Becker Muscular Dystrophy; Congential Muscular Dystrophy (including Ullrich, Bethlem and Fukuyama, Muscle-Eye-Brain and Walker Warberg Syndrome); Distal Muscular Dystrophy; Duchenne Muscular Dystrophy; Emery-Dreifuss Muscular Dystrophy; Facioscapulohumeral Muscular Dystrophy; Limb-Girdle Muscular Dystrophy; Manifesting carrier of Becker or Duchenne Muscular Dystrophy; Myotonic Dystrophy Types 1 and 2; Occulopharyngeal Muscular Dystrophy; • Spinal Muscular Atrophy (SMA) - all types including: Type 1 Infantile Progressive SMA/Werdnig Hoffmann Disease; Type 2 Intermediate SMA; Type 3 Juvenile SMA/Kugelberg-Welander syndrome; Type 4 Adult SMA; Spinal Bulbar Muscular Atrophy (SBMA) / Kennedy's Disease and X-linked SBMA ; Spinal Muscular Atrophy with Respiratory Distress (SMARD1) / Distal SMA Type 1 (DSMA1) / Distal Hereditary Motor Neuropathy. Charcot-Marie-Tooth Disease (CMT)
(Hereditary Motor and Sensory Neuropathy); Dejerine-Sottas Disease (CMT Type 3); Hereditary Sensory Neuropathy; Dermatomyositis; Juvenile Dermatomyositis; Polymyositis; Inclusion Body Myositis; Myasthenia Gravis; Lambert-Eaton Syndrome; Congential Myasthenic Syndrome; CANVAS; Friedreich Ataxia (FA); Spinocerebellar Ataxia (SCA) - all types; Andersen-Tawil Syndrome; Central Core Disease; GNE Myopathy/Hereditary Inclusion Boby Myopathy/Distal Myopathy; Hyperthyroid Myopathy; Hypothyriod Myopathy; Myofibrillar Myopathy; Myotonia Congenita (Thomsen's and Becker's Disease); Myotubular Myopathy; Nemaline Myopathy; Paramyotonia Congenita; Periodic Paralysis Types 1 and 2; PROMM (Proximal Myotonic Myopathy)/ Myotonic Dystrophy Type 2; McArdle's Disease (Phosphorylase Deficiency); Pompe Disease (Acid Maltase Deficiency); Tarui's Disease (Phosphofructokinase Deficiency); Cori or Forbe's Disease (Debrancher Enzyme Deficiency); Mitochondrial Myopathy (including MELAS, MERRF, NARP and MIDD); Carnitine Deficiency; Caritine Palmityl Transferase Deficiency; Phosphoglycerate Kinase Deficiency; Phosphoglycerate Mutase Deficiency; Lactate Dehydrongenase Deficiency; Myoadenylate Deaminase Deficiency; Central Cavernous Hemangioma; Neurofibromatosis Type 1 and 2; Schwannomatosis; Tuberous Sclerosis; Von Hippel Lindau Syndrome; Adrenoleucodystrophy; Adrenomyeloneuropathy; Metachromatic Leucodystrophy

Website: www.mda.org.nz

Facebook: www.facebook.com/MDANationalOffice/