The household of Bruce Willis says frontotemporal dementia “is a cruel disease that many of us have never heard of and can strike anyone.”
WASHINGTON — The household of Bruce Willis shared Thursday that the beloved actor has been identified with frontotemporal dementia, referred to as FTD.
The announcement comes one 12 months after his household mentioned he’d been identified with aphasia and could be stepping away from his decades-long appearing profession as a result of it was impacting his cognitive skills.
“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,” his family said Thursday.
What is frontotemporal dementia?
According to the Mayo Clinic website, frontotemporal dementia “is an umbrella term for a group of brain disorders that primarily affect the frontal and temporal lobes of the brain.”
While dementia principally impacts individuals over the age of 65, frontotemporal dementia tends to begin at a youthful age with most circumstances identified in individuals between 45-65 years outdated, according to the U.K. National Health System.
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The most typical signs and indicators of frontotemporal dementia contain excessive adjustments in habits and character together with, lack of judgement, more and more inappropriate social habits, repetitive compulsive habits and extra.
Frontotemporal dementia is the reason for 10% to twenty% of dementia circumstances, based on the Mayo Clinic.
As Bruce Willis’ household defined: “FTD is a cruel disease that many of us have never heard of and can strike anyone.”
Are there any therapies for frontotemporal dementia?
Unfortunately, there is no remedy or particular therapy for frontotemporal dementia, the Mayo Clinic explains on its website.
Willis’ household mentioned Thursday it is a actuality they hope can change within the years forward.
“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 household assertion added. They inspired those that have been lucky sufficient to not have any private expertise with FTD to take the time to find out about it and support The Association for Frontotemporal Degeneration’s mission.
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