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Muscle disease patients 'failed' | Muscle disease patients 'failed' |
(20 minutes later) | |
Up to 3,000 patients with muscle degenerating diseases are being failed by the Welsh NHS, a report says. | Up to 3,000 patients with muscle degenerating diseases are being failed by the Welsh NHS, a report says. |
The Muscular Dystrophy Campaign claims a lack of specialist services means life expectancy for sufferers is lower than Scotland and England. | The Muscular Dystrophy Campaign claims a lack of specialist services means life expectancy for sufferers is lower than Scotland and England. |
Sufferers have to travel to England for certain services or receive general, non-specific physiotherapy. | Sufferers have to travel to England for certain services or receive general, non-specific physiotherapy. |
The Welsh Assembly Government says it will consider the findings as part of an ongoing review of neurosurgery. | The Welsh Assembly Government says it will consider the findings as part of an ongoing review of neurosurgery. |
Diseases such as muscular dystrophy can lead to rapid weakening of a patient's body. | Diseases such as muscular dystrophy can lead to rapid weakening of a patient's body. |
Care needs to be regular and specific to their needs, but Wales lacks a specialist centre, forcing patients to either go for treatment in England or accept physiotherapy which may not be the most appropriate. | Care needs to be regular and specific to their needs, but Wales lacks a specialist centre, forcing patients to either go for treatment in England or accept physiotherapy which may not be the most appropriate. |
CAMPAIGN REPORT Services are "variable" across Wales, with almost three out of four local health boards failing to support a muscle clinic for adults or childrenPatients in Wales are currently being forced to travel to London and Winsford, Cheshire to receive essential treatmentThe services which exist are "vulnerable" due to a dependence on a handful of leading clinicians, who could move on or retireVentilation prolongs life but is "not provided in a systematic way" across WalesFunding constraints stop one health board commissioning services from a specialist centre in OswestryFunding for diagnostic tests for Welsh patients at recognized specialist centres in England is not consistentSource: Building on the Foundations: The Need for a Specialist Neuromuscular Service Across Wales | CAMPAIGN REPORT Services are "variable" across Wales, with almost three out of four local health boards failing to support a muscle clinic for adults or childrenPatients in Wales are currently being forced to travel to London and Winsford, Cheshire to receive essential treatmentThe services which exist are "vulnerable" due to a dependence on a handful of leading clinicians, who could move on or retireVentilation prolongs life but is "not provided in a systematic way" across WalesFunding constraints stop one health board commissioning services from a specialist centre in OswestryFunding for diagnostic tests for Welsh patients at recognized specialist centres in England is not consistentSource: Building on the Foundations: The Need for a Specialist Neuromuscular Service Across Wales |
The report highlights difficulties involving access to specialist services and the distances patients have to travel for treatment. | |
Seven-year-old Rhys Jenkins and his family travel from the Vale of Glamorgan to Hammersmith in London twice a year so he can receive specialist treatment for Duchene muscular dystrophy. | |
As the journey takes three hours each way, the family has to spend the night in London, taking time off from school and work. | |
His mother, Helen Jenkins, said the specialist clinic at hospital offers a range of professionals, including physiotherapists as well as specialists in respiratory and cardiac medicine. | |
She said: "We would simply be seeing a neuromuscular consultant in Cardiff. | |
"She works alone, she is not able to benefit from the team of professionals and the input that the neuromuscular consultants benefit from at the Hammersmith. | |
"We would be missing out on people like the family officer as well." | |
Steve Higginson, from Colwyn Bay, has spent 10 years making the two-hour round trip to Cheshire for treatment for Becker muscular dystrophy. | Steve Higginson, from Colwyn Bay, has spent 10 years making the two-hour round trip to Cheshire for treatment for Becker muscular dystrophy. |
"I found many parts Wales to be a desert for the treatment of patients with conditions like mine," he said. | "I found many parts Wales to be a desert for the treatment of patients with conditions like mine," he said. |
'Huge advances' | |
The report by a lobbying group of doctors and patients says investment is needed to catch up with the rest of the UK, as the life expectancy of Welsh patients is falling behind. | The report by a lobbying group of doctors and patients says investment is needed to catch up with the rest of the UK, as the life expectancy of Welsh patients is falling behind. |
Dr Louise Hartley, a consultant paediatric neurologist, said: "We know that in the past two decades there have been huge advances in the improvement of care for these patients, improving both survival dramatically and quality of life." | Dr Louise Hartley, a consultant paediatric neurologist, said: "We know that in the past two decades there have been huge advances in the improvement of care for these patients, improving both survival dramatically and quality of life." |
At the best centres in the UK, in Scotland and England, survival had been increased from late teens well into adulthood, accompanied by a dramatically improved quality of life, she said. | At the best centres in the UK, in Scotland and England, survival had been increased from late teens well into adulthood, accompanied by a dramatically improved quality of life, she said. |
But, she added: "Children in Wales and adults in Wales are not experiencing that improval by any means." | But, she added: "Children in Wales and adults in Wales are not experiencing that improval by any means." |
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