Daycare Owner, 23, Charged with Murder After Allegedly Slamming 8-Month-Old Infant’s Head into Floor Over Frustration.
A baby boy is dead, and a young daycare owner faces capital murder charges following a shocking incident in Little Rock, Arkansas.
On Dec. 30, 8-month-old Elijah Flowerday was found unresponsive at the home-based daycare run by 23-year-old Erin Sauls. Emergency responders performed CPR on the infant before rushing him to a nearby hospital, where he later died. Police quickly determined that Elijah’s injuries were consistent with homicide.
According to authorities, Sauls allegedly admitted to slamming Elijah’s head on the floor multiple times while changing his diaper. In a police interview, she reportedly stated she acted out of frustration and because she had a headache. The assault caused skull fractures and brain bleeds, consistent with the infant’s fatal injuries.
Sauls was arrested the same day, and on Dec. 31, she appeared in court, entering a not guilty plea to capital murder. The judge denied a request for bail, ordering her to remain in custody pending trial.
Elijah’s family has been left devastated by the loss. Relatives identified the child as Elijah Flowerday, and a GoFundMe page has been set up to help cover funeral expenses. “This tragedy has left Isaac, Trinity, and their son Laylon heartbroken as they grieve the loss of their son and little brother,” the fundraiser reads. “The days ahead will be incredibly difficult as they try to find comfort and healing together as a family.”
The incident has shocked the local community, raising urgent questions about the safety and oversight of home-based daycare facilities. Authorities are continuing to investigate the circumstances surrounding Elijah’s care and the events leading up to the fatal injuries.
This case highlights the devastating consequences of caregiver frustration and the importance of proper training and support in childcare settings. Experts say any signs of stress, fatigue, or potential abuse must be addressed immediately to prevent tragedies.
Sauls’ legal team has not publicly commented. The case remains under investigation, and no further details have been released about the potential trial timeline.
Elijah’s death has prompted an outpouring of grief online, as friends, neighbors, and parents expressed shock and sympathy for the family. The GoFundMe fundraiser, created shortly after the tragedy, has drawn widespread support, demonstrating the community’s desire to help the family navigate the financial and emotional aftermath.
Authorities emphasize that anyone witnessing signs of child abuse or unsafe caregiving practices should report them immediately. The case is a stark reminder of the vulnerability of children in daycare settings and the critical responsibility placed on caregivers entrusted with their lives.
As the community mourns Elijah Flowerday, officials and advocates continue to call for awareness, support for families, and accountability in childcare environments.
Man Sentenced to 40 Years for Killing Gay College Student, Allegedly to Hide Romantic Relationship; Victim’s Family Seeks Justice After Years of Waiting.
A University of Mississippi student’s life was cut tragically short, and justice has finally been served.
Sheldon “Timothy” Herrington Jr., 25, was sentenced to 40 years in prison on Dec. 2, 2025, after pleading guilty to second-degree murder and tampering with evidence in the death of 20-year-old Jimmie “Jay” Lee. Prosecutors claimed the killing was an attempt to conceal a romantic relationship between the two men.
Lee, a prominent member of Ole Miss’ LGBTQ+ community, went missing on July 8, 2022. His disappearance sparked immediate concern among family, friends, and the university community. Investigators soon discovered sexually explicit messages exchanged between Lee and Herrington, along with online searches on Herrington’s device asking, “how long it takes to strangle someone,” according to the Associated Press.
In the months following Lee’s disappearance, his car was found abandoned in a parking lot, and security footage showed him leaving near Herrington’s apartment in Oxford, Mississippi. A judge eventually ruled Lee legally dead in absentia, though his remains were not recovered until February 2025.
Herrington initially faced capital murder charges, but a trial in December 2024 ended in a mistrial after jurors failed to reach a verdict. His attorney had argued that a conviction was impossible without a body, highlighting the challenges prosecutors faced in proving the case.
The sentencing marks a long-awaited moment for Lee’s family, who have spent years seeking answers and justice. Friends described Lee as vibrant, engaged, and deeply involved in the university’s LGBTQ+ community, whose loss left a lasting impact on everyone who knew him.
Prosecutors described the crime as both violent and premeditated, emphasizing that
Herrington’s actions were intended to hide the relationship and the events leading to Lee’s death. By pleading guilty to second-degree murder and evidence tampering, Herrington avoided a potential capital murder trial, but the sentence ensures decades behind bars.
The case also underscores broader conversations about violence against LGBTQ+ individuals, particularly young men who may face threats in their personal and social lives. Advocates stress that education, awareness, and support systems are vital to preventing similar tragedies.
In court, Lee’s family expressed relief that Herrington had been held accountable, though grief and loss remain deeply felt. For the Ole Miss community, the sentencing provides closure while honoring the memory of a young man taken too soon.
The story of Jimmie “Jay” Lee serves as a reminder of the risks LGBTQ+ individuals can face, the importance of vigilance by friends and family, and the long path to justice when a life is violently ended.
Authorities continue to stress the importance of reporting suspicious activity or threats to prevent further tragedies. Lee’s legacy, both as a student and a beloved member of his community, is remembered through scholarships, advocacy, and the memories of those who loved him.
Two Children Born with Severe Heart Defects Defy All Odds, Surviving Life-Threatening Surgeries and Inspiring Families with Their Remarkable Courage and Resilience.
Wyatt and Harper entered the world carrying battles no child should ever face. Both were born with severe congenital heart defects, and doctors warned their families that survival was uncertain. Yet, through courage, love, and relentless care, the siblings defied the odds in ways that inspire everyone who hears their story.
Wyatt’s fight began the moment he took his first breath. His heart was so weak that without immediate intervention, he would not survive. At just two months old, he underwent a heart transplant, the first of many surgeries that would define his early life. The procedure was risky, and every second in the hospital was fraught with fear. His tiny body struggled to recover, battling infections, complications, and the constant threat of organ rejection.
Through it all, Wyatt’s parents stayed by his side, holding onto hope with every beep of the monitors tracking his fragile body. They watched as their son faced each challenge with determination. Months turned into years, and Wyatt’s condition stabilized. By the age of five, he was running races, something his doctors had once thought impossible. Today, at nine, Wyatt competes in 5K races, a living testament to human resilience and the power of perseverance.
Harper’s journey, though different, was no less extraordinary. Her heart condition was complex and unclear, leaving doctors adjusting her treatment plan constantly. At four months old, she underwent a life-saving surgery to strengthen her heart, facing risks similar to Wyatt’s. Recovery was slow, with infections and complications threatening her progress, but Harper’s parents never let fear overshadow their hopes.
They surrounded her with love, laughter, and encouragement, speaking to her as if she were already the joyful, energetic child they envisioned. Harper thrived in this environment, building strength day by day. Today, she is a healthy, active child, defying the odds that once seemed insurmountable.
The stories of Wyatt and Harper are more than just tales of medical triumph. They highlight the resilience of children and the vital role families, doctors, and caregivers play in the fight for life. Each milestone, every step, every laugh, every race is a victory, not just for the children, but for everyone who has supported them along the way.
Experts say congenital heart defects are among the most challenging conditions to treat in infants, requiring careful monitoring and sometimes multiple surgeries over several years. Wyatt and Harper’s survival and progress illustrate both the advancements in pediatric cardiac care and the extraordinary determination of children and their families.
Wyatt and Harper’s stories serve as a reminder that hope, love, and courage can move mountains even when the odds seem impossible. Their journeys inspire families facing similar battles, showing that even in the darkest moments, life and joy can prevail.
Father Survives Four Heart Stops After Surgery, Daughter’s Touch Brings Him Back, Family Now Prays for Miracle Recovery.
Ricardo Garza’s life has been a fight from the very start of his open-heart surgery. While the procedure itself was critical, his family believed the worst was behind them once he was moved to the ICU. But fate had more challenges in store.
In the days following surgery, Ricardo’s heart stopped not once, but four times. Each time, doctors worked tirelessly to bring him back, performing life-saving interventions as every second passed like an eternity. Family members waited in the tense silence of the ICU, hearts heavy with fear, hoping their loved one would survive each ordeal.
It was during this desperate time that his daughter, Thalia, became a source of light in the dark. Sitting at his bedside, she gently spoke to him, her voice filled with love and reassurance. In a moment that seemed almost miraculous, Ricardo opened his eyes and squeezed her hand. That small gesture was more than a sign of life; it was a signal of hope, a reminder to everyone in the room that his fight was not over.
“Seeing him respond to Thalia, even just for a moment, gave us the courage to keep believing,” a family member said. For the Garza family, every heartbeat and every breath became a small victory. Each passing hour was a reminder of how fragile life can be, and yet how precious every moment is when filled with love.
The road to recovery remains uncertain. Ricardo’s organs, his heart, and his brain have endured tremendous strain, and doctors caution that the days ahead will require careful monitoring and patience. But the family refuses to give in to despair. Instead, they are turning to faith, asking friends, community members, and prayer groups to support Ricardo with their prayers and positive thoughts.
Thalia, in particular, has become a voice for hope. She believes in the power of prayer to strengthen her father, knowing that while medicine can do much, some things are beyond human hands. “God can do what only He can,” she said, holding onto faith as a lifeline through the uncertainty.
Ricardo’s story is a testament to resilience, love, and the human spirit. It reminds us that even in the most critical circumstances, connection, care, and hope can make a difference. For families facing similar battles, his journey underscores the importance of holding on to every moment, cherishing gestures of love, and finding strength in community and faith.
For now, the Garza family continues to pray, waiting for the day Ricardo will fully recover and return home. Every heartbeat, every small response, and every act of love brings them one step closer to that day. And in that hope, they find courage.
WOMAN WHO MARRIED A RAGDOLL ANNOUNCES THE BIRTH OF HER.FOURTH CHILD.
Meirivone Rocha Moraes, the Brazilian woman who captured international attention for marrying a life-sized ragdoll, has once again made headlines this time to announce the arrival of her “fourth child.”
Moraes’ story first emerged years ago when she revealed that she had found the “man made for her” after venting to her mother about being single and frustrated at not having a dance partner. In a creative attempt to cheer her up, her mother crafted a life-sized ragdoll named Marcelo. What began as a playful gesture soon transformed into a unique relationship that Moraes says has been life-changing.
Over the years, Moraes has documented her unusual life online, sharing images of her wedding to Marcelo, family celebrations, and the “births” of their children. She maintains that Marcelo is her husband, and she treats the ragdoll as a full member of her family.
The latest announcement comes with staged, hospital-style photographs showing Moraes holding what she describes as her newest “child,” wrapped in blankets just like a newborn baby. The images follow the same format as her previous posts, blending humor, creativity, and her personal vision of family.
“I am happy to share the arrival of our newest family member,” Moraes told local media. “Our love and family continue to grow, and we celebrate every moment together.” She says that Marcelo has been a consistent presence in her life, supporting her through personal milestones, creative projects, and now the ongoing expansion of her family.
Moraes’ story has sparked a mixture of fascination, amusement, and curiosity online. Social media users have shared memes, debated the concept of unconventional family structures, and expressed both admiration and disbelief at her commitment to Marcelo. Despite the attention, Moraes remains unbothered by criticism, emphasizing that her life choices bring her joy and fulfillment.
Experts in psychology and social behavior note that Moraes’ relationship, while unusual, highlights broader conversations about companionship, loneliness, and the ways people create meaning and connection in their lives. While skeptics may question the logistics of raising a family with a ragdoll, Moraes’ posts suggest that for her, the boundaries of love and family are defined by personal happiness rather than convention.
As Moraes celebrates the arrival of her “fourth child,” her social media channels continue to showcase the family’s daily life, creative photoshoots, and whimsical celebrations. Whether viewed as performance art, a personal statement, or an unconventional family narrative, her story continues to captivate audiences worldwide.
In a world increasingly open to different ways of forming bonds and defining family, Moraes’ story is a reminder that joy, love, and commitment can take forms that challenge expectations and that happiness, for some, may come in the most unexpected packages.
Ore. Man Killed His Ex-Girlfriend. Then He Put Her Body in Her Own Car and Crashed It While Drunk.
An Oregon man was sentenced to life in prison after pleading guilty to murdering his ex-girlfriend and then attempting to conceal the crime in a shocking, reckless act.
Tyler Holman, 25, entered a guilty plea to second-degree murder in connection with the 2025 death of Ashley Gandolfi. On Jan. 14, 2026, a Marion County court handed down a life sentence, with Holman eligible for parole after 25 years.
The circumstances of Gandolfi’s death stunned authorities. On the day of his arrest, Holman was involved in a rollover crash in Polk County while driving Gandolfi’s car. Inside the vehicle, police discovered her body. Initial reports indicated that she had not been killed in the crash itself, but subsequent investigation revealed she had died from a gunshot wound before the vehicle accident occurred.
Prosecutors said that Holman, who had been in a relationship with Gandolfi and shared a child with her, had been intoxicated at the time of the crash. The child was reportedly living with Gandolfi’s parents at the time of the murder. Court records and news outlets also confirmed that a second individual involved in the case pleaded guilty to tampering with evidence and abuse of a corpse in March 2025.
Holman faced additional charges for weapons violations, tampering with evidence, and abuse of a corpse, but these were dropped following his guilty plea to second-degree murder. The case highlighted not only the tragic loss of Gandolfi’s life but also the enduring consequences for her family and the child she shared with Holman.
According to court documents, investigators pieced together the timeline of events, determining that Gandolfi was killed prior to the car crash. Authorities described the case as both tragic and unsettling, given the lengths Holman went to attempt covering up the crime.
The sentencing marks the conclusion of a case that gripped the local community and raised questions about domestic violence, alcohol-related crimes, and the protection of vulnerable family members. District attorneys emphasized that the court’s decision reflected both the severity of the crime and the need for justice for Gandolfi and her loved ones.
“This was a case of a senseless, preventable loss,” a representative from the Marion County District Attorney’s Office said. “While nothing can undo the harm caused, today’s sentence ensures accountability and the possibility of justice for the victim’s family.”
Gandolfi’s family, who had been caring for her child during the investigation, said they were relieved that the legal process had concluded but continue to mourn her loss.
As Holman begins his life sentence, the case serves as a sobering reminder of the dangers of domestic violence and the lengths some individuals may go to hide violent acts. Authorities urge communities to remain vigilant, report concerns early, and provide support to those in potentially abusive situations.
Single Mom Diagnosed with Rare Blood Cancer Urges Help as Only One Stem Cell Match in the World Can Save Her Life.
A single mom from Wales is fighting for her life after receiving a diagnosis that left her stunned and fearful. Sian Chathyoka, 56, discovered last September that she has a rare and aggressive form of blood cancer called myelofibrosis. Now, she is urging people around the world to consider becoming stem cell donors because only one matching donor in the world can save her.
Chathyoka, a mother of two teenagers, had always led an active life. She managed a family seaside campsite and frequently swam in the cold waters of Swansea Bay. But over the summer of 2025, something changed. Extreme fatigue left her unable to complete her usual activities, and she noticed rapid, unexplained weight loss. “Since August, I’ve just been lying in bed because I’ve had no energy. It’s been quite scary,” she said.
Her symptoms prompted further medical investigation. Tests revealed an enlarged spleen and abnormalities in her bloodwork, leading doctors to refer her to haematology specialists. After a series of scans, she received the life-altering diagnosis of myelofibrosis, a rare blood cancer where a stem cell becomes malignant, crowding out healthy blood cells and damaging bone marrow.
“I couldn’t stop crying,” Chathyoka recalled. “My condition is very rare, and I’ve been told my disease is aggressive as well.” Since then, she has undergone weekly blood and platelet transfusions and treatment to shrink her spleen.
The real challenge came this month when Chathyoka learned that there is only a single stem cell donor in the entire world who matches her. A successful transplant from that one donor could be her only chance at survival. “It’s absolutely petrifying. But you’ve got to forget about that and be positive,” she said.
Chathyoka’s story also highlights the importance of awareness. She explained that many friends and even her own community were unaware of how critical stem cell donations can be. “Just signing up to the register, you can literally save a life. I feel really emotional because that’s as powerful as it is,” she said.
Despite the fear and uncertainty, Chathyoka remains hopeful. She wants her experience to encourage others to join the stem cell register, share their stories, and support life-saving research. “I’m lucky. I’m grateful that there is the possibility of a cure through a stem cell transplant,” she said.
For now, Chathyoka continues her treatments while waiting for her match. Her journey is a poignant reminder of both the fragility of life and the extraordinary power of generosity—how one person’s willingness to donate could literally save a life.
9-Year-Old Girl Suffered Back and Leg Pain for Weeks Before Being Diagnosed with Rare Blood Cancer.
A 9-year-old girl from Scotland has been diagnosed with a rare form of blood cancer, after weeks of suffering from back and leg pain. Ava Ferguson’s story is a stark reminder of how quickly childhood illnesses can turn serious and how crucial early intervention can be.
In December 2025, Ava began complaining of discomfort in her back and legs. Her parents, Jamie and Sam Ferguson, initially attributed it to growing pains, but the severity and persistence of her symptoms quickly raised concern. “It was more than just normal growing pains,” family friend Laura Gillespie told Edinburgh Live. “Her mom was up every hour massaging her legs to try and give her some comfort and relief from the pain.”
Doctors initially suspected post-viral reactive arthritis, a temporary condition that can follow infections in children. But as Ava’s symptoms persisted, blood tests were carried out shortly before Christmas, revealing a much more serious diagnosis: acute lymphoblastic leukemia (ALL), a rare cancer of the blood cells.
“It’s brutal, and it’s very intense,” Gillespie said. ALL develops when abnormal blood cells form in the body, crowding out healthy cells, and requires immediate treatment. While more common in children under the age of four, Ava’s case highlights that older children can also be affected.
Ava began chemotherapy almost immediately after her diagnosis. The treatment has been aggressive, causing fatigue and hair loss, and requiring bone marrow harvesting and blood transfusions. Gillespie explained that Ava recently celebrated her birthday, but her energy and joy have been curtailed by the intensity of her treatment.
The impact of the diagnosis extends beyond Ava. Her parents, who are from New Zealand and have no nearby family, must balance supporting Ava with caring for her younger sister, Zoe. Gillespie set up a GoFundMe to assist the family with medical costs and to support Ava’s dream of visiting the Capybara Cafe in Tokyo. “Her treatment journey has already started, but there’s a long road ahead for Ava and her family,” she wrote.
Despite the challenges, Ava remains spirited. She loves sushi and is already planning her dream trip, a symbol of hope and resilience amidst uncertainty. The GoFundMe has raised over $1,000 toward a $3,355 goal, demonstrating the power of community support in times of crisis.
Ava’s story serves as a powerful reminder to parents and caregivers: persistent pain, even when it seems minor, should never be ignored. Early attention and advocacy can make a life-saving difference. For Ava Ferguson, timely medical tests revealed a rare condition just in time to begin treatment giving her a fighting chance and a future filled with hope.
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