
Thinking about taking a stab at IV therapy? Ask some questions first
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.
How many IV clinics are there?
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.
What should customers know about IV therapy clinics?
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.
Why are regulators concerned?
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.
Is there too much patient involvement?
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.
What's the big picture?
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.
'Usually within eight hours, all that expensive therapy (is) peed out,' he said.
___
The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute's Science and Educational Media Group. The AP is solely responsible for all content.
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Los Angeles Times
24 minutes ago
- Los Angeles Times
Why People Delay Dental Visits, and What It Means for Their Health
Missing or putting off dental appointments may seem harmless in the short term but over time those delays can have long term consequences – not just for your teeth but for your overall health. From cavities in toddlers to infections in cancer patients, understanding why people put off treatment is the first step to changing those habits. Research shows those delays are rarely about laziness – they're more often about cost, anxiety, lack of support and access barriers with lack of dental insurance or not being covered by a dental plan being a common reason for delay. Table of Contents Dental delays are more common than you think. A 2025 cross-sectional study found that over 71% of preschoolers with cavities didn't get treated right away. The average delay? Nearly four months—117.5 days [1]. Reasons ranged from financial hardship and logistical challenges to caregivers not knowing their child had a problem until it got worse. Dependents like children rely on caregivers to find the right dental care and meet the requirements for timely treatment. And it's not just kids. During the COVID-19 pandemic, nearly half of U.S. adults admitted to putting off dental care [4]. What's interesting is that urban residents—despite having more dentists nearby—were more likely to delay treatment than those in rural areas. That means it's not just about distance; stress, work schedules and transportation logistics may be just as big of a factor. Fear is a powerful barrier. A 2023 study found that dental anxiety and low self-efficacy—the belief that one can't handle the stress or logistics of dental treatment—were stronger predictors of delay than simple procrastination [3]. In plain terms, some people aren't avoiding the dentist because they don't care—they're overwhelmed, nervous, or unsure how to take the first step. In older adults, social support can make all the difference. Research from China on oral cancer patients found that those who lived with their adult children were less likely to delay treatment [2]. When people feel supported, they're more likely to seek care promptly. We hear all the time about the importance of early dental visits for kids but the data tells a more complicated story. A 2012 Medicaid study found no significant difference in outcomes between kids who had their first dental visit before 18 months and those who started later [5]. Early care is important but maybe not as early as some programs suggest. Dental benefits and dental coverage for kids are based on state Medicaid policies and kids have to qualify for these services according to specific criteria. That could help us target our prevention efforts more effectively. Meanwhile dental neglect—intentional or not—remains a big problem. States vary in how they provide dental services and preventive services to kids through Medicaid. A global review found 34-56% of kids and teens are affected by dental neglect [8]. Whether it's financial strain or caregivers not knowing the signs of dental disease, the takeaway is clear: education and access matter just as much as timing. Dental health doesn't exist in isolation. For patients undergoing cancer treatment, a minor dental issue can be life threatening. If a dental problem is left untreated it can complicate or delay cancer therapy. A 2018 systematic review found a high rate of untreated dental infections like pericoronitis in oncology patients [9]. These infections can delay or complicate chemotherapy and radiation. That's why cancer care teams are working more closely with dental professionals – often involving a dental practice to treat emerging oral health issues as they arise – to catch problems early and avoid preventable setbacks. If a tooth has been neglected for too long many people assume the only option is to extract and replace. But is that always the best choice? The goals of dental treatment should include both preserving natural teeth whenever possible and patient preferences for long term outcomes. A 2013 review compared long term outcomes of preserving compromised teeth vs replacing them with implants. Surprisingly well maintained natural teeth lasted longer than implants [10]. This finding supports the value of early conservative treatment – acting sooner means saving teeth rather than replacing them. Not directly related to delays but a 2022 Cochrane review on full-mouth disinfection for periodontitis brings up a related question: timing matters but so does method. Not all periodontitis cases need antibiotics and overtreatment should be avoided. Full-mouth treatment is meant to be aggressive but the evidence didn't show it was superior to step-by-step scaling and root planing [6]. It raises the question of overtreatment especially when antibiotics are involved. This applies outside of dentistry too. A 2025 study on statin therapy in diabetic patients found that delays in preventive care even when not related to teeth led to worse outcomes [7]. The lesson applies across all medical disciplines: proactive care is better. Delaying dental care isn't about being lazy—it's about fear, finances, logistics and sometimes just lack of information. What's clear is that delays are costly in dollars and in health. Fixing this requires a multi-faceted approach: Timely dental care doesn't just save smiles it saves overall health and quality of life. [1] Huang, J., Sun, J., Ji, Y., Chen, C., Yang, Z., & Zhao, H. (2025). Analysis of factors influencing delayed treatment seeking for dental caries in preschool children: a cross-sectional study. BMC public health, 25(1), 1669. [2] Yang, Y., Ning, H., Liang, B., Mai, H., Zhou, J., Yang, J., & Huang, J. (2024). Exploring Factors Influencing Patient Delay Behavior in Oral Cancer: The Development of a Risk Prediction Model in Western China. Healthcare (Basel, Switzerland), 12(22), 2252. [3] Steinvik, L. M., Svartdal, F., & Johnsen, J. K. (2023). Delay of Dental Care: An Exploratory Study of Procrastination, Dental Attendance, and Self-Reported Oral Health. Dentistry journal, 11(2), 56. [4] Kranz, A. M., Gahlon, G., Dick, A. W., & Stein, B. D. (2021). Characteristics of US Adults Delaying Dental Care Due to the COVID-19 Pandemic. JDR clinical and translational research, 6(1), 8–14. [5] Beil, H., Rozier, R. G., Preisser, J. S., Stearns, S. C., & Lee, J. Y. (2012). Effect of early preventive dental visits on subsequent dental treatment and expenditures. Medical care, 50(9), 749–756. [6] Jervøe-Storm, P. M., Eberhard, J., Needleman, I., Worthington, H. V., & Jepsen, S. (2022). Full-mouth treatment modalities (within 24 hours) for periodontitis in adults. The Cochrane database of systematic reviews, 6(6), CD004622. [7] Shah, N., Lan, Z., Brown, C. J., Martin, S. S., & Turchin, A. (2025). Impact of Statin Nonacceptance on Cardiovascular Outcomes in Patients With Diabetes. Journal of the American Heart Association, 14(11), e040464. [8] Khalid, G., Metzner, F., & Pawils, S. (2022). Prevalence of dental neglect and associated risk factors in children and adolescents-A systematic review. International journal of paediatric dentistry, 32(3), 436–446. [9] Hong, C. H. L., Hu, S., Haverman, T., Stokman, M., Napeñas, J. J., Braber, J. B., Gerber, E., Geuke, M., Vardas, E., Waltimo, T., Jensen, S. B., & Saunders, D. P. (2018). A systematic review of dental disease management in cancer patients. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 26(1), 155–174. [10] Levin, L., & Halperin-Sternfeld, M. (2013). Tooth preservation or implant placement: a systematic review of long-term tooth and implant survival rates. Journal of the American Dental Association (1939), 144(10), 1119–1133.


USA Today
5 hours ago
- USA Today
How Trump's tax bill could cut Medicaid for millions of Americans
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The legislation amounts to "the biggest rollback in health care coverage in the history of the United States," said Joan Alker, a research professor and executive director and co-founder of Georgetown University's Center for Children and Families. Vice President JD Vance, who cast the tiebreaking vote July 1 to pass the Senate bill 51-50, said in social media posts the Medicaid cuts are "immaterial" compared to savings the bill will fund through bolstered immigration enforcement. The House is scheduled to consider the legislation on July 2 in advance of Trump's self-imposed July 4th deadline for his signature domestic policy legislation. How will the legislation cut Medicaid? The legislation would require states to double eligibility checks to twice a year. And states, which administer Medicaid, would have to set up systems to verify a person's employment or exemption status. The legislation requires "able-bodied" Medicaid recipients to work 80 hours a month or qualify for an exemption, such as being a student, caregiver or having a disability. The original House version limited the work requirement to low-income adults without children, but the Senate version added the work requirement to parents of children older than 13. The legislation defines "able-bodied" people as those not medically certified as physically or mentally unfit for employment. The legislation also would strip coverage from undocumented immigrants who get Medicaid through state-funded programs. Health policy experts say more frequent eligibility checks and red tape will add administrative costs and cut off people who qualify but fall through the cracks because of administrative miscues. What do hospitals and doctors think of bill? Medicaid insures 83 million low-income children and adults, according to KFF, a health policy nonprofit. That represents more than 1 in 5 Americans. Health policy experts have warned the cuts could harm rural hospitals and doctors who serve a higher percentage of people enrolled in Medicaid. The Senate bill added a $50 billion rural health care fund, double the amount that an earlier version of the legislation proposed. Still, hospitals are "deeply disappointed" the bill cleared the Senate, said Rick Pollack, president and CEO of the American Hospital Association, a trade group. Pollack said the $1 trillion in Medicaid cuts would cause "irreparable harm to our health care system," and reduce access to care for all Americans. Hospitals are required to diagnose and stabilize anyone who visits an emergency room. Eliminating coverage of nearly 12 million Americans will "drive up uncompensated care for hospitals and health systems," Pollack said. Pollack said hospitals might be forced to cut services and staff, and patients could face longer wait times in emergency rooms. 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A KFF survey found nearly 2 in 3 people on Medicaid are employed full or part time, and others would qualify for an exemption from the work requirement because they are caregivers or students. Just 8% were not working due to inability to find work, retirement or other reasons, KFF said. While the bill doesn't mandate work requirements before January 2027, states will likely need to plan for big changes before then, said Jennifer Tolbert, deputy director of the KFF program on Medicaid and the uninsured. States will need to prepare for smaller Medicaid payments from the federal government while adding the extra administrative duties of verifying an enrollee's work or volunteer status. "Some states are anticipating this reduced revenue," Tolbert said. "At the same time, they are also required to make pretty costly changes to their eligibility systems." 'Death by a trillion cuts': Health care workers lobby Republicans in Congress Johannah Alabi's days usually consist of feeding, bathing, and caring for residents at two nursing homes in Bloomfield, Conn. She said most of her patients depend on government health insurance programs, so she is concerned about what will happen to them and her job if Trump signs the bill into law. Medicaid is the primary payer for 63% of nursing home facility residents and an additional 13% rely on Medicare as their primary payer, according to KFF, a health policy nonprofit headquartered in San Francisco. 'If some of that money is going to be taken away, something has to give,' Alabi said. 'It's going to come down to the resident care. It's going to come down to the food. It's going to come down to the activities.' That's why she was inspired to join Service Employees International Union members to lobby lawmakers to vote against the bill last week. They arrived at the Capitol with signs reading, 'Death by a trillion cuts,' and wearing shirts with the message, 'Republican cuts kill.' Jennifer Woods, another SEIU member who works in the claims department at Kaiser Permanente, ran into Sen. Ted Cruz, R-Texas, during her trip to Washington. She said she tried to explain how cuts could 'ruin people's lives' and potentially lead to some patients' deaths as she followed him through the Capitol building. 'He just shook his head and would keep going,' Woods said. 'He didn't really say anything. None of them did.'
Yahoo
9 hours 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. At 19, she met her future husband, Kane, and they lived in Seattle, where they dreamed of building a life and starting a family. But those dreams came with difficult questions. Genetic testing revealed a 50% chance their children could inherit LAD. Still, the couple moved forward with hope. At 21, Madison became pregnant with their first child, a boy. But what should have been a joyful milestone quickly turned to fear: during their first ultrasound, doctors couldn't find the baby's left arm. "I remember we went home and we cried," Madison, now 34, tells PEOPLE exclusively. "It was a terrifying pregnancy. I didn't share it with anyone — not out of shame, but for my own emotional protection. I needed to hold on to some normalcy." Genetic testing during the pregnancy showed no signs of LAD. Even so, doctors raised concerns about the baby's quality of life due to his missing limb. Until 24 weeks, some even discussed termination. But Madison held firm in her belief that her son was healthy and whole. When Ryker was born, he was missing his left arm and was later diagnosed with hearing loss. But the biggest moment came after birth: postnatal genetic testing confirmed he had inherited LAD. 'It was really shocking to us,' Madison says. 'We thought we had beaten the odds.' Even knowing the challenges ahead, Madison and Kane still felt their family wasn't complete. In early 2020, they began preparing for in vitro fertilization (IVF) to reduce the risk of passing on LAD. Then the COVID-19 pandemic hit, and everything was put on hold. Once clinics reopened, they resumed the IVF process — until life took another unexpected turn: Madison became pregnant naturally. 'Honestly, we were terrified,' she says. 'After everything with Ryker, we didn't know what to expect.' Their second son, Rhett, was born with differences in both arms and was completely deaf. Two months after his birth, the weight of it all hit Madison during a quiet drive home with Rhett in the backseat. 'I called Kane, sobbing on the freeway,' she remembers. 'And he said, 'Whatever is meant to be has already been written. It is what it is. We just keep moving forward.' ' That mindset has carried them ever since. Today, Madison and Kane, also 34, focus on empowering their boys — celebrating what they can do rather than dwelling on what they can't. Over the years, they've watched Ryker, now 11, learn to use his feet for everything from writing and eating to playing video games. His growing confidence inspired the family to begin sharing their journey on social media, where they've built a following of nearly 46,000 people. 'He loves showing people what he can do,' Madison says. 'He's really the one who started all this. Just this morning, as I dropped him off at school, he said, 'Mom, maybe tonight we can take a video of me playing video games so I can show everyone how I do it.' ' One recent video of Ryker figuring out how to open a car door on his own drew more than 10 million views and nearly 9,000 comments. Another, showing Ryker and Rhett, 3, helping Madison make burgers with their feet, garnered 8.6 million views and 10,000 comments. 'Some people think using your feet is gross or dirty,' Madison says. 'But what they don't realize is that Ryker washes his feet constantly. The first thing he does when we get home is wash them. Before dinner, he washes his feet. Just like someone else would wash their hands — he washes his feet. Honestly, they're probably cleaner than most people's hands.' 'So many of the comments we get are negative — people saying Ryker is going to struggle his whole life," she adds. "But that's exactly why we share the adaptive tools and show how he does things. 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. The only time he might ask for help is when his foot gets tired.' One of their biggest adaptive wins is a custom shower setup — a large sponge filled with soap that attaches to the wall. Ryker can press against it to wash his back, shoulders and even his hair. But being outside the home comes with different challenges. 'Right now, we're not doing sleepovers or letting him go to friends' houses unless we're really close with the family,' Madison says. 'He's good about asking for help, but he's at a vulnerable age. We want to protect his dignity and independence as much as we can.' 'At home, he uses a bidet and has a solid routine," she adds. "At school, he goes to the nurse's office. They've created a comfortable system for him, and he's really confident with it.' Rhett's routine is different. He attends multiple therapy sessions each week — sometimes three in a single day — and recently started preschool for deaf and hard-of-hearing children. Since he's young, he still doesn't understand much yet. "I think with Rhett, I don't think he'll have as hard of a time because his brother is like him and he thinks his brother is the coolest person in the entire world," Madison adds. "Anything that his brother does, he wants to do, he wants to dress the same, he wants to act the same, he wants to do the same things." Through it all, Madison and Kane have leaned on a strong support system that has helped them stay grounded. 'We're really lucky,' she adds. 'Our family is amazing — they love our boys like their own. They've been a huge part of our journey, and we feel incredibly fortunate to have that kind of support.' 'I also had a lot of surgeries and doctor visits growing up, and I always felt a little different,' she continues. 'So I can relate to my kids. But more than anything, it's helped me understand that having a physical disability doesn't mean something is wrong. My boys are thriving. 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