Africa Hip-Hop Songs #GIVE by Young City Ft. Lizkid
Thursday, 4 February 2016
Sunday, 24 January 2016
Tuesday, 27 October 2015
election Tanzania : Government ministers suffer shock defeat in Tazanian Election
Seven Tanzanian
government ministers have lost their parliamentary seats to the
opposition Ukawa coalition, partial results from Sunday's vote show.
It is the biggest shock of the election so far which is the most competitive in the country's history.The BBC's Muliro Telewa in the main city Dar es Salaam says the news will worry the governing CCM party that has been in power for 54 years.
The electoral commission has until Thursday to announce the final results.
Observers from the European Union have given a positive assessment of the polls.
But they raised several concerns - including the apparent failure of state media to give fair and equitable coverage to the opposition in the build-up to the election.
- seniorgstar.blogspot.com live new
Residents on the islands also voted for their own president and members of the Zanzibar parliament on Sunday.
CUF, one of four parties which make up Ukawa, has accused the Zanzibar electoral commission of only releasing results from constituencies where the CMM candidate has won.www.google.com
King Ooni of IfeYoruba Nigeria New King
King Ooni of IfeYoruba Nigeria (www.facebook.com New King)
He is a prince from one of the ruling houses in the Ife kingdom.
A 40-year-old accountant has been named the new Ooni of Ife - a revered monarch in south-west Nigeria.
Adeyeye
Enitan Ogunwusi is the new king, one of the most influential among the
Yoruba people, Nigeria's second biggest ethnic group, who number about
35 million in West Africa.He is a prince from one of the ruling houses in the Ife kingdom.
Sunday, 24 May 2015
Thursday, 14 May 2015
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President Barack Obama Surprises 3 women
To celebrate Mother’s Day, the White House has released a very sweet video of the president calling up a few moms …
Wednesday, 18 February 2015
Thursday, 2 October 2014
Why I haven’t lost my Vir gi nity – Sexy Adokiye o...
Why I haven’t lost my Vir gi nity – Sexy Adokiye o...: “I have a boyfriend now, But what we share is AGAPE love; no s ex kind of love. But I know I want to settle down and have kids. I heard...
Monday, 22 September 2014
It's Kemi Filani's blog...: Very Gigantic Fish Washes Up On Alpha Beach Lagos ...
It's Kemi Filani's blog...: Very Gigantic Fish Washes Up On Alpha Beach Lagos ...: This very gigantic fish washed up on Alpha Beach according to eye witnesses. You will recall that earlier on this month, Lagos state...
It's Kemi Filani's blog...: Shocking confessions from ex-boko haram who is now...
It's Kemi Filani's blog...: Shocking confessions from ex-boko haram who is now...: My name is Sheik Sani Haliru. I am from Niger Republic, but my mother is from Bornu State of Nigeria and I grew up in Wulari, Maidugur...
Friday, 5 September 2014
Shrinking my 17stone legs: Hope for woman whose limbs wouldn't stop growing after doctors develop pioneering treatment
Shrinking my 17stone legs: Hope for woman whose limbs wouldn't stop growing after doctors develop pioneering treatment
- Mandy's condition has caused her legs to grow uncontrollably her whole life
- DNA study revealed it is the first known case of its kind in the world
- Cambridge doctors have developed a medication they hope will reverse it
Doctors have told a woman whose legs won't stop growing that they have developed a promising treatment for her after mapping her DNA.
Mandy Sellars, 38, has a condition that has caused her legs to grow uncontrollably her whole life.
She even had her massive left leg amputated after it became infected with septicaemia. But the stump soon started growing again and within three years measured a metre in circumference and weighed 3stone.
Ms Sellars has now been told it has no name after genetic testing revealed it was the first case of its kind in the world.
The condition makes it incredibly difficult for Mandy to move around and she is housebound during the week. She travels in a specially reinforced wheelchair.
'I find it incredibly frustrating,' Ms Sellars, from Huncoat in Lancashire, said.
'I have such a zest for life and I really want to get out there and live it.'
This could now be a possibility, after scientists at Cambridge University took an interest in Ms Sellars' case.
Over the past year, Dr Robert Semple has mapped her DNA from blood and tissue samples. Ms Sellars' presumed she had a rare form of Proteus Syndrome - the condition that affected the Elephant Man. However, the analysis revealed she had a unique disorder.
'I'm the first person in the world with it and it hasn't even got a name yet,' Ms Sellars told ITV's This Morning.
'I keep suggesting Dr Semple call it Sellars Syndrome!'
As a result, Dr Semple's team have come up with a medication aimed at replacing her unique mutated gene with a therapeutic gene.
'I started taking it in September and the aim was to stop my limbs growing further. Actually they have started to shrink a little,' Ms Sellars' said.
'I just kind of accepted my condition would get worse and keep growing but I am more optimistic following the discovery.'
Ms Sellars, who is a size 12 on her top half, has had to deal with her one in seven billion condition her whole life.
'There was clearly something
dramatically different about me when I was born as my legs were so much
bigger than my body. Doctors didn't know what it was and whisked me away
- they didn't let my mother see me for two weeks. They didn't think I
would survive.'
Her left leg was three inches longer than her right, and both were out of proportion. But Mandy flourished despite their dire prognosis.
'I could walk around and play football as a child,' she said.
'I had friends and went to a comprehensive school for my GCSE's. But I found it harder to deal with as a teenager as you become more aware. Some people would stare and laugh at me. I find that easier to deal with now.'
Her parents encouraged her to be independent and she moved out of home at 19. She went to the University of Central Lancashire where she gained a BSc in Psychology.
She has volunteered in the past at the RSPCA but had not been able to work full-time due to her health condition. She has suffered arthritis, deep vein thrombosis (DVT) and had a blood clot in her leg.
The condition makes it incredibly difficult for Mandy to move around and she is housebound during the week. She travels in a specially reinforced wheelchair.
Doctors had hoped to fit her with a
prosthetic leg but as her stump kept growing, new legs had to be made
and to date she is still unable to walk.
Mandy Sellars, pictured on This Morning in her electric wheelchair, said she has a 'zest for life'
'I have such a zest for life and I really want to get out there and live it.'
This could now be a possibility, after scientists at Cambridge University took an interest in Ms Sellars' case.
Over the past year, Dr Robert Semple has mapped her DNA from blood and tissue samples. Ms Sellars' presumed she had a rare form of Proteus Syndrome - the condition that affected the Elephant Man. However, the analysis revealed she had a unique disorder.
'I'm the first person in the world with it and it hasn't even got a name yet,' Ms Sellars told ITV's This Morning.
'I keep suggesting Dr Semple call it Sellars Syndrome!'
As a result, Dr Semple's team have come up with a medication aimed at replacing her unique mutated gene with a therapeutic gene.
'I started taking it in September and the aim was to stop my limbs growing further. Actually they have started to shrink a little,' Ms Sellars' said.
'I just kind of accepted my condition would get worse and keep growing but I am more optimistic following the discovery.'
Ms Sellars, who is a size 12 on her top half, has had to deal with her one in seven billion condition her whole life.
Ms Sellars with the medication she hope may reverse her condition
Dr Robert Semple studies Mandy Sellars over-sized right leg. He mapped her DNA and found out her condition was unique to her
Her left leg was three inches longer than her right, and both were out of proportion. But Mandy flourished despite their dire prognosis.
'I had friends and went to a comprehensive school for my GCSE's. But I found it harder to deal with as a teenager as you become more aware. Some people would stare and laugh at me. I find that easier to deal with now.'
Her parents encouraged her to be independent and she moved out of home at 19. She went to the University of Central Lancashire where she gained a BSc in Psychology.
She has volunteered in the past at the RSPCA but had not been able to work full-time due to her health condition. She has suffered arthritis, deep vein thrombosis (DVT) and had a blood clot in her leg.
He even struggles to eat due to his rare condition.
"The teacher say other kids are scared of my hands," Kaleem said.
"When I used to go to school many of them would say, 'Let's beat up the kid with the large hands'.
"Some of them have beaten me and would go after me often."
Kaleem's undiagnosed condition has seen his hands hit a staggering weight of 1st 4lb.
His mother Haleema, 27, said: "When Kaleem was born his hand was twice the size of a normal baby's.
"Initially his fists were small but began to grow large as well and his fingers also kept growing.
"We have tried several places with no solutions so far."
“The teacher say other kids are scared of my hands”Mohammad Kaleem
Monday, 18 August 2014
Olusoga Sofolahan, Nigeria Scout CC has been appointed as one of the Vice Chairman
Olusoga Sofolahan,
Nigeria Scout CC has been appointed as one of the Vice Chairman for
Commonwealth Scout Association. This is a good news for Nigerians and a
big step forward. The election was held at ongoing World Scout
Conference in Ljubljana. Congratulation
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