Supporting individuals living with neuromuscular diseases
We support individuals living with the following diagnoses.
- Becker muscular dystrophy (BMD)
- Bethlem CMD
- Fukuyama CMD
- Muscle-eye-brain diseases (MEBs)
- Rigid spine syndromes
- Ullrich CMD
- Walker-Warburg syndromes (WWS)
- Duchenne muscular dystrophy (DMD)
- Emery-Dreifuss muscular dystrophy (EDMD)
- Facioscapulohumeral muscular dystrophy (FSHD)
- Limb-girdle muscular dystrophies (LGMD)
- Myotonic dystrophy (DM)
- Oculopharyngeal muscular dystrophy (OPMD)
- ALS (amyotrophic lateral sclerosis)
- Spinal-bulbar muscular atrophy (SBMA)
- Spinal muscular atrophy (SMA)
- Andersen-Tawil syndrome
- Hyperkalemic periodic paralysis
- Hypokalemic periodic paralysis
- Becker congenita
- Thomsen congenita
- Paramyotonia congenita
- Potassium-aggravated myotonia
- Friedreich’s ataxia (FA)
- Kearns-Sayre syndrome (KSS)
- Leigh syndrome (subacute necrotizing encephalomyopathy)
- Mitochondrial DNA depletion syndromes
- Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
- Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
- Myoclonus epilepsy with ragged red fibers (MERRF)
- Neuropathy, ataxia and retinitis pigmentosa (NARP)
- Pearson syndrome
- Progressive external opthalmoplegia (PEO)
- Cap myopathies
- Centronuclear myopathies
- Congenital myopathies with fiber type disproportion
- Central core disease
- Multiminicore myopathies
- Myosin storage myopathies
- Myotubular myopathy
- Nemaline myopathies
- GNE myopathy/Nonaka myopathy/hereditary inclusion-body myopathy (HIBM)
- Laing distal myopathy
- Markesbery-Griggs late-onset distal myopathy
- Miyoshi myopathy
- Udd myopathy/tibial muscular dystrophy
- VCP Myopathy / IBMPFD
- Vocal cord and pharyngeal distal myopathy
- Welander distal myopathy
- Hyperthyroid myopathy
- Hypothyroid myopathy
- Dermatomyositis
- Inclusion-body myositis
- Polymyositis
- Acid maltase deficiency (AMD, Pompe disease)
- Carnitine deficiency
- Carnitine palmitoyltransferase dificiency
- Debrancher enzyme deficiency (Cori disease, Forbes disease)
- Lactate dehydrogenase deficiency
- Myoadenylate deaminase deficiency
- Phosphofructokinase deficiency (Tarui disease)
- Phosphoglycerate kinase deficiency
- Phosphoglycerate mutase deficiency
- Phosphorylase deficiency (McArdle disease)
- Myofibrillar myopathies (MFM)
- Scapuloperoneal myopathy
- Congenital myasthenic syndromes (CMS)
- Lambert-Eaton myasthenic syndrome (LEMS)
- Myasthenia gravis (MG)
- Charcot-Marie-Tooth disease (CMT)
- Giant axonal neuropathy (GAN)
