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37-year-old woman arrested after posing as a 12-year-old girl and living with an adoptive family for over a year while behaving like a child

A woman has been arrested after posing as a 12-year-old girl and living with an unsuspecting family for more than a year.

According to investigators, the suspect, initially known to the family as Gabriele, was welcomed into the home of a couple who believed she was a vulnerable child in need of care. The family reportedly developed a close emotional bond with her, celebrating birthdays and treating her as their own daughter.

Authorities later identified the suspect as Amanda Maria Sousa Oliveira, a 37-year-old woman.

Police said the deception came to light when officers arrived at the family’s home and arrested her following an investigation into her identity.

According to investigators, the suspect first approached a church in Joinville, Brazil, claiming she had fled an abusive situation in the northern state of Pará. Members of the religious community reportedly provided financial assistance and helped arrange accommodation before she was eventually taken in by the family.

Police stated that she lived with the family for approximately 14 months while maintaining the false identity.

Investigators allege that Oliveira claimed to suffer from autism and other medical conditions to explain her adult appearance. She also reportedly told the family that she had been forced to take hormones as a child due to abuse, which she said contributed to her mature features.

To sustain the deception, police said she adopted childlike behavior, including using baby bottles, dummies, and a comfort blanket. She also allegedly feigned panic attacks and spoke in a high-pitched voice to gain sympathy and attention.

The family reportedly became so attached to her that they celebrated what they believed was her 12th birthday, paid for medical treatments, and even considered formally adopting her.

Detective Rodrigo Bueno Gusso said the suspect consistently avoided discussions about official adoption procedures and never produced identification documents. Investigators also claim she persuaded the family not to enroll her in school by alleging that her abusive father could track her down.

The alleged scam was eventually uncovered after a relative alerted authorities, prompting a police investigation.

During questioning, police said Oliveira confessed to the deception and was subsequently charged with fraud and false identity offenses before being taken to Joinville Regional Prison.

Authorities further revealed that she has previously been linked to similar cases in several Brazilian states, including São Paulo, Rio de Janeiro, Minas Gerais, Rio Grande do Sul, and Goiás.

In one case from 2023, investigators allege that she posed as a 12-year-old girl named “Maria Eduarda” and convinced community members to provide housing and support. Police claim she fabricated stories of abuse and inserted needles into her own body in an attempt to support her allegations.

Although she was detained in connection with that case, she was later released under court-imposed precautionary measures.

Officials noted that several previous investigations involving different identities remain open due to her frequent relocation between states and use of multiple aliases.

As of now, Oliveira remains in custody at Joinville Regional Prison while facing the latest charges against her.

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I Can’t Use Water on My Face, and I Can’t Even Drink Plain Water – Woman Allergic to Water Laments

A woman living with an extremely rare medical condition has opened up about the daily struggles she faces after revealing that even a small amount of water touching her skin can trigger painful allergic reactions.

Kimberlee Mills, from Houston, has been diagnosed with Aquagenic Urticaria, a rare condition in which contact with water—regardless of its temperature—causes itchy, painful hives, redness, or swelling on the skin.

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Because of the condition, Kimberlee said she has drastically changed her daily routine, including how often she washes her face and the way she stays hydrated.

According to her, she only washes her face with water once or twice a month and relies on water-free skincare products to reduce the risk of painful flare-ups. She also explained that she avoids drinking plain water because it makes her feel extremely nauseous.

Speaking about how the condition has transformed her daily life, she said:

“Aquagenic Urticaria affects almost every part of my life.

“My mornings look completely different from most people’s.

“I only wash my face with water once or twice a month because even that can trigger a painful reaction.

“Most days I rely on rinse-free cleansers and waterless skincare products.

“Before I leave the house, I check the weather.

“If it’s hot, humid or looks like it might rain, I have to think about whether it’s worth going out at all.

“Something as simple as sweating can leave me covered in hives.

“Most people don’t think about water.

“I have to think about it every single day.

“Everything has to be planned.

“I don’t shower every day like the average person.

“Even brushing my teeth requires planning to keep water exposure to a minimum.

“I don’t drink plain water because it makes me extremely nauseous, so I stay hydrated through other beverages and foods that I tolerate better.”

She also revealed that the reactions can sometimes become severe enough to require emergency medical attention.

“In severe situations I’ve experienced swelling and symptoms serious enough to require emergency medical treatment.

“The severity isn’t always predictable.”


Kimberlee explained that she first started experiencing symptoms when she was just 12 years old. For many years, doctors struggled to determine the cause of her reactions because the condition is so uncommon.

Initially, both she and medical professionals believed soaps, shampoos, or chemicals in the water were responsible.

However, after years of consultations with different specialists, she eventually underwent a water challenge test that confirmed she had Aquagenic Urticaria.

Recalling her long journey to receiving a diagnosis, she said:

“In the beginning everyone thought I was reacting to soap, shampoo or something in the water.

“Over time I realised it wasn’t the products, it was the water itself.

“After years of searching for answers and seeing multiple specialists, I finally underwent a water challenge test that confirmed I had Aquagenic Urticaria.

“The first thing I noticed was intense itching, burning and hives after showering.

“I also reacted after being caught in the rain and eventually realised I reacted to sweat too.

“It took more than a decade to finally get a diagnosis because the condition is so rare that most of the doctors I saw had never encountered it before.

“It was a very long and frustrating battle.

“I was relieved because I finally had an answer after so many years of wondering what was wrong with me.

“At the same time it was heartbreaking because I learned there wasn’t a cure.

“Having a diagnosis finally made me feel like I wasn’t crazy.

“It gave a name to something that had affected my life for years.”
Kimberlee said living with the rare disorder has affected not only her physical health but also her emotional well-being and family life.

She explained that activities many parents enjoy with their children have become difficult because sweating, rain, humidity, or even water rides can trigger painful reactions.

She shared:

“Living with Aquagenic Urticaria has affected both my mental health and my confidence in ways I never expected.

“It doesn’t just stop me from swimming; it impacts almost every aspect of my life.

“I can’t freely play outside with my children on hot days because sweating can trigger a reaction

“I have to think twice about taking them to water parks or theme parks because rides, splash zones, rain or even the heat and humidity can leave me in pain.

“Some of the memories parents dream about making with their children simply aren’t possible for me.

“Sometimes it feels like the world was designed around something my body can’t tolerate.

“It can also make me feel like a burden because my family has to help me with things many people take for granted.

“I’ve had to grieve the freedom I thought I’d have.

“The hardest part isn’t being allergic to water, it’s losing the freedom that comes with it.

“I can’t be spontaneous; I have to think about the weather, my surroundings, how long I’ll be outside and whether I’ll sweat.

“Water is something most people never think about but I have to think about it every single day.”
Kimberlee also spoke about the skepticism she has faced over the years, revealing that many people—including some medical professionals—found it difficult to believe that someone could be allergic to water.

She said:

“Most people think I’m joking.

“Once they realise I’m serious, they’re fascinated and have lots of questions.

“Others don’t believe me because it sounds impossible.

“That’s one of the reasons I share my journey online.

“As a child I constantly felt dismissed.

“Some people thought I was exaggerating my symptoms.

“Others assumed I simply didn’t want to bathe.

“As I got older, I still dealt with skepticism.

“There were doctors who laughed when I suggested I might be allergic to water or questioned the research I had done instead of listening to what I was experiencing.

“It was incredibly dehumanising.

“I knew something was wrong with my body and I was simply looking for answers.

“Receiving a diagnosis validated years of experiences that so many people had dismissed.”

Kimberlee said she now shares her story publicly to educate people about rare diseases and invisible illnesses, hoping her experience can help others receive earlier diagnoses and greater understanding.

She concluded:

“I want people to understand that it isn’t just about being allergic to water.

“It affects every part of my life and requires constant planning.

“I also hope people remember that just because a disease is rare doesn’t mean it isn’t real.

“My goal has never been to gain sympathy; it’s to raise awareness.

Kimberly face without allergies

“If sharing my story helps someone receive a diagnosis sooner, encourages people to believe someone living with a rare disease or helps others understand invisible illnesses, then every vulnerable moment has been worth it.

“Water is something most people never have to think twice about.

“For me, it’s something I have to think about every single day.”

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Woman Left With £15,000 Dental Repair Bill After Traveling to Turkey for Veneers

Celebrity makeup artist Vanessa Thornton-Yates, from Cheshire, has shared her experience after travelling to Istanbul, Turkey, for cosmetic dental treatment, saying what she hoped would be a smile makeover turned into a painful ordeal.

Vanessa explained that she chose to have the procedure abroad after learning it would cost around £15,000 to have similar treatment in the United Kingdom.

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She admitted that the decision came during one of the most difficult periods of her life, shortly after losing her mother to cancer.

She said:

“At the time, I had just suddenly lost my mum to cancer and wasn’t in a good place emotionally.

“Looking back, travelling abroad for cosmetic dentistry was a flippant decision that I didn’t fully think through.

“My natural teeth were healthy but they were slightly misaligned and not as white as I wanted them to be.

“The cost in the UK was considerably higher than treatment abroad, which was one factor in my decision.

“I was also impatient and didn’t want to wait up to 18 months, which is something I now deeply regret.

“Some days the teeth are very uncomfortable, which can stop me eating altogether, so as not to make the situation worse.”

According to Vanessa, she decided to use the clinic after seeing its five-star Google reviews and positive feedback from previous patients.

She initially planned to have 20 teeth treated but said the dentist advised increasing the number to 24, explaining that she had a wide smile and that all of the teeth would be fitted with zirconia crowns.

During her stay in Istanbul, her natural teeth were shaved down and temporary restorations were fitted. However, she said she became alarmed later that day when her gums began bleeding and turned what she described as a “grey colour.”

Vanessa later learned that gum contouring had also been carried out during the procedure, something she believes was not clearly explained to her beforehand.

She said:

“Throughout the entire process, my understanding remained that I was receiving 24 individual crowns.

“At no point do I recall anyone explaining that multiple teeth would be permanently joined together as bridges.

“Cosmetically, I was delighted with the result.”

Although she was pleased with the appearance of her new smile, Vanessa said she continued to experience pain and extreme sensitivity. Believing it was a normal part of the recovery process, she endured the discomfort for about six months.

As the pain worsened and her gums began bleeding more frequently, she sought advice from her dentist in the UK.

According to Vanessa, her dentist immediately suspected she had undergone treatment overseas.

She recalled:

“My dentist immediately asked whether I had received my treatment abroad.

“In his opinion, 16 of what I believed were individual crowns were actually connected together as multiple bridges.

“These included bridges joining my four upper front teeth, my four lower front teeth, and additional bridges joining teeth on both sides of my mouth.

“My dentist explained that he believed this treatment wasn’t appropriate in my case because joining the teeth together makes it impossible to floss properly or clean between each individual tooth.

“He diagnosed gum disease and advised that the connected bridges should be removed and replaced with individually restored teeth.

“I was completely shocked.

“I genuinely believed I had paid for and received 24 individual zirconia crowns.

“Discovering that 16 of those restorations were actually connected bridges was devastating.

“I felt angry, disappointed and incredibly upset.

“I also blamed myself for not carrying out more research before making such an irreversible decision.

“Every day I worry about what’s happening underneath the restorations and whether my natural teeth are deteriorating.”

Vanessa said that since undergoing the procedure in September 2024, her gum recession has progressed rapidly, while persistent pain in her teeth and gums has continued both day and night.

Her UK dentist reportedly believes the crowns were fitted too tightly against her gum line, contributing to the ongoing problems.

She has now been informed that removing the bridges and replacing them with individual restorations could cost between £8,000 and £15,000, although she is still waiting for a final estimate.

Despite everything she has experienced, Vanessa said she is not trying to blame the clinic or the dentist who carried out the treatment and has chosen not to publicly identify them.

She said:

“My concerns only arose later when I began experiencing ongoing problems and sought advice from my UK dentist.

“I’m sharing my experience because I want people to understand that cosmetic dentistry isn’t just about how your smile looks on the day you leave the clinic.

“It’s also about the long-term health of your teeth and gums.

“I wish I’d taken the longer route in the UK and preserved the health of my natural teeth.

“My aim isn’t to stop people travelling abroad for treatment or to attack one particular clinic.

“My aim is simply to educate people about the risks of choosing what can appear to be a quick fix, so they can make a genuinely informed decision before undergoing irreversible dental treatment.”

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Who Is Melissa Sloan? Meet the World Most Tattooed Woman Who Claims Her Looks Got Her Banned From Churches and Schools

British woman Melissa Sloan, who became widely known for covering almost her entire body in tattoos, has once again spoken about the challenges she says she faces because of her appearance.

Over the years, Melissa has repeatedly shared how her tattoos have affected different aspects of her life, claiming they have made it difficult for her to secure employment and participate in everyday activities.

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She previously disclosed that she lost her job, was asked to leave her daughter’s school because of her appearance, and has also been turned away from churches. According to her, she has even been told not to return to some Halloween parties because of the way she looks.

Despite the difficulties, Melissa said she has no intention of giving up tattoos, describing them as an addiction she can no longer control.

She said:

“I have three tattoos a week. It’s like when you have a fag or a drink, you get addicted. I can’t stop it now, it’s addictive, for me anyway. I just can’t stop it.

“I carry the tattoo g*n around with me in the boot, I’ll get one in the car or anywhere. My boyfriend does them, he does my tattoos prison style.”

Speaking about her struggle to find employment, Melissa explained that employers have repeatedly rejected her because of her appearance.

She said:

“I can’t get a job. They won’t have me. I applied for a job cleaning toilets where I live and they won’t have me because of my tattoos.”

Melissa has also previously revealed that she often feels isolated because of public perception, claiming she is rarely invited to social gatherings and sometimes avoids public attention by hiding in bushes.

Reflecting on how people react to her appearance, she said:

“People say I don’t need a costume because I’m scary enough,” “They don’t know the inside of me, bless them.

“I just take no notice of them as there’s nothing I can do, nothing I can do. I just carry on with the tattoos, more tattoos.

“I’ve never been invited to a Halloween party, I’d love to be invited but that’s not happened. I’d scare them all when I walk through the door.

“I would dress up as Freddy Kruger because you can’t see me underneath,” Melissa explained. “I’ll have a red and grey jumper with a mask – can’t see me then, can you!”

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My Boyfriend Left Me Because of Vitiligo – Nigerian Woman Shares Her Emotional Journey After Her Diagnosis

A Nigerian woman, Blessing Opeyemi Oduola, has shared the emotional challenges she faced after being diagnosed with vitiligo, revealing that her relationship ended shortly after she developed the skin condition.

Blessing spoke openly about her experience, explaining that in addition to dealing with the diagnosis, she also had to confront misconceptions and stigma from people who misunderstood the condition.

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According to her, some people believed her vitiligo was linked to spiritual causes rather than a medical condition. She said several individuals suggested she may have offended traditional deities and advised her to perform rituals to seek forgiveness.

Speaking about the experience, she said:

“My former boyfriend left me because of Vitilgo people always feel like okay it was a fire accident and they would be telling me (Her future would never rise again oh) because a lot of people have misconception that okay it is caused by a deity called obatala that maybe i have done an abomination, I have eaten what i am not supposed to eat that I need to appease the gods”

Blessing also recounted how she first noticed unusual changes to her skin in 2024, long before she knew she had vitiligo.

She explained:

” My vitiligo started 2024 the first sign i noticed was on my scalp and that was when i was preparing to make my hair for my POP and it was like an Injury so i felt like okay maybe hairstylist over struck my scalp because i have a very soft scalp so i was not really paying attention I felt it was going to go.

“So In november I was preparing for my birthday shoot so i did a makeup few days after, it started like an eczema I was angry at my makeup artist, I felt like she did not sterilize the Instruments she used that i was reacting to it so after few days, it came like a bigger eczema It was not white, New patches would come very light before they turn to white and people were telling me I need to see a dermatologist and i could not see a dermatologist because seeing a dermatologist in nigeria is a war and I booked an appointment in UCH (University colleage hospital, Ibadan) they told me they are fully booked for the year…… Unfortunately, i saw a private clinic online so i went there in Ibadan that was where i met doctor bello and that was when she officially diagnosed me with Vitiligo and I did series of test to check if my liver is functioning well before she can place me on the medication and at some point I was seeing improvement but when emotional stress came in, the Vitiligo started spreading so fast and it made the medications not effective again so I stopped this year, i stopped taking the medication, I was just spending money i was not seeing any effective of the medication so i stopped”

See video below…………

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Meet Elaine Davidson, the Woman with Over 15,000 Piercings Who Says She Has No Plans to Stop

Elaine Davidson, the woman recognized by Guinness World Records as the world’s most pierced person, has revealed that she is still adding to her remarkable collection of body piercings despite already wearing more than 15,000.

Speaking about her journey, Elaine disclosed that approximately 2,500 of her piercings are located in her private area, adding that she has no intention of slowing down. Instead, she is working toward an even bigger milestone—reaching 20,000 piercings.

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The former nurse first gained international attention in May 2000, when Guinness World Records officially recognized her for having the highest number of body piercings. At the time, officials confirmed that she had 462 piercings, including 192 on her face. Over the years, that number has grown dramatically as she continued pursuing her passion.

In a previous television interview with presenters Alison and Dermot, Elaine addressed questions about the health risks associated with having so many piercings. Responding to concerns about infections, she explained that proper care has helped her avoid serious problems.

“No, you need to be extremely careful because if you’re not, they can get infected. I use vinegar, and I have an amazing doctor who’s very understanding and supportive,” she said.

When asked whether any of the piercings ever fall out, Elaine simply replied:

“No.”

She also reflected on the mixed reactions she receives from people because of her appearance, saying she has learned to accept both praise and criticism.

“Some people like it, some people don’t, but I get used to the good comments and the bad as well.”

Elaine revealed that her fascination with Guinness World Records began when she was young, describing it as a lifelong dream.

“It started when I was very young. I always wanted to be in the Guinness World Records book. For me, it was my passion—everything. It was my dream.”

She added that achieving the record remains one of the proudest moments of her life.

“After a long time trying, I managed to meet the people from Guinness World Records, and they made me part of the family. It was amazing—one of the best things to happen to me.”

More than two decades after making history, Elaine Davidson continues to push the boundaries of body modification, with her sights now firmly set on becoming the first person to reach 20,000 body piercings.

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People Always Ask Why I Look Like This, and Some Even Stare at Me – Lady Born With Goldenhar Syndrome Laments

Nineteen-year-old fraternal twin sisters Liz and Maddie Adams from New York are touching hearts across social media after opening up about their unique journey growing up together.

While the sisters share an inseparable bond, Liz was born with Goldenhar syndrome, a rare craniofacial condition that resulted in a missing ear, an underdeveloped eye, an underdeveloped jaw, and facial asymmetry.

Liz and maddie when they were kids

Despite the challenges she has faced since childhood, Liz has continued to inspire many through her confidence and determination.

During an interview with Truly, Liz spoke candidly about the questions she regularly receives from strangers because of her appearance.

She said:

” I am missing a ear on my right side, my right eye is under developed my jaw is underdeveloped”

Liz and maddie

Liz explained that growing up was not always easy, especially when other children questioned why she looked different.

She recalled:

“We always used to play princesses all the girls in my class and there wasn’t a princess for me to play and i get hit with questions that what’s wrong with your face ow why do you look like that.

‘When i was 4 years old i didn’t know how to answer that kids don’t know how to include people that looked so different and that was when i realised “Oh my gosh” I look really different, I really didnt start to have a lot of self confidence until High school, I found theater and I loved being on stage, i am so used to people staring at me but the beautiful thing of being on stage is that they are staring at you for a good reason so thats where my confidence came from”


Maddie shared that she never noticed any difference between herself and her sister until they both started school.

She said:

“As a kid I never realized that liz looked different until we got to school and I realized that other kids had no idea why she looked the way she did or what the story was”
Liz also revealed that she continues to receive insensitive questions and negative comments, especially during livestreams.

She said:

“I get a lot of questions like what is wrong with my face and that might seem like an harmless question but its the connotation that different equals wrong… I get people asking ‘why do you look like that why were you born’ really nasty comments like that”

Liz and her dad when she was a baby

Despite the negativity, Liz hopes people will begin to see beyond physical appearance.

She added:

“I wish people would know that people with facial differences can live happy lives we can be happy with the way that we look I think beauty is a feeling rather than a characteristic It is not about what you are wearing or how you look its about how you feel”


Maddie described Liz as one of the strongest people she knows and praised her resilience throughout the years.

She said:

“I admire liz’s courage, I admire her perservance and also her outlook on life,eventually i think we would branch out and do different things i think in a perfect world we would work together in some capacity i think we would really make some great team”

Liz became emotional as she reflected on the unwavering support she has received from her twin sister.

She said:

“I dont know if i would be here if i didn’t have Maddie as a sister she has been my bestfriend my therapist, she has just walked through life with me the whole time and i am so grateful and to have such a fierce advocate and protector next to me has made this condition so much easier I think everything happens for a reason and i think she was meant to be my twin to help me out”

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Meet Mary Magdalene, the Influencer Who Turned Her Eyes Yellow and Became Famous for Her Extreme Body Modifications Before Her Death

Popular Canadian-Mexican body modification influencer Mary Magdalene, who gained international attention for her dramatic physical transformations, has reportedly died following a fall from a high-rise apartment.

Elizabethblog could recall that the social media personality died on December 13, 2025, after allegedly falling from the ninth floor of an apartment building.

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Mary became widely recognized online for her extreme body modifications, including covering large portions of her body with black tattoos and tattooing the whites of her eyes yellow.

Before her reported death, Mary opened up about one of the biggest challenges she faced after undergoing extensive body modifications.

Mary before the modification

In 2025, she revealed that she had nearly become homeless after losing access to her OnlyFans account. According to Mary, the platform’s facial recognition system was no longer able to recognize her following her decision to tattoo both of her eyes in May 2024.

She explained that the issue prevented her from accessing her account, affecting her primary source of income and leaving her in financial difficulty until the matter was eventually addressed.

Mary Magdalene built a massive online following by documenting her body modification journey and openly sharing the risks, criticism, and personal experiences that came with her lifestyle.

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England Fan Left Heartbroken After Spending £550 on a World Cup Winners Tattoo Before Argentina Ended England’s Dream

An England football fan has become the center of attention on social media after getting a £550 tattoo celebrating England as the 2026 World Cup champions before the team’s semi-final clash with Argentina.

The tattoo featured the inscription “England world cup winner 2026”, reflecting the fan’s confidence that England would go all the way and lift the trophy.

Explaining why he decided to get the tattoo before the outcome of the tournament was known, he said:

“I’m just impulsive really. The longer it goes on in your head, the more you talk yourself out of it.”

The supporter also revealed that he had confidently predicted England would defeat Argentina 3-0 in the semi-final before going on to beat Spain 2-1 in Sunday’s final.

However, his prediction did not come true, as England’s World Cup journey ended following a 2-1 defeat to Argentina in the semi-final.

Rather than removing the tattoo, the fan has already come up with a humorous solution. Sean, who now has nine tattoos, plans to add the words “only kidding” beneath the inscription to turn the mistake into a joke.

Speaking after England’s elimination, he said:

“It’s not the end of the world, it’s just a tattoo.

“I called the shop and they were busy, but when I explained what I wanted the lady said “wow, yeah, I’ll fit you in”

Jamie Taylor, the manager of the tattoo studio that carried out the artwork, recalled Sean’s enthusiasm and said:

“He is a lovely guy and was the life and soul of the studio that day. I’m very happy we did it.

“I was unsure at first, but he was adamant and to him it was a bit of fun and he would get it done anyway.”

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I Regret Having Triplets at 55 – Woman Cries Out

A woman, Sharon Cutts, has opened up about her regrets over undergoing IVF at the age of 55 after her relationship with her husband, Stuart Reynolds, ended two years ago.

Sharon and her ex with their triplets when they were babies

Speaking in an interview with The Sun, Sharon, now a grandmother and mother of seven, said she does not regret having her triplets but wishes she had not gone through IVF, considering how her marriage eventually turned out.

She said:

“I was shocked when Stuart said he wanted a divorce, but we hadn’t been getting on, probably because you don’t get a minute to talk about anything other than kids when you’ve got triplets.

“I’d get the kids to bed and I was exhausted from everything — food shops, cooking, cleaning, gardening.

“All I wanted to do was crawl into bed. Our sex life came to a standstill then we just stopped talking. It’s sad but it happens.”

Reflecting on her decision to have children later in life, she added:

“Do I regret the decision to have had IVF aged 55? Yes, I do regret it, seeing how things have turned out. I absolutely wouldn’t do it again.

“But that doesn’t mean I’m not glad I’ve got the triplets as they, along with my grown-up children, are my absolute world.”

Sharon revealed that she took out a £22,000 loan to pay for the IVF treatment because she wanted to fulfil Stuart’s dream of becoming a father. She later paid off the remaining £8,000 by accessing part of her NHS pension after the triplets were born.

She also shared that she underwent Botox treatments in 2016 to help her feel confident while raising her young children.

Despite criticism over becoming a mother at 55, Sharon insisted she was physically fit and active.

“People said I was selfish having them at 55 but I went to the gym four times a week then and I still do.

Sharon Triplets now grown

“When I’m in the park with the kids after school, I’m going down the slides with them and they often end up pushing me on the swings.

“Younger mums just seem to sit on their phones looking bored. The beauty of being 65 is that you know what’s important and what isn’t.”

She described the early years of raising triplets as demanding, saying she and Stuart handled all childcare themselves while juggling work.

“We were doing 24 feeds a day and 21 nappy changes. It was pretty intense.”

The couple married in 2018 in a small ceremony attended by close family members, but Sharon said the demands of raising three young children, working, and managing the household gradually left little time for their relationship.

A former Navy nurse, Sharon credited her military background for helping her establish routines that made parenting easier.

Now living separately from Stuart following their split, she said the stress of the divorce has even contributed to hair loss, although she continues to focus on raising her children and rebuilding her life.

She also made it clear that she has no plans to enter another relationship.

“While I love being a mum, I’ll definitely be spending the rest of my life old, free and single.

“There won’t be any more men in my life — and that way you can guarantee there’ll be no more kids on the cards.”

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I saw Lilith beside the devil — Influencer Araceli Ordaz claims she saw Satan and his wife Lilith during foot massage after baptism

Influencer Araceli Ordaz, who has been sharing content about her faith journey, has recounted a spiritual experience she says occurred shortly after her baptism in December 2025.

She claimed the incident happened during a foot massage, just one day after she became a Christian through baptism.

According to her account, the experience began unexpectedly during the massage session, which she described as a moment of sudden awareness and fear.

Speaking about what she believed she saw, she said:

“The massage started and when she got to my feet, it’s like I woke up.

“Beside her was Satan and Lilith, who is the Devil’s wife

“I start telling her ‘they’re behind you, they’re behind you’, but she didn’t react.

“She continued with my feet, moved towards my head, started massaging my head, and that’s when I reacted.

“Crying, I told her ‘hug me, hug me please, hug me.

“I know this is a spiritual battle because I had just been baptised the day before.

“They are angry that I’m no longer in their world.”

She also said she later sought guidance from her pastors, who linked a red female figurine she had received earlier to what she described as “Lilith.”

She added:

“I remembered that someone gave me a Lilith.

“It was a red woman, I didn’t know until that day because the pastor told me ‘it’s Lilith, the Devil’s wife’.

“I then started throwing everything out.”

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