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• Region: East Midlands East of England London North East North West Northern Ireland Scotland South East South West Wales West Midlands Yorkshire and the Humber
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• Are you?: Employed Employed (part time) Self-employed Student Unemployed
• Date of birth: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 January February March April May June July August September October November December 1900 1901 1902 1903 1904 1905 1906 1907 1908 1909 1910 1911 1912 1913 1914 1915 1916 1917 1918 1919 1920 1921 1922 1923 1924 1925 1926 1927 1928 1929 1930 1931 1932 1933 1934 1935 1936 1937 1938 1939 1940 1941 1942 1943 1944 1945 1946 1947 1948 1949 1950 1951 1952 1953 1954 1955 1956 1957 1958 1959 1960 1961 1962 1963 1964 1965 1966 1967 1968 1969 1970 1971 1972 1973 1974 1975 1976 1977 1978 1979 1980 1981 1982 1983 1984 1985 1986 1987 1988 1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010
• Ethnicity: African Asian other Bangladeshi Black African Black Caribbean Chinese Indian Other Pakistani Roma White European White other
• Highest level of education: GCSE College/Further Education HND Degree Masters PHD/Doctorate
• Neuromuscular condition (if any): Anderson deficiency Becker muscular dystrophy Bethlem myopathy Carnitine deficiency Carnitine palmityl transferase deficiency Central core disease Centronuclear myopathy Charcot-Marie-Tooth/HMSN/PMA Congenital muscular dystrophy (merosin negative) Congenital muscular dystrophy (merosin positive) Congenital fibre-type disproportion myopathy Congenital muscular dystrophy Congenital myasthenic syndromes Congential myopathy Congenital myotonic dystrophy Debrancher enzyme deficiency (Cori or Forbes Disease) Dermatomyositis Duchenne muscular dystrophy Emery-Dreifuss syndrome/muscular dystrophy Facioscapulohumeral muscular dystrophy Familial periodic paralysis Glycogen Storage Diseases of muscle Inclusion body myositis Juvenile dermatomyositis Limb girdle muscular dystrophy Manifesting carrier of Duchenne McArdle disease (myophosphorylase deficiency) Minicore (multicore) myopathy Mitochondrial myopathies Multi-minicore disease Myasthenia Gravis Myoadenylate deaminase deficiency Myofibrillar myopathies Myositis Ossificans Progressiva (MOP) Myotonia congenita Myotonic dystrophy type 1 & 2 Myotubular myopathy Nemaline myopathy Neuromyotonia Ocularpharyngeal muscular dystrophy (OPMD) Paramyotonia congenita Periodic paralysis (muscle channelopathies) Peroneal muscular atrophy Phosphofructokinase deficiency (Glycogen storage disease type 7/Tarui’s disease) Polymyositis Acute post infective polyneuropathy (Guillain Barre syndrome) Pompe's disease Pseudomyotonia Scapuloperoneal myopathy Schwartz-Jampel syndrome Spinal muscular atrophy, adult Spinal muscular atrophy, dominant variants Spinal muscular atrophy, Intermediate Spinal muscular atrophy, mild (Kugelberg Welander disease) Spinal muscular atrophy, severe (Werdnig Hoffman disease) Spinal muscular atrophy Spinal muscular atrophy, X-linked bulbospinal neuropathy (Kennedy’s syndrome) Non-specific myopathy Ullrich congenital (UMCD) Unspecified condition

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