Advanced filters Filter results Content type - Any -BlogNewsPress releasePublicationYour story Topic - Any -AdvocacyCampaignsCare & SupportCovid-19FundraisingInformation for professionalsMuscular Dystrophy UKPowerchair FootballResearchVolunteeringYour stories Conditions - Any -All conditionsBecker muscular dystrophyBethlem myopathyCentral core diseaseCharcot-Marie-Tooth disease Congenital fibre type disproportionCongenital muscular dystrophy (CMD)Congenital muscular dystrophyCongenital myasthenic syndromeCongenital myopathyCongenital myotonic dystrophyDisorders of the neuromuscular junctionDuchenne muscular dystrophyEmery-Dreifuss muscular dystrophyFacioscapulohumeral muscular dystrophyFacioscapulohumeral muscular dystrophy (FSH)Fibrodysplasia ossificans progressivaGNE myopathyInclusion body myositisInflammatory and autoimmune neuropathiesJuvenile dermatomyositisLimb girdle muscular dystrophyLimb girdle muscular dystrophy 1B (LGMD1B)Limb girdle muscular dystrophy 1C (LGMD1C)Limb girdle muscular dystrophy 2A (LGMD2A)Limb girdle muscular dystrophy 2B (LGMD2B)Limb girdle muscular dystrophy 2I (LGMD2I)Limb girdle muscular dystrophy 2L (LGMD2L)LMNA-CMDManifesting carriers of Duchenne and Becker muscular dystrophyMcArdle diseaseMerosin-deficient congenital muscular dystrophyMinicore (multicore) myopathyMitochondrial myopathyMiyoshi myopathyMulti-minicore myopathhyMyasthenia gravisMyofibrillar myopathiesMyotoniasMyotonic dystrophyMyotonic dystrophy type 2Myotubular and other centronuclear myopathiesNemaline myopathyNondystrophic myotonic disordersOculopharyngeal muscular dystrophyPeriodic paralysis (muscle channelopathy)Periodic paralysesPolymyositis and dermatomyositisRigid spine syndrome – SEPN1 related myopathySarcoglycanopathies: LGMD2C, LGMD2D, LGMD2E and LGMD2FSpinal muscular atrophyUllrich congenital muscular dystrophy News British Science Week 2020While muscle-wasting conditions affect around 70,000 people in the UK, the conditions MDUK supports…Read more