: "width=1100"' name='viewport'/> THUNDERSTORM: November 2020

Monday, November 30, 2020

22 Year Old Pakistan Man Wants To Marry For Fourth Times .

Adnan with his three wives Shumbal, Shubana and Shahida    

A 22 years old Pakistan man wants to marry for the fourth times and his three wives helping him to find a new bride .

Adnan got married for the first time when he was only 16-years-old. At that time, he was a student. He married for the second time when he was 20 and the third wedding took place last year when he was 21 years of age .

The 22-year-old also has a condition that his fourth wife must meet him first and that her name should begin with an 'S' to match the initials of the rest of his wives, Shumbal, Shubana and Shahida. Adnan has fathered five children with them, three with his first wife Shumbal, and two with Shubana. Out of Shubana's two children, one has been adopted by Shahida.

On being asked about how he manages the expenses of all his wives, Adnan revealed that he stays in a house, which has six bedrooms, a drawing room and a storeroom. He has no problem in managing expenses as he is of the opinion that his finances flourished after his first marriage. The expenditure per month for the family is between a lakh to one and a half lakh Pakistani rupees.

Furthermore, Adnan revealed that all three of his wives adjust well with each other. The only complaint the women have from him is that each one of them believe that he is not spending adequate time with the other wives. He claims that all three of his wives love him and he too loves them very much. Source : News18 .
 

Sunday, November 29, 2020

United Kingdom set to approve Pfizer-BioNtech vaccine within very short time


 United Kingdom  is poised to become the first European  country to approve a Covid-19 vaccine, with the independent regulator set to grant approval within few days. 

Deliveries of the vaccine developed by BioNTech and Pfizer would begin within hours of the authorisation, according to government officials. The first injections could take place from December 7 . 2020 .

Vaccines would normally be authorised by the European Medicines Agency until the end of the Brexit transition on December 31. 

The same process could be applied to the vaccine developed by Oxford and Astrazeneca . The government ask the regulator to review the Astrazeneca and Oxford vaccine .

An emergency US approval could come as soon as 8-10 December, with shipments across the country starting within 24 hours of the announcement, according to US media reports.

Saturday, November 28, 2020

AstraZeneca , Moderna and Pfizer Covid Vaccines


 AstraZeneca , Moderna and Pfizer all three giants have said they will seek regulatory clearance in order to offer their vaccines to million of people of all over the world . The drugmakers have moved at record speed, and the first shots of the Pfizer and Moderna vaccines could be given in the coming weeks. The path for the AstraZeneca vaccine is less clear .

The FDA has emergency authority to issue temporary approvals of medical products to get them to the public more quickly during public health emergencies. Such authorizations require less data and can be done more rapidly than full approvals. Since February, the FDA has used this power to authorize hundreds of Coronavirus  tests and a few treatments. But it has authorized a vaccine that way only once in its history — in 2005, against anthrax — and that was under sharply different circumstances.

Some experts have expressed qualm about using that process for a coronavirus vaccine that would be given to hundreds of millions of people, but those criticisms have become stopped as the pandemic has raged, killing thousands of Americans a week. 

The vaccines could begin to be distributed as soon as mid-December to those in high-risk groups — an estimated 200 million people — who will receive priority, according to a framework devised by an advisory committee to the Centers for Disease Control and Prevention. Government officials said that if both the Pfizer and Moderna vaccines are authorized, they anticipate having enough doses for 20 million people by year’s end.

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