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Ex-Johnson aide makes scathing attack on U K government Covid response

Ex-Johnson aide makes scathing attack on U.K. government Covid response Adela Suliman © Provided by NBC News LONDON A former chief adviser to British Prime Minister Boris Johnson lambasted the government s handling of the Covid-19 pandemic on Wednesday, arguing the response was inadequate. Dominic Cummings, caricatured by British tabloids as a Svengali-like advisor to Johnson, was the leading strategist behind the 2016 Brexit campaign and Johnson s landslide election win in 2019. He was quizzed on on Wednesday by British lawmakers on the lessons learned from the pandemic. In a blistering attack on the government he once served, Cummings s said the United Kingdom s government had failed the British public and fell disastrously short in its handling of Covid-19.

Community Scoop » Health Access Must Be Based On Need Not Diagnosis As Disease Does Not Discriminate

Press Release – Rare Disorders NZ Rare Disorders NZ (RDNZ) supports Patient Voice Aotearoas nationwide Lie Down for Life to call for better access to modern medicines for genetic, undiagnosed and rare disorders. Anyone, anytime, could find themselves or a loved one having … Rare Disorders NZ (RDNZ) supports Patient Voice Aotearoa’s nationwide ‘Lie Down for Life’ to call for better access to modern medicines for genetic, undiagnosed and rare disorders. “Anyone, anytime, could find themselves or a loved one having to cope with the symptoms of a genetic rare disorder,” says RDNZ Chief Executive Lisa Foster. “It makes no sense to provide access to medicine based on greatest numbers. All children and adults deserve access to assessed medications that can improve their lives.”

Health Access Must Be Based On Need Not Diagnosis As Disease Does Not Discriminate

Thursday, 6 May 2021, 1:25 pm Rare Disorders NZ (RDNZ) supports Patient Voice Aotearoa’s nationwide ‘Lie Down for Life’ to call for better access to modern medicines for genetic, undiagnosed and rare disorders. “Anyone, anytime, could find themselves or a loved one having to cope with the symptoms of a genetic rare disorder,” says RDNZ Chief Executive Lisa Foster. “It makes no sense to provide access to medicine based on greatest numbers. All children and adults deserve access to assessed medications that can improve their lives.” “That’s why our genetic, undiagnosed and rare disorder collective will stand alongside the families dealing with disease types such as

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