For in-depth information on a range of neuromuscular disorders, please visit The Loop. You can even tailor and save a condition guide specific to you that you can share with others.
Becker Muscular Dystrophy (BMD)
Congential Myopathies
- Central Core Disease
- Nemaline Myopathy (Rod Body Disease)
- Myotubular Myopathy (Centronuclear Myopathy)
Charcot-Marie-Tooth Disease (CMT)
- Also known as Hereditary & Motor Sensory Neuropathy (HMSN)
- And also as Peroneal Muscular Atrophy
Distal Muscular Dystrophy
Duchenne Muscular Dystrophy (DMD)
Emery-Dreifuss Muscular Dystrophy
Facioscapulohumeral Muscular Dystrophy (FSHD)
Friedreich’s Ataxia (FA)
Idiopathic Inflammatory Myopathies
- Dermatomyositis (DM)
- Polymyositis (PM)
Inclusion Body Myositis (IBM)
Limb Girdle Muscular Dystrophy
Motor Neurone Disease
- Amyotrophic Lateral Sclerosis (ALS)
- Progressive Muscular Atrophy
- Progressive Bulbar Palsy
Myasthenia Gravis
- Myasthenia Gravis (MG)
- Lambert-Eaton Myasthenic Syndrome (LES)
- Congenital Myasthenic Syndrome (CMS)
Myopathies (other)
- Myotonia Congenita (Thomsen’s disease and Becker type)
- Paramyotonia Congenita (Eulenberg’s disease)
- Periodic Paralysis
Myotonic Dystrophy (DM)
Spinal Muscular Atrophy (SMA)
- SMN-Related SMA
- Non-SMN SMA
- Spinal-Bulbar Muscular Atrophy
Muscular Dystrophy Foundation Australia
c/- Muscular Dystrophy NSW
80 Betty Cuthbert Drive, Lidcombe NSW 2141
chairperson@mdaustralia.org.au
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Muscular Dystrophy Foundation Australia acknowledges the Traditional Owners of Country throughout Australia and recognises their continuing connection to land, waters and culture. We pay our respects to their Elders past, present and emerging.
