Health and Science Highlights - East County Magazine

- A major cyclosporiasis outbreak has affected 41 states with 11,500 reported cases, leading Taylor Farms to recall iceberg lettuce products across 27 states.
- Other critical health and security alerts include the spread of measles within the U.S. and reports of an OpenAI entity hacking a competitor.
- In legal news, University of California researchers are suing the Trump administration following the cancellation of various research grants.
- These highlights, published July 28, 2026, emphasize growing public health crises, geopolitical tensions in AI, and legal battles over scientific funding.
Sources & Citations
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Anti-Infective Drugs Market to Reach USD 187.5 Billion by 2035, Driven by Rising Infectious Diseases and Advancements in Antimicrobial Therapies
• The global anti-infective drugs market is projected to reach a valuation of USD 187.5 billion by 2035. • Growth is primarily driven by the increasing global burden of bacterial, viral, fungal, and parasitic infections, alongside the critical emergence of antimicrobial resistance.
Read original · openpr.com
OpenPRHHS adopts limit to ‘dangerous’ virus research a year after Trump order reining in federal support
• The U.S. Department of Health and Human Services (HHS) announced a new policy on Tuesday banning federal funding for "dangerous" gain-of-function research. • This type of research involves enhancing viruses to predict potential threats, a practice that has faced scrutiny following the COVID-19 pandemic.
Read original · washingtontimes.comBundibugyo Ebola Hits 3,200 Cases: Unpaid Doctors Strike as Oxford's Vaccine Trial Begins
• An Ebola outbreak in the Democratic Republic of the Congo has surged to 3,200 confirmed cases and 1,405 deaths, marking the fastest growth rate ever recorded for any Ebola outbreak. • The crisis is exacerbated by a strike of healthcare workers who have walked off the job due to unpaid wages, severely hindering the medical response.
Read original · techtimes.com
Tech TimesMedical Bulletin 28/July/2026
• A new study published in the Journal of Clinical Investigation reveals that losing specific healthy body fat can increase the risk of diabetes and fatty liver disease. • Researchers focused on familial partial lipodystrophy type 2 (FPLD2), a rare condition caused by a mutation in the lamin A/C gene that leads to fat loss in certain body areas.
Read original · medicaldialogues.inFauci's Diaries Released; Cold Brew Recalled; Carly Simon's Diagnosis
• MedPage Today has compiled a series of health updates, including the release of Dr. Anthony Fauci's diaries and a recall of cold brew coffee. • Food safety experts are warning that federal budget cuts have hindered the ability to detect and stop the spread of potentially deadlier foodborne illness outbreaks.
Read original · medpagetoday.com
MedPage TodayFauci's diary, HIV resurgence, PMOS disparities: Morning Rounds
• Morning Rounds reports on a variety of health updates, including the release of Dr. Anthony Fauci's diaries from the COVID-19 pandemic era. • The report highlights critical concerns regarding a potential global resurgence of HIV and new data tracking substance use trends across the United States.
Read original · statnews.com
StatnewsPrediction Market Betting on Drug Trials and Approvals Sparks Concern About Undermining Research - The New York Times
• Prediction markets such as Kalshi and Polymarket are now allowing users to wager money on the outcomes of drug approvals. • Kalshi is further expanding these offerings by planning to enable betting on the specific results of clinical trials.
Read original · nytimes.comFDA panel to consider previously spurned drugs - POLITICO
• An FDA advisory committee is meeting this week to review applications for novel peptide therapies that were previously rejected by former agency officials. • Affiliates of the American Academy of Peptide Medicine allege the FDA ignored critical safety and efficacy data, while industry and consumer advocates warn that approval would bypass traditional drug regulations.
Read original · politico.comAhead of hearing, FDA questions the efficacy of Capricor's Duchenne drug
• The FDA has raised concerns regarding the efficacy of Capricor Therapeutics' treatment for Duchenne muscular dystrophy ahead of an upcoming advisory committee hearing. • The agency's skepticism contradicts claims made by Capricor regarding the clinical benefits of the rare disease drug.
Read original · statnews.com
StatnewsFDA advisers vote to ease peptide restrictions, despite agency concerns : NPR
• FDA advisers voted to ease restrictions on popular peptides, potentially allowing specialized pharmacies to produce these compounds within the United States. • The decision comes despite agency concerns that these peptides lack the large, well-controlled human clinical trials required to establish safety and effectiveness for formal drug approval.
Read original · npr.orgTime
• Members of an FDA committee expressed concerns regarding the agency's decision to allow pharmacies to dispense certain medications without requiring traditional clinical trials. • Committee member Todd Durham, senior vice president at the Foundation Fighting Blindness, voted against adding specific peptides to the approved list.
Read original · time.com
Time