‘In Awe Of The Love So Many People Have For My Papa’: Scout Willis Thanks Fans After Father’s Dementia Revealed
Scout Willis, Bruce Willis’ 31-year-old daughter with ex-wife Demi Moore, Posted a message To all those who offered sympathy following the disclosure that her father had dementia.
Scout Willis was joined at the end by Rumer, Tallulah and Tallulah, her sisters. They pounced on her message to support its sentiments.
“Feeling emotionally tired and a bit overwhelmed, yet also very in awe of the love so man people have for my papa,” Scout Willis posted on Instagram.
“Second this Scouter feeling the abundant love for our guy and our family,” Tallulah, 29 years old, added, and Rumer, 34-year-old, echo it. “I third this Scouter and Buusk feeling so deeply grateful and in awe of the love for our sweet Daddio.”
Last year, Willis’ family released a Statement announcing he had been diagnosed with aphasia.
On Thursday, Bruce Willis’ wife Emma Heming, Moore, and his five daughters and posted a message on The Association for Frontotemporal Degeneration’s website.
“Since we announced Bruce’s diagnosis of aphasia in spring 2022, Bruce’s condition has progressed and we now have a more specific diagnosis: frontotemporal dementia (known as FTD). Unfortunately, challenges with communication are just one symptom of the disease Bruce faces. While this is painful, it is a relief to finally have a clear diagnosis,” The family stated.
“FTD is a cruel disease that many of us have never heard of and can strike anyone. For people under 60, FTD is the most common form of dementia, and because getting the diagnosis can take years, FTD is likely much more prevalent than we know. Today there are no treatments for the disease, a reality that we hope can change in the years ahead. 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,” They added.
Bruce’s family stated that he would like FTD awareness.
“Ours is just one family with a loved one who suffers from FTD, and we encourage others facing it to seek out the wealth of information and support available through AFTD (@theaftd, theaftd.org). And for those of you who have been fortunate enough to not have any personal experience with FTD, we hope that you will take the time to learn about it, and support AFTD’s mission in whatever way you can,” They said.
The family thanked everyone for their support during this difficult time and concluded by thanking them all.
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