Thoughtful neighbour has created a parking spot for an NHS nurse who is working on the front-line of the battle against coronavirus
Image by: Steve Chatterley
A thoughtful neighbour has created a parking spot for an NHS nurse who is working on the frontline of the battle against coronavirus.
The space was marked out in white spray paint directly outside the health worker's house so she does not have to search for a gap when returning from long shifts.
The nurse, who does not want to be named, is working in a hospital to treat patients with coronavirus in Greater Manchester.
A sign put up by the neighbour next to the spot read: “SPACE RESERVED. Polite notice. Please respect the sign and give our NHS workers a change. Thanks.”
The nurse's husband, who also does not wish to be named, first saw the paint after his wife had gone to work on Saturday morning (28 March) and said she was “incredibly touched” by the small act of kindness.
He said she often has to park further away from her home when she gets back from her work at the hospital.
Image by: Steve Chatterley
He posted on Facebook: “What absolutely gorgeous caring neighbours who have done this for her. Such a caring touch.
“She was emotional when the street clapped for the NHS in the week, this will do her in! Let's keep supporting our nurses and NHS.”
Critical staff are starting to be tested today (Mon) to see whether they have coronavirus, with tests for A&E staff, paramedics and GPs set to follow.
Last week more than 20,000 former NHS staff applied to return to the health service to join the fight against Covid-19.
Yesterday (Sun) Prime Minister Boris Johnson also thanked 750,000 volunteers who had put their names down to support doctors and nurses however they can.
On Saturday NHS consultant Amged El-Hawrani, 55, was the first hospital frontline worker to die after testing positive for the virus.
Meet the orangutan who decided to take an outdoor vacation in -7°C
Image by: Jake Kubie
A canny orangutan was not going to let a little freezing weather stop him enjoying a ten day treetop holiday - and even took his own blanket to keep him toasty.
Wild orangutans, which hail from the steamy continent of Asia, never encounter cold weather.
Captive orangutans in breeding programmes around the world tuck up inside their zoo enclosures to wait out the winter months.
But 12-year-old Sumatran orangutan Jaya had different plans and braved the perishing cold in the freezing winter of Denver, Colorado, with his trusty blanket.
Jaya threw caring zookeepers of Denver Zoo into a panic when he left the comfort of his indoor retreat and took a 10-day holiday up a tree - in JANUARY.
Zookeeper Cindy Cossaboon said: “We don't know what spooked him, but he retreated into the yard, climbed up a tree and refused to come back inside.
Denver winters can be perishingly cold, so zoo staff rallied to try and coax Jaya back inside.
Cindy, 43, added: “They say the way to a man’s heart is through his stomach. It’s normally much the same with apes.
“We tried a lot of novel foods with him. He loves dried fruit nuts and juices but nothing was working. He just wouldn’t come down.
“Jaya’s favorite thing is whipped cream. We give him that occasionally for an extra special treat, but even that didn’t persuade him.
“We had two big doors that were left open for him at all times, but he simply refused to come back inside.”
The zookeepers were concerned that Jaya would get frostbite, so they monitored him around the clock to keep him safe.
Image by: Jake Kubie
Image by: Jake Kubie
Image by: Jake Kubie
Cindy added: “We set up a giant heater out there and gave him bedding and hay and sleeping bags and comforters and tarps, everything we could think of to keep him warm.
“We sent up warm drinks and warm foods and the night keepers checked on him throughout the night, every night.
“It’s like having a kid. The animals feel like family and we care about them very much. When he was outside it was probably harder on us than it was on him.
“I wasn’t sleeping. We were all so worried about him. I kept checking with the night keepers every night, asking, ‘how’s Jaya doing?’
“We were lucky because it was quite mild this year, fortunately it was in the 40s in the day (4.5 Celsius) but there were a couple of nights when it got down to 20 (-7 Celsius)
“On those colder nights I didn’t sleep at all. We like to joke that we’re their mothers, their nurses, their restaurants and their house maids. Working with orangutans is about building relationships.
“Everything is about clear, honest and consistent communication. We treat them with respect and give them choices.
"You can’t force them to do anything. We work for them and it’s a real privilege for us.”
Jaya finally decided to end the outdoor experience after 10 days and vacated his treetop home and loped back into the warm.
Cindy added: “We were so relieved. It was a rough couple of weeks.”
Jaya is now happily settled at the zoo and has formed a firm friendship with a female orangutan called Eirina of the same age.
Cindy said: “Eirina absolutely loves him, she follows him everywhere. They play together all day. They like to hang by their feet upside down and wrestle.
“We’re hoping that in the future it’ll become a romantic relationship, but they are too young to breed effectively at the moment.
“When orangutans have children too young they don’t become the best parents, so the recommendation is that they don’t have their first baby until they are 15-years-old.
“But we really hope that in a few years we’ll have some babies to celebrate.”
Video by: Ashley Moran
These amazing photographs show how an ingenious bird has built a cosy nest for its chicks - inside a set of city centre traffic lights
Image by: Dan Rowlands SWNS
These amazing photographs show how an ingenious bird has built a cosy nest for its chicks - inside a set of city centre traffic lights.
An industrious mistle thrush piled up a cluster of leaves and twigs on a visor below the middle amber light at the top of a metal post.
It was built in Leeds, West Yorks, and is home to five young chicks.
It's thought the unusual spot was chosen by the bird because of the warmth given off from the light, as chicks need supplementary warmth until they are fully feathered.
Image by: Dan Rowlands SWNS
Image by: Dan Rowlands SWNS
Image by: Dan Rowlands SWNS
Dozens of passersby and motorists have been spotted inspecting the nest, which sits at the centre of a busy junction close to Leeds Beckett university.
The mistle thrush is a large songbird with pale grey-brown upper parts, a greyish-white chin and throat, and black spots on its pale yellow and off-white under parts.
Generally found if wood and parkland, the creature feeds on a variety of invertebrates, seeds and berries.
Their favoured food is mistletoe fruit, which is reflected in its name.
Mistle thrush's incubate their eggs for around two weeks, which is when chicks are usually mature enough to fledge.
Video by: Gabriella Petty
PIPING A HERO - Former Labour advisor Alastair Campbell serenades dedicated NHS nurse on bagpipes as she returns home from gruelling hospital shift.
Image by: Jon Mills
Former Labour advisor Alastair Campbell serenaded a hero nurse home on the bagpipes after she finished a gruelling shift on a busy hospital ward.
Matilda 'Sissy' Bridge battled leukaemia from the age of two-and-a-half and joined the NHS to work with those who helped her beat the cancer and care for others.
Sissy, 27, now works as a nurse on the asthma ward at Whittington Hospital, Upper Holloway, London.
She and Campbell's comedian daughter Grace, 25, have been neighbours and friends since birth.
Image by: Jon Mills
Accomplished piper Alastair said: "Sissy and grace are great friends. Sissy had childhood leukaemia and was hospitalised for quite a while. That is part of the reason she became a nurse.
"It was an honour to march a heroine home from the front line - well done Sissy.
"And we did a nice hymn for the whole street who came out to thank Sissy and all who work in our wonderful NHS.
"We were also serenading Sissy's loving family, mum Victoria and older sister Florence, who worry about her every minute of every day.
"#clapforNHS. And, of course, the wonderful @RoyalFreeNHS."
Alastair, inspired by Sissy's childhood cancer battle, ran the marathon for Bloodwise charity in her honour.
He said: "I ran the marathon for leukaemia research in 2003 and her family donated £50k. I raised over £1million in the end."
Video by: Ellis Wylam
An arcade owner has put toilet roll, soap and hand sanitiser as prizes - in GRABBER machines
Image by: Adam Harnett
An arcade owner has put toilet roll, soap and hand sanitiser as prizes - in GRABBER machines.
Rob Braddick, 48, owns Ho Barts Amusement Arcade and noticed that stocks of toilet roll were running low in his local supermarket.
He then decided to buy as many as he could, and used his stock to replace the toys and teddy bears in his grabbing machines.
Rob said that there were still products available to buy in his area, but hoped that people would flock to his amusement arcade in Westward Ho!, Devon, when they got desperate.
Image by: Adam Harnett
Image by: Adam Harnett
Image by: Adam Harnett
Rob said: "We evicted the character from Frozen and the Peter Rabbit teddy bears and replaced them with hand sanitiser and toilet rolls.
"We also have a large machine that used to have a Spider Man doll, but now there is a large Curex soap in there - that's the Rolls-Royce of hand sanitisers.
"We test it, it's possible to win them but it is hard. We've lad people coming in to have a go but I don't think anyone has won yet.
"It's been a bit quiet so far but I think people will start coming in to have a look.
"There are still some toilet rolls on the shelves around here so I guess people aren't that desperate yet."
Rob also owns the nearby Braddick Holiday Centre, which employs around 100 people.
He said that they are taking the coronavirus scare very seriously, and have implemented a strict hand-washing policy for staff.
Rob continued: "We have a lot of staff at the holiday centre and the arcade, and we've put in measures where people have to wash their hands every half hour.
"So far the effect of the outbreak is unclear, we're still getting people ringing up and booking holidays - but it's early days and things could get worse."
Baker creates a LIFE-SIZED Karl Lagerfeld cake to mark the one-year anniversary of his death
Image by: Matthew Newby SWNS
A British baker has created a LIFE-SIZED cake of German fashion designer Karl Lagerfeld to mark the one year anniversary of his death.
Confectionary artist Debbie Wingham, 38, used 195 eggs, 44lbs of sugar paste, 13 bags of flour and over 15,000 baby marshmallows to create the edible sculpture - which stands at 5'10 tall and weighs 287 pounds.
"I made it with all the vital statistics of the late, great Karl Lagerfeld," said Wingham, who spent 11 days building the creation for an unnamed German businesswoman.
“The person who commissioned it shares my passion for this legend in couture,” added Wingham.
The cake was even made to taste like the late Karl's favorite food, toasted corn bread.
"It is a sweet corn bread cake with honey salted butter frosting," said Wingham.
The sugary model depicts Lagerfeld in his signature black sunglasses, monochromatic
suit, fingerless gloves, and starched, detachable collar.
“Every detail in this cake embodies King Karl,” said Wingham who sculpted the legs from rice crispy treats, bonded with butter and marshmallows.
Image by: Matthew Newby SWNS
Image by: Matthew Newby SWNS
Image by: Matthew Newby SWNS
The facial likeness of the former Chanel honcho was achieved with the help of Israeli sculptor Mike Viner, who traditionally works in clay, but turned his hand to modeling chocolate on Wingham’s request.
“Working in modeling chocolate is a little different from what I’m used to, and I was somewhat worried when I accepted the challenge,” said Viner.
Adding: “But the result of both mine and Debbie’s sculpting skills together are the perfect combination.”
Wingham is hailed as one of the top sugar artists in the world, with clients including Drake, Tim Burton and Justin Bieber.
In 2018 she famously made a “cake-a-like of Kim Kardashian.
“
Sculpting Kim Kardashian’s curves in cake was no easy job,” she said.
“But making Karl was even more difficult.
“I have always had much admiration for Karl and every job I do is always important to me, but to date this cake was definitely my most important edible creation.
"I hope Karl would have approved.”
Karl Lagerfeld died in Paris, France on 19 February 2019 at the age of 85 after a battle with cancer.
Video by: Ashley Moran
GARDEN HORROR - A dad-of-two almost died after catching a rare flesh eating bug when he cut his hand GARDENING
Image by: Steve Palmer
A dad-of-two almost died after catching a rare flesh eating bug when he cut his hand GARDENING.
Steve Palmer, 34, nicked the middle finger on his right hand while clearing debris which had swept into his garden from a river during the recent floods.
He thought nothing of it until the next morning when his finger appeared red and swollen.
Steve went to work with his father-in-law but was stunned when his hand ballooned in size and his arm had turned black.
He was rushed to hospital where doctors diagnosed him with necrotising fasciitis, a potentially fatal flesh-eating bacteria.
Image by: Steve Palmer
Image by: Steve Palmer
Image by: Steve Palmer
He was transferred to the Queen Elizabeth Hospital in Birmingham where surgeons operated to remove the dead and infected tissue from his arm.
A plastic surgeon was able to save his arm from being amputated and Steve is expected to take a year before making a full recovery.
Steve, who worked as an air conditioning engineer, has posted graphic pictures of his blackened arm on Facebook in a bid to warn others.
He said: “It was terrifying, it was like something from a horror movie. I could literally see my entire arm turning black.
“When the surgeon looked at my hand all the blood vessels in my knuckles had turned to mush.
“I just want to warn people to be careful and to wear gloves while gardening, particularly now that people will probably be spending more time in their gardens due to the coronavirus lockdown."
Steve was gardening with his wife Laura, 34, at their home in Polesworth, Warks., on March 7 when he cut his finger.
He said: "Me and my wife were in the garden tidying up.
“We live on the back of the River Anker which had flooded a couple of weeks earlier and messed the garden up a bit.
“We’d waited for the weather to get better so we could clean up.
"While I was clearing reeds which had been swept into the garden from the river I got a
little nick on my finger.
“I didn’t even notice it, I get little cuts all the time at work and just cracked on but there must have been all sorts of bacteria from the floods which got into the cut.
"The next morning I was meant to help my father-in-law do some cementing at his farm but when I looked at my middle finger it had swelled up and was red.
“I felt a bit soft for saying I couldn’t help him but went round anyway and played with the kids and on the piano but I could hardly move my finger.
“I said to Laura 'that starting to look a bit infected'.
"When I got home my knuckles were swollen and the infection had started to spread up my arm."
Image by: Steve Palmer
Image by: Steve Palmer
The next day Steve was taken to Good Hope Hospital in Sutton Coldfield, West Mids., by his friend and was told to wait in A&E.
Steve, who is dad to three-year-old Jacob and seven-year-old Charlie, said: “The doctor said he thought it might be sepsis and cellulitis so put me on a saline drip overnight
and gave me paracetamol because my temperature was very high.
“The next day I was transferred to hand specialists at the QE in Birmingham where a surgeon told me again he thought it was sepsis.
“I was taken down to surgery and was operated on for four-and-a-half hours.
“When I came round doctors told me that they discovered it was actually necrotising fasciitis which is quite rare.
“The blood vessels under my knuckles were mush so the surgeons had to wash all of the infection away and pull down skin from my forearm onto the tendons before taking a skin graft from my leg onto my arm.
“I was very lucky and could easily have died. The surgeons saved my life and my arm.
“I’m back home but I’ve been told it’ll take 10 to 12 months before I can hold tools again. I’ve got two per cent use of my hand at the moment.
“It’s going to be a long long journey back to recovery. I just want to warn everyone now to wear gloves in the garden.
“It was a tiny cut I had on my hand but it was enough to let the bacteria in which almost killed me.”He was transferred to the Queen Elizabeth Hospital in Birmingham where surgeons operated to remove the dead and infected tissue from his arm.
A plastic surgeon was able to save his arm from being amputated and Steve is expected to take a year before making a full recovery.
Steve, who worked as an air conditioning engineer, has posted graphic pictures of his blackened arm on Facebook in a bid to warn others.
He said: “It was terrifying, it was like something from a horror movie. I could literally see my entire arm turning black.
“When the surgeon looked at my hand all the blood vessels in my knuckles had turned to mush.
“I just want to warn people to be careful and to wear gloves while gardening, particularly now that people will probably be spending more time in their gardens due to the coronavirus lockdown."
Steve was gardening with his wife Laura, 34, at their home in Polesworth, Warks., on March 7 when he cut his finger.
He said: "Me and my wife were in the garden tidying up.
“We live on the back of the River Anker which had flooded a couple of weeks earlier and messed the garden up a bit.
“We’d waited for the weather to get better so we could clean up.
"While I was clearing reeds which had been swept into the garden from the river I got a
little nick on my finger.
“I didn’t even notice it, I get little cuts all the time at work and just cracked on but there must have been all sorts of bacteria from the floods which got into the cut.
"The next morning I was meant to help my father-in-law do some cementing at his farm but when I looked at my middle finger it had swelled up and was red.
“I felt a bit soft for saying I couldn’t help him but went round anyway and played with the kids and on the piano but I could hardly move my finger.
“I said to Laura 'that starting to look a bit infected'.
"When I got home my knuckles were swollen and the infection had started to spread up my arm."
Image by: Steve Palmer
Image by: Steve Palmer
The next day Steve was taken to Good Hope Hospital in Sutton Coldfield, West Mids., by his friend and was told to wait in A&E.
Steve, who is dad to three-year-old Jacob and seven-year-old Charlie, said: “The doctor said he thought it might be sepsis and cellulitis so put me on a saline drip overnight
and gave me paracetamol because my temperature was very high.
“The next day I was transferred to hand specialists at the QE in Birmingham where a surgeon told me again he thought it was sepsis.
“I was taken down to surgery and was operated on for four-and-a-half hours.
“When I came round doctors told me that they discovered it was actually necrotising fasciitis which is quite rare.
“The blood vessels under my knuckles were mush so the surgeons had to wash all of the infection away and pull down skin from my forearm onto the tendons before taking a skin graft from my leg onto my arm.
“I was very lucky and could easily have died. The surgeons saved my life and my arm.
“I’m back home but I’ve been told it’ll take 10 to 12 months before I can hold tools again. I’ve got two per cent use of my hand at the moment.
“It’s going to be a long long journey back to recovery. I just want to warn everyone now to wear gloves in the garden.
“It was a tiny cut I had on my hand but it was enough to let the bacteria in which almost killed me.”
A space engineer has built her own cell phone with a ROTARY DIAL because she hates smartphones and texting
Image by: Adam Gray SWNS
A space engineer has built her own cell phone with a ROTARY DIAL because she despises smartphones and texting.
Justine Haupt, 34, spent three years creating the old school device which fits into her pocket with a battery that lasts up to 30 hours.
When she wrote about the retro cell phone on her website, so many people visited the post that her site crashed.
Justine has since been inundated with requests from fellow smartphone haters begging for their own version of the phone and she is now offering build-it-yourself kits.
The astronomy instrumentation engineer, at Brookhaven National Laboratory in New York, was inspired to make the phone because she dislikes the culture of smartphones and has never even owned one.
“I work in technology but I don’t like the culture around smartphones,” she said.
“I don’t like the hyper connected thing.
“I don’t like the idea of being at someone’s beck and call every moment and I don’t need to have that level of access to the internet.
“Whenever I want to look something up, I’m more than happy to do so when I am at my computer.
“I’ve never texted and building this phone was in part so that I would have a good excuse for not texting.
“Now I can hold up this phone and say, ‘No, I can’t text.’”
While Justine did once buy a Samsung Galaxy smartphone for her mother and played around on it herself, she said she got rid of the device after a month.
“I thought I would give it a try but I lasted less than a month with it.
“I went back to my flip phone.
“I’m an engineer, I love technology, but the phone is not the way I want to do it.”
She is also not a fan of the interface on a smartphone or the touch screen.
“The interface is absolutely horrible,” she said.
“When you open an application and then you want it to go away but you don’t know if it is closed - that grates against the fibre of my being.”
Justine’s appreciation of rotary dials inspired her project.
“Rotary dials are neat and I wanted to include them in a project.
“I had had a flip phone for a long time and it can technically text so I wanted an even more dumbed down phone.
“I thought: ‘why not make a rotary dial phone?’
“I wanted it to fit in my pocket, be sleek, something I could actually use.”
The project was stop-start until two months ago when she decided to finally finish the device.
“I had the idea three years ago.
“I started putting it together and then I lost interest and it was in a box in the closet for a while.
“It was only about two months ago that I said: ‘I’m going to finish this thing’.”
Image by: Adam Gray SWNS
Image by: Adam Gray SWNS
Image by: Adam Gray SWNS
Image by: Adam Gray SWNS
Image by: Adam Gray SWNS
Justine sourced a rotary dial from an old Trimline telephone, making sure the dial was small enough to fit on a phone which would slip into her pocket.
“I was particular about getting one that could be as compact as possible.”
She bought a cell phone radio development board from hardware company Adafruit and the first cell phone prototype was very basic with wires showing.
“I did it just to prove it could work,” she said.
“I then designed my own circuitry.”
Justine used a 3D printer to create the cell phone case and added speed dialing buttons so she could call her husband, David Van Popering, 57, and her mother, Lorraine Labate, 60, at the click of a button.
The button for David is labelled ‘Da’ and Lorraine’s button is ‘La’, an abbreviation of Llama, Justine’s nickname for her mother.
“If I want to call my husband, I can call him by pushing a single button. I can call people more quickly on this phone than on my old phone.
“In rare cases when I want to call a new number, I do use the rotary dial and it is a fun, tactile experience.”
Justine added an e-paper display to the phone so that she could see messages and missed calls.
“It’s actual e-paper, the same material that you find on Kindles.
“Those kinds of displays are cool and are under utilised in technology.”
The phone takes an AT&T prepaid sim card which is compatible with the cell phone radio.
The device is 4 inches tall, 3 inches wide and 1 inch thick - easily fitting into Justine’s pocket.
“The battery lasts for a solid 24 hours, maybe 30 hours.
“It is actually my phone - I don’t carry my flip phone with me anymore.
“It fits into my pocket and, in total bulk, I don’t think it is much bigger than a large smartphone with a protective case on it.”
Justine published a post about the cell phone on her website on February 10 and so many people visited her site that it crashed under the demand.
“I never expected to go viral with this,” Justine said.
“There was so much demand.
“I didn’t want to sell it at first but everyone was clamoring and I got so many emails from people begging to buy a phone.
“Finally someone suggested I should at least make a kit.
“I very quickly put together a new version of the circuit that would be a little more robust.”
Justine created another version of the cell phone with a turquoise case.
Customers can buy the kit, which includes the circuit board and the 3D printed parts, from Justine’s company Sky’s Edge for $170, but they will have to source their own rotary dial.
“Now I’m looking at making a more inclusive kit that will come with everything you need,” Justine added.
“In a week, I’ve had around 30 orders.”
Justine admitted that the phone’s popularity has baffled her.
“I’m not totally sure why people responded to it the way they did.
“Maybe they see it as a hipster gadget which I hate because to me, it’s an actual phone.
“But there’s a surprising number of people who have identified with my philosophy of not liking smartphone culture - I’m pleasantly surprised that those people are out there.”
Video by: Gabriella Petty
A mother lost both FEET after a life-threatening labour ordeal which left her bleeding heavily and infected with sepsis
Image by: Callie Colwick
A mother lost both her FEET after a life-threatening labour ordeal which left her bleeding heavily and infected with sepsis.
Callie Colwick, 30, suffered from a rare condition called placenta accreta while pregnant with her son Quinn.
The serious complication occurs when the placenta detaches from the uterine wall after delivery and causes severe blood loss.
She tragically lost her newborn son and contracted sepsis which left her fighting for her life as her organs failed.
Doctors had no choice but to amputate both of Callie’s legs, her left thumb and forefinger and remove her uterus as the tissue had ‘died’ due to the loss of blood.
The graphic designer, from McKinney, Texas, said: “My limbs started to die.
“My legs were black and shriveled up, my toes looked like raisins.”
When Callie finally returned home after spending over a year in the ICU, her health insurance refused to cover the $11,000 custom wheelchair she needed to move around freely.
The mother of Kenzi, four, couldn’t push herself around in a standard wheelchair and was forced to wear diapers as she wasn’t able to go to the bathroom alone.
Callie was astounded to receive an Instagram message on December 31 2019 from a kindhearted stranger offering to raise the funds to buy her the special wheelchair.
Amy Bernhard, 32, set up a GoFundMe campaign and within just one day she had raised a staggering $20,980 for Callie’s chair with the extra money going towards installing ramps in her home.
Callie and husband Kevin, 30, a web developer, were delighted to discover that Callie was pregnant with Quinn, their second child, in November 2016.
But when Callie began experiencing heavy bleeding at work when she was 15 weeks pregnant, she went to hospital.
“I’d had light bleeding from day one,” Callie said.
“But what made me go to the doctor was the heavy abdominal bleeding.
“I was passing blood clots.
“I was at work about to go into a meeting and I felt this gush of liquid - my pants were soaked in blood.
“I went straight to hospital and called Kevin.”
Image by: Callie Colwick
Image by: Matthew Newby SWNS
Image by: Callie Colwick
Doctors told Callie that Quinn could be born at any time and that tragically he would not survive the birth.
“They put me in the pregnancy wing.
“Here we were in this room, surrounded by women giving birth and babies crying and we were told that Quinn had no chance of survival and we were just waiting to give birth to him.
“It was a solemn few weeks.”
Callie lay in the Trandelenberg Position with her feet elevated above her head in a last ditch attempt to help her baby survive.
“I hung like a bat trying to keep him inside through gravity,” she said.
“I was afraid of sneezing or going to the restroom in case my waters broke and he was born.
“It was a terrifying few weeks with nothing to do in the hospital but just wait.”
Doctors induced labour on December 26 2016 and little Quinn was stillborn, weighing just half a pound.
“I was fading in and out of consciousness,” Callie said.
“I wasn’t responsive, my eyes would roll to the back of my head and I was burning up.
“My fever had spiked way too high and they were packing ice onto me.
“They broke my waters and he was born.
“Quinn was too tiny to survive; he went straight to heaven.
“My husband was stuck between mourning the loss of his son and making all these medical decisions.”
During the delivery Callie lost so much blood that a trauma doctor was flown in from Dallas.
“My uterus was hemorrhaging blood.
“Doctors were pumping blood into me as soon as it was flowing out.”
But Callie developed septic shock in her uterus and the infection soon spread leaving doctors no choice but to remove her uterus.
She said: “My world went black.
“That infection overrode my entire body.
“They had to take out my uterus.
“The sepsis shut down my kidneys and my lungs so I was on a breathing machine.”
Two months later, doctors decided that they would have to amputate Callie’s legs below the knee and part of her left hand as the tissue was so damaged due to lack of blood.
“I remember coming to, in extreme pain and confusion.
“My husband had to explain what happened.
“I had everything minus my uterus and my feet.”
Image by: Callie Colwick
Image by: Callie Colwick
Image by: Callie Colwick
Callie spent more than a year in the ICU and finally in March 2018 she was able to return home.
She had been refused prosthetics by her health insurance and struggled to adjust to life as an amputee in a bulky wheelchair that she could not push herself in.
“The wheelchair they sent me home in was a basic chair off of Amazon.
“Kevin had to dress my wounds every day.”
Callie was finally able to stand on her knees for the first time on January 15 2019.
“Until then, Kevin had been picking me up and putting me in my chair.”
In April 2019 she was finally approved for prosthetics and she applied for a custom chair in October.
“My doctor put in the order and they denied my chair.
“It is just insane.
“I don’t have feet and I can’t put my prosthetics on by myself.”
She shared her frustration on Instagram where Amy, a business coach, from Lafayette, Louisiana, came across her story.
“I glanced at Callie’s page and as I watched her videos, I had tears come down my face,” Amy said.
“I had trouble sleeping because I could not stop thinking about what this woman had gone through.”
She reached out to Callie and offered to start a GoFundMe campaign for her chair, but Callie at first turned down the offer.
Callie explained: “I messaged her back and said: ‘No thanks’.
“I was still hoping that my insurance would approve it.
“But she just kept messaging me and then when my request was declined again for the chair, I agreed.
“I said: ‘Yes, do what you think is best’.”
The next morning Amy launched the fundraising campaign and Callie was amazed to see how quickly people donated.
“It was shared like wild fire,” she said.
“This generous gift from a complete stranger gives me the ability to make my home completely accessible.
“It’s a lightweight custom built chair so I can pick it up by myself.
“I can actually wheel myself around in it.
“Imagine being trapped in a chair - for me, this chair is the difference between a chair that has wheels and one that doesn’t.”
The two women met in person for the first time on January 24 when Amy flew to Dallas for work.
They bonded over a sushi dinner where Callie told Amy just how big a difference the baby pink chair had made to her life.
“She shared with me what that wheelchair would actually do for her,” Amy said.
“She told me that it was the first time in three years that she was able to go to the bathroom herself.”
Callie added: “I felt like I had known Amy my whole life.”
Despite all her health struggles, Callie says she is keen to make the most of her life.
She said: “My hope is to help and inspire others.
“I was 27 when this happened - no one expects a 27-year-old mom to die.
“I truly feel like I am living on borrowed time now.”
Video by: Callie Colwick
HEARTBREAKING DANCE - Dad has shared a heartbreaking video showing the final dance he shared with his four-year-old girl before she suddenly passed away
Image by: John Newton
A grieving dad has shared a heartbreaking video showing the final dance he shared with his four-year-old daughter before she suddenly passed away last week.
Doting John Newton, 39, can be seen dancing around the room with his poorly daughter, Charlotte Grace, laughing and smiling in his arms.
The emotional footage was captured before Charlotte, who suffered from several medical issues, died on Wednesday evening (April 22).
John, from Barnsley, South Yorks., said despite the problems Charlotte faced, she never let them hold her back and always lived life to the fullest.
The video, John added, shows his daughter as he would like her to be remembered and taken a few months before she died.
He said: "She was such a happy little girl who woke up each day with a love for life, a beautiful little girl who brought joy into the lives of everyone she encountered in life.
"The video of us dancing shows what an amazing girl she was, always smiling."
Charlotte battled numerous health issues from birth, including stage five kidney disease, liver disease, a rare genetic disorder and heart problems.
Last Wednesday she was at home with her family, including mum Rachel, 37, and sister Emily, seven, when her condition drastically deteriorated and she suddenly died from complications relating to her various illnesses.
John said only five minutes before Charlotte she fell ill and was rushed to hospital she was speaking to her grandparents on FaceTime.
Image by: John Newton
Image by: John Newton
Image by: John Newton
At the time of her death the four-year-old girl, who loved Disney films and Spiderman, was on the transplant list for a combined liver and kidney transplant.
The potentially life-changing operation would have taken place at Birmingham Children's Hospital.
John said: "The sudden loss of our baby girl has been devastating and heartbreaking for us and has left us in complete bits.
"We knew from the time Charlotte was born that every minute with her would be precious, we tried to remain positive and look to the future.
"We had always hoped that she would be one of those miracle cases, who lives a long and happy life but it wasn't to be."
John, who is training to be a teacher, said he broke the news to his other daughter Emily, who is autistic and deaf, this week.
He added: "We told her Charlotte isn't hurting anymore and that she is a star up in the sky.
"The two of them had such a wonderful bond so we will have to see how Emily is affected."
John said he shared the dancing video to show the world what kind of girl Charlotte was.
He added: "We would like everyone to know how beautiful and loved she was."
A fundraising page has been set up in memory of Charlotte, to help support the Newton family through the tragedy.
Donate here: https://www.gofundme.com/f/charlottes-go-fund-me
Video by: John Newton
