Once considered nearly eradicated in the United States, measles is making a troubling comeback. As of early April, nearly 600 confirmed cases have been reported across multiple states, with Texas emerging as the outbreak’s epicenter. The resurgence of this highly contagious, vaccine-preventable disease is being linked to declining immunization rates, misinformation surrounding vaccines, and weakened public health infrastructure following recent federal budget cuts.
Experts warn that unless aggressive intervention strategies are employed—including increasing vaccination coverage and restoring epidemiological support—the current outbreak could not only persist for months but also jeopardize the U.S.'s measles elimination status achieved in 2000.
In a candid and critical moment of reflection, U.S. Health Secretary Robert F. Kennedy Jr. urged Americans to get vaccinated against measles, even as he admitted on national television that he was unaware of the full impact of significant public health funding cuts enacted during his early tenure. The statement comes amid one of the largest measles outbreaks in recent U.S. history—now spanning multiple states and threatening to reverse decades of progress in infectious disease control.
As of this week, over 595 cases of measles have been confirmed across Texas, New Mexico, Oklahoma, and Kansas. Texas has borne the brunt of the outbreak with 505 cases reported in 21 counties, including urban spillovers that concern local officials. New Mexico has reported 56 cases, Oklahoma 10 (with two still under investigation), and Kansas 24, some of which are believed to be linked to the same source.
The outbreak’s epicenter is Gaines County, Texas—a rural region with low vaccination coverage and limited public health infrastructure. Public health authorities are scrambling to contain the virus, which is known for being highly contagious—transmissible to 90% of unvaccinated individuals in proximity to an infected person.
In his first network television interview since joining President Donald Trump’s cabinet, RFK Jr. sat down with CBS News’ Dr. Jon LaPook for a revealing conversation that quickly became the focus of nationwide scrutiny.
LaPook confronted Kennedy with the administration’s decision to implement $11 billion in cuts to programs targeting infectious diseases, childhood vaccinations, mental health, and addiction support.
“You proposed more than $11 billion in cuts... Did you personally approve those cuts?” asked LaPook.
Kennedy replied, “I’m not familiar with those cuts… Those were mainly DEI cuts, which the president ordered.”
LaPook countered with a specific example, “About $750,000 of a University of Michigan grant into adolescent diabetes was cut. Did you know that?”
“I didn’t know that, and that’s something that we’ll look at,” Kennedy responded, acknowledging that while some reinstatements had occurred, important studies may have been unintentionally defunded due to the sweeping nature of the restructuring.
The CDC’s local partnerships and lab capacities have been severely strained by the budget reductions. Several local health departments, particularly in Texas and New Mexico, have stated that their ability to track, test, and isolate measles cases has been weakened due to the loss of funding and trained personnel.
These challenges are compounded by HHS restructuring, which has resulted in the layoff of more than 10,000 employees under a new directive led by Kennedy in collaboration with the Musk-supported Department of Government Efficiency (DOGE).
“HHS’s job is to make America healthy. We’re spending $1.9 trillion a year and people are not getting healthy,” Kennedy said during the interview. “When you do a disruption of this scale… you may make mistakes in 20% of cases, and then you go back and fix them.”
Yet critics argue that the stakes are too high to risk such large-scale experimental reforms, especially in areas concerning communicable diseases.
Despite his controversial past as a prominent vaccine skeptic, Kennedy used the same interview platform to strongly endorse measles vaccination—a surprising but much-needed pivot.
“We are urging all families in outbreak areas to ensure their children are vaccinated with the MMR vaccine,” Kennedy said, echoing guidance issued by the CDC earlier this week.
The Texas Department of Health Services is now encouraging parents in outbreak zones to get the second MMR dose for children aged 1–4 as soon as possible. Infants between 6–11 months are also eligible for an early dose, with two more to follow on the standard schedule.
The CDC emphasized that 12% of all measles cases this year have required hospitalization, making the situation even more urgent. Experts warn that if the outbreak continues for over 12 months, it could jeopardize the measles elimination status the U.S. achieved in 2000.
The outbreak has cast a spotlight on the fragile state of public health infrastructure, and Kennedy’s remarks have amplified the debate around how to fund and manage it effectively. Though he has promised to revisit specific defunded studies, public health experts remain cautious.
“What we need now is a full restoration of support—not just funds, but trust,” said Dr. Erin Thomas, an infectious disease specialist based in Houston. “These cuts sent a message that infectious disease prevention was no longer a national priority. This outbreak is the direct consequence.”
The statement by the Department of Health and Human Services last week, calling COVID-19 a “non-existent pandemic” and labeling response efforts as wasteful spending, further illustrates the administration’s departure from traditional public health principles.
Robert F. Kennedy Jr., the U.S. Secretary of Health and Human Services, is facing strong backlash after making sweeping comments during a recent press conference regarding autism and its supposed causes. As the CDC released a report revealing a rise in autism diagnoses among U.S. children — now affecting 1 in 31 8-year-olds — Kennedy doubled down on discredited theories linking autism to environmental exposures and vaccines, while portraying the disorder in stark, stigmatizing terms.
His remarks — including claims that children with autism “will never hold a job,” “never pay taxes,” or “never use a toilet unassisted” — were swiftly condemned by parents, medical experts, and advocacy groups alike for reinforcing outdated stereotypes and misrepresenting the broad and diverse autism spectrum.
Autism spectrum disorder (ASD) is not a single condition with uniform symptoms or outcomes. Rather, it is a neurological and developmental condition characterized by challenges in social interaction, communication, and repetitive behaviors. The key word is "spectrum" — and it exists for a reason.
Some individuals with autism may be nonverbal and need lifelong support, while others live independently, excel in careers, write books, or even hold public office. “Autism is not a disease,” said actress and autism advocate Holly Robinson Peete in a video statement, responding to Kennedy. “It is a developmental difference — and it is important to get that right.”
Her son, RJ, diagnosed 25 years ago, has “shattered a lot of 'never' off that list,” she said, referring to Kennedy’s grim portrayal. Countless parents echoed this sentiment on social media, stating that Kennedy’s generalizations erase the lived realities, milestones, and accomplishments of their children.
The CDC’s Autism and Developmental Disabilities Monitoring (ADDM) Network reported that 1 in 31 8-year-olds in the U.S. were diagnosed with autism in 2022, compared to 1 in 54 in 2016. But experts stress that this increase is not necessarily cause for alarm. It is, in fact, a sign of progress.
"The rise in autism rates is driven largely by improved awareness, broader diagnostic criteria, and increased access to evaluations and services," said Dr. Jessica Martin, a developmental pediatrician based in Boston. “We are identifying children earlier and more accurately — that’s a good thing.”
Kennedy, however, rejected this explanation as “indefensible” and announced plans for a directive to the National Institutes of Health to investigate “environmental exposures” as the root cause — reigniting long-debunked concerns about vaccines and toxins.
Despite overwhelming scientific consensus debunking any link between vaccines and autism, Kennedy has long been associated with promoting vaccine hesitancy. His latest comments, veiled in language about “environmental exposures,” once again hint at this discredited narrative.
Leading medical organizations, including the American Academy of Pediatrics and the World Health Organization, have repeatedly emphasized that vaccines are safe, effective, and have no causal relationship with autism. “Resurrecting these claims only spreads fear and confusion,” said Dr. Shana Vick, an epidemiologist. “It undermines public health and harms autistic people by framing their existence as a preventable tragedy.”
Perhaps the strongest rebuke came from parents of autistic children themselves. Samantha Taylor, whose 20-year-old son is on the spectrum, told Good Morning America, “Autism doesn’t destroy families — misinformation does.” In a viral Facebook post, she added, “What truly causes damage is the relentless portrayal of autism as something catastrophic, rather than a different way of experiencing the world.”
Kennedy’s comments, they say, not only ignore the complexity of the condition but strip children of their dignity and potential.
“Statements like ‘they’ll never write a poem’ deny the creative genius that so many autistic individuals demonstrate,” said Peete. “It’s dangerous, it’s harmful, and it’s simply false.”
While Kennedy has promised answers by September through federally backed studies, medical experts warn that his rhetoric may set back years of advocacy and research by framing autism as an “epidemic” akin to an infectious disease.
Autism is not something to be eradicated, it’s something to be understood, supported, and embraced. Families deserve resources, not fearmongering.
In the last two decades, the medical community has shifted toward neurodiversity — a perspective that recognizes neurological differences like autism as natural variations of the human genome. This philosophy emphasizes inclusivity, respect, and strength-based approaches rather than medicalizing difference.
At a time when public trust in institutions is fragile, the words of public officials matter deeply. Kennedy’s comments have triggered a reckoning not only about how autism is portrayed in the media and politics but also about how society chooses to value — or devalue — people who are different.
Advocates stress the need for policies rooted in science, not stigma, and for leadership that uplifts rather than marginalizes.
As the national conversation around autism continues, one thing is clear: the autism community — parents, children, adults on the spectrum, clinicians, and allies — is not going to stay silent in the face of outdated narratives.
Credits: Canva
On World Liver Day, which is observed on April 19, to spread awareness about liver health and the life-saving power of organ donation, let us look at one such real-life story. This is where doctor's prompt's action and one's selfless donation saved one human's life.
When the 30-year-old Delhi-based man walked into the hospital, he had yellow eyes and dangerously high liver enzymes. He was admitted in Max Super Speciality Hospital, Patparganj. That moment, he rarely knew that his life was, in fact, hanging by a thread. The man was diagnosed with acute liver failure, which was caused by viral hepatitis. His body was slowly shutting down. The frequency of his body shutting down had increased. The doctors also quickly informed the family. This was the one last hope of survival - a liver transplant.
His sister was family's first ray of hope. She was also willing and had a compatible liver whose part of it could be donated. However, pre-surgery tests revealed that her liver size was too small to ensure a safe transplant. The family then proposed the patient's brother-in-law - a second-degree relative, as the next donor. His liver was a better match, but since he was not an immediate blood relative, there had to be special regulatory approvals which were required.
However, the worsening condition of the patients allowed no such time.
The hospital too scrambled to get clearance for the brother-in-law. All this while, the patient suffered a cardiac arrest. The situation turned dire within minutes. Doctors performed CPR to revive him. He was immediately put on ventilator support. The decision had to be taken soon.
With no time in hand, the doctors decided to go ahead with the sister as the donor, though there were risks there too.
A team of highly skilled hepatobiliary surgeons, anesthesiologists, and critical care specialists took over. In a high-risk, nine-hour surgery, they removed the patient’s failing liver and replaced it with part of his sister’s.
“This was one of the most challenging cases we’ve handled,” said Dr. Ajitabh Srivastava, Director – HPB Surgery & Liver Transplant. “When the patient collapsed, our team acted within seconds. Every decision, every move mattered. His survival was truly a team triumph.”
The patient is now recovering well.
As per the National Institute of Diabetes and Digestive and Kidney Diseases, a liver transplant is a surgical procedure to replace a diseased liver with a healthy one from a donor. It’s often the last resort when liver failure occurs—whether due to chronic illness or sudden injury.
People may need a liver transplant for:
The most common type, where a full or partial liver is taken from someone who has recently died.
A healthy person donates a portion of their liver—typically a close relative. Both the donor’s and recipient’s liver regenerate to normal size in a few weeks.
A rare and fatal brain disease with a 100% mortality rate has gripped Hood River County, Oregon, raising concerns within the medical community and eliciting intense probes by local and federal health officials. It is called Creutzfeldt-Jakob Disease (CJD), and it has killed two people and impacted a third in eight months—a terrifying cluster in a county of only slightly more than 23,000 people.
On April 14, the Hood River County Health Department reported one case of Creutzfeldt-Jakob Disease and two more probable cases. Although only one case has been confirmed by a diagnosis through an autopsy, the other two are presumptive and await post-mortem confirmation through examination of brain tissue and cerebrospinal fluid. Such examination, as explained by Trish Elliott, Director of the Hood River County Health Department, may take months.
Although the origins of these three cases are still unknown, the cluster is epidemiologically significant. The U.S. experiences about 350 cases of CJD each year, or 1 to 2 cases per million individuals globally. For Hood River County, with only 23,000 people, to see three cases over such a brief time span is an epidemiologic outlier.
Creutzfeldt-Jakob Disease is a rapidly advancing and always lethal neurodegenerative disease resulting from misfolded proteins known as prions. Initially documented in the 1920s by German physicians Hans Gerhard Creutzfeldt and Alfons Jakob, CJD causes sponge-like holes to form within the brain, destroying its structure and function.
CJD is a member of the larger family of prion diseases, which also encompasses other rare but fatal disorders like kuru and fatal familial insomnia. Similar to bovine spongiform encephalopathy (BSE), commonly referred to as mad cow disease, CJD irreversibly destroys the brain and has no cure.
The symptoms of CJD are extreme and worsen quickly. Early symptoms may involve confusion, disorientation, personality changes, memory loss, visual disturbances, and stiffness of the muscles. Later in the disease, patients can develop hallucinations, difficulty speaking or swallowing, seizures, and sudden jerky movements.
Death typically occurs within a year of the onset of symptoms, usually as a result of complications such as pneumonia, heart failure, or problems arising from neurological deterioration such as falls and choking.
Symptoms in the early stages of sporadic CJD usually resemble other dementias but worsen with terrifying rapidity. The majority of individuals with sporadic CJD are between 50 and 80 years of age, but some genetic forms can occur earlier, even in some people as young as 30.
CJD comes in several types:
Sporadic CJD (sCJD): This type is the most prevalent, affecting about 85% of the cases. This type happens spontaneously when healthy proteins in the brain misfolded into prions for unknown reasons.
Genetic CJD (fCJD): Due to mutations in the PRNP gene, this form is inherited and represents about 10–15% of the total cases. The PRNP gene codes for the prion protein (PrP), a protein involved in neuronal communication and protection.
Acquired CJD (also referred to as iatrogenic or variant CJD): This is a rare type that involves outside sources of infection, such as eating infected beef (BSE/mad cow disease) or through tainted medical equipment or transplanted tissue.
In spite of concerns, authorities from Hood River County stressed that the present cases do not seem to have resulted from infected cows. "At this point in time, there is no cause identified between these three cases," the department noted. They also pointed out that CJD cannot be transmitted via air, touching, social contact, or water.
The Hood River County Health Department, in collaboration with the Oregon Health Authority and the Centers for Disease Control and Prevention (CDC), has launched an "active and ongoing investigation" into the three reported cases.
“We’re trying to look at any common risk factors that might link these cases,” Trish Elliott told The Oregonian. “But it’s pretty hard in some cases to come up with what the real cause is.”
Although risk to the general population is "extremely low," the health department continues to monitor it. Since CJD cannot be definitely diagnosed until after death, real-time monitoring is not easy, and so robust surveillance is essential.
Although there is no treatment or cure to prevent the development of CJD, the U.S. has established strict public health measures to minimize the risk of acquired CJD, especially through food supply control and medical safety measures.
Federal authorities have maintained since the 1990s a prohibition against feeding cattle which could be contaminated with BSE, and employment of high-risk material in foods is strictly barred. Sterilization processes of surgical devices as well as strict donor screening in transplantation and transfusions are all undertaken to cut back on iatrogenic spread.
While medical officials wait for further verification and possible connections between the three patients, the attention is on education, surveillance, and reassurance to the public.
Although it is reassuringly ominous to witness a disease of this kind emerging in a small American community, the risk at the international level remains low, especially with measures presently in place. Nevertheless, the cases are a sobering reminder of the enigma that prion diseases continue to pose to modern medicine.
Health officials are still keeping an eye on the matter and are asking people not to panic but to remain updated. "The health department will remain vigilant and inform you of any public health risk," officials promised in a statement.
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