skills etc. His wife, Emma Heming Willis, noted early signs were subtle changes in his speech, initially mistaken for a resurgence of his childhood stutter.
A family’s support means a lot during this time and the gracious efforts of his close ones, has inspired and drawn many people close to them. The Willis family provides regular updates on Bruce's condition. Demi Moore described his health as "stable" in December 2024, emphasizing the importance of meeting him where he is. Tallulah Willis acknowledged the "painful days" but highlighted the "love" within the family. Emma Heming Willis spoke about the challenges of caregiving and the emotional toll FTD takes on the entire family. His daughters and wife share photos and videos to mark special events.
According to Johns Hopkins Medicine, Frontotemporal dementia, or FTD, is a group of brain problems. It happens when brain cells in certain parts of the brain die. These parts, called the frontal and temporal lobes, then get smaller. This shrinking can cause changes in how a person acts, their personality, how they talk, and how they move. FTD often affects people younger than other types of dementia, usually starting between 40 and 65 years old, but it can happen to anyone.
It affects men and women the same. There are different kinds of FTD. One type, called the frontal variant, mainly changes a person's behavior and personality. Another type affects how a person communicates. This type has two forms: one makes it hard to speak properly, and the other makes it hard to understand words. A less common form of FTD affects movement, causing problems like those seen in Parkinson's disease.
We don't know exactly what causes FTD. Some cases are linked to genes that run in families. Sometimes, tiny clumps of abnormal protein, called Pick bodies, are found in brain cells. Having a family history of FTD is the main risk. However, most people with FTD don't have anyone in their family with it.
Symptoms of FTD develop slowly and get worse over time. They vary from person to person. Common symptoms include changes in behavior and personality, such as acting impulsively, saying rude things, or not caring about personal hygiene. People might also have trouble using or understanding language, like forgetting words or having trouble speaking. They might become less interested in things they used to enjoy and withdraw from others. Some people with FTD also have physical problems, such as tremors, muscle weakness, or trouble walking. They might also experience mood changes, agitation, and increased dependency on others.
The average life expectancy for someone with FTD is seven to 13 years after diagnosis. The disease progresses over time, affecting cognition and behavior. The Willis family continues to share their experiences, raising awareness about FTD and the challenges it presents.
Rumer Willis provided an update on her father, Bruce Willis, who is battling frontotemporal dementia (FTD). Despite the challenges, he is doing "great," considering the circumstances. The family emphasizes their close bond and how they support each other. Rumer highlighted that her parents, even after their divorce, always prioritized their children, fostering a strong family unit. While this is a very tough disease to go through, working together helps ease the pain and makes the process smoother. If you are struggling to cope with a loved one’s diagnosis, reach out to support groups and do not hold back on therapy as it can go a long way.
© 2024 Bennett, Coleman & Company Limited