Wife of Bruce Willis Shares Emotional Post as Husband Struggles with Dementia on 17th Anniversary

Emma Heming Willis recently marked her 17th anniversary with⁤ Bruce Willis,⁤ sharing a deeply emotional message on social⁢ media. In her post, she‍ reflected on the challenges ‍they face ​following Bruce’s diagnosis with aphasia in 2022, and later dementia, which she described ‍as a debilitating condition. ⁣She expressed that⁣ anniversaries, which onc brought joy, now ⁢evoke feelings of sadness and anger.However,she emphasized the‌ importance of unconditional love in their⁣ relationship,stating ⁢she would​ choose to ​go through it all again if given the ⁤chance.

Emma pointed out⁤ her grief yet acknowledged the blessings ⁤of their ⁢love, stating, “what is… is ⁣unconditional ⁤love.” She emphasized that they focus ⁤on living⁢ fully each day,despite the difficulties posed by Bruce’s health issues. Emma has committed to advocating⁣ for ​awareness around frontotemporal dementia,using her experiences‍ to support others affected by similar⁣ challenges. She ‌expressed hope for⁣ the future and shared her determination ‍to fight against the disease while cherishing the loving memories they’ve created ​together.


In a post filled with pathos, the wife of actor Bruce Willis noted their 17th anniversary together.

Willis left acting in 2022 after being diagnosed with aphasia. In February 2023, his family said Willis was suffering from dementia, according to Fox News.

“17 years of us,” Emma Heming Willis wrote Sunday on Facebook.

“Anniversaries used to bring excitement — now, if I’m honest, they stir up all the feelings, leaving a heaviness in my heart and a pit in my stomach. I give myself 30 minutes to sit in the ‘why him, why us,’ to feel the anger and grief. Then I shake it off and return to what is,” she wrote.

“And what is… is unconditional love. I feel blessed to know it, and it’s because of him. I’d do it all over again and again in a heartbeat,” she added.

When Willis’s family members announced his condition, they posted a message on the website of the Association for Frontotemporal Degeneration.

“FTD is a cruel disease that many of us have never heard of and can strike anyone,” the post said.

“As Bruce’s condition advances, we hope that any media attention can be focused on shining a light on this disease that needs far more awareness and research,” the post said.

“Bruce always believed in using his voice in the world to help others, and to raise awareness about important issues both publicly and privately,” they wrote.

“We know in our hearts that — if he could today — he would want to respond by bringing global attention and a connectedness with those who are also dealing with this debilitating disease and how it impacts so many individuals and their families,” they added.

“Bruce has always found joy in life — and has helped everyone he knows to do the same,” the post continued.

“It has meant the world to see that sense of care echoed back to him and to all of us. We have been so moved by the love you have all d for our dear husband, father, and friend during this difficult time. Your continued compassion, understanding, and respect will enable us to help Bruce live as full a life as possible,” the post concluded.

In a post on Instagram, Willis’s wife said she would do what she could to fight for those with frontotemporal dementia.

“FTD doesn’t get to write my family’s story — I do. Advocacy has been my lifeline, transforming grief into action,” she d.

“It’s my way of giving FTD the middle finger and making it clear that powerful advocates, care partners, researchers, scientists, medical professionals, and community leaders are coming for it — and I’m right there with them. I’m looking forward to seeing what 2025 has in store for us,” she wrote.




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