UK Government issues new plan to tackle ‘rare diseases in England’

UK Government issues new plan to tackle 'rare diseases' in England

UK Government issues new plan to tackle 'rare diseases' in England. Image: DC Studio/

THE UK government published a new Rare Diseases Action Plan for England on Tuesday, February 28, which builds on the ‘first-ever plan’ published in 2022.

The new Rare Diseases Action Plan for England “will ensure those living with these conditions receive better care and treatment, fairer access to testing and have continued support,” the UK government announced.

As noted, the first plan published in 2022 “developed digital tools to put information on rare diseases at the fingertips of healthcare staff and helped 1,000 new complex diagnoses for people with rare diseases to be made thanks to advances in genomic research, helping to inform appropriate clinical care for patients.”

Within the new plan, 13 actions are listed that “have been developed with the rare diseases community focussing on faster diagnosis, increased awareness of rare diseases among healthcare staff, better coordination of care and improved access to specialist care, treatments, and drugs,” according to the statement.

It added: “Although rare diseases are individually rare, they are collectively common, with 1 in 17 people affected by a rare disease at some point in their lives, such as spinal muscular atrophy, haemophilia A, epidermolysis bullosa or Huntington’s disease.

“This new plan will increase data sharing so we can, for the first time, get a full picture of how people are tested for genetic diseases across England and help get patients a diagnosis faster.

“With more than 7,000 rare diseases affecting an estimated 3.5 million people in the UK, it is vital that healthcare professionals have the right training to care appropriately for their needs.

“The new plan will collect evidence on health inequalities faced by people living with rare diseases so they can be addressed by health services, for instance for people not living in areas where specialist centres exist.”

Following the announcement of the new Rare Diseases Action Plan for England, UK Health Minister Helen Whately said: “Rare diseases are individually rare but collectively common, affecting 3.5 million people in the UK.

“We’ve made huge progress in the last year, making 1,000 complex new diagnoses thanks to advances in genomic research.

“But there is still more to do. Our Rare Diseases Action Plan will reduce health inequalities, help people participate in research and join up specialist services better for patients.”

While Lucy Chappell, Chief Scientific Adviser Professor, said: “The impacts of rare diseases on individuals and their families are wide-ranging. Our research plays an important underpinning role in furthering the understanding, diagnosis, treatment and care for people living with rare diseases.

“The Action Plan highlights significant advances in rare disease research supported through our funding. There is always more to do and our commitments will be supported by the recently announced funding for ground-breaking research into the NIHR Biomedical Research Centres and the Medical Research Council (MRC)-NIHR UK Rare Disease Research Platform.”

She added: “This research will continue to drive progress and foster collaboration to translate scientific breakthroughs into clinical advances.”

Professor Sir Stephen Powis, NHS England medical director, said: “We’ve made great progress in securing new medicines for people with a range of rare conditions, including life-saving gene therapy, advancements in genomic testing and sequencing, made possible through the NHS Genomic Medicine Service, where we are a truly world-leading health system.

“As well as being an adopter of innovation today, the NHS is developing a strategic approach to prepare for the breakthroughs of tomorrow and enable rapid patient access to future tests and treatments for rare conditions.”

Dr Ellen Thomas, Deputy Chief Medical Officer at Genomics England, said: “A decade on from the launch of the ground-breaking 100,000 Genomes Project, it’s vital that we continue to harness the potential of genomics to deliver benefits in diagnosis, treatment, and care for those living with rare conditions.

“Connecting research and clinical care and doing both at a national scale is crucial to this and great strength of the approach we are taking as a country.

“In 2022, thanks to this link and work carried out in the National Genomic Research Library, we returned over 1,000 new, complex diagnoses for people with rare conditions to the NHS to help inform the most appropriate clinical care.

“We must continue to build on this progress, working alongside national delivery partners across the health system and in close consultation with the rare disease community, to deliver on our shared vision to improve the lives of people living with rare conditions across the UK.”

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Written by

Matthew Roscoe

Originally from the UK, Matthew is based on the Costa Blanca and is a web reporter for The Euro Weekly News covering international and Spanish national news. Got a news story you want to share? Then get in touch at