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Dad Brings Home ‘Strange’ Prescription To Help Daughter Sleep, Other Parents Order Too.

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Being scared of the dark is a common childhood fear, one that most of us can remember.

I can remember hiding under the bedsheets believing I saw monsters in my room at night, I was so scared I just couldn’t sleep.

In order to help his sweet little girl, this amazing dad decided to do something to help her get a good night’s sleep.

Now all other parents are copying his clever solution, read on to find out what he did.

Mya, his daughter was so scared of monsters it prevented her from getting to sleep at night.

Clever dad from British Columbia, Canada, went to the local pharmacy to get a prescription to rid the room of these scary creatures for good.

He picked up a spray bottle and asked if they would kindly print out a prescription label for Mya to create her own bottle of monster spray!

The confused pharmacist was happy to oblige.

This magical bottle of monster spray is quality stuff and great for dealing with about 120 monsters.

Or perhaps make them drowsy enough so they won’t bother her.

This little girl now holds the power to turn the tables on these pesky monsters who now fear the two-year-old with her magic potion to eliminate them.
It does what it says on the bottle and she is one happy little customer now.

Watch the reaction from the girl in the video below.

Feel free to SHARE this clever idea  with other parents on Facebook.

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Father takes picture of little girl posing with horse, cant stop laughing when he looks closer.

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Photographs are a great way to make a memory for any occasion, like births, marriage and holidays.

The task can be a difficult one trying to coax your subjects into striking a pose.

But should leave you with an amazing photo collection, if you’re really lucky you may even encounter an epic photobomb.

This is precisely what happened to this little girl on a day out with her family turned her and one happy horse into instant viral celebrities.

The photobomb photo was originally uploaded to Reddit which has the internet in stitches ever since.

The information available is limited, but it’s pretty easy to see what preceded the memorable image.

This little girl seems to be enjoying a beautiful day of festivities, as she spends time with her family watching large Clydesdale horses parading around.

Its most likely she spent the whole day checking out the large creatures, hesitant about whether to approach them while feeling a mixture of awe at the same time.

After building up the courage to give the horses a few soft pats on their head, it’s likely that one of her parents asked her to turn around a smile for a photo.

The young girl stood before the beautiful creature, awaiting the flash.

As the person behind the camera calls out “Say ‘cheese!

There you have it the picture is snapped, the ultimate Clydesdale photobomb!

Share if you liked this classic photobomb.

Published By Trending Stylist.

Son hides camera on carer as his mom is acting strange, images seen make his heart break

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When my grandmother was placed in a retirement home I wasn’t that old.

We all knew she didn’t have long to live as she was very unwell.

I used to call her in the early morning when neither my mother or father had awakened as I loved her so much.

She always answered, claiming she was not asleep.

I realized years later that most of the time I was actually waking her, but she still answered every time, just so she could speak to me.

It’s really important not to stop appreciating your elderly family members.

That’s why you should read this story, despite it being rather sad.

When my grandma moved into the retirement home there was something that was abundantly obvious, she didn’t like getting help with things she could do herself previously.

She was embarrassed that she was losing her independence and could not manage on her own.

The most difficult aspect of her condition was having to wear adult diapers.

There have been previous reports of abuses on the elderly, what you’re about to read is probably the worst case we’ve come across.

Camille’s mother suffered from Alzheimer’s and he thought he’d found great accommodation for her.

Loving and caring are how the home was described.

Camille began to suspect that something was off after a while– something about the place that just felt wrong.

Then, one day, he had enough as he discovered his mother Helen with a black eye so he installed a hidden camera.

Soon enough Camille discovered the unthinkable.

He continued to hope and feel it was unlikely that anything wrong was taking place despite having installed a camera.

Camille discovered after watching the recordings, that not just one, but several of the home’s staff were abusive toward his mother.

We see many things in the video below including how one staff member blows his nose with Helen’s bed sheets.

Two employees are also seen heavily making out in her room while clearly uncomfortable Helen watches on.

Other residents of the home take her possessions when they enter Helen’s room, none member of staff prevent this happening.

Helen gets a washcloth full of feces propped up in her face.

It leaves one sick to imagine that this is the case for other residents of this home.

Home director Alan Cavell, he acknowledged that they failed when Camille revealed the films to him.

He promised that kind of behavior will never be repeated again and he will greatly improve security at the home.

Camille decided that he no longer wanted his mother there, all the staff involved have been fired, though one of them was reinstated.

Following the incident, the manager was fired.

However, much to the disappointment of Camille, not one single staff member was prosecuted.

Helen was the wonderful mother of seven children passed away in September 2016.

During World War II she was a nurse before she had to flee the Nazis and emigrate to Canada.

Helen had a dignified end thanks to her vigilant son.

You can view the mistreatment in the video below.

Police have since arrested and charged many of the suspects on video and were quoted saying ” They have never seen anything like this ”

This is unacceptable, no one should have to experience anything like this.

Share this post if you have a loved one in care.

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You have one of these in your house and you will not believe the danger it poses to your children.

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Courtney N Davis from Glasgow, KY, United states is a normal loving mom like the rest of us.

On September 29th 2017, something happened to her 19 month old child that would change both their lives forever.

She could never have imagined that something like this would happen to her and her family.

But everybody always thinks the same until it actually happens.

Posting on Facebook, Courtney stated that she did not want to post this until she had posted in a mom’s group and found out from that group that many parents don’t think twice about the dangers of a phone charger.

On September 28th, 2017, her 19 month old child had stuck the mom’s phone charger into her mouth.

Courtney then rushed the child to the Doctor who confirmed it was an electrical burn and there was nothing he could do due to her being able to lick it.

Courtney said that any other day, her charger would have been plugged in out of reach of the 19 month old but due to a lot of stuff going on that day, she didn’t have time to move it, it only took a few seconds for her to get burned.

Courtney also added, “She had never tried to put it in her mouth and she had never messed with it. The one day it isn’t moved she stuck it in her mouth and got a severe burn. She doesn’t feel it thank God hasn’t acted like it bothers her at all.”

It seemed to have progressively got worse.

By Friday morning the poor child had a very nasty looking burn.

Courtney took to Facebook to warn Parents, Grandparents, babysitters, mothers and fathers and since she posted this on the 4th of October 2017, the post has gone viral reaching over 300,000 shares and over 68,000 likes.

Please take the time to comment on this and send your good wishes to this poor child and don’t forget to SHARE so people know the potential dangers.

8-year-old boy celebrates beating stage 4 brain cancer – everyone sends him love and support

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The incredible capabilities of modern science always amaze me.

With each passing year improvements for treatment for all kinds of illnesses emerge that that wouldn’t have been possible over a decade ago.

Take eight year old Cameron Scott, who is being hailed a true hero after beating stage 4 brain cancer thanks to the help of the amazing staff at St. Jude Children’s Research Hospital.

Young Cameron was diagnosed with Medulloblastoma, a high-risk tumor which had spread to his spine.

In order to remove the tumor, the 8-year-old underwent surgery before being sent to St. Jude’s for follow-up treatment.

“He’s my hero,” his father, explains.

The doctors at St. Jude’s, did in fact discover that Cameron had not only one disease, but four.

However, it was also at St. Jude’s, that the hospital’s pioneered gene sequencing of Cameron’s cancer allowing them to begin a much more effective treatment.

Cameron did endure six months of chemotherapy and radiation, but he remained strong in the face of adversity.

I feel amazing now,” Cameron explains, “I feel like I’ve been through everything.”

If you agree this little boy is brave then please SHARE this post with others on Facebook.

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Vet frees chained horse, doesn’t realise he’s about to get the ultimate thank you.

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Animal cruelty stories are always so heartbreaking to hear but thankfully the animal heroes that dedicate their lives making positive changes in the animal kingdom.

In Romania, wild horses are sometimes found with their front or hind legs chained to prevent them from escaping.

A vet from the company Four Paws released one of these majestic animals from her barbaric chains, and received quite the thank you.

The video below shows the moment when vet Ovidiu Rosu from Four Paws’ freed a horse from its chains but it was the horse’s moving reaction that caused it to go viral…

Naturally the horse was a little nervous at first, however Ovidiu made an effort and took his time approaching the grateful animal.

The vet works to calm the horse down in order to remove the painful chains, which have left marks on the horse’s legs.

In was a touching moment when another member of the herd came forward and touched his nose, almost a gesture to thank him for helping his friend.

Four Paws has been carrying out this animal rescue work for years, The video notes, that this is “a typical practice in parts of Romania … to join the front or hind legs of horses with chains.”

According to Animal Channel “These horses were first brought to Romania around 300 to 400 years ago by the Tatars. The Tatars left many horses behind, and they started roaming freely through the area.

Many horses were also set free in 1989, after the agricultural cooperatives in the area broke apart. This led to a huge population boom—by 2010, there were as many as 1,500 horses living in the Danube Delta.”

The horses were moved to the protected Letea Forest where their numbers increased, environmentalists and local authorities wanted to help control the population.

Four Paws offered to carry out a program and stepped in to give contraceptives to mares to control the numbers.

Thanks to their efforts which have paid off after an aerial census in 2017  revealed there were less than 500 horses in the Letea Forest.

The organisation also administer vaccinations to the horses and still unfortunately finds themselves removing these chains.

Have a look at the amazing work that Ovidiu and his team have carried out in the clip below.

If you were moved by this story then please SHARE it with your friends and family on Facebook.

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Rare monkeypox virus has started reappearing – here’s what you need to look out for.

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Our health is often  something we all take for granted. You feel fit and active one moment, then all of a sudden you could be suffering from a cold, flu or even worse.

Social media has a great advantage these days as it allows us to read the mass warnings about health issues that might possibly go under the radar until it’s too late.

This is a problem that has apparently been around for quite a while now, however it has began to spread again.

Monkeypox is a virus that generally occurs in central and west Africa, however in the last fortnight two possibly unrelated cases have been discovered in the UK.

Public Health England confirmed the news that both of the sufferers recently travelled to Nigeria.

According to the reports, this illness is rare, where many cases exhibit symptoms similar to fever, muscle aches, and a rash. However, more serious cases could be dangerous.

Deputy director of the National Infection Service,Nick Phin, admitted that the new cases are rare, however proper measures are being taken to reduce spreading.

It is very unusual to see two cases in such a relatively short space of time. We are working hard to contact individuals, including healthcare workers, that might have come into contact with the individual to provide information and health advice,” he said.

It is likely that monkeypox continues to circulate in Nigeria and could, therefore, affect travelers who are returning from this part of the world,” Phil continued.

In 1970 the first human case of monkeypox was diagnosed which maintains a death rate of 10%.

The disease can be transmitted from animals to humans, humans to humans, through bodily fluid or possibly by air.

What to look out for?

As ever, it’s always  important for people to be aware of the symptoms and signs to look out for.

The most prominent symptoms in the scenario would include fever, headaches, aching muscles, back pain, and swollen lymph nodes.

Usually a rash accompanies the virus, meanwhile, one which leaves scabs.

Naturally with many of these symptomatic problems of the body, if you are worried it’s always better to be checked out by a medical professional.

Help us by spread awareness of the dangers and share this article with your friends on Facebook. 

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New Mother Reveals What It Was Like Having Her MIL Carry Her Baby

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This couple Kayla and Cody Jones were more than ready to start a family.

When Kayla was a teen she had a partial hysterectomy, leaving her unable to carry children.

The Arkansas, couple had been searching for the perfect surrogate since they were married in 2012.

They delighted couple accepted a unique offer from Cody’s mom, Patty Resecker, who volunteered to carry their unborn baby after a number of options didn’t work out.

You heard it right—the baby’s grandmother was going to be the gestational carrier.

(It’s important to note that gestational carrier is the correct term in a case like this, where a woman carries a baby made from another woman’s egg. A surrogate is someone who carries a baby made from her own egg for another couple.)

Kayla comments “At first I thought the doctors may think I was a bit crazy, but as I researched I found other grandmothers who had been surrogates. After much testing, my mother-in-law was cleared to carry our baby!

The couple had an embryo transferred into Resecker’s uterus in March 2017, After undergoing IVF in October 2016, but it didn’t take on this occasion.

In May 2017 they gave it a second attempt and transferred another embryo where this time Resecker at age 50 became pregnant.

Kayla and Cody were able to do the initial pregnancy test at home themselves to make the experience extra special.

The day we found out was the second best day of my life (the first best day was the day Kross was born!)”

Kayla tells us “Patty left a urine in a specimen cup on her porch before she left for work,”

I picked it up and my husband and I tested at home. I cannot describe the feeling of seeing two pink lines!” she said.

All went well with the pregnancy and baby Kross Allen Jones was born on 30th December via c- section.

Resecker claims it was a privilege and a rewarding experience to carry her own grandchild for her son and daughter-in-law.

This is something that has blessed not only me and my family but also Kayla’s family,” she said.

Also adding “A child is a lifetime commitment and I knew there weren’t two more deserving people than them. To see them with Kross and see the parents they’re already becoming thrills my soul.”

Kross is thriving and the family reports that Resecker has recovered extremely well following her pregnancy and surgery.

“Words cannot describe how thankful we are. I never thought I would have children, so this has truly been such a blessing, God found us a way to Kross,” the new mom explains.

If you moved by this touching story then please SHARE this post with your loved ones on Facebook.

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Kids With Terminal Illness Reveal What Really Matters In Life.

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Recently a paediatrician finished an assignment where he questioned kids in relation to their terminal illness and what gives their lives true meaning.

He also asked them what they really enjoy in life and what comforts them. Be forewarned, as their answers will play with your heart strings and very likely will bring a tear to your eye. Get those tissues ready!

Dr. Alastair McApline, is a palliative paediatrician (specialising in medical care for children with serious illnesses) who comes from Cape Town, South Africa.

He decided to share the valuable lessons the children gave him because he thinks we can all benefit from their wise words of wisdom.

McAlpine shared the results from his assignment online via Twitter.

As you can probably guess, one of the main factors that were important to the kids was spending time with loved ones – dad, mom, siblings and family pets.

Perhaps one thing to note about these children is that they love spending time with their families and friends – bedtime stories, making sandcastles at the seaside, and doing activities that take their minds off being sick.

What is another meaningful part of life? How they feel when surrounded by the people that love them.

More often than not, the most memorable family moments are the ones that seem completely normal.

Children that are surrounded by people that they love the most will always feel loved.

At the end of the day, that is exactly how we all feel.

It at times appears like our present generation of parents is continually endeavoring to go out of their way.

We are overcome with giving our youngsters every one of the additional items we couldn’t have as children: costly Disney get-aways, amazing birthday parties, the most recent cutting edge devices.

Also, having the capacity to give those things feels extraordinary, without a doubt.

But many of those things can be quite amazing, to be sure – but they do not give life its true meaning.

Well not to children, anyhow.

Children prefer the small things in life such as, snuggling up with their moms, playing sports with their dads, playing with the family pets or having fun with their siblings around the house.

It is these very moments that give a child stability, a sense of security and the feeling of love that ensures them to want for life even when faced with the toughest of circumstances.

“I was inspired to share the thread because there was so much negativity on my timeline,” McAlpine explains.

My brave patients were countering it all with such beautiful and profound insights, that they immediately brightened my day, and I hoped that they would do the same for others.”

If you were inspired by this touching story then please SHARE this post with friends and family on Facebook.

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Mom Warns Others About Disease That Left 8-Year-Old Son Left Unable to Walk or Talk.

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Every parent dreads this time of the year when the cold and flu season is in full swing. It is very hard for children to avoid succumbing to this illness, meaning parents will undoubtedly have to brace themselves for a few days off school.

When 8-year-old Jamie Jones took ill  with what seemed like common flu symptoms, it turned into a potential life threatening situation. Jamie’s mother, Jessica, now wants to educate other parents around the world on how to spot the warning signs.

It all began one day when Jamie returned from school with a sore throat. It started with a fever,” said Jessica. “We took him to multiple ERs and urgent cares and they kept telling us it was just a viral infection.” She was not very worried about it at the time.

Then, out of nowhere, Jamie’s neck swelled up on one side and became incredibly painful. This was the initial sign for Jessica that something was seriously wrong with her child.

It was not long before more symptoms started to appear. His heart started to beat very rapidly, a fever set in, and his lymph nodes became very swollen. Even after a course of antibiotics, there was no improvement in Jamie’s condition.

“He couldn’t walk, couldn’t talk and I knew something was off with him because he just wasn’t getting better,” said Jessica. Her concern grew.

Jamie was always very fond of sports, his favorite being wrestling. His keen interest in sport was something he shared with his father, but now Jamie was so tired and sick that he remained in bed all day.

In his first year, he finished first and second at local events and went on to place sixth in his weight class. Now, to see him sick and unable to do what he loved was heartbreaking for his parents.

After numerous hospital visits and countless misdiagnosis, one doctor finally saw the signals. He diagnosed Jamie with Kawasaki disease. This is a disease in young children with an unknown cause, giving rise to a rash, glandular swelling, and sometimes damage to the heart if left untreated.

Jessica was very taken back by the news. Director of pediatric cardiology at Peyton Manning Children’s Hospital, Dr. Sanjay Parikh, said that people don’t realize how prevalent Kawasaki disease actually is.

The treatment Jamie would have to undergo would be very intense. Sadly, tests later revealed that Jamie’s little heart had already suffered damage due to the illness. Doctors found several aneurysms in his arteries.

For almost eight months Jamie had to be given daily injections in his stomach to keep to thin the blood and help him avoid developing new blood clots. “Our lives went from normal, carefree, to worry about every single thing, ” said Jessica. Jamie will have to live a different life now, one without wrestling.

If Jamie had been diagnosed a week into his illness then the heart damage could have been avoided. Jamie is not one to lay down and let this beat him though, he has now found a new love in swimming.

He gained inspiration from Australian junior world record holder and Olympic gold medalist, Kyle Chambers, and decided to take up swimming. He must be careful though, he cannot get any bumps or bruises.

Lately, Jamie has befriended many kids with Kawasaki disease on Facebook. Like the true warrior he is, he asked his mom if he could send a book to one of these friends to try and cheer him up. He has now sent well over 20 books to his new friends.

Jessica is actively trying to raise awareness about this disease. “If you feel like something is not right or your child’s not getting better, question it,” she said. “If they have a fever for five days, bring up Kawasaki disease. It doesn’t hurt to question it.”

If you were touched by this little boy’s story then please SHARE this post with others on Facebook.

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