News
Survey shows more support needed for Muscular Dystrophy
The Muscular Dystrophy Campaign highlight poor access to services in their document “State of the Nation: The 2008 National Survey.” Launched prior to Muscle Awareness Week (20 – 27 September 2008), the survey reveals a postcode lottery of care with many being denied essential health and social care services. The survey canvassed details from 4000 people throughout the UK living with muscle disease. The main findings were that half had to pay for their own wheelchairs. Three quarters of carers had no access to respite and that half of all patients did not have contact with any relevant specialists. A similar number being unemployed. The full document is available at www.muscular-dystrophy.org. Muscular Dystrophy Campaign must be congratulated on such a comprehensive and thought provoking study that should be the catalyst for much needed improvement of services.Philip Butcher, Chief Executive of the Muscular Dystrophy Campaign, commented that:“Our survey reveals that there are significant inequalities in access to vital specialist care across the UK. For some families, access to specialist care can be a matter of life or death. Their plight is made worse by the considerable delays and variations in the provision of essential equipment and the barriers that exist to living independently”. Attending the Liberal Democrat conference, Shadow Secretary of State for Health Norman Lamb MP, is quoted on the website as commenting that: “Despite the Government’s numerous published commitments to ensuring patients with chronic conditions can access the right care and support, it is clear from today’s report that this simply isn’t happening for thousands of families across the UK.”