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People Question Medical Standards After Bruce Willis’ Wife Gets Disturbing Call From Top Doctor
People Question Medical Standards After Bruce Willis’ Wife Gets Disturbing Call From Top Doctor
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People Question Medical Standards After Bruce Willis’ Wife Gets Disturbing Call From Top Doctor

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As Bruce Willis remains absent from the spotlight due to health issues, his wife Emma Heming opened up about an unexpected call she received from a “prominent doctor.”

Her revelation came a few days after she shared an important message related to the passing of Gene Hackman and his wife, Betsy Arakawa.

In a recent Instagram video, Emma narrated the conversation she had with the doctor over the phone.

Highlights
  • Bruce Willis’ wife Emma Heming narrated an unexpected conversation she had with a “prominent doctor.”
  • “Doctors need to do better,” she said in the video.
  • Her revelation came shortly after she shared an important message related to the passing of Gene Hackman and Betsy Arakawa.
BP Daily - Your Source for Unbiased Reporting

    Bruce Willis’ wife Emma Heming narrated a conversation she had with a “prominent doctor”

    Couple sitting outdoors, man in orange vest, woman in black jacket, nature setting. Keywords: Bruce Willis, dementia.

    Image credits: emmahemingwillis

    The doctor spoke to her about a patient’s diagnosis of young-onset Alzheimer’s and their family, which includes three children aged 10, 12, and 14.

    “He needs all of my resources, any contacts,” Emma said as she explained the doctor’s request.

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    “And I was like: ‘Huh?’” she added.

    Woman in glasses shares news about actor's dementia diagnosis in a home setting.

    Image credits: emmahemingwillis

    Emma revealed that she was more than happy to share her contacts and resources with the doctor, but she was surprised they didn’t already have the resources to help their patient.

    “The thing that just boggles my mind is how do our doctors not already have a Rolodex of ways to support caregivers,” she told her audience.

    Emma said she couldn’t understand how doctors do not already have a Rolodex of resources

    Man and woman close together in low light; related to actor’s dementia battle discussion.

    Image credits: emmahemingwillis

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    She also noted how she receives messages from family members dealing with dementia diagnoses, who also have questions about resources.

    Sometimes, these families might not even be in the same city or state as her, she noted.

    When the action hero received his diagnosis, all that Emma received was a “pamphlet”

    Couple embracing near a snowy riverbank, highlighting actor's dementia battle.

    Image credits: emmahemingwillis

    “It’s just like, they need to do better. Doctors need to do better,” she said. “Doctors really do need to have a road map of just some support.”

    She revealed that she touches upon the subject in her upcoming book The Unexpected Journey: Finding Hope And Purpose On The Caregiving Path.

    Bruce Willis' wife discussing a call from a doctor about dementia, wearing glasses and a white sweater with text overlay.

    Image credits: emmahemingwillis

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    When her action hero husband Bruce received his diagnosis, she admitted that a pamphlet was all she got.

    “I was not handed one resource and we gotta put an end to that,” she added.

    “Doctors need to do better,” said the Die Hard actor’s unwavering partner

    Emma’s brief heart-to-heart came shortly after she spoke about the late Gene Hackman and his longtime wife and caregiver, Betsy Arakawa.

    Betsy’s decomposing body was found in their Santa Fe home on February 26.

    Officials believe she passed away on February 11 from hantavirus, which spreads by contact with rodents or their urine or feces.

    Emma touched upon the passing of Gene Hackman and Betsy Arakawa in a recent video

    A woman and man posing for a photo at a formal event, smiling and wearing blazers.

    Image credits: Jim Smeal/Ron Galella Collection

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    Gene, who was in the advanced stages of Alzheimer’s disease and might not even have been aware of his wife’s passing in the same house, is believed to have passed away on February 18 from hypertensive atherosclerosis cardiovascular disease.

    After details about their passing were released, Emma said in a video that the discovery is a reminder of how caregivers need care too.

    Emma said there is a “broader story” in the discovery of Gene and his wife’s bodies

    A man and woman in swimsuits standing in the ocean at sunset.

    Image credits: emmahemingwillis

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    “The tragic passing of Mr. and Mrs. Hackman” made her “think of this broader story,” she said.

    “Caregivers need care too,” she told her audience. “And that they are vital, and that it is so important that we show up for them so that they can continue to show up for their person.”

    She asserted that it’s a “misconception” that caregivers have “got it figured out [or] they’re good.”

    “I think that we need to be showing up for them so that they can continue to show up for their person,” she concluded.

    Emma married Bruce in March 2009 and welcomed two daughters, Mabel Ray, 12, and Evelyn, 10, with him.

    The Die Hard star is also a father to daughters Rumer, 36, Scout, 33, and Tallulah, 31, whom he shares with ex-wife Demi Moore.

    The action hero shares three daughters with ex-wife Demi Moore and two daughters with Emma Heming

    Woman sitting with a man on a recliner, appearing engaged and comforting him amid his dementia battle.

    Image credits: demimoore

    Bruce retreated from the spotlight in 2022 after his family announced in March 2022 that he was diagnosed with aphasia, a condition that affects one’s ability to communicate.

    They later said in February 2023 that the Hollywood icon has frontotemporal dementia (FTD), which can include speaking and writing challenges associated with the effects of aphasia.

    Weeks after the announcement, she requested that paparazzi stop photographing her husband when he was out and about.

    “This one is going out to the photographers and the video people that are trying to get those ‘exclusives’ of my husband out and about,” she said in March 2023. “Just keep your space.”

    Requesting photographers not yell or ask her how he’s doing, she asked them to allow Bruce and whoever he is accompanied by to “safely” get from “point A to point B.”

    Bruce’s family announced that he has frontotemporal dementia (FTD) in 2023

    Group photo of Bruce Willis with family, smiling outdoors, amid his dementia battle.

    Image credits: demimoore

    Back in September 2022, Emma was branded a “drama queen” by internet trolls after sharing a post about her husband’s health on National Grief Awareness Day.

    She said the grief was “paralyzing,” but noted she discovered new hobbies along the way and stayed active.

    Emma has long been vocal about her journey since her husband’s diagnosis

    Family playtime on the floor, sharing a joyful moment in their home.

    Image credits: emmahemingwillis

    After criticism for her comments, she clapped back at haters, who asked her to “stop whining” because she could “cope just fine with his $$$.”

    “When you marry an old man DECADES older than you are, you become their caregivers,” read one of the messages. “That’s what you signed up for deal with it and stop complaining.”

    A group of people, including Bruce Willis, sitting on outdoor furniture surrounded by lush plants.

    Image credits: emmahemingwillis

    Emma shared screenshots of the hateful comments and wrote, “When you’re not allowed to talk grief, self-care, or being human in the world on grief awareness day.”

    “My gawd,” she added. “But in the words of the great, philosophical, insightful Bruce Willis … ‘Ah, f*** em.’”

    Netizens agreed that “caregiver burnout is real” after watching Emma’s video

    Comment on doctors’ role beyond diagnosis in dementia care.

    Comment on caregiver burnout with heart emoji amid Bruce Willis dementia news.

    Comment on medical support amid Bruce Willis' dementia battle.

    Comment from a nurse discussing dementia care challenges and the lack of resources for families.

    Bruce Willis’ wife shares a doctor’s call about losing memory, emphasizing the need for resources in dementia care.

    Instagram comment discussing Alzheimer's diagnosis experience related to Bruce Willis' dementia.

    Comment thanking Emma for highlighting dementia caregiver challenges, with a message of support for Bruce Willis and family.

    Comment on doctors' lack of dementia resources, highlighting care challenges.

    Comment expressing sadness over lack of doctor support for dementia families, related to Bruce Willis' health battle.

    Instagram comment praising Bruce Willis' wife for supporting caregivers amid his dementia battle.

    Instagram comment expressing surprise at doctors' knowledge amid Bruce Willis' dementia battle.

    Comment on doctors and technology, mentioning frustration with information sharing.

    Comment on Bruce Willis' wife's call for help amid actor's dementia battle.

    Comment highlights lack of dementia awareness among doctors, thanking Bruce Willis’ wife for advocacy.

    Comment on providing support to caregivers and families in dementia care.

    Comment on social media about challenges in healthcare systems in the US and Canada.

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    Binitha Jacob

    Binitha Jacob

    Writer, Entertainment News Writer

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    At Bored Panda, I dive into breaking celebrity news, Hollywood updates, and viral pop culture stories that spark global conversations. My background as a reporter at International Business Times and Latin Times gave me experience covering fast-moving entertainment stories for international audiences. Today, my work regularly appears on Google News, AOL, and MSN, reaching millions of readers. What excites me most is capturing the pop culture moments that people can’t stop talking about.

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    Binitha Jacob

    Binitha Jacob

    Writer, Entertainment News Writer

    At Bored Panda, I dive into breaking celebrity news, Hollywood updates, and viral pop culture stories that spark global conversations. My background as a reporter at International Business Times and Latin Times gave me experience covering fast-moving entertainment stories for international audiences. Today, my work regularly appears on Google News, AOL, and MSN, reaching millions of readers. What excites me most is capturing the pop culture moments that people can’t stop talking about.

    What do you think ?
    Rouch Houz
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    It's the whole health system, doctors aren't to blame individually! They aren't superheroes, they're humans too and they can't be an expert at everything?! (Written by someone also HUGELY let down by the health system!)

    Roni Stone
    Community Member
    Premium
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    I have been have been a full time caregiver for a couple of years now and yesterday, I had to go on anxiety medication. With my own physical limitations and slighter disabilities, I'm at the end of my rope all the time and it's terrifying no knowing if there is anyone to catch me should I lose grip.

    LakotaWolf (she/her)
    Community Member
    Premium
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    I spent my life age 18 to age 39 being the primary caregiver for my completely-disabled father. He had a catastrophic brain injury from an accident, and was bedridden, had a feeding tube, was in diapers, etc. Caregiver burnout is real, and it is devastating. I attempted su!cide twice during the 21 years I helped care for him. He died in 2021 and I'm still not okay. And I loved my father deeply and was happy to stay living at home and pause my entire life to help care for him... but it destroyed my life and it destroyed me. There are very few resources to help family caregivers out, even in supposedly "advanced" countries like America. If you're a caregiver for a family member, please try to take care of yourself as much as possible <3

    Doodles1983
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    This. And ensure access to respite care regularly. Even if it's a few hours. For yourself to regroup. It's not failure. It's not selfishness. It actually enables you to refresh, get new perspective, have some you time and provide better tlc to the person you're responsible for in the long term. This counts for carers of any kind. AND the person being cared for. A change of face can distress some people but it can also reinvigorate THEM. And this goes for parenting too, actually. All the best.

    Load More Replies...
    Patricia Rudolph
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    My LO has been diagnosed with Alzheimer's officially for 5 years. Memory was lost, didn't remember his mother, or past life, acted like a 12 yr old. he was 75, He had some terrible night as he kept asking to go to the bathroom and get up at night. The doctor prescribed a sleeping pill (zolpidem), but it had a very bad side effect on him (delusions and hallucinations) and we decided not to give it any more and went for the Neuro X program that was introduced to us by his primary care doctor, he was on the Neuro X program for Alzheimer’s disease from Uine Health Centre for 6 months. The treatment relieved symptoms significantly, After the treatment he’s all of a sudden back active again, almost all his symptoms are gone, no signs of agitations, his sleeps pattern are back to normal. His memory loss has greatly improved and he tells stories about his past life, we got the Neuro X program from uinehealthcentre. com.

    Libstak
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    As a care giver to my father who had vascular dementia I support this message. I am caring for mum now who is showing signs of memory issues. However, in terms of Gene Hackman...how does a couple with many millions available not have nursing assistance at home daily or at least 3 to 4 times a week fgs? The wife seems to have isolated them both.

    H. B. Nielsen
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    Did they really need to say "Gene Hackman's decomposing body" effiing disgusting BP. Do better.

    Doodles1983
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    Not sure why she's shocked. If all she got was a pamphlet then had to educate herself... Doctors, due to increasing demand, and population and that we are getting better at diagnostics etc, can't oversee entire patient journeys anymore. And honestly? It is too much for one person. If one person caring for one family member and keeping track of everything is struggling, imagine doctors trying to juggle 10 patients with dementia from diagnosis, to care pathways, support, decline and eventually death. We MUST become better versed about our own health needs. And our elected governments should ensure the supporting packages exist with appropriate people leading them. It truly DOES take a village.

    Bryn
    Community Member
    9 months ago (edited) Created by potrace 1.15, written by Peter Selinger 2001-2017

    I'm having issues believing this... A "prominent" doctor calls some random person (and yes I know she's married to a celeb but still, she's not a doctor!) and discusses a patient with them?! I'd be reporting that doctor the minute I got off the phone with them.

    tameson
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    He was asking about resources. There is nothing that says he revealed anything about his patient.

    Load More Replies...
    Rouch Houz
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    It's the whole health system, doctors aren't to blame individually! They aren't superheroes, they're humans too and they can't be an expert at everything?! (Written by someone also HUGELY let down by the health system!)

    Roni Stone
    Community Member
    Premium
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    I have been have been a full time caregiver for a couple of years now and yesterday, I had to go on anxiety medication. With my own physical limitations and slighter disabilities, I'm at the end of my rope all the time and it's terrifying no knowing if there is anyone to catch me should I lose grip.

    LakotaWolf (she/her)
    Community Member
    Premium
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    I spent my life age 18 to age 39 being the primary caregiver for my completely-disabled father. He had a catastrophic brain injury from an accident, and was bedridden, had a feeding tube, was in diapers, etc. Caregiver burnout is real, and it is devastating. I attempted su!cide twice during the 21 years I helped care for him. He died in 2021 and I'm still not okay. And I loved my father deeply and was happy to stay living at home and pause my entire life to help care for him... but it destroyed my life and it destroyed me. There are very few resources to help family caregivers out, even in supposedly "advanced" countries like America. If you're a caregiver for a family member, please try to take care of yourself as much as possible <3

    Doodles1983
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    This. And ensure access to respite care regularly. Even if it's a few hours. For yourself to regroup. It's not failure. It's not selfishness. It actually enables you to refresh, get new perspective, have some you time and provide better tlc to the person you're responsible for in the long term. This counts for carers of any kind. AND the person being cared for. A change of face can distress some people but it can also reinvigorate THEM. And this goes for parenting too, actually. All the best.

    Load More Replies...
    Patricia Rudolph
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    My LO has been diagnosed with Alzheimer's officially for 5 years. Memory was lost, didn't remember his mother, or past life, acted like a 12 yr old. he was 75, He had some terrible night as he kept asking to go to the bathroom and get up at night. The doctor prescribed a sleeping pill (zolpidem), but it had a very bad side effect on him (delusions and hallucinations) and we decided not to give it any more and went for the Neuro X program that was introduced to us by his primary care doctor, he was on the Neuro X program for Alzheimer’s disease from Uine Health Centre for 6 months. The treatment relieved symptoms significantly, After the treatment he’s all of a sudden back active again, almost all his symptoms are gone, no signs of agitations, his sleeps pattern are back to normal. His memory loss has greatly improved and he tells stories about his past life, we got the Neuro X program from uinehealthcentre. com.

    Libstak
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    As a care giver to my father who had vascular dementia I support this message. I am caring for mum now who is showing signs of memory issues. However, in terms of Gene Hackman...how does a couple with many millions available not have nursing assistance at home daily or at least 3 to 4 times a week fgs? The wife seems to have isolated them both.

    H. B. Nielsen
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    Did they really need to say "Gene Hackman's decomposing body" effiing disgusting BP. Do better.

    Doodles1983
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    Not sure why she's shocked. If all she got was a pamphlet then had to educate herself... Doctors, due to increasing demand, and population and that we are getting better at diagnostics etc, can't oversee entire patient journeys anymore. And honestly? It is too much for one person. If one person caring for one family member and keeping track of everything is struggling, imagine doctors trying to juggle 10 patients with dementia from diagnosis, to care pathways, support, decline and eventually death. We MUST become better versed about our own health needs. And our elected governments should ensure the supporting packages exist with appropriate people leading them. It truly DOES take a village.

    Bryn
    Community Member
    9 months ago (edited) Created by potrace 1.15, written by Peter Selinger 2001-2017

    I'm having issues believing this... A "prominent" doctor calls some random person (and yes I know she's married to a celeb but still, she's not a doctor!) and discusses a patient with them?! I'd be reporting that doctor the minute I got off the phone with them.

    tameson
    Community Member
    9 months ago Created by potrace 1.15, written by Peter Selinger 2001-2017

    He was asking about resources. There is nothing that says he revealed anything about his patient.

    Load More Replies...
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