On June 12, 2026, the FDA cleared the first over-the-counter continuous glucose monitor (CGM) for children age 2+ who do not use insulin. Here’s what the device can do, the key safety limits FDA emphasized, and practical steps for families to use glucose data responsibly.
A new UK randomized trial found that adults with long COVID–related brain fog who received 10 telehealth sessions of goal-focused cognitive rehabilitation reported better day-to-day functional goal attainment at 3 months—an improvement that remained at 6 months. Here’s what the program involved, what seemed to improve most, and how U.S. readers can use CDC guidance to decide next steps.
CMS’ updated Hospital Price Transparency requirements for 2026 begin on Jan. 1, 2026, with enforcement of those updates starting Apr. 1, 2026. Rural patients can use the posted “shoppable services” display and the new median/percentile allowed-amount data to plan questions for insurers and hospitals—without expecting a perfect cost match.
Wisconsin extended BadgerCare Plus postpartum coverage from 60 days to up to about 12 months for many full-benefit members, effective in 2026. Because the state uses an “end of the month” rule, your exact coverage end date matters—especially for follow-up care, mental health support, and treating complications that can arise months after delivery.
On July 14, 2026, the FDA updated a Class I correction for Baxter Volara System single-patient-use circuits. The concern: possible air and medication leakage from the nebulizer cup when the cup isn’t properly locked after medication is added. Here’s how to check if your circuits are affected, what to do before each home therapy session, and when to get urgent help.
If a school or child care notice says there may have been measles exposure, timing and your child’s documented MMR doses matter. CDC guidance focuses on urgent, time-limited post-exposure options—often an MMR within 72 hours, or immune globulin for certain higher-risk people within 6 days.
New federal rules take effect June 8, 2026, and schools can expand fluid milk options again. Here’s what changes for families—plus a checklist for requesting lactose-free or a nutritionally equivalent nondairy substitute.
An NIH-highlighted Cell study suggests that, in some people with long COVID, the immune system may react to nervous-system-related targets—pointing to possible biologic subgroups. But CDC guidance remains clear: in the U.S., long COVID is diagnosed clinically, and there is still no definitive lab test for routine use.
Starting April 1, 2026, CMS enforcement begins for updated Hospital Price Transparency requirements tied to the CY 2026 machine-readable file. Here’s what changed for hospitals’ data (allowed amounts percentiles, attestation updates, and Type 2 NPI encoding) and what that does—and doesn’t—mean for patients’ bills.
If your bottle shows Lot 5950 with a best-by/expiration date of 02/2028, stop using it. FDA linked this lot to potential Aspergillus contamination and recalled it. People with weakened immune systems or certain lung diseases should be especially alert for concerning symptoms and seek medical care promptly if they develop them.
CDC’s “Activity Levels” turn community respiratory-virus surveillance into five labels (Very Low → Very High). Here’s how to interpret the signals—wastewater, emergency department/ARI activity, and severe-illness context—and what families, schools, and workplaces can do next without panic.
If your family used Nara Organics Whole Milk Organic Powdered Infant Formula, the FDA says stop using it now. Know the warning signs of infant botulism, preserve lot/use-by info, and get emergency care right away if symptoms appear.
If you may have been exposed to Andes virus through the 2026 U.S. cruise-ship outbreak and you develop fever or breathing symptoms, contact a clinician and public health promptly. CDC and WHO interim guidance explains the monitoring window after exposure, common symptom patterns, and how labs use coordinated testing—when different tests are most useful.
On July 1, 2026, the FDA expanded Casgevy (exagamglogene autotemcel) so some children age 2 and older with sickle cell disease (SCD) can be evaluated for the gene-edited, stem-cell therapy—previously approved for older children. Here’s what the FDA change does and does not mean, what benefits were seen in pediatric data, and what risks and long-term monitoring families should discuss.
CMS’s June 2026 Hospital Price Transparency FAQs update what hospitals must post online (including machine-readable expectations) and how consumers can use CMS’s enforcement-actions page. Here’s how to interpret what you find—and why those posted “prices/charges” may still not equal what you’ll personally pay with insurance.
IHS is ending mercury-containing dental amalgam use by 2027. If you’re offered a filling during 2026–2027—or you’re thinking about replacing an existing “silver” filling—these questions can help you make an informed choice about materials, risks, benefits, and dental need.
On June 10, 2026, the FDA approved label updates for OTC alli (orlistat) 60 mg that add clearer warnings about rare but serious kidney risks, including kidney stones. If you have a history of kidney disease or kidney stones, the label advises asking a health care provider before using alli—and stopping alli and seeking medical guidance promptly if symptoms appear.
CDC’s national wastewater dashboard updates every Friday. Learn what “wastewater viral activity” means, what it can’t tell you about individuals, and how families can use the signal to plan everyday prevention and keep vaccines up to date.
Seeing an FDA recall record for an implanted deep brain stimulation (DBS) neurostimulator can be alarming. Here’s what the specific FDA record for Medtronic Kinetra model 7428 describes, how to check your device identifiers, and when symptom changes should trigger urgent care.
ACOG’s pregnancy vaccine schedule and CDC’s vaccine-table view can look mismatched at first glance—especially for COVID-19. Here’s how to use ACOG for the “what to plan,” then use CDC’s dedicated pregnancy pages to confirm the timing logic for RSV (Abrysvo) and COVID-19.
FDA updated its AI-Enabled Medical Devices list on June 16, 2026. Here’s how patients, caregivers, and clinician-adjacent readers can check whether an AI-enabled medical device is FDA-authorized—and what the list and linked FDA entries do (and don’t) tell you.
In 2026, the American Cancer Society labeled blood-based colorectal cancer screening tests as “not preferred.” Here’s what that means for everyday decisions—what to ask if a clinic offers a blood test, and why a positive result still requires timely colonoscopy follow-up.
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