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Columbine Survivor Dies 25 Years Later of Complications From Shooting

Columbine Survivor Dies 25 Years Later of Complications From Shooting

Yahoo18-02-2025
Anne Marie Hochhalter, who was shot in the back during the 1999 Columbine shooting, was found dead in her home Sunday, according to the Denver Post.
Sue Townsend, whose stepdaughter Lauren was killed in the shooting, formed a close relationship with Hochhalter after the shooting, which left 15 people dead. She and her husband told the Post that Hochhalter's death appears to be from complications she suffered from the shooting.
'She was fiercely independent,' Sue Townsend told the newspaper. 'She was a fighter. She'd get knocked down — she struggled a lot with health issues that stemmed from the shooting — but I'd watch her pull herself back up. She was her best advocate and an advocate for others who weren't as strong in the disability community.'
Hochhalter was a 17-year-old junior at Columbine High School in Colorado eating lunch outside when one of the two shooters shot her in the back. Hochhalter told People in 2004 that when she was first shot, she thought it was from a paintball gun.
'I was bleeding to death,' Hochhalter told People in 2004. 'It didn't look bad on the outside, but inside it felt wrong — it felt wet.'
The shooting left Hochhalter paralyzed and wheelchair-bound.
In 2016, Hochhalter wrote in a Facebook post that she holds no bitterness toward Sue Klebold, the mother of one of the shooters.
'It's been a rough road for me, with many medical issues because of my spinal cord injury and intense nerve pain, but I choose not to be bitter towards you,' Hochhalter wrote. 'A good friend once told me, 'Bitterness is like swallowing a poison pill and expecting the other person to die.' It only harms yourself. I have forgiven you and only wish you the best.'
School shootings have risen over the past 25 years, according to the American Academy of Pediatrics and in 2024, then-U.S. Surgeon General Vivek Murthy declared gun violence to be a public health crisis.
If you or someone you know needs help, call or text 988 or chat 988lifeline.org for mental health support. Additionally, you can find local mental health and crisis resources at dontcallthepolice.com. Outside of the U.S., please visit the International Association for Suicide Prevention.
Teen And Friends Held At Gunpoint After 'Ding-Dong Ditch' Gone Wrong, Police Say
This 'Degrassi' Plotline Was Inspired By Columbine — And It's Just As Relevant Today
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Kate Middleton opens up about life after cancer. ‘Really, really difficult'
Kate Middleton opens up about life after cancer. ‘Really, really difficult'

Miami Herald

time17 hours ago

  • Miami Herald

Kate Middleton opens up about life after cancer. ‘Really, really difficult'

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She Was Told to Terminate Her Pregnancy. Now She's Raising 2 Sons Who Are Inspiring Millions (Exclusive)
She Was Told to Terminate Her Pregnancy. Now She's Raising 2 Sons Who Are Inspiring Millions (Exclusive)

Yahoo

time2 days ago

  • Yahoo

She Was Told to Terminate Her Pregnancy. Now She's Raising 2 Sons Who Are Inspiring Millions (Exclusive)

Madison Sisson was born with leukocyte adhesion deficiency (LAD syndrome) Despite the diagnosis, Madison's childhood felt surprisingly "normal." At 19, she met her future husband, Kane, and they lived in Seattle, where they dreamed of building a life and starting a family However, genetic testing revealed a 50% chance their children could inherit LAD. Still, the couple moved forward with hope and at 21, Madison became pregnant with their first childFrom the moment Madison Sisson was born, life presented challenges. She arrived with only four fingers on her left hand and, unbeknownst to doctors, a rare immune disorder that wouldn't be diagnosed until she was 9 months old. The condition — leukocyte adhesion deficiency (LAD syndrome) — is so rare that most people have never heard of it. It's present from birth and affects the body's ability to fight infections. Despite the diagnosis, Madison never saw herself as different. 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We want to change the way people view disability. It's not about living a horrible life or struggling forever." As much as Ryker now enjoys sharing his abilities with the world, Madison remembers the quiet, early moments when he first began to understand his differences. She shares that Ryker didn't really start putting two and two together about his arm until he was around 4 years old. "He would look at himself in the mirror and say, 'Ryker has one arm and Mommy has two,' " Madison recalls. "Honestly, it was never something we had to explain or make a big deal about — it just was." It wasn't until he was about 7 or 8 that mother and son had their first real conversation about it. One night, he got emotional and started crying, asking Madison, 'Why am I like this?' "That was a really hard moment as a parent," she adds. "I sat with him and told him, 'God makes everybody different — sometimes on the outside, sometimes on the inside. No two people are exactly the same. You can see your difference, like how you have one arm and Mommy has two, or how I have four fingers and Daddy has all of his. But everyone has something that makes them unique.' ' That emotional night marked a turning point — not in how Madison saw her son, but in how she began guiding him through moments of doubt while nurturing his growing independence. As Ryker grows, that independence continues to blossom, though some tasks still require creative solutions. He attends a public school and is in general education classes. He has a paraprofessional available if needed, but Madison says he rarely uses the support. The family is currently testing dressing sticks to help with clothing, and Ryker is adapting quickly. At home, they've installed wall hooks that allow him to pull his pants up and down on his own. 'For the most part, he's got it down,' she says. 'He writes with his feet, so he has a special chair at his desk and another one at lunch for positioning. 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They're just like any other kids — they might do things differently or need a little more help, but they're just as capable.' One of Madison's biggest goals is not only helping her sons feel proud of who they are, but helping others see their abilities, not just their differences. When children stare, seem scared or appear unsure, Madison redirects their focus with positivity and curiosity. 'Ryker has always handled it really well," Madison says. "He'll just shrug it off like it's no big deal. He doesn't like to make it a thing. He'll say, 'Yeah, they're looking at me,' and move on. But me? I get a little mama bear when it's adults. I'll say something like, 'He's really cute, huh?' just to break the tension.' 'I'll say, 'Want to know something really cool? He does everything with his feet,' " she adds. " 'He eats, writes, colors, plays video games — all with his feet. He doesn't even need hands.' And suddenly, they're fascinated. They'll be like, 'What?! That's so cool!' And next thing you know, they're trying it themselves. It's hilarious.' As for the future, Madison says the family plans to continue sharing their journey online. And while negativity still finds its way in, the overwhelming love and support has made a lasting impact. 'There have been thousands of amazing comments,' she says. 'I was reading Ryker's page the other night and just started bawling because I was like, 'Oh my God — the amount of good humans there are.' Life can feel really heavy sometimes, and the world can feel really heavy. But then you read comments from people who think your kid is just incredible.' She adds. 'Some of Ryker's favorite comments are things like, 'You're the coolest kid on the Internet,' or, 'You're the coolest kid on this app.' He loves those — they've been really special. People say his superpower is using his feet, which is so cute. And there are so many others who say things like, 'God bless your family,' or, 'We love your videos.' It's overwhelming in the best way. Just so many people saying how much they love our kids — it means the world to us.' 'The whole point is to raise our kids to be as independent as possible — to give them the confidence and tools they need to one day leave the nest, build a family, and live a full life on their own,' she adds. 'I don't want them to rely on me or anyone else. I want them to feel capable, just like their peers." Read the original article on People

Thinking about taking a stab at IV therapy? Ask some questions first

time2 days ago

Thinking about taking a stab at IV therapy? Ask some questions first

IV therapy clinics are springing up around the country, touting quick ways to recover from a hangover or a hard workout. But doctors and regulators preach caution. The services have been on a growth spurt since the COVID-19 pandemic, offering drips that promise to boost energy, gird immune systems or relieve joint pain. This is done from bags of intravenous fluids normally seen hanging next to hospital beds. Customers must be willing to fork over as much as couple hundred dollars for each session — in some cases for a mixture of vitamins and supplements that would be considerably cheaper in pill form. Proponents say this approach helps customers hydrate faster and absorb more of a vitamin or supplement than they would by swallowing pills. But Dr. Sam Torbati, co-chair of emergency medicine at Cedars-Sinai Medical Center in Los Angeles, says the therapy mostly helps people create 'expensive urine,' with the body clearing what it doesn't use. They're hard to count, partly because some businesses just provide IV therapy while others offer it as part of a medical spa. The practice grew popular during COVID-19, when access to doctors became limited and people grew more concerned about their immune system health, according to the American IV Association, an industry group. Regulators in Ohio are following the trend closely in their state, which now has around 200 clinics. These businesses were largely unheard of there before the pandemic, said Cameron McNamee, a spokesman for the Ohio Board of Pharmacy. Doctors say there are some good questions to pose before any treatment starts. Customers should ask the person starting the IV how long they have been doing their job and what sort of training they have, said Torbati. They also should know what's in the IV drip. For instance, 'Wonder Juice' treatment offered by the Restore Hyper Wellness franchise combines six vitamins and supplements that are available, in oral form, on the pharmacy store shelves. Knowing all the ingredients comes in handy if someone has an allergic reaction. Also ask where the company gets its drugs, if any are used. The answer should be a licensed pharmaceutical wholesaler, according to McNamee. Otherwise, the drug could be counterfeit or substandard. Ohio regulators have suspended the licenses of businesses that purchased drugs on Facebook. Customers also should make sure the clinic is in decent shape when they visit. 'If the office isn't clean, then the IV room's probably not clean either,' McNamee said. They don't like that a nurse or a paramedic often helps a customer decide on an IV therapy and then delivers the treatment. Rules can vary, but many state regulators say a doctor, physician assistant or nurse practitioner should be involved. The clinics often run on standing orders, which are issued by a doctor with the idea that they give the nurse or paramedic permission to treat patients according to certain protocols. Hospital emergency rooms regularly operate on the same kind of orders, according to Dr. Chris Seitz, an emergency physician and chairman of the American IV Association's scientific advisory board. 'Many nurses saw patients before I ever could get to them in the emergency department and initiated care like IV fluids,' he said. Regulators also worry about the role customers play in picking their own treatments. 'A patient cannot enter a doctor's office or hospital and demand an IV any more than a patient can direct his or her own appendectomy,' Kentucky officials said in a March statement. But Seitz says there should be a partnership between any care provider and the patient, with the provider helping the patient make the right decision. 'Patients have a requirement and a need to be the CEO of their own health,' he said. Patient choice feeds another worry: the mixing of ingredients for specific treatments, a practice known as compounding. South Carolina regulators said in a 2023 statement that this should result from a valid care provider order, 'not from a patient-driven menu akin to a fast-food restaurant.' However, proponents say the addition of vitamins or drugs to an IV treatment should not be confused with mixing prescription drugs in a lab. 'It's just pretty simple low-hanging fruit in terms of clinical complexity,' said Jeff Cohen, a co-founder of the American IV Association. IV therapy clinics do provide some care. They can help cancer patients or pregnant women stay hydrated. Some treatments offer relief from migraine pain. But many drips require the creation of a sterile, soluble vitamin or supplement that is safe to put into someone's veins. That's more expensive to make than a vitamin that may cost a few cents a pill, Torbati noted. Customers will need to determine whether the added expense is worth it. 'Usually within eight hours, all that expensive therapy (is) peed out,' he said. ___

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