February 02, 2016

Mother hears dead baby's heartbeat inside 4 year old transplant recipient

A woman whose seven-month-old son died after being reportedly abused by a babysitter's boyfriend donated his organs - and has now heard the boy's heartbeat in a young girl.

Heather Clark couldn't hide her emotions as she listened to the heart of four-year-old organ recipient Jordan Drake at Phoenix Children's Hospital.

Donate Life Arizona wrote on Facebook Saturday: 'Amid the unthinkable grief of losing her son Lukas, Heather made a decision that saved three lives.

'Jordan received Lukas' precious heart when she was just 18 months old. 'Yesterday, Heather heard her son's heartbeat for the first time in nearly three years.'


Clark and Drake's mother, Esther Gonzalez, were filmed by KDVR crying and hugging while meeting one another for the first time.

Gonzalez was heard telling Clark: 'I just can't believe this is happening.'

Jordan gifted Clark with a red teddy bear covered in pink hearts that when pressed made a heartbeat sound.

'That's Lukas' heartbeat,' Gonzalez explained, leading to Clark crying. 'Thank you, Jordan,' Clark said. 'It's perfect.'


Clark also put on a stethoscope and placed it upon Jordan's chest, listening to her late son's heart beating.

'It's so strong,' Clark was filmed saying. When she was done, Clark gave Jordan a hug and a kiss.


Jordan later used the stethoscope herself, and heard Clark's heartbeat.  Clark also shared photographs of Lukas at the emotional meeting.

At one point, Clark told Gonzalez in the footage:

'And another amazing thing with donating his organs is it gave me the chance to hold him again.'



Clark said in a January 22 post on the Facebook page Justice For Lukas Scot:

'One week from today I will be listening to Lukas' heartbeat once again. 'I will be holding Jordan in my arms showering her with love and kisses!'





A baby has been born in this Italian town For the first time in 28 years

Since the 1980s, the Italian town of Ostana had not seen the birth of a single baby.
But last week, a dream came true, as the mayor of the small town said. A baby was born. The first in 28 years.
According to La Stampa, the town has only 85 inhabitants, including newborn Pablo. Its population has continuously fallen -- a fate shared by many other Italian towns and villages.

"The real decline started in 1975, with 17 babies between 1976 and 1987, when the last boy was born - until little Pablo,"


Mayor Giacomo Lombardo was quoted as saying. A party will be held to celebrate what he hopes will be the start of a reversal of that trend.

But the population decline will be hard to stop, no matter what ideas Lombardo comes up with.

Younger Italians in particular say there are few attractive job prospects in rural areas. Many have moved to cities, leaving their hometowns to the elderly. Ostana, which is in northern Italy, has only one shop, a bar and two restaurants, according to the Italian news site the Local.

Some parts of northern Italy have been hit harder than others. But the south, including the island of Sicily, has faced more dramatic demographic changes in recent decades.

The arrival of baby Pablo has certainly been welcomed in Ostana, according to the mayor. "It's great to finally have someone born here, and it shows that our efforts to reverse population decline are slowly working," Lombardo was quoted as saying.

Lombardo has tried to create jobs in order to prevent other young people from leaving the town. Pablo might be the first indication that his strategy is working. His parents wanted to move away several years ago but stayed after they were offered the opportunity to work at a mountain refuge.

Source: Washington Post

Graphic photos of a Female suicide bomber who tried to attack Dikwa village in Borno

Search and Rescue officers in NEMA, today evacuated the body of a Lone female suicide bomber intercepted along Dikwa Maiduguri Road, Borno state. The explosives strapped to her exploded before she gained access to target location‎.



 




Zika virus is now an international public health emergency - W.H.O

The World Health Organization has declared the spread of Zika virus an international public health emergency and has freed funds to combat the disease.

“This is an extraordinary event,” said WHO Director General Margaret Chan at a press conference on  Monday. “It poses a public health threat to other parts of the world and a coordinated international response is needed.”

Margaret Chan cited the pattern of the disease’s spread, the lack of a vaccine, and the large global population of mosquitoes that can carry the virus as factors that contributed to the declaration.

The declaration, only the fourth in WHO’s history, comes just days after the organization said the number of cases could hit 4 million by the end of the year. The virus has spread rapidly throughout the Americas infecting people in more than 20 countries. 

Officials in Brazil, the hardest hit country, have estimated 1.5 million infections. 

The Zika virus is spread to people through mosquito bites and causes genetic mutation in babies. The most common symptoms of Zikavirus disease are fever, rash, joint pain, and conjunctivitis (red eyes). The illness is usually mild with symptoms lasting from several days to a week.

Photos: Danish woman rescues little boy who was accused of withcraft and left to die in Uyo


On Sunday, a Danish woman, Anja Ringgren Loven, a Philanthropist an founder of African Children's Aid Education and Development Foundation ( ACAEDF) who lives with her partner and son in Uyo rescued a little boy who had been abandoned by his family because they claimed he was a 'witch'. She took him into her care, fed him, gave him clothes and he is currently receiving some medical attention. This was what she shared on her Facebook page.







Today she gave an update on the boy whom she named Hope. 

We should be proud to be Danes. We are a loving people and we're taking good care of each other. We are always together when there is need our help. When natural disasters hit, famine ravaging and civil wars devastate affects us deeply. We Danes are among the world's most generous. We are the best to donate money to charity, help others and do volunteer work. More than every other of us Danes gives money to charity and help people we don't know. And we must be proud!


Right now we danes hung out in the foreign media. Incorrect or not, media account certainly not the true picture of US DANES. For when it comes to love there are no countries can match us! So let us give the media something new to write about. Something to really show them who we danes are!


Just 2 DAYS HAVE DINNØDHJÆLP RECEIVED 1 million dollars to help little hope!!! Let me repeat that: 1 million Danish kroner is donated to dinnødhjælp in just 2 DAYS!!!


My feelings are sitting without his clothes! I'm so overwhelmed! I'm so grateful and touched by all the love, care and huge support there just pouring here to Nigeria all the way from Denmark! I want as long as I live thank you all every day! I forget simply never! With all the money we can besides giving hope the very best treatment now also build a doctor clinic on the new land and save many more children out of torture! It's just so great! The building must be called hope clinic - donated city Denmark!! They say thanks is just a poor words, but for me means thank you life! And to those who says otherwise, then we can today together prove to the whole world that charity indeed still exists in Denmark!heart emoticon


Hope's condition is stable now. He's taking food for himself, and he responds to the medicine he gets. Today he has had powers to sit up and smiling at us. He's a strong little boy. To see him sit and play with my own son is without doubt the greatest experience of my life! I just don't know how to describe it in words. This is what makes life so beautiful and valuable and therefore I will let the pictures speak for themselves:


Today we "groundbreaking" ceremony at the construction site. Ground breaking ceremony where we are so lucky to the Danish Ambassador here in Nigeria participates as a guest of honour and the keynote speaker. I can't believe our ambassador and his sweet wife comes entirely from the capital Abuja to our little village where dinnødhjælp builds a new orphanage and participating in our ceremony. It's so big and I am very pleased to see the ambassador again. Today during the ceremony I will think of our architect Martin from engineers without borders and his working group as in more than half a year now worked every day for putting together and draw dinnødhjælps orphanage in cooperation with our Nigerian engineers. I very much look forward to show you all the outcome when the construction is finished. About 1 years running little hope around on dinnødhjælps new orphanage and play with all the other children.


Where there is love, there is life




 


Anja with her son,  David Jnr


Photos: Village doctor with no legs offers home visit in mountainous area for 15 years



A woman who had her legs amputated due to a traffic accident has gone on to become a doctor who takes care of more than 1,000 villagers in a mountainous county in southwest China's Chongqing Municipality.



Li Hongju, 37 has "worn out" 24 wooden step stools when practicing medicine on over 6,000 call outs in 15 years.



One afternoon in March 1983, the 4-year-old Li Hongju was on her way to nursery school. She was hit by a large truck and ended up trapped underneath it. After the amputation, she was left with less than 3 cm of her legs.


When she was eight years old she learnt to "walk" on her hands by supporting her entire upper body using wooden step stools. Having experienced such pain, Li Juhong decided to help save the lives of others.

February 01, 2016

British scientists granted permission to genetically modify human embyros

British scientists have been granted permission to genetically modify human embryos by the fertility regulator. The Francis Crick Institute could begin thecontroversial experiments as early as March after the Human Fertilisation and Embryology Authority(HFEA) gave the green light this morning.

The scientists want to deactivate genes in leftover embryos from IVF clinics to see if it hinders development.

It will only be the second time in the world that such a procedure has been undertaken and the first time it has been directly approved by a regulator. A Chinese team carried out similar experiments last year to widespread outcry.

Currently around 50 per cent of fertilised eggs do not develop properly and experts believe that faulty genetic code could be responsible.

If scientists knew which genes were crucial for healthy cell division, then they could screen out embryos where their DNA was not working properly, potentially preventing miscarriages and aiding fertility.

The initial pilot, which will also have to pass an ethics evaluation, will involve up to 30 embryos and the team would like to work on a further three genes, which could bring the total of to 120.

Critics warn that allowing embryos to be edited opens the door to designer babies and genetically modified humans.

But lead scientist Dr Kathy Niakan said that the research could fundamentally change our understanding of human biology and give hope to prospective parents.

“We would really like to understand the genes that are needed for an embryo to develop into a healthy baby,” she told a briefing in central London last month.


“Miscarriage and infertility are extremely common but they are not very well understood. We believe that this research could improve our understanding of the very earliest stages of human life.


“The reason why I think this is so important is that most human embryos fail to reach the blastocyst stage. Over 50 per cent will fail so this window is absolutely critical.


“If we were to understand the genes, it could really help us improve infertility treatment and provide crucial insights into the causes of miscarriage.”

The team at Francis Crick are already in talks with fertility clinics across the country to use their spare embryos.

Sir Paul Nurse, director of the Crick, said:

“I am delighted that the HFEA has approved Dr Niakan’s application. Dr Niakan’s proposed research is important for understanding how a healthy human embryo develops and will enhance our understanding of IVF success rates, by looking at the very earliest stage of human development - one to seven days.”

Currently it is not illegal to edit human embryos for research purposes although it has never been done before because they technology has not been available.

When China announced it had carried out similar experiments last year there was a widespread outcry.

A spokesman for the HFEA said:

“Our Licence Committee has approved an application from Dr Kathy Niakan of the Francis Crick Institute to renew her laboratory’s research licence to include gene editing of embryos.

“The committee has added a condition to the licence that no research using gene editing may take place until the research has received research ethics approval.

“As with all embryos used in research, it is illegal to transfer them to a woman for treatment.”


All cells in a human embryo have the same DNA code, but they divide into specialised cells depending on gene expression.

Between day five and seven of human development and embryo has around 200 cells of three different types. One set will go on to form the foetus , while another type becomes the placenta, and the third kind the yolk sac which nourishes growing baby. The aim of the new project is to find out what causes the cells to turn into different kinds, a process known as ‘lineage specification.’

The new genetic editing technique, called Crispr, acts like molecular scissors to snip out part of the DNA code so that scientists can see if it was needed.

“Crispr is so efficient and precise that it can go inside a single volume, open up, a specific page, identify a single word, and alter a single letter,” added Prof Niakan.

The first gene that the team is planning to deactivate is OCT4, which in mice appears to be crucial for the healthy development of foetal cells.

However British scientists were among 150 experts who in November called for a worldwide ban on genetic editing of embryos claiming the practice could open the door to ‘irrevocably altering the human species.’

Dr Calum MacKellar, Director of Research of the Scottish Council on Human Bioethics said: “Allowing the gene editing of embryos opens the road to genetically modifying all the descendants of a person as well as full blown eugenics which was condemned by all civilised societies after the Second World War.”

“It is the very future of the way in which societies accept persons with disabilities that is at play since such gene editing procedures infer that they should not have been brought into existence.”

Gene therapy has been available since the 1970s but it is only recently that scientists have developed technology which can snip out parts of genetic code

The technique could permanently remove harmful mutations which lead to inherited diseases like Huntingdon’s, cystic fibrosis and haemophilia, critics say it could have unexpected side effects any may damage healthy strands of DNA.

Alastair Kent, Director of Genetic Alliance UK, said: "“Understanding the crucial process of embryo development could help us to understand causes of infertility, miscarriage and some genetic diseases.

"The team at the Crick Institute have explained to the HFEA why they would like to use genome editing to investigate embryo development and the HFEA have authorised the research to proceed. We hope that this avenue of research is fruitful, and that genome editing is as powerful a research tool as it currently seems to be." 


Photos: Man uses 100 kilograms of paper boxes to make a transformer for son



Recently a 35-year-old man named Xu Ou went viral in Ziyang city, southwest China's Sichuan province. He made a transformer with more than 100 kilograms of discarded paper boxes. At the noon of Jan. 30, Xu carried the super transformer out from home and displayed it in the plaza of Sanxian Park.



Together with his friends, Xu spent over 20 days to make this transformer using more than 100 kilograms of waste paper boxes and 1,000 screws.

"The inspiration of making an 'Optimus' occurred in my mind suddenly when I sent my son to learn drawing. I made the transformer—the embodiment of justice and gave it to my son and other children as a Spring Festival gift," said Xu.

"My son is studying painting in a fine arts training class. He often wastes things in daily life. I want to let him know that we can take advantage of the discarded materials to make pleasant things rather than buy them with money. When I finished the work, my son and his friends all liked it very much and the photo of the transformer was widely spread in the WeChat circle," Xu told the reporter of West China Metropolis Daily.




"The inspiration of making an 'Optimus' occurred in my mind suddenly when I sent my son to learn drawing. I made the transformer—the embodiment of justice and gave it to my son and other children as a Spring Festival gift," said Xu.


"My son is studying painting in a fine arts training class. He often wastes things in daily life. I want to let him know that we can take advantage of the discarded materials to make pleasant things rather than buy them with money. When I finished the work, my son and his friends all liked it very much and the photo of the transformer was widely spread in the WeChat circle," Xu told the reporter of West China Metropolis Daily.

Four Nigerian banks among top 500 banking brands in the world in 2016

According to the 2016 Top 500 banking brands ranking published in the February edition of The Banker magazine of Financial Times Group in conjunction with Brand Finance, London, United Kingdom, First Bank of Nigeria is in 320th position out of 500 top banks in the world in 2016. It has moved up from it's former position of 336th from last year.

First Bank of Nigeria Limited retained its number one banking brand ranking in Nigeria for the fifth consecutive year in the global ranking of banks by The Banker magazine.

A press release from the Country Representative of The Banker magazine in Nigeria, Kunle Ogedengbe, added that three other Nigerian banks also made the ranking of the top 500 banks in the World.
First Bank of Nigeria is in 320th position out of 500 top banks in the world in 2016
Guaranty Trust Bank is 389th in the world from 417th in 2015
Zenith Bank dropped from 392nd in the world in 2016
United Bank for Africa is in the 447th position.

Of the five countries in Africa that made the ranking, Nigeria has the highest brand value increase of $249 million. 
Egypt moved up by $239 million
Togo gained $134 million while South Africa and Morocco lost $878 million and $213 million respectively.
Globally, Wells Fargo of the United States of America retained the number one banking brand in the world for the fourth consecutive year with a brand value $44.1 billion for 2016

Walmart heiress Alice Walton is the richest woman in the world

With a net worth of $33.2 billion, Alice Walton isn't just the wealthiest woman on our list of the 50 richest people on earth, she's also a member of one of the richest families in the world.
Alice, along with older brothers Jim and Rob, who also graced the list, produced with Wealth-X, a company that conducts research on the superwealthy, have a combined net worth of $101.5 billion, thanks primarily to their stake in retail giant Walmart.
Unlike her brothers, 66-year-old Walton never took an active role in running the retail empire her father started in 1962, though she's still managed to become the target of pushback from minimum-wage Walmart employees who view her highfalutin lifestyle as insensitive and ignorant to the plight of many workers.
Instead of spending time at Walmart, Walton became a patron of the arts at a young age. When she was just 10 years old, Walton saved up her allowance to buy a reproduction of Picasso's "Blue Nude," she told The New Yorker.
"Collecting has been such a joy, and such an important part of my life in terms of seeing art, and loving it,” she said.
She began buying watercolor pieces in the 1970s and adorning the walls of her Rocking W Ranch with them. From there she moved on to more serious original works, particularly those by classic American artists; her immense personal collection now includes pieces from Andy Warhol, Norman Rockwell, and Georgia O'Keefe, among others.
In 2011, she opened the $50 million Crystal Bridges Museum in Arkansas to house her $500 million collection. When it opened, Crystal Bridges already had four times the endowment of the famous Whitney Museum in New York.
Before delving into the art realm, Walton made a brief career as an equity analyst and even founded her own investment bank, Llama Company, in 1988. The company closed about 10 years later, shortly after Walton was arrested for driving under the influence of alcohol (not for the first time).
Twice divorced with no children, Walton is also a lover of horses, which she breeds at Rocking W Ranch, located in Texas, and rides competitively. The 1,456-acre ranch, however, is currently for sale for nearly $20 million.
Walton is one of just four women to make our list of the 50 richest people on earth — and each inherited their fortune. The next wealthiest woman is 93-year-old Liliane Bettencourt, the French heiress to the L'Oreal fortune, with a net worth of $29 billion.

Family struggles to find answers for boy with rare stiff skin syndrome

Compared with the developmental and emotional problems Jaiden suffered from the time he was born, the odd patch of skin that appeared on his right thigh when he was 7 seemed minor.
He noticed it first. It was about the size of a postage stamp and looked no different than the surrounding skin. But it felt as hard as pavement.
Natalie and Tim Rogers — Jaiden's legal guardians — weren't particularly worried, and neither was his pediatrician. But a specialist ordered a biopsy and told Natalie to sit down before giving her the news over the phone.
She imagined cancer. The doctor gave her a different diagnosis: stiff skin syndrome.

It sounded so innocuous, until she learned more about it.
In healthy people, a protein known as fibrillin helps form the elastic fibers that enable skin and ligaments to stretch. But in people with the syndrome, a genetic mutation causes abnormal production of the protein, thickening of the skin and limited joint movement.

In the worst cases, hardening tissue can squeeze vital organs.
The syndrome is extremely rare. Since it was identified in the early 1970s, fewer than 50 cases have been documented worldwide.
Having so little experience with the disease, doctors said they had no way of knowing how it would affect Jaiden. There is no cure.
Alone at her computer, Natalie searched online for other families afflicted by the disease — to compare notes about possible treatments, or just to commiserate. But she found none.
"If you have cancer, there are places you can go ," she said.
::
Natalie had her own health problems. Doctors advised her long ago that pregnancy would be too risky.
So she had her husband set out to find another way to make a family. They adopted. A baby girl who grew up to become a physical therapist. And a 12-year-old orphan from Russia who now serves as an officer in the U.S. Air Force.

"It didn't matter if I had my own kids," said Natalie, 49. "There were kids out there that needed me, and I love them as much as any child that I could have given birth to."


She had stayed in touch with her daughter's biological family, including a sister with a 2-year-old boy named Jaiden and too many problems of her own to take care of him.
Natalie offered to do it. At the time, she and her husband were living in Minnesota, where Tim was a manager in the federal prison system. Their plan was to eventually retire on an 80-acre plot they had purchased near Alamosa, a tiny town in Colorado.
Jaiden had already been diagnosed with fetal alcohol syndrome, attention problems and autism. Those problems never scared Natalie, who simply saw an easygoing little boy, she said.
And soon those issues would be overshadowed.
By early 2013, a few months after the first hard patch of skin appeared, it had grown to cover Jaiden's entire thigh.
He began struggling to walk because hard skin coated the backs of his legs. He was already using a wheelchair when the family moved to Colorado that fall.
The hard patches continued to grow, spreading across his back. Eventually they spread to his neck, left shoulder and much of his stomach.

Most worrisome, Jaiden began having breathing difficulties as a result of the skin around his chest tightening. Last summer he began using an oxygen tank, and soon after stopped going to school because his medicines left him so drowsy that he would drift into sleep during class and topple out of his wheelchair.
The school district now sends a tutor to the house.

The couple have turned over the master bedroom to him — the only room with enough space for maneuvering a wheelchair.

It wasn't the retirement that Natalie and Tim had imagined.
It is difficult living with such a rare disease so far from a major city and medical specialists.
Mikaila Pence, a pediatrician in Alamosa, keeps up with the literature on stiff skin disease and in close touch with Jaiden's specialists in Denver.

"He came to me with a diagnosis I don't know anything about — I've never heard of," Pence said. "I'm not only having to learn about a new patient and a new family, but having to learn about a new disease."


Treatment options have been limited. Natalie and Tim raised $85,000 in an online charity campaign to install a heated pool so Jaiden could do water exercises aimed at maintaining his range of motion in his arms and legs.
For a time, he took a drug normally used to treat leukemia that seemed to slow the disease's progression. But doctors stopped the drug after a year and a half, when the side effects became too severe.

At least once a month, Natalie drives Jaiden to Denver. The four-hour journey starts on gravel county roads that link up with the highway, most of it two-lane, running east through the Sangre de Cristo Mountains to the interstate that leads north.
His pediatric dermatologist there recently tried another leukemia drug. It is too soon to know whether it is working.
Now 10, Jaiden weighs 105 pounds and stands 4 feet 7. He often rides in a large stroller, which he started using after falling out of his wheelchair during bouts of tiredness.
Yet he also enjoys many of the things healthy children do, especially video games.

"He likes his picnics and he likes to sit in the grass," Natalie said. "We have chickens, and every once in a while he likes to see the chickens. He likes to roast marshmallows and sit out by the fire pit."


He calls Natalie and Tim his parents and says he would like them to adopt him, something they have been reluctant to do out of fear that it would threaten his Medicaid benefits.
"We're going to consider him our son whether we adopt him or not," Natalie said. "We're going to love him no matter what. I'm going to fight for him no matter what."

West Ham sign Nigerian footballer Emmanuel Emenike

Emmanuel Emenike has signed for top English club West Ham on loan from Fenerbahce till the end of the season. The footballer who retired from the Super Eagles last year agreed to join the club in the late hours of Sunday, 31st of January, barely 24hours till the end of the transfer window.

The Nigeria international has been on loan at Qatari club Al Ain this season.

"I'm very happy and very excited that I'm here," 28-year-old Emenike told the club's official website. "I have always known West Ham as a great club. I have known [manager Slaven] Bilic for years and thank God we are here together." he said


Emenike, who has scored nine goals in 37 international appearances for Nigeria, is the club's second signing of the January transfer window.