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No Deal Brexit could endanger lives of four million Brits with rare diseases


No Deal Brexit could endanger lives of four million Brits with rare diseases
Updated: 12 Dec 2020, 3:35
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A NO-DEAL Brexit would have a detrimental impact on the care received by the four million Brits who suffer from a rare disease, a group of leading clinicians have said.
The warning comes after Prime Minister Boris Johnson said on Friday it was very, very likely the UK would be leaving the UK without a deal in place.
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The treatment received by four million Brits with a rare disease would suffer in the event of a no-deal Brexit, a group of clinicians have saidCredit: Getty Images - Getty ....

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No deal Brexit could endanger the lives of four MILLION Britons


No deal Brexit could endanger the lives of four MILLION Britons
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If the UK slams out of Europe without a deal it could leave the four million Britons with rare diseases with subpar medical treatment, experts have warned. 
A total of 53 leading clinicians and 20 patient support groups have signed a letter warning of the impact No Deal will have. 
They say that without a deal the UK will lose access to the 24 European Reference Networks (ERNs) built to inform and aid research into rare diseases. 
A rare disease that qualifies for these networks is anything that affects fewer than one in 2,000 people. ....

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No deal Brexit could have detrimental impact for people in UK living with a rare disease


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Experts have warned that a no deal Brexit will result in the exclusion of the UK from the 24 European Reference Networks (ERNs) that were established to improve the care of patients bearing the lifelong burden of a rare disease, which require highly specialised diagnosis and treatment.
One in 17 UK citizens lives with a rare disease, which are defined as conditions that affect fewer than one in 2,000 people in the general population. A group of experts has written to
The Lancet highlighting their concerns about the detrimental impact a no deal Brexit will have on these individuals.
Rare diseases are rare, and experts are rarer still, said Dr Marc Tischkowitz from the University of Cambridge, who helped coordinate the letter. European Reference Networks were set up because no single country has the expertise or resources to cover all of the known rare diseases, which number in the thousands. They ve played a pivotal role in harnessing the collective k ....

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