
Emma Heming Willis is opening up about the emotional toll of caring for her husband, Bruce Willis, as he battles frontotemporal dementia (FTD). In a new interview with People published September 3, the 49-year-old shared how isolating and overwhelming the early days felt, describing a period filled with sadness, uncertainty, and fear.

For Heming Willis, stepping into the role of caregiver meant not only adjusting to the changes in her husbandâs health but also finding her own strength in the midst of heartbreak.
Heming Willis Talks About Mental Health Struggles as a Caregiver

âEarly on, I was very isolated. I was too scared to say anything to anyone,â she admitted. âI was in so much sadness and darkness for so long. I ended up becoming very singular in this and it felt like what was happening was only happening to us.â
Over time, Heming Willis realized sharing their story could help others. By opening up publicly, she hopes to encourage families to pursue medical care sooner and connect with resources such as clinical trials.
How Bruceâs Symptoms First Appeared

Heming Willis recalled that she first noticed subtle but troubling changes in her husbandâs communication. âI started noticing his stutter started to come back [and] conversations werenât really aligning anymore,â she explained.
âThings just got very cloudy in our relationship, which just so wasnât like our relationship. Things just started to shift gradually over time.â
She admitted she never considered dementia as a possibility. âI never in a million years thought that was a symptom of FTD,â she said.

The family first announced Bruceâs aphasia diagnosis in 2022 before revealing the progression to FTD the following year. âThere was relief in understanding, âOh, okay, this wasnât my husband, it was that this disease was taking parts of his brain,ââ Heming Willis said of receiving a clear diagnosis. âI just softened.â
Turning Pain Into Purpose
Despite the ongoing grief, Heming Willis has found strength in reframing her experience. âWhile the grief and sadness and trauma is here all the time, I have learned itâs okay for me to also enjoy our life,â she shared. âBruce would want that for me and for our kids, to not wallow in the sadness of it, but also rise to it.â
She said her mission now is to make sure other families donât feel as alone as she once did. âThe only way I can get through this is to help someone else feel less alone,â she explained.
Advocating for Awareness & Support
FTD is the most common form of dementia for people under 60, yet it often goes undiagnosed for years.
âDoctors arenât thinking about dementia in those years so itâs very confusing. ⦠Itâs just not on anyoneâs radar,â Heming Willis explained.
She also noted the lack of support after Bruceâs diagnosis. âAfter Willis was diagnosed, we were sent out into the world with no support, no help, no nothing, which was very traumatic,â she said.
Now, with her book, The Unexpected Journey: Finding Strength, Hope, and Yourself on the Caregiving Path, set to release on September 9, Heming Willis hopes to provide comfort and guidance for caregivers walking the same difficult path.
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