Indian-origin White House official Raj Shah quits Trump administration

Agencies
January 16, 2019

Washington, Jan 16: Raj Shah, an Indian-origin top spokesman in the White House press office, has left US President Donald Trump’s administration to join an arm of a lobbying firm, becoming the latest of several senior officials to quit in recent months.

Shah, 34, White House deputy spokesman and a former researcher at the Republican National Committee, was in the administration since president Trump took office in January 2017.

His portfolio recently included helping prepare Justice Brett M Kavanaugh for his Senate confirmation hearings to the Supreme Court.

Shah will lead the Media Group, the press wing of Ballard Partners, a lobbying firm with offices in Florida and Washington, The New York Times reported.

He will work with Jamie Rubin, a Democrat who was a spokesman for Madeleine Albright, the former secretary of state, the report said, quoting the officials.

His departure comes as the White House press and communications teams have been depleted. Several aides have moved on to roles at government agencies or have left the Trump administration entirely.

Shah was born in 1984 to Indian parents of Gujarati origin. His parents moved to Chicago in 1970s and then moved to Connecticut where he was born and raised.

Shah joined the White House right from the day the Trump administration took charge. He was made the Deputy Communications Director at the White House. Previously, he was director of Opposition Research in the Republican National Committee.

Shah is the latest in a number of top officials to leave the Trump administration.

Former Defence Secretary James Mattis left Trump’s Cabinet last month, after former Attorney General Jeff Sessions was pushed out in November. Former Secretary of State Rex Tillerson was unceremoniously fired in March and national security adviser H R McMaster was replaced last year.

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News Network
March 13,2020

Mar 13: Canadian Prime Minister Justin Trudeau and his wife announced they were self-isolating Thursday as she undergoes tests for the new coronavirus after returning from a speaking engagement with "mild flu-like symptoms."

Sophie Gregoire-Trudeau's symptoms have subsided since she recently got back from Britain, but as a precaution the prime minister "will spend the day in briefings, phone calls and virtual meetings from home," according to a statement.

Trudeau also cancelled a meeting Thursday and Friday with Canada's provincial and territorial leaders in Ottawa, but still planned to speak with them and world leaders by phone about measures being taken to curb the spread of the virus in Canada.

Gregoire-Trudeau's symptoms had included "a low fever late last night." She immediately sought medical advice and testing.

Trudeau has exhibited no symptoms, and was advised by doctors "to continue daily activities while self-monitoring."

"However, out of an abundance of caution, the prime minister is opting to self-isolate and work from home until receiving Sophie's results," said his office.

Since the novel coronavirus first emerged in late December 2019, 127,070 cases have been recorded in 115 countries and territories, killing 4,687 people, according to an AFP tally compiled at 1200 GMT on Thursday based on official sources.

Canada has so far reported more than 100 cases in six provinces, and one death.

Also Thursday, the Canada's Juno music awards cancelled its upcoming gala show, planned for Sunday evening in Saskatoon, Saskatchewan.

"We are devastated to cancel this national celebration of music, but at this time of global uncertainty, the health, safety and well-being of all Canadians must stand at the forefront of any decisions that impact our communities," organisers said in a statement.

And in Quebec province, Premier Francois Legault unveiled a series of measures to prevent the spread of the coronavirus, including placing all travellers returning from overseas under quarantine for two weeks.

Quebec also banned indoor gatherings of more than 250 people.

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News Network
July 20,2020

Paris, Jul 20: Two coronavirus vaccine candidates have proven safe for humans and produced strong immune reactions among patients involved in separate clinical trials, doctors said on Monday.

The first trial among more than 1,000 adults in Britain found that the vaccine induced "strong antibody and T cell immune responses" against the novel coronavirus.

A separate trial in China involving more than 500 people showed most had developed widespread antibody immune response.

The studies, published in The Lancet medical journal, constitute a major step on the road towards a COVID-19 vaccine that is effective and safe for widespread use.

The authors of the studies said that they encountered few adverse side-effects from the vaccine candidates.

However, they cautioned that more research was needed, particularly among older adults, who are disproportionately at risk of dying of COVID-19.

Co-author Sarah Gilbert from the University of Oxford said the results "hold promise".

"If our vaccine is effective, it is a promising option as these types of vaccine can be manufactured at large scale."

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News Network
March 28,2020

Washington, Mar 28: A US-based lab has unveiled a portable test that can tell if someone has COVID-19 in as little as five minutes, it said in a statement Friday.

Abbot Laboratories said the US Food and Drug Administration (FDA) had given it emergency authorization to begin making the test available to healthcare providers as early as next week.

The test, which is the size of a small toaster and uses molecular technology, also shows negative results within 13 minutes, the company said in a press statement.

"The COVID-19 pandemic will be fought on multiple fronts, and a portable molecular test that offers results in minutes adds to the broad range of diagnostic solutions needed to combat this virus," said Abbot president and chief operating officer Robert Ford.

The test's small size means it can be deployed outside the "traditional four walls of a hospital in outbreak hotspots," Ford said, and Abbott is working with the FDA to send it to virus epicenters.

The test has not been cleared or approved by the FDA, and has only been authorized for emergency use by approved labs and healthcare providers, the company said.

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