logo
Covered California pushes for better healthcare as federal spending cuts loom

Covered California pushes for better healthcare as federal spending cuts loom

Yahoo26-04-2025

Faced with potential federal spending cuts that threaten health coverage and falling childhood vaccination rates, Monica Soni, the chief medical officer of Covered California, has a lot on her plate — and on her mind.
California's Affordable Care Act health insurance exchange covers nearly 2 million residents and 89% of them receive federal subsidies that reduce their premiums. Many middle-income households got subsidies for the first time after Congress expanded them in 2021, which helped generate a boom in enrollment in ACA exchanges nationwide.
From the original and enhanced subsidies, Covered California enrollees currently get $563 a month onaverage, lowering the average monthly out-of-pocket premium from $698 to $135, according to data from Covered California.
The 2021 subsidies are set to expire at the end of this year unless Congress renews them. If they lapse, enrollees would be on the hook to pay an average of $101 a month more for health insurance — not counting any premium hikes in 2026 and beyond. And those middle-income earners who did not qualify for subsidies before would lose all financial assistance — $384 a month, on average — which Soni fears could prompt them to drop out.
At the same time, vaccination rates for children 2 and under declined among 7 of the 10 Covered California health plans subject to its new quality-of-care requirements. Soni, a Los Angeles native who came to Covered California in May 2023, oversees that program, in which health plans must meet performance targets on blood pressure control, diabetes management, colorectal cancer screening and childhood vaccinations — or pay a financial penalty.
Lack of access to such key aspects of care disproportionately affects underserved communities, making Covered California's effort one of health equity as well. Soni, a Harvard-trained primary care doctor who sees patients one day a week at an urgent care clinic in Los Angeles County's public safety net health system, is familiar with the challenges those communities face.
Covered California reported last November that its health plans improved on three of the four measures in the first year of the program. But childhood immunizations for those under 2 declined by 4%. The decline is in line with a national trend, which Soni attributed to postpandemic mistrust of vaccines and 'more skepticism of the entire medical industry.'
Most parents have heard at least one untrue statement about measles or the vaccine for it, and many don't know what to believe, according to an April KFF poll.
Health plans improved on the other three measures, but not enough to avoid penalties, which yielded $15 million. The exchange is using that money to fund another effort Soni manages, which helps 6,900 Covered California households buy groceries and contributes to more than 250 savings accounts for children who get routine checkups and vaccines. Some of the penalty money will also be used to support primary care practices around California.
In addition to her bifurcated professional duties, Soni is the mother of two children, ages 4 and 7.
KFF Health News senior correspondent Bernard J. Wolfson spoke with Soni about the impact of possible federal cuts and the exchange's initiative to improve care for its enrollees. This interview has been edited for length and clarity.
Q: Covered California has record enrollment of nearly 2 million, boosted by the expanded federal subsidies passed under the Biden administration, which end after this year. What if Congress does not renew them?
A: Our estimates are that it will approach 400,000 Californians who would drop coverage immediately.We hear every day from our folks that they're really living on the margins. Until they got some of those subsidies, they could not afford coverage.
As a primary care doctor, I am the one to treat folks who show up with preventable cancers because they were too afraid to think about what their out-of-pocket costs would be. I don't want to go back to those days.
Q: Congress is considering billions in cuts to Medicaid. How would that affect Covered California and the state's population more broadly, given that more than 1 in 3 Californians are on Medi-Cal, the state's version of Medicaid?
A: Those are our neighbors, our friends. Those are the people working in the restaurants we eat at.
Earlier cancer screenings, better chronic disease control, lower maternal mortality, more substance use disorder treatment: We know that Medicaid saves lives. We know it helps people live longer and better.
As a physician, I would be hard-pressed to argue for rolling back anything that saves lives. It would be very distressing to watch that come to California.
Q: Why did Covered California undertake the Quality Transformation Initiative?
A: We were incredibly successful at covering nearly 2 million, but frankly we didn't see improvements in quality, and we continue to see gaps for certain populations in terms of outcomes. So, I think the question became much more imperative: Are we getting our money's worth out of this coverage? Are we making sure people are living longer and better, and if not, how do we up the ante to make sure they are?
Q: There's a penalty for not meeting the targets, but no bonuses for meeting them: You meet the goals or else, right?
A: We don't say it like that, but that is true. And we didn't make it complicated. It's only four measures.
It's things that as a primary care doctor I know are important, that I take care of when I see people in mypractice. We said get to the 66th percentile on these four measures, and there's no dollars that you have to pay. If you don't, then we collect those funds.
Q: And you use the penalty money to fund the grocery assistance and child savings accounts.
A: That's exactly right. We had this opportunity to think about what would we use these dollars for and how we actually make a difference in people's lives. So, we cold-called hundreds of people, we sent surveys out to thousands of folks, and what we heard overwhelmingly was how expensive it is to live in California; that folks are making trade-offs between food and transportation, between child care and food — just impossible decisions.
Q: You will put up to $1,000 a child into those savings accounts, right?
A: That's right. It's tied to doing those healthy behaviors, going to child well visits and getting recommended vaccines. We looked at the literature, and once you get to even just $500 in an account, the likelihood of a kid going to a two- or four-year school increases significantly. It's actually because they're hopeful about their future, and it changes their path of upward mobility, which we know changes their health outcome.
Q: Given the rise in vaccine skepticism, are you worried that the recent measles outbreak could grow?
A: I am very concerned about it. I was actually reading some posts from a physician colleague who trained decades earlier and was talking about all the diseases that my generation of physicians have never seen. We don't actually know how to diagnose and take care of a number of infectious diseases because they mostly have been eradicated or outbreaks have been really contained. So, I feel worried. I've been brushing off my old textbooks.
Wolfson writes for KFF Health News, a national newsroom that produces in-depth journalism about health issues and is one of the core operating programs at KFF — an independent source for health policy research, polling and journalism.
Sign up for our Wide Shot newsletter to get the latest entertainment business news, analysis and insights.
This story originally appeared in Los Angeles Times.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Opinion - How thousands of unreviewed ingredients got into our food — and what FDA can do about it
Opinion - How thousands of unreviewed ingredients got into our food — and what FDA can do about it

Yahoo

time6 hours ago

  • Yahoo

Opinion - How thousands of unreviewed ingredients got into our food — and what FDA can do about it

At least 1,000 ingredients in food products on our grocery store shelves have never been checked for safety by the Food and Drug Administration. Dozens have raised serious safety concerns among experts. How did the FDA allow this? The answer can be found in the agency's lax interpretation of a little-known legal designation that lets companies decide for themselves if ingredients in their products are safe. Fortunately, there are steps the agency can take right now to stem the flow of potentially unsafe ingredients into our food supply. Environmental Defense Fund outlined these steps in a letter we recently sent to the agency, but first let's take a closer look at how we got here. 'Generally Recognized as Safe' is a designation Congress created in 1958 to allow commonly used food ingredients to bypass the FDA's pre-market safety review process. It was meant for food substances — such as oils, vinegar, baking soda and common spices — that were widely considered safe due to their long history of everyday use. Since 1958, this status has been coopted to cover a universe of foods that extends far beyond its original intent. According to FDA regulations, a chemical can receive the designation if experts widely agree that scientific evidence shows its use to be safe. But because 'Generally Recognized as Safe' wasn't meant for newer ingredients, Congress allowed ingredients so designated to skip the FDA's premarket approval process — despite requiring similar evidence for other additives. Under the agency's current interpretation, companies can designate the use of a substance as safe and take products with that substance to market without informing the FDA or the public of its decision. While companies may voluntarily submit a notice to FDA offering safety evidence, they are not required to — and often don't. Our organization estimated that manufacturers have notified FDA of fewer than half of the ingredients they market as safe under the 'Generally Recognized' standard. Companies that do bother to submit a notice to the FDA are free to withdraw it at any point and take their product to market, provided they can cite evidence of its safe use. But this 'evidence' is often far from independent. Companies can, and often do, enlist their own employees or handpicked consultants to conduct their safety assessments. The result is a process riddled with conflicts of interest that lets unsafe foods into Americans' homes. We analyzed 'Generally Recognized as Safe' notices received by the FDA, obtained via a Freedom of Information request, and found that of the 1,163 submitted by companies between 1997 and April 2024, 192 were later withdrawn, with safety concerns cited in at least a dozen cases. We also identified 31 ingredients that companies have advertised to be recognized as safe, such as in press releases, trade publications and on their own websites (see the Appendix of our letter). However, we were unable to find the scientific evidence required under this standard to demonstrate these ingredients are commonly regarded as safe among experts. This raises red flags that FDA should be taking seriously. Although a comprehensive fix to the 'Generally Recognized' standard will require legislation from Congress, there are significant steps the FDA can take right away to ensure a more rigorous determination process that better protects Americans' health. Starting today, the FDA can use existing authority to remove safe designations from ingredients it deems unsafe and take them off the market. It can also notify manufacturers, importers, distributors and retailers that the substance is no longer recognized as safe. In addition, the FDA can enforce the requirement that companies base safety designations on publicly available data. Although this won't curtail companies' ability to self-declare substances as safe, it will require those who do to be transparent in citing their evidence. Third, the FDA can enforce the requirement that safety assessments consider vital health information such as a substance's dietary sources, potential cancer risks and the cumulative health effects of similar substances. Finally, the FDA can make companies revise and resubmit their data for review when they submit 'Generally Recognized as Safe' notices that fail to comply with the criteria. The 'Generally Recognized as Safe' designation is far from a perfect system, but it can work better if it is interpreted and enforced more comprehensively. If the FDA is serious about protecting public health, it should start by fully exercising the tools already at its disposal. Maria Doa is senior director at the Chemicals Policy at Environmental Defense Fund. Maricel Maffini is an independent consultant focused on human and environmental health and chemical safety. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

In Lansing, Democrats warn Medicaid and SNAP cuts would be a 'perfect storm' for the poor
In Lansing, Democrats warn Medicaid and SNAP cuts would be a 'perfect storm' for the poor

Yahoo

time7 hours ago

  • Yahoo

In Lansing, Democrats warn Medicaid and SNAP cuts would be a 'perfect storm' for the poor

U.S. Sen. Elissa Slotkin (D-Holly) and U.S. Rep. Kristen McDonald Rivet (D-Bay City) at a June 6, 2025 town hall in Lansing. | Kyle Davidson Members of the Michigan Democratic Party laid out the impacts of congressional Republicans' 'big beautiful bill' at a town hall on Friday, calling on residents of Michigan's 7th Congressional District to help educate their friends and family as well. A few hundred supporters packed into the gym of Everett High School in Lansing as U.S. Sen. Elissa Slotkin (D-Holly), U.S. Rep. Kristen McDonald Rivet (D-Bay City) and Michigan Democratic Party Chair Curtis Hertel detailed how the Trump administration's policies would impact everyone, particularly individuals with limited income. The Michigan Democratic Party has hosted several similar events in Republican districts throughout the state, Hertel said, noting House Republicans had been instructed to avoid town halls with their constituents. 'The most basic thing for a public servant is to be able to sit and answer questions. … The least someone can do is sit down with people and explain their votes' Hertel said. And the 7th Congressional District's current representative, Tom Barrett (R-Charlotte) has a lot of explaining to do, Hertel said, slamming Barrett for supporting Republican's spending plan, and arguing the representative failed to stand up to the President and make himself available to his constituents A Barrett spokesperson did not respond to a request for comment. Prior to taking questions, McDonald Rivet slammed the Republican spending effort, telling audience members that it would take away healthcare and raise the cost of medicine, education and energy in order to deliver a tax break to the wealthy. 'Oh, and by the way, it's going to increase the deficit by several trillion dollars,' She said. Slotkin looked back on the president's first term, when Trump was looking to overturn the Affordable Care Act, which expanded access to Medicaid and barred insurance providers from denying people coverage or charging them due to preexisting health conditions. 'It was the first thing he talked about when he got sworn in, he even had the House of Representatives vote to repeal Obamacare. And now we not only still have it, we expanded it, and how? Because we educated people,' Slotkin said. However, rather than cutting people's healthcare outright, Slotkin argued Trump is aiming to hide those cuts by requiring individuals to reregister for Medicaid every six months, making it harder to qualify and more difficult to sign up. While the current proposal would implement work requirements for Medicaid recipients, Slotkin noted it also raises the age limit for those requirements to 64. According to KFF, an independent health policy organization, 92% of medicaid recipients under 65 are already working full or part time. The nonpartisan Congressional Budget Office estimated that Republican's budget plan would result in 10.9 million additional people being uninsured in 2034, with 7.8 million fewer individuals on Medicaid due to the policy's proposed work requirements. Even individuals who are not on Medicaid will feel the impacts of cuts to the program, Slotkin said, noting that nursing homes, hospitals and mental health facilities all rely on Medicaid funding. 'I would just say this bill is designed to really be a perfect storm for poor people. If you are living at or below the poverty line, you're getting hit in every direction. Medicaid, your health care; SNAP your food; a bunch of programs, right, that you depend on. … They are paying for those tax benefits for the most wealthy by really the perfect storm of cuts for the poorest among us,' Slotkin said. On top of cutting SNAP benefits by $300 billion, the Department of Government Efficiency had canceled $1 billion in funding to programs supporting school meals and food banks, McDonald Rivet said. 'So you're that hungry kid and you have lost access to a food bank. You have lost access to food at school, and now you don't have SNAP benefits. This is the America that this bill creates,' McDonald Rivet said. Alongside questions on cuts to SNAP and Medicaid, audience members asked the lawmakers about the legal challenges levied against the Trump administration, and Democrats' plans to counter Republicans heading into the 2026 mid-term election. On Friday, the Trump Administration backed down in its resistance of a Supreme Court order demanding that the administration facilitate the return of Kilmar Abrego Garcia, who was wrongly deported to El Salvador three months ago. However, the fight goes beyond Abrego Gracia, into whether the executive branch needs to obey orders from the Supreme Court, Slotkin said. 'Now, we haven't had to deal with this issue in the years past because Democrats and Republicans have largely said, 'Huh, if the Chief Justice of the Supreme Court issues a court order, we're going to follow it.' Trump is pushing the boundaries on all the democratic values and principles most of us grew up with,' Slotkin said. Should an individual defy a federal court order, U.S. marshals would eventually be sent to enforce that order, Slotkin said. However, the U.S. marshals are controlled by the United States attorney general. Should the U.S. marshals receive a request to enforce a Supreme Court order against the president, Slotkin raised the question on whether Attorney General Pam Bondi, a Trump loyalist, would approve it. 'We've needed to have this fight. We need to have it out. We need a court order that he needs to obey, and we need to precipitate this conversation on the U.S. marshals. But today was an important sign that they don't want to get to that point. They don't want to wait until the U.S. marshals are potentially getting an order to activate,' Slotkin said. In preparing to take on the Trump Administration, Slotkin said she'd gone back to her roots in national security and crafted a war plan in the form of a 17-page powerpoint, with plans to lay out her vision of the nation's future under Democratic leadership. 'It's about facing our problems head on and saying the only way we do well as a country, the only way that we have a strong middle class going forward, the American Dream going forward, is if we face these issues and have a vision. And it's economic, it's about national security, and it's about our democracy,' Slotkin said. SUBSCRIBE: GET THE MORNING HEADLINES DELIVERED TO YOUR INBOX

How thousands of unreviewed ingredients got into our food — and what FDA can do about it
How thousands of unreviewed ingredients got into our food — and what FDA can do about it

The Hill

time8 hours ago

  • The Hill

How thousands of unreviewed ingredients got into our food — and what FDA can do about it

At least 1,000 ingredients in food products on our grocery store shelves have never been checked for safety by the Food and Drug Administration. Dozens have raised serious safety concerns among experts. How did the FDA allow this? The answer can be found in the agency's lax interpretation of a little-known legal designation that lets companies decide for themselves if ingredients in their products are safe. Fortunately, there are steps the agency can take right now to stem the flow of potentially unsafe ingredients into our food supply. Environmental Defense Fund outlined these steps in a letter we recently sent to the agency, but first let's take a closer look at how we got here. 'Generally Recognized as Safe' is a designation Congress created in 1958 to allow commonly used food ingredients to bypass the FDA's pre-market safety review process. It was meant for food substances — such as oils, vinegar, baking soda and common spices — that were widely considered safe due to their long history of everyday use. Since 1958, this status has been coopted to cover a universe of foods that extends far beyond its original intent. According to FDA regulations, a chemical can receive the designation if experts widely agree that scientific evidence shows its use to be safe. But because 'Generally Recognized as Safe' wasn't meant for newer ingredients, Congress allowed ingredients so designated to skip the FDA's premarket approval process — despite requiring similar evidence for other additives. Under the agency's current interpretation, companies can designate the use of a substance as safe and take products with that substance to market without informing the FDA or the public of its decision. While companies may voluntarily submit a notice to FDA offering safety evidence, they are not required to — and often don't. Our organization estimated that manufacturers have notified FDA of fewer than half of the ingredients they market as safe under the 'Generally Recognized' standard. Companies that do bother to submit a notice to the FDA are free to withdraw it at any point and take their product to market, provided they can cite evidence of its safe use. But this 'evidence' is often far from independent. Companies can, and often do, enlist their own employees or handpicked consultants to conduct their safety assessments. The result is a process riddled with conflicts of interest that lets unsafe foods into Americans' homes. We analyzed 'Generally Recognized as Safe' notices received by the FDA, obtained via a Freedom of Information request, and found that of the 1,163 submitted by companies between 1997 and April 2024, 192 were later withdrawn, with safety concerns cited in at least a dozen cases. We also identified 31 ingredients that companies have advertised to be recognized as safe, such as in press releases, trade publications and on their own websites (see the Appendix of our letter). However, we were unable to find the scientific evidence required under this standard to demonstrate these ingredients are commonly regarded as safe among experts. This raises red flags that FDA should be taking seriously. Although a comprehensive fix to the 'Generally Recognized' standard will require legislation from Congress, there are significant steps the FDA can take right away to ensure a more rigorous determination process that better protects Americans' health. Starting today, the FDA can use existing authority to remove safe designations from ingredients it deems unsafe and take them off the market. It can also notify manufacturers, importers, distributors and retailers that the substance is no longer recognized as safe. In addition, the FDA can enforce the requirement that companies base safety designations on publicly available data. Although this won't curtail companies' ability to self-declare substances as safe, it will require those who do to be transparent in citing their evidence. Third, the FDA can enforce the requirement that safety assessments consider vital health information such as a substance's dietary sources, potential cancer risks and the cumulative health effects of similar substances. Finally, the FDA can make companies revise and resubmit their data for review when they submit 'Generally Recognized as Safe' notices that fail to comply with the criteria. The 'Generally Recognized as Safe' designation is far from a perfect system, but it can work better if it is interpreted and enforced more comprehensively. If the FDA is serious about protecting public health, it should start by fully exercising the tools already at its disposal. Maria Doa is senior director at the Chemicals Policy at Environmental Defense Fund. Maricel Maffini is an independent consultant focused on human and environmental health and chemical safety.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store