Federal judge dismisses lawsuit over medicaid oversight but allows amended complaint
A federal judge this week dismissed a lawsuit alleging the state failed to provide adequate oversight of Medicaid managed-care plans that care for people in their homes, but he gave plaintiffs three weeks to file an amended complaint.
The lawsuit, filed in September on behalf of five adults with disabilities such as quadriplegia, Alzheimer's disease and debilitating genetic disorders, contends managed-care plans have not provided adequate information about decisions to reduce or deny services. Also, it contends a Florida Agency for Health Care Administration hearing process for appeals does not hold the plans accountable.
But, siding with the state agency, U.S. District Judge Robert Hinkle's ruling said the plaintiffs lacked legal standing because none of them alleged they are not receiving services they need or are facing a reduction or denial of services.
Hinkle gave the plaintiffs until April 24 to file an amended lawsuit and instructed them to 'address head-on the lack of a concrete, imminent injury to the plaintiffs themselves that is traceable to' the state health-care agency.
The lawsuit alleged that notices sent to plaintiffs about benefits did not include enough information, failed to include policies or were received late. 'But none of the plaintiffs are currently facing a reduction in benefits.
It is speculative that any plaintiff will face a reduction or denial of benefits in the future. It is even more speculative that the various issues they experienced in the past related to the notices will recur.
Moreover, even in the past instances where the notices were allegedly insufficient, the plaintiffs for the most part ultimately succeeded in challenging the reduction or denial either before the plan or before AHCA,' Hinkle wrote in the 18-page ruling Wednesday.
In addition, the judge said 'the issues with the notices are not traceable' to the state agency, which has contracts with the managed-care providers requiring that their plans comply with federal law.
The plaintiffs also alleged that benefits were reduced while the review process was ongoing, which the secretary of the agency acknowledged 'is not supposed to happen,' Hinkle wrote. 'There apparently is no nonspeculative basis to believe it will happen again,' the judge wrote, adding 'there is also no reason to believe' the issue was traceable to the agency.
Click here to download our free news, weather and smart TV apps. And click here to stream Channel 9 Eyewitness News live.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
15 minutes ago
- Yahoo
50+ Alabama groups urge Gov. Ivey, legislators to oppose cuts to Medicaid, ACA coverage
MONTGOMERY, Ala. (WHNT) — A slew of organizations are urging Gov. Kay Ivey and state lawmakers to oppose healthcare cuts in the U.S. House's budget reconciliation bill. In a letter initiated by the Cover Alabama Coalition, 52 organizations are asking state policymakers to contact members of Congress and express concerns about the bill's negative impact on Alabama's families and budgets. 'This legislation would undermine Alabama's ability to manage its Medicaid program, limit our future options and increase barriers to coverage for families across our state,' the letter reads. On May 22, the U.S. House approved a huge budget bill, 215-214. The groups contend the bill — which among its provisions extends and creates new tax cuts and creates new spending for a border wall and immigration enforcement — would also either drive the costs of healthcare up or make it inaccessible for millions of people. 📲 to stay updated on the go. 📧 to have news sent to your inbox. 'The bill … would allow the enhanced Affordable Care Act (ACA) subsidies to expire, making Marketplace plans less affordable for more than 400,000 Alabamians,' the letter reads. 'This would result in coverage losses and higher uninsured rates, especially among working families who don't qualify for Medicaid but can't afford full-price private plans.' Expiration of enhanced ACA tax credits would cost Alabama an estimated 10,000 jobs and $1.14 billion in GDP in 2026, the groups contend. The groups also say if the budget bill is given final approval it would cost Alabama $619 million in extra federal funding that would help cover the first two years of Medicaid expansion. The bill would also freeze provider taxes at current levels, which would limit the state's future options for funding Medicaid by forbidding legislators to increase fees on nursing homes, ambulance services and other providers. The groups say the bill would also would reduce the retroactive Medicaid coverage period from three months to just one. This change could leave many pregnant women and other Alabamians in greater medical and financial risk. It also would undermine a new law that the Legislature passed this year to remove red-tape barriers to Medicaid coverage for thousands of mothers who are expecting. The letter encourages state policymakers to reach out to Alabama's congressional delegation and urge them to oppose the bill. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.


Axios
18 minutes ago
- Axios
Senate GOP eyes Medicare cuts with Trump's blessing
President Trump gave Republican senators a green light to explore ways to save money on Medicare during a meeting at the White House, senators said Thursday. Why it matters: Changes to save money on Medicaid have already proven contentious with some Republicans. Medicare could open a new can of worms. "The president is willing to eliminate any waste, fraud and abuse anywhere," Sen. Ron Johnson (R-Wisc.) told Axios about the White House meeting Wednesday night that he attended, "which opens up Medicare, as well," he added. "What the president made clear is he does not want to see any cuts to beneficiaries, but to go after... the waste, fraud and abuse," said Sen. Steve Daines (R-Mont.), clarifying that Trump opened up Medicare as an option at the meeting. Politico first reported on the Medicare discussions. What to watch: One possibility being floated is a bill from Sen. Bill Cassidy (R-La.), which would get savings from the Medicare Advantage program. The measure would crack down on an insurer practice known as "upcoding," where health insurers classify patients as sicker in order to secure higher government payments. Cracking down on the practice has some support from Democrats as well, but would be sure to draw the opposition of the health insurance industry.


Boston Globe
31 minutes ago
- Boston Globe
RFK Jr. wants to allow more experimental therapies, acknowledging health risks and threat of ‘charlatans'
'And of course you're going to get a lot of charlatans, and you're going to get people who have bad results,' he added. 'And ultimately, you can't prevent that either way. Leaving the whole thing in the hands of pharma is not working for us.' Advertisement Kennedy cited his own experience at a clinic in Antigua, where he said he received a stem cell treatment that 'enormously' eased his neurological condition, spasmodic dysphonia, which affects his voice and has few treatment options. Get Starting Point A guide through the most important stories of the morning, delivered Monday through Friday. Enter Email Sign Up If Kennedy does permit broader use of unauthorized or experimental therapies, he would be reversing long-standing efforts by the FDA to monitor and sometimes police the emerging field. Experts, including some who support alternative medicine, worry that without safeguards, an expansion of such treatments could undermine legitimate development of new therapies. The FDA now narrowly permits stem cell therapies to treat blood and immune disorders. Nearly a decade ago, the field was so loosely regulated that the agency pursued court actions to shut down rogue clinics using unauthorized treatments for a wide array of ailments. Some providers in the United States and in other countries continue to offer experimental stem cell therapies for everything from autism to Alzheimer's to erectile dysfunction. Advertisement The latest move reflects an expansion of Kennedy's drive to dismantle federal health policy to reflect his long-held views, which had so far focused mainly on vaccines, chronic diseases, food dyes and fluoride. A push to open up the field of unregulated stem cell infusions meshes with his oft-stated contention that the FDA is a 'sock puppet' for major drug companies and faces a crisis of distrust. Wellness industry products, he has claimed, are unfairly sidelined. A spokesperson for the Department of Health and Human Services did not respond to requests for comment. Kennedy's statements alarmed experts on the field of sometimes dangerous stem cell infusions -- who noted that many of Kennedy's allies endorse wellness products ranging from red-light therapy to magnetism. 'It's a complete abdication of protection of the public, letting these grifters go forward,' said Timothy Caulfield, a research chair in health law and policy at the University of Alberta in Canada. 'For him to say, 'There are problems with Big Pharma, so we want our opportunity to be bad actors too,' it doesn't make any sense.' One leading expert group, the International Society for Stem Cell Research, reviewed Kennedy's podcast statements and condemned the approach as potentially allowing products that are 'sometimes contaminated with pathogens and are often marketed with scientifically implausible claims.' 'It is critical that the FDA maintain its regulatory authority to protect Americans from these potentially harmful and deceptive products,' the society said in a statement. Advertisement On Thursday, a panelist appearing at an FDA meeting on cell and gene therapies raised a concern about 'snake oil' treatments. Dr. Vinay Prasad, the agency's director of the center for biologics evaluation research, responded, 'We have to regulate the bad actors. We can't let that taint what we do here at the FDA.' Kennedy, who also attended the event, voiced full support for the researchers and biotech executives working on gene therapies for rare diseases, including those who made history by creating a custom gene therapy for an infant named KJ. 'We're going to do everything in our power to sweep away the barriers from you getting those solutions to market and getting them funded, and do everything that we can to support you all,' Kennedy said. On Brecka's podcast in May, Kennedy cited other products that he'd like to see more of, including chelation treatment, which was discussed in a 2015 book edited by him that focused on widely debunked theories about mercury in vaccines and autism and cites 'evidence of chelation's benefits' from a few small studies. One 5-year-old Pennsylvania boy died in 2005 from cardiac arrest after a doctor tried to treat his autism with chelation. Neither Kennedy nor the FDA has released a formal plan to change agency standards for stem cell treatments, which have typically been reviewed by the agency as individual therapies to treat a specific disease. Widening overall access could also happen informally if the agency decided to relax enforcement, an approach the FDA used in the past to indicate that it wouldn't crack down on unauthorized products. During the pandemic, for example, the agency allowed providers to retrofit infusion pumps and ventilators to treat hordes of sick patients. Advertisement During the first Trump administration, the agency's commissioner, Dr. Scott Gottlieb, escalated enforcement against stem cell providers whom he described in 2017 as 'unscrupulous actors who have seized on the clinical promise of regenerative medicine.' The FDA followed through with lawsuits seeking to stop some stem cell providers, including one case that the government won on appeal in the fall. In that case, the agency alleged that one provider, the California Stem Cell Treatment Center, was offering a drug without FDA approval by taking stem cells from a person's fat, manipulating them and infusing them as a remedy for Alzheimer's disease, cancer and arthritis. The agency classifies stem cell treatments as a 'biologic' and approves them much like a drug after careful studies of safety and effectiveness. But the FDA does make exceptions: It does not regulate some treatments if providers say they are extracting and then reinserting a person's cells with minimal manipulation. In March, Kennedy convened a meeting with leaders in the stem cell field. Two people who attended said the gathering was a fact-finding effort to explore a safe way to increase access. To Dr. Noah Raizman, who attended the meeting on behalf of the American Academy of Orthopaedic Surgeons, Kennedy's new pronouncement 'sounds a little more casual and a little bit more emboldened.' In the podcast, Kennedy said that consumers should be able to navigate the industry's claims. 'We don't want to have the Wild West,' Kennedy said. 'We want to make sure that information is out there. But we also want to respect the intelligence of the American people -- the capacity of people who explore the outcomes that are going to benefit them the most.' Advertisement In recent years, stem cell treatments have caused harm in the United States and abroad. Experts at the Pew Research Center tallied more than 350 cases of side effects including life-threatening blood infections, heart attacks and tumors. One Boston neurosurgeon discovered a huge mass of bloody tissue in the lower spine of a man who had received unproven stem cell treatments in Mexico, China and Argentina. Three patients were blinded after stem cell treatments at a Florida clinic. The FDA prevailed in getting a court order to stop the clinic from operating. The field of stem cell treatments is so complex that the Harvard Medical School created a free course to help doctors navigate patient questions, said Insoo Hyun, the director of life sciences at the Museum of Science in Boston. More than 110 stem cell clinical studies are advancing under regulatory oversight. In one, scientists at the National Institutes of Health are using retinal cells developed from patients' blood to try to treat vision loss in older adults -- and follow them for 15 years. In another study aimed at helping patients with Parkinson's disease, researchers at a biotech company in California are exploring the safety of infusing dopamine-producing neurons in a region of the brain that controls the body's movements. A Chinese company is studying a treatment for heart failure that involves transplanting cardiac muscle cells into the heart. Some providers sidestep the costly, yearslong process of careful work that can lead to an FDA approval. Among them is Dr. Chadwick Prodromos, a Chicago doctor who offers stem cell treatments in Antigua. Kennedy welcomed him warmly at the March meeting, Raizman recalled. Reached for comment, Prodromos' office said that he was in Antigua doing treatments and was not available. Advertisement In an April interview on YouTube, Prodromos said that he was still in touch with the FDA about stem cell treatments that could help people 'without allowing scams and things that aren't valid. And you know, it's a tricky proposition.' A website for Prodromos' clinic says that he and colleagues offer injections in Antigua into the joints, back, neck, scalp, penis and pelvic floor for an array of conditions including autism, thinning hair and lupus. He uses AlloRX cells, which are derived from the umbilical cord, in a manner that in the United States would require an FDA-cleared clinical trial. People can seek out unregulated treatments using their own cells that are processed, purified and amplified in different ways. They can also find treatments using others' cells that vary widely in quality and sterility. Some low-quality clinics process cells in a back room, which is the opposite of a clinical-grade cell processing site. Hyun said he recently toured one in the Netherlands that used specialized air filtering, layers of gowns and a ban on bacteria-laden cellphones in their sterile area. 'It's kind of like you're entering a space station,' he said. Ultimately, Caulfield said, many unauthorized stem cell providers adopt the language of biotech and regenerative medicine, post glowing patient testimonials and exploit patients who are desperate for a cure. This article originally appeared in .