Parent’s devastating decision – forced to pull the plug on 13-year-old daughter after sleepover horror

Devastated parents forced to pull the plug on their 13-year-old daughter after sleepover horror. They’ve now issued a warning to spare others from the same tragedy.
When Esra Haynes died, she was just 13 years old, and the reason for her tragic death is bizarre.

This young girl who was referred to as “determined, fun, cheeky and talented” by the Montrose Football Netball Club that she co-captained, got caught in a viral craze called chrominghttps://comsoftvn.com/in-order-to-pick…a-tiny-stray-dog/, which involves inhaling toxic chemicals through the mouth or nose to get high.

Esra was an athlete and lead a healthy life, racing BMX bikes with her brothers, and leading her team to a national aerobics’ championship in Queensland. But all that was taken away from her after a wrong decision she made on March 31 during a sleepover at a friend’s house.

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As she wanted to be part of the viral trend, Esra inhaled a toxic amount of aerosol deodorant and went into cardiac arrest, sustaining irreparable brain damage.

Her parents were devastated. Appearing on A Current Affair with host Ally Langdon, they spoke of the heartbreak and the fatal consequences of inhaling toxic chemicals in an attempt to prevent something similar from happening to other naive young people.

“It was just the regular routine of going to hang out with her mates,” her mom Andrea, told Langdon in the interview. Her father Paul added, “We always knew where she was and we knew who she was with.

It wasn’t anything out of the ordinary…To get this phone call at that time of night, (it) was one of the calls no parent ever wants to have to receive, and we unfortunately got that call: ‘Come and get your daughter.’”

Initially, her friends weren’t aware how serious Esra’s condition was. They only thought she was having a panic attack, not aware that their friends was dying right in front of their eyes. “But after inhaling deodorant, her body was actually starting to shut down, she was in cardiac arrest and no one at the sleepover used cardiac arrest,” Langdon explained.

When her mom arrived by Esra’s side, paramedics were trying to revive her and told Andrea that her daughter had been chroming, a word that the scared mother heard for the first time ever.

Esra was transferred to the hospital and was placed on life support, but just eight hours later, the parents were told that her brain was damaged beyond repair and that needed to make a decision to turn the life support off.

Knowing there was nothing that could be done, Andrea and Paul called relatives and family members to say their final goodbyes. “It was a very, very difficult thing to do to such a young soul. She was put onto a bed so we could lay with her. We cuddled her until the end.”

Esra’s siblings, Imogen, Seth and Charlie are have been shattered ever since their sister is gone.

“It was really devastating, devastating for everyone involved, all her friends as well,” Paul said. “It’s been the most difficult, traumatic time any parent could go through. We haven’t been sleeping, we’ve hardly been eating, we haven’t been smiling–we’re not ourselves…But it’s not just affected us, it’s the community as well.”

Following Esra’s passing, Andrea and Paul are doing all in their power to put an end to the crazy viral craze that took their daughter’s life.

Speaking to 7 News, Paul said he wished he knew of chroming when Esra was still alive, so he could have warned her of the dangers: “If we were educated and the word had been put out there, we would have had the discussion around our kitchen table for sure.

“We need to ramp it up and let these kids find out the information first-hand, and not through friends, and not through social media–then they’re given the right advice off the bat.”
Esra isn’t the first victim of chroming. Over the years, a number of young people lost their lives from the consequences of it as it can easily lead to seizures, heart attack, suffocation, sudden sniffing death, coma, and organ failure.

“We’ve got the pictures in our mind which will never be erased, you know, of what we were confronted with,” Paul told Langdon. “Our gut was ripped out.”

We are so very sorry for this family’s loss and we wish no parent ever experiences such heartbreak.

Baby Born With Unusual Syndrome – 22 Years Later She Looks Amazing

These young, allegedly productive qualities are seen in the 99-63-91 body, which stands 1.68 meters tall.

In reality, though, a woman’s level of fertility would rely on a multitude of factors, with physical type playing a relatively minor role.

Despite the fact that obesity has been linked to miscarriages, pregnancy difficulties, and infertility in women, infertility problems can affect anyone, regardless of size.

Mary’s pregnancy and delivery had proceeded without any complications. There were no signs that their daughter Michelle experienced any problems when she was born. Yet the moment she opened her eyes, the physicians realized something wasn’t quite right. They didn’t figure out what it was until they perused medical texts and talked to a geneticist at a different hospital.

Michelle’s face was large and innocent. She had a nose like a little beak, and she was balding. It was discovered that she had Hallermann-Streiff syndrome, a hereditary illness of which there are only 250 known cases worldwide.

Michelle was born at Children’s Memorial Hospital, where no one had ever seen it in person.

When the doctor told us we had Hallermann-Streiff syndrome, my heart fell. “I was concerned about how we were going to care for our child who had a rare genetic disease that was one in five million,” Michelle’s mother said.

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Michelle exhibits 26 of the 28 symptoms that are associated with the condition. Although the sickness affects only one in five million people, it can lead to a variety of health issues.

Michelle is just two years older than her sister, yet she can barely reach over her waist because of Hallermann-Streiff syndrome and dwarfism.

Because of her illness, Michelle needs a lot of help, including an electric wheelchair, a respirator, a hearing aid, a probe, and visual aids. Michelle and her family have also had to spend a lot of time in the hospital as a result of the illness. She may be mistaken for a toddler while being 25 years old due to her appearance.

As a 20-year-old, Michelle is happier than ever and as intelligent as a poodle. She is among the happiest twentysomethings I’ve ever met.Her mother Mary continued, saying:

She brightens people’s days with her happiness. She is aware of her differences, but she refuses to let them define her.

Michelle is a great, distinctive young woman despite her challenges. Among other things, she aspires to date and become like her older sister. She doesn’t mind his height because practically everyone is taller than her, but she wished his hair was longer.

Her goal is to become a doctor as well!

Kindly SHARE this article and send her best wishes!

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