logo
Health officials prepare for measles spread as disinformation threatens already low vaccination rates

Health officials prepare for measles spread as disinformation threatens already low vaccination rates

CNN14-03-2025

When Pastor Landon Schott attended a school board meeting for Mercy Culture Preparatory Academy last week, he found the room filled with balloons and T-shirts.
The celebratory shirts read: #1 school in Texas for least amount of vaccinations.
Schott, who has more than 48,000 followers on Instagram, posted a video to congratulate all the families at the school who have chosen to 'embrace freedom of health and they are not allowing government or science projects to affect how you live and lead your life.'
State Rep. Nate Schatzline also shared the news with his over 17,000 followers on X. His video says that the school is in his district and that his children attend there.
'Why haven't we celebrated this sooner?' the Republican asked.
The Fort Worth-area school has the lowest measles vaccination rate in Texas: Just 14% of incoming kindergartners had measles-mumps-rubella (MMR) coverage last school year, according to data from the state health department.
But low vaccination rates across Texas are leaving many communities vulnerable amid a measles outbreak centered in the western part of the state, one of the largest the United States has seen since the disease was declared eliminated in the country in 2000.
In efforts to prevent even broader spread, public health officials in Texas, New Mexico and Oklahoma are working around the clock to raise vaccination rates and otherwise help protect vulnerable communities – work that is challenged by the spread of disinformation.
'They are stressed and stretched beyond belief,' Terri Burke, executive director of the Immunization Partnership, a nonprofit focused on improving vaccination coverage in Texas, said at a briefing Thursday. 'The biggest thing I'm hearing is the need for more resources.'
One public health director in a county that has been hit by the outbreak told Burke she had been working more than a month straight without a day off.
'We spoke at six o'clock at night, and she told me she had started at 4:30 that morning,' she said.
Overall, the MMR vaccination rate among kindergartners in Texas was 94.3% for the 2023-24 school year, just below the 95% target that federal agencies have set to prevent epidemics. But about half of all school districts in the state have coverage that falls below this threshold, including nearly a quarter that have a vaccination rate of less than 90%. And Mercy Culture Preparatory Academy is one of more than a dozen schools where coverage was less than 50%.
The school did not immediately respond to CNN's request for comment on its vaccination coverage.
Tarrant County, home to Mercy Culture Preparatory, has not reported any measles cases this year, but local health officials there and in many parts of the state are preparing for what seems inevitable.
'We're kind of a more high-risk area, if you will,' Russ Jones, chief epidemiologist with the Tarrant County Public Health Department, said at a county commissioners' meeting Tuesday, referencing the county's vaccination rate of 91.5%. 'At this level, we'll have some cases.'
He also noted that there are pockets of the county where even larger shares are unvaccinated, including children at Mercy Culture Preparatory.
'Those would be particularly vulnerable if that network of cases crosses with our unvaccinated population,' he said. 'If it doesn't happen, there won't be a problem. If it does, then we could have many cases, depending on the population it crosses with.'
To prepare, the county health department is communicating directly with schools and day cares and coordinating with hospitals and other local health care providers. Vaccines are available at community clinics, too.
'There is a heightened vigilance across our state because of this outbreak,' Burke said.
As public health experts work to curb the spread, there's concern about the ways anti-vaccine messaging can hinder their efforts.
'There has been a lot of misinformation [and] disinformation on social media,' said Dr. Philip Huang, director of the Dallas County Health and Human Services Department. 'On social media, you can put some of that info out there without any fact checks, and incorrect information is just as readily available as correct information.'
He also attributed decreasing vaccination rates to a distrust in government and politicization over vaccinations in general.
'There are these pockets of communities that are anti-vax, and so you can get a lot of people together that aren't vaccinated, and that's the biggest … dangerous situation,' Huang said.
As in Tarrant County, Huang's department has hosted informational sessions with school nurses, physicians and hospitals to make sure everyone is up to speed on measles. He has sent letters to public and private school officials who are in districts with low vaccination rates and offered to provide vaccines.
Across the state line in New Mexico, which has also seen dozens of measles cases, officials are providing vaccines through free clinics. Jimmy Masters, the Southeast regional director with the New Mexico Department of Public Health, says the driving message is 'to be proactive.'
His region has set up clinics not only in Lea and Eddy counties, where there are current cases, but in neighboring Chaves County. Residents are encouraged to check their vaccination status if they are unsure whether they ever received a dose of the MMR vaccine.
New Mexico has administered nearly twice as many MMR vaccines as last year. In the past six weeks, there have been nearly 10,000 doses given, compared with about 5,300 in the same time frame last year.
Primary care physicians can also play a key role in getting ahead of the measles outbreak by addressing questions and concerns directly with patients and families.
'We have a number of parents today who have concerns about all the vaccines their children receive. We'd recommend they talk to their primary care physician,' Tarrant County's Jones said.
Some pediatricians – both in counties that have reported cases and in those that haven't – are reaching out to families directly to raise their awareness of the ongoing outbreak and encourage them to get their children vaccinated.
'I think it's very important for all of us – and especially on an individual level – to continue to be the voice of truth, if you will, but also the voice of strength and endurance and commitment to our families and our children in Texas,' Dr. Ana Montanez, a pediatrician in Lubbock, said at the briefing Thursday.
Learning about how many vaccinations had been administered in New Mexico bolstered her determination to continue the work she's been doing to keep her patients and their families safe.
'That extra effort is being made, and there is a difference that is coming out from that, although it may be small and tied up in little experiences,' she said. 'But it is making a difference.'

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Sad reason 31-year-old woman has never had a boyfriend
Sad reason 31-year-old woman has never had a boyfriend

New York Post

timean hour ago

  • New York Post

Sad reason 31-year-old woman has never had a boyfriend

My life has always been marked by a strange duality. I was Dux of my high school, but I had no best friend to trade secrets and friendship bracelets with. Advertisement I graduated with a double-degree, but I couldn't make eye contact with the cute guys in my classes. I work professionally and was headhunted for a PhD scholarship, but at age 31 I've still never had a boyfriend. 6 Elena Filipczyk, 31, who has not had a boyfriend yet, was diagnosed as autistic at age 28. elenafilipczyk/Instagram The shame of my difference was all-consuming until I was diagnosed as autistic at age 28. Advertisement Finally, my life made sense: my sensory quirks, mental health struggles, and especially my 'social awkwardness'. For many women like me, an autism diagnosis comes later in life – if we're ever diagnosed at all. According to recent research, nearly 80% of autistic females remain undiagnosed at age 18. Advertisement For a long time, autism was considered a 'male' condition, with four times as many boys diagnosed as girls. Now, though, experts are realizing that autism is much more common in girls and women than previously thought. 6 Finally, my life made sense: my sensory quirks, mental health struggles, and especially my 'social awkwardness,' Filipczyk says. elenafilipczyk/Instagram Still, the diagnostic criteria for autism remains male-centric, meaning girls and women often remain undiagnosed and unsupported. Advertisement Yet even with a diagnosis, autistic women often face barriers receiving appropriate support. Take, for example, my experience with the National Disability Insurance Scheme (NDIS). According to the NDIS, the scheme prioritizes participant 'choice and control' and supports that are 'reasonable and necessary' to improve disabled people's quality of life, independence, and social skills. Applying to the NDIS, I was hopeful I'd finally get some help – support I need particularly because of my social isolation. I have no partner, and both of my parents have died. After a year of waiting on my application, I got a life-changing call from a sunshine-voiced woman. 'Just calling to let you know that you are now a participant of the NDIS,' she said. Advertisement Relief flooded through me, but it was short-lived. In my first planning meeting, an NDIS worker asked me what supports I would like. 'Psychosexual therapy and pelvic floor physiotherapy,' I responded. 'And maybe a hearing aid for my left ear.' Advertisement 'How are those related to your autism?' she asked. Awkwardly, I explained how my social anxiety and trauma are stored in my pelvic muscles, a condition called vaginismus. 6 Filipczyk deals with social anxiety and trauma that are stored in her pelvic muscles, which is a condition called vaginismus. Elena Filipczyk/Twitter These therapies, I clarified, will mean one day I'll have the confidence and physical ability to have a normal romantic, sexual relationship, just like everyone else. Advertisement 'Not everyone who has autism experiences trauma,' she said. 'There's no direct link from autism to psychosexual therapy or pelvic floor physiotherapy for your vaginis… whatever'. Shame swept over me. 'These are considered medical treatments,' she continued, 'So they're not covered by the NDIS but by Medicare.' Advertisement It took all my courage to point out that neither of these therapies are covered by Medicare. Later, I found out that both psychosexual therapy and physiotherapy can be covered by the NDIS. At the end of the call, the NDIS planner offered me access to a speech therapist and support worker, despite the fact I have no speech impediment and am comfortable going out alone. As a disability scholar, I know why I've fallen through the cracks. Like many services that aim to help autistic people, the NDIS is biased by years of male-centric diagnostic and treatment rhetoric. 6 'Like many services that aim to help autistic people, the NDIS is biased by years of male-centric diagnostic and treatment rhetoric,' Filipczyk says. Elena Filipczyk/Twitter This underlying current of medical misogyny fuels ignorance about how autism presents in girls and adult women, and therefore what 'reasonable and necessary' supports might be. In other words, because I'm autistic, I was offered speech therapy and a support worker, which I understand is common for autistic men. But I'm an autistic woman, and I don't need speech therapy. I need physical and mental therapy so I can build my confidence and heal my traumatized body, so that relationships aren't terrifying and so that sex isn't painful. 6 'I need physical and mental therapy so I can build my confidence and heal my traumatized body, so that relationships aren't terrifying and so that sex isn't painful,' Filipczyk says. And I'm not alone in struggling with romance and sex. Research shows that autistic women often have poorer levels of overall sexual functioning, feel less well in sexual relationships than autistic men, and are also at greater risk of becoming a victim of sexual assault or abuse. According to a recent study, 9 out of 10 autistic women have experienced sexual violence. I am among them. 6 Young Elena Filipczyk. elenafilipczyk/Instagram Despite statistics like these, support for autistic women is scarce and hard to access, even for so-called 'high-functioning' autistic people like me. Reflecting on my NDIS experience, I think 'it shouldn't be this hard'. But it is. And it has real-life implications. In a pub where the noise worsens my hearing impairment, I can't properly hear the guy who approaches me to talk. He eventually gives up and politely excuses himself, walking away. I have a panic attack and leave. On Facebook, I see old school peers post about their partners and children. On Instagram, I see one of my oldest friends announce her engagement. 'Congrats!!!' I comment, crying tears of envy. At the gynaecologist, I fail a cervical exam in searing pain. Alone, I remember lying in a man's bed, paralyzed with fear and the shame of my inexperience. I wonder what a speech therapist would say. Elena Filipczyk is an autistic writer and PhD candidate.

The science of sleep paralysis, a brain-body glitch making people see demons and witches
The science of sleep paralysis, a brain-body glitch making people see demons and witches

Yahoo

time6 hours ago

  • Yahoo

The science of sleep paralysis, a brain-body glitch making people see demons and witches

Sign up for CNN's Sleep, But Better newsletter series. Our seven-part guide has helpful hints to achieve better sleep. Baland Jalal lay in bed terrified, experiencing his own real-life horror film. Newly awake, the 19-year-old could see his surroundings but couldn't move or speak, and he didn't know why. He thought, ''My God, what do I do?'' Jalal, now 39, said of that moment in 2005. 'I tried to call my mom (and) dad, but no words would emerge from my throat. … I had this ominous presence of a monster, and it lifted my legs up and down. 'It strangled me, trying to kill me. And I was 100% sure that I was going to die,' Jalal added. 'It literally feels like all the evil of the universe is condensed into a bubble, and it's in your bedroom.' This type of hallucination is a hallmark for many people with sleep paralysis. It occurs during transitions into or out of rapid eye movement, or REM, sleep, similar to a traffic jam at a busy intersection — your brain, awake and alert, and body, still asleep and immobilized, collide momentarily, said Dr. Matthew P. Walker, director of the Center for Human Sleep Science at the University of California, Berkeley, via email. Following deep sleep, REM sleep is the next critical phase of sleep cycles, characterized by more dreaming that's also extra vivid and lifelike, and by faster heart rate and breathing. It's essential for memory, concentration, mood regulation and immune function. Jalal's experiences propelled him to study this phenomenon around the world. He aimed to discover the cause of sleep paralysis, he said, and why some people with the diagnosis 'have these powerful encounters where it feels like evil of epic proportions.' He has since earned a doctorate in psychiatry and is now a researcher in Harvard University's psychology department and a leading expert on sleep paralysis. He also treats patients struggling with it. An estimated 30% of people worldwide experience at least one episode of sleep paralysis in their lifetime, according to the Cleveland Clinic. How many of those people have recurring and impairing sleep paralysis isn't clear, but the percentage is likely low, Jalal said. Here's what else you should know about sleep paralysis and how it can be managed. In REM sleep, our bodies are paralyzed so we don't act out our dreams and risk hurting ourselves or others, Jalal said. Sleep paralysis episodes are usually only a few minutes long but can last up to 20 minutes, according to the Cleveland Clinic. During sleep paralysis, however, 'we regain consciousness before the muscles regain their freedom from REM-induced paralysis,' said Walker, who is also a professor of neuroscience and psychology at the University of California, Berkeley About 40% of people with sleep paralysis have visual, auditory or tactile hallucinations, such as pressure on one's chest or feeling out of body, Jalal said. For about 90% of those individuals, the illusions are terrifying. They can include ghosts or cat- or alien-like creatures, and their actions can be as innocuous as simply approaching them or as nefarious as molesting or trying to kill them. In Jalal's academic travels, he discovered the contents and interpretations of hallucinations, views on what causes sleep paralysis, and episode frequency and duration can all also have a cultural basis. People living in Egypt and Italy, for example, would often see witches and evil genies, hold them responsible and think they could die from sleep paralysis, Jalal said. People in Denmark, Poland and parts of the United States, on the other hand, have less supernatural or exotic explanations and less fear. 'Why do we see these monsters? Is it the dreaming imagery … that's spilling over into conscious awareness?' Jalal said. 'My answer to that is, according to my research, no, not exactly. But it's part of it.' When you're aware yet paralyzed and confused, your natural reaction is to escape that situation. Your brain is bombarding your body with signals to move, but your body can't return any feedback. Jalal's theory, in short, is that your brain says, 'to hell with it' and concocts a story it thinks your body must be facing to be experiencing such bizarre symptoms. The reduced activity in your prefrontal cortex — responsible for reason and logic — also contributes to hallucinations becoming 'extremely realistic and emotionally charged, amplified by an overly active amygdala, the brain's emotional alarm center,' Walker said. Though scientists know that wake-sleep glitch is what's happening during a sleep paralysis episode, they're not entirely sure why. But there are several factors that can increase the risk of fragmented sleep and sleep paralysis. Those factors include stress and related conditions such as anxiety, post-traumatic stress disorder (PTSD), bipolar disorder and panic disorder, experts said. Much of Jalal's sleep paralysis occurred when he was in school. Now when he has an episode once or twice per year, it's usually during a high-stress period, he said. (Once you've experienced sleep paralysis, you can be conscious of that during an episode but still feel afraid.) Other common contributors are sleep deprivation, jet lag, an irregular sleep schedule, sleep disorders such as narcolepsy, and genetic factors, Walker and Jalal said. Obstructive sleep apnea, substance use disorder and some medications — such as those for attention deficit hyperactivity disorder — can also raise risk, according to the Cleveland Clinic. As scary as sleep paralysis may sound, it's not actually dangerous, experts said. But depending on how recurring it is, sleep paralysis can be a sign of an underlying sleep disorder, Jalal said. Regular episodes can also lead to anxiety around sleep and then avoidance of sleep, Jalal said. This pattern can interfere with your daily energy and ability to function. And if you often have frightening hallucinations, that can lead to anxiety or trauma-like symptoms. Sleep paralysis can be significantly alleviated with several practices or treatments, Walker said — starting with healthy sleep habits, for one. That includes seven to nine hours of restful sleep nightly. Maintaining a sleep schedule consistent in quality and quantity 'acts like tuning your internal clock, reducing the chance of disruptive wake-sleep overlaps — much like ensuring all parts of an orchestra are synchronized for perfect harmony,' Walker said. Also prioritize stress management, by using, for example, mindfulness and relaxation exercises, Walker said. Therapies can relieve certain underlying issues triggering sleep paralysis, including cognitive behavioral therapy, especially the version for people with insomnia. In more serious situations, medications are sometimes used, Walker said. Those include SSRI (selective serotonin reuptake inhibitor) or tricyclic antidepressants that can help manage a smooth flow between sleep stages or even reduce the REM phase of sleep. Generally, boosting the brain's serotonin levels somehow compensates for the loss of the REM phase, Jalal said. But rarely, long-term antidepressant use has been linked with REM sleep behavior disorder. While the aforementioned treatments can help reduce the frequency or length of sleep paralysis episodes, there isn't yet a gold-standard treatment that can stop an episode once it's happening. Jalal has been trying to officially create one over the past decade, though, and it's self-inspired. Called meditation relaxation therapy, the treatment reduced sleep paralysis by 50% after eight weeks for six people with narcolepsy, compared with a control group of four participants, found a small pilot study Jalal published in 2020. He currently has another study of the same treatment with more participants underway at Harvard. And the steps of Jalal's therapy are as follows: Cognitively reappraise the meaning of the attack. Close your eyes and remind yourself that your experience is common and you won't die from it. Emotionally distance yourself from it. Tell yourself that since your brain is just playing tricks on you, there's no reason for you to be scared or risk the situation getting worse because of your own negative expectations. Focus on something positive. Whether it's praying or imagining a loved one's face, this refocusing can make thoughts more pleasant rather than monstrous. Relax your muscles and don't move. Some experts say trying to slightly move your fingers or toes one by one may help you come out of an episode sooner. But Jalal's fourth step advises against this movement since you'd still be sending signals to paralyzed muscles and maybe triggering hallucinations. Viewing your own biology in a more objective way by learning more about the scientific basis of sleep paralysis is also helpful, Jalal said.

Mom Captures Moment With Toddler, Just Days Later She'll Be Gone
Mom Captures Moment With Toddler, Just Days Later She'll Be Gone

Newsweek

time11 hours ago

  • Newsweek

Mom Captures Moment With Toddler, Just Days Later She'll Be Gone

Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. A mom from Ontario, Canada, captured a moment with her toddler, not knowing it would be one of the last memories together. Tamara Spearing, 31, posted a reel on Instagram holding and kissing her daughter. Days later, Gwendolyn was gone. Spearing told Newsweek that she was pregnant with Gwendolyn at 26. She had just bought her first home and was working two jobs. From left: Tamara Spearing holds her toddler daughter in her arms and kisses her head in dark lighting. From left: Tamara Spearing holds her toddler daughter in her arms and kisses her head in dark lighting. @tamaraspearing_ Spearing's days were full—friends, family, healthy living and big dreams. "I had full trust in the universe and what life was going to look like for me," she said. "That was until my life drastically changed within a matter of days." Gwendolyn was what Spearing called her "pleasant surprise." While her pregnancy was unplanned, she said she quickly embraced it. "I remember daydreaming what my child would look like; who they would grow up to be," Spearing said. "For me, my pregnancy was just the beginning of something amazing, and I was so, so excited to be a mama." At 28 weeks and five days, Spearing went into premature labor—a terrifying experience that unfolded while she was visiting Gwendolyn's father, who had recently been admitted to the ICU after a serious accident. "I didn't want to believe it as I was hardly into my third trimester," she added. Spearing walked herself to the labor and delivery floor, where she was met by a team of specialists. "I faintly remember looking over to the bedside nurse, asking her what I should expect and begging and pleading for a safe arrival of my baby," Spearing said. "I told the nurse, 'That wasn't my birth plan. I don't even have a nursery at home.' "She looked at me and said, 'Hunny, there is no such thing as a birth plan'," Spearing said. Within two hours and just three pushes, Gwendolyn was born at 2 pounds, 10 ounces. What followed were months of medical hurdles. Gwendolyn was diagnosed with Esophageal Atresia with Tracheoesophageal Fistula (EA/TEF)—a rare congenital condition where the esophagus doesn't connect to the stomach. Gwendolyn's prematurity brought additional complications: brain bleeds, underdeveloped lungs, multiple surgeries, code blues (where a patient requires resuscitation or is in need of immediate medical attention) and long hospital stays. Overall, Gwendolyn spent 170 days in hospital before being cleared to go home. Against the odds, she was thriving and hitting every milestone, according to her mom. "Appointments were further and farther between; she was attending playgroups and making friends; she was learning and discovering as a child should be at her age," Spearing said. "For the first time in her life, she was able to be just a kid." Then, on April 5, their world came crashing down. "For us, it was a normal day," Spearing added. "Little did I know this day would change my life forever." That evening, Gwendolyn's heart stopped. The autopsy provided no definitive cause. Some specialists suspect a catastrophic seizure or undetected heart failure. Spearing explored genetic counseling in the aftermath but was overwhelmed by the lack of answers. "I may never know why my daughter passed, and although I know now sometimes things just aren't meant to have an explanation, I still lay awake at nights contemplating the days leading up to her death and wondering if there was something I missed and if there was something apparent; maybe I could have saved her," Spearing said. Now, three years later, grief remains a constant companion. Spearing said that she barely remembers anything after Gwendolyn passed. "I was very angry. I lost trust in the universe and I questioned my beliefs," she added. "I wanted nothing more than to wake up from this nightmare that I was living in. I couldn't understand why a beautiful, innocent soul, who fought so hard to be here, only to be taken so abruptly." Out of her grief, Spearing created The Gwen Effect, a foundation honoring her daughter's legacy. It supports premature infants and children with complex medical conditions, funds research, and offers community support for grieving families. "I found a way of turning my pain into a purpose," Spearing said. "I continue to speak on grief and life after loss as I truly believe it is something that needs to be talked about more." The foundation's mission is clear: raise awareness, provide resources and create spaces where both grief and hope can coexist. Through it, Gwendolyn continues to touch lives. "Gwen was a ray of sunshine," Spearing said. "She was born tiny but mighty. Her passion for life while in and out of hospital showed us and many others how precious our time is. She was strong and brave."

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