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Gene Hackman death investigation: Doctor claims Betsy 'didn't know how sick she was' in final days

Gene Hackman death investigation: Doctor claims Betsy 'didn't know how sick she was' in final days

Fox News18-03-2025
Gene Hackman's wife, Betsy Arakawa-Hackman - who was initially thought to have died on or around Feb. 11 due to hantavirus pulmonary syndrome - allegedly did not know the extent of her illness in her final days.
In an exclusive interview with Fox News Digital, Dr. Josiah Child - a physician who oversees Cloudberry Health, the medical practice that Betsy called on Feb. 12 according to preliminary phone records - said the late classical pianist did not initially express symptoms of hantavirus pulmonary syndrome.
"[Betsy] had actually made an appointment to have an initial visit with one of our doctors on the 12th," Dr. Child said. "She called on the 10th saying that her husband was ill or wanted to take care of her husband. She wanted to cancel that appointment. She called back on the 12th and [looking for] advice. She said, 'I have some congestion and I just want some advice. What can I do for it.?' She had no shortness of breath or chest pain or fever or anything like that. Our receptionist spoke to the doctor and the doctor said, 'Well, I've never met her. We have to have an initial appointment.'"
On Monday, the Santa Fe Sheriff's Department confirmed that Betsy's last cell phone activity was Feb. 12, the day after she was initially presumed to have died.
"We can now confirm that Mrs. Hackman's phone was utilized on the morning of February 12 to call a medical center in Santa Fe, Cloudberry Health," the sheriff's department told Fox News Digital. "A total of three calls were made that morning, all to the medical center. One incoming call was made to Mrs. Hackman from the same medical center that afternoon."
According to Dr. Child, the practice scheduled Betsy for a 1 p.m. appointment on Feb. 12 after she called that morning, but she never showed up. The practice then called Betsy, but there was no answer.
"If we had known the patient and known that they had a medical condition or something, then if we try and call them and they didn't call back, we would be more aggressive about finding out what's going on," said Dr. Child. "But in this case, I think, since the doctor had never seen the patient, it was unclear whether maybe she found another doctor or went somewhere else."
"We assumed since she'd never come before that she'd gone somewhere else or maybe to her previous doctor," he added.
Dr. Child said it sounded like Betsy was "starting to feel ill" but was not fully aware of how sick she was actually becoming.
"I don't know whether it was because she was focusing on her husband or because it was a rapidly progressive disease, or she was just one of those people that didn't really feel a lot of discomfort. No one will ever know," he said. "But for some reason she didn't recognize that she was becoming very ill with the second phase of Hantavirus, which invades the lungs."
"She just didn't know how sick she was becoming," he added.
"But for some reason she didn't recognize that she was becoming very ill with the second phase of Hantavirus, which invades the lungs. She just didn't know how sick she was becoming."
Betsy died due to hantavirus pulmonary syndrome, which is transmitted from animals to humans and is commonly found in rodents, the New Mexico Department of Health confirmed.
Hantavirus is characterized by "flu-like symptoms consisting of fever, muscle aches, cough, sometimes vomiting and diarrhea that can progress to shortness of breath and cardiac or heart failure and lung failure," Chief Medical Investigator Dr. Heather Jarrell explained during the news conference.
Hackman died due to hypertensive atherosclerosis cardiovascular disease, with Alzheimer's disease as a significant contributing factor, New Mexico officials confirmed one week ago. He was likely alone in the home for about a week until he died around Feb. 18, which was the last time activity was recorded on his pacemaker.
WATCH: GENE HACKMAN AND WIFE'S CAUSE OF DEATH REVEALED
On Monday, the Hackman estate was awarded a temporary restraining order against the release of records regarding the deaths of Gene and Betsy.
The order stated the "Office of the Medical Investigator and the Santa Fe County Sheriff's Office, including each entities' agents, assigns, and employees are hereby temporarily restrained from disclosing through IPRA or other means, any and all photographs or videos containing images of the following: the body of Gene Hackman, the body of Betsy Arakawa-Hackman, the interior of Mr. and Mrs. Hackman's residence."
Additionally, "any lapel video footage," including the Hackmans' bodies or footage of "images of any deceased animals at the Hackman residence," was added to the temporary restraining order.
The Office of the Medical Investigator was temporarily restrained from disclosing the autopsy and/or death reports, according to the order. A hearing was set for March 31.
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My Son And I Were Turned Away From Ikea's Play Area For A Disturbing Reason. Here's What They Don't Understand.
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My Son And I Were Turned Away From Ikea's Play Area For A Disturbing Reason. Here's What They Don't Understand.
My Son And I Were Turned Away From Ikea's Play Area For A Disturbing Reason. Here's What They Don't Understand.

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My Son And I Were Turned Away From Ikea's Play Area For A Disturbing Reason. Here's What They Don't Understand.

In late June, a few days before Disability Pride Month began, I took my 7-year-old child on an outing to an Ikea store. As I filled out a waiver so he could enter the store's small play area, I noticed I was the only parent present. It turned out that parents typically drop off their children while they shop, but that wasn't an option for me. My son has a rare, severe form of epilepsy called Dravet syndrome, among other medical conditions, and he can't be without a grown-up carrying his seizure rescue medication, as I was. The scary reality is that around one in five children with Dravet syndrome die in childhood because the seizures can be so severe. There is currently no cure. I explained this to a staff member and told her that I'd need to be in the room with my child. She informed me that no parents were allowed into the play area. 'But isn't there a policy for kids with disabilities?' I asked. She told me a service dog could accompany a child, but a parent could not. I stopped signing the form. I said to the staff member, 'That's discrimination against kids with disabilities.' She didn't respond. I hadn't known about the store's play area before this visit, and I had been happy to see that it wasn't a playground ― just a space with toys like a train set and dart board. Since my son had a seizure at an indoor playground a year ago, I'd stopped taking him to them. But now, even this play space was not an option for him. My child and I were both upset. He loves going to Ikea to walk through the showroom and eat in the cafeteria ― a place open enough that it was the only indoor restaurant he ate in during our four years of masking during the COVID-19 pandemic. We have several Ikea furniture items, including bunk beds, a coat/shoe cubby and a toy chest. He helped us build them all. Since his severe seizures began about two years ago, he's had to change his life in significant ways. Heat, sports, just running around to play, illness and excitement have all become triggers for him. Summer is especially hard — on hot days, he can't be outside. In fact, we had driven the hour to Ikea in traffic just so he could walk and have a change of scenery in a large, air-conditioned space because the temperature outside was dangerous for him. I told him, 'This isn't OK.' He said, 'We should talk to someone.' I was proud of him. After talking to a few staff members, we spoke with a manager, who said he wasn't familiar with the policy, and he'd get back to me the next day. He didn't. Later, I looked online, and there was a section on the Ikea website directing caretakers of children with disabilities to start a conversation with the Ikea store manager about how the child can best have their needs accommodated in the play area. I was hopeful that when we went in the future, we could show the policy to the staff. However, that doesn't undo the pain my child felt after hearing that he wasn't welcome in that play space because of his disabilities. During the hour-long car ride home afterward, we talked a lot about discrimination. I reinforced that what happened wasn't OK, and that the more than 3 million kids with disabilities in our country deserve to be included. I told him about my older sister, his late aunt, who had microcephaly and faced various barriers to equal access too, like having to sit on the sidelines of playgrounds in her wheelchair. It upset me. When I was 10 in 1993, I read about new accessible playgrounds in an issue of Scholastic News, and I hoped we could build one for her. Sadly, she died a few weeks later, but in her memory, my family and I worked with the Cincinnati Parks Department to build an accessible playground. My son thought that was cool. I also explained that many groups of people face discrimination for reasons such as gender, race, sexual orientation, immigration status and more, and we need to be allies and stand up against all forms of discrimination. I also told him that one way to help is to make disabilities more visible and raise awareness, as we have done in his school class for the past three years. This June, for Dravet Syndrome Awareness Month, he and I held a neighborhood lemonade and cupcake fundraiser and donated money to the Dravet Syndrome Foundation, which helps fund the kind of critical epilepsy research that the Trump administration has recently cut. After our experience at Ikea, as one of his bedtime books, we re-read the picture book All the Way to the Top, about a child who protested and helped advocate for the Americans with Disabilities Act, which passed 35 years ago. Afterward, I told him about children with disabilities who went to Congress this summer, asking their leaders not to make it harder for them to go to the doctor and get the medicine and treatment they need. Unfortunately, President Donald Trump's domestic policy bill has since passed, and many people, including children with disabilities, will be harmed as a result. Two days after the bill passed, my child woke up and said, 'I want to make a sign about disabilities.' He asked for my help with spelling before writing the words 'People with disabilities are important' in pencil and then tracing over them with marker. He stood by our Disability Pride yard sign, and then, since the temperature was cooler out, he walked down our street and held it up for cars passing by. He said that when he grows up, he wants to be an 'activist' and 'protester.' I told him that he already is. [Editor's Note: HuffPost reached out for a response, and Ikea US issued the following statement: 'At IKEA, we strive to offer a safe and inclusive environment for children to play while in our stores. Our Småland policies are in place to keep children safe when they are in our space. Regarding this family's recent experience in our College Park, MD store, we are incredibly sensitive to feelings of exclusion, and so we have shared information with the family about our accommodations process, so that they may have a more positive experience at IKEA. We are constantly working to improve how we create an inclusive space while maintaining policies that keep all children safe.'] This article originally appeared on HuffPost in July 2025 and was updated in August 2025.

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