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La plupart des gens ne se souviennent pas de leur naissance. Moi, si. Parce que je suis née deux fois. À huit mois les médecins ont annoncé à mes parents que j'étais atteinte d'une maladie génétique, une maladie évolutive. Je souffrais d'amyotrophie spinale, ma mort était programmée, je ne dépasserais pas l'âge de trois ans… Et j'ai fêté mes cinq ans. Puis sept. Puis dix. Je n'étais pas décidée à mourir. II faut dire que, les chemins tout tracés, ça n'a jamais été mon truc. Le parcours a été difficile, il a été long, il y a eu des obstacles, il y a eu de la souffrance… Mais surtout il y a eu de la joie, il y a eu de l'amour et des rires. Aujourd'hui j'ai vingt-neuf ans, et de toutes ces années à ne pas pouvoir regarder vers demain, j'ai gardé l'urgence de vivre ici et maintenant et d'aller au bout de mes projets. Et des bâtons qu'on m'a mis dans les roues, des clichés qu'on m'a opposés quand j'ai eu le front de refuser de rentrer dans la case que la société avait prévue pour moi, j'ai gardé la rage de montrer qui je suis : je m'appelle Lucie Carrasco, je suis créatrice de mode, je suis folle amoureuse de l'homme avec lequel je vis, j'ai une famille et des amis fantastiques, et je suis passionnée par la vie.
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NEUROMUSCULAR JUNCTION --- MUSCLE, SKELETAL --- ELECTRIC STIMULATION --- AMYOTROPHIC LATERAL SCLEROSIS --- POSTPOLIOMYELITIS SYNDROME --- MUSCULAR ATROPHY, SPINAL --- NEUROMUSCULAR JUNCTION --- MUSCLE, SKELETAL --- ELECTRIC STIMULATION --- AMYOTROPHIC LATERAL SCLEROSIS --- POSTPOLIOMYELITIS SYNDROME --- MUSCULAR ATROPHY, SPINAL
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Kinesitherapie --- Kinesitherapy --- Kinésithérapie --- Mechanotherapy --- Movement cure --- Mécanothérapie --- Spinal Muscular Atrophies of Childhood --- Muscular Atrophy, Spina --- Muscular Dystrophy, Duchenne --- Muscular Atrophy, Spinal --- Duchenne muscular dystrophy --- Spina bifida --- Spinal muscular atrophy --- Duchenne, Myopathie de --- Spina-bifida --- Atrophie musculaire progressive --- Spinal Muscular Atrophies of Childhood. --- Muscular Dystrophy, Duchenne. --- Muscular Atrophy, Spinal. --- Paralysis --- Treatment
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Movement Disorders. --- Muscular Atrophy, Spinal. --- Neuromuscular Diseases. --- Motor neurons --- -Movement disorders --- Dyskinesia --- Dyskinesias --- Motor disorders --- Disabilities --- Nervous system --- Anterior horn cells --- Brain motor cells --- Motoneurons --- Brain --- Neurons --- Spinal cord --- Cramp-Fasciculation Syndrome --- Fasciculation-Cramp Syndrome, Benign --- Foley-Denny-Brown Syndrome --- Oppenheim's Disease --- Amyotonia Congenita --- Oppenheim Disease --- Benign Fasciculation-Cramp Syndrome --- Benign Fasciculation-Cramp Syndromes --- Cramp Fasciculation Syndrome --- Cramp-Fasciculation Syndromes --- Fasciculation Cramp Syndrome, Benign --- Fasciculation-Cramp Syndromes, Benign --- Foley Denny Brown Syndrome --- Neuromuscular Disease --- Oppenheims Disease --- Syndrome, Cramp-Fasciculation --- Syndrome, Foley-Denny-Brown --- Syndromes, Cramp-Fasciculation --- Adult Spinal Muscular Atrophy --- Adult-Onset Spinal Muscular Atrophy --- Amyotrophy, Neurogenic Scapuloperoneal, New England Type --- Distal Spinal Muscular Atrophy --- Hereditary Motor Neuronopathy --- Muscular Atrophy, Adult Spinal --- Myelopathic Muscular Atrophy --- Myelopathic Muscular Atrophy, Progressive --- Progressive Myelopathic Muscular Atrophy --- Progressive Proximal Myelopathic Muscular Atrophy --- Proximal Myelopathic Muscular Atrophy, Progressive --- Scapuloperoneal Spinal Muscular Atrophy --- Spinal Amyotrophy --- Spinal Muscular Atrophy, Distal --- Spinal Muscular Atrophy, Oculopharyngeal --- Spinal Muscular Atrophy, Scapuloperoneal --- Spinal Muscular Atrophy, Scapuloperoneal Form --- Bulbospinal Neuronopathy --- Oculopharyngeal Spinal Muscular Atrophy --- Progressive Muscular Atrophy --- Scapuloperoneal Form of Spinal Muscular Atrophy --- Spinal Muscular Atrophy --- Adult Onset Spinal Muscular Atrophy --- Amyotrophies, Spinal --- Amyotrophy, Spinal --- Atrophies, Progressive Muscular --- Atrophy, Myelopathic Muscular --- Atrophy, Progressive Muscular --- Atrophy, Spinal Muscular --- Bulbospinal Neuronopathies --- Hereditary Motor Neuronopathies --- Motor Neuronopathies, Hereditary --- Motor Neuronopathy, Hereditary --- Muscular Atrophies, Progressive --- Muscular Atrophy, Myelopathic --- Muscular Atrophy, Progressive --- Neuronopathies, Bulbospinal --- Neuronopathies, Hereditary Motor --- Neuronopathy, Bulbospinal --- Neuronopathy, Hereditary Motor --- Progressive Muscular Atrophies --- Spinal Amyotrophies --- Linguofacial Dyskinesia --- Movement Disorder Syndromes --- Oral Dyskinesia --- Oral-facial Dyskinesia --- Tardive Dyskinesia --- Tardive Dystonia --- Tardive Oral Dyskinesia --- Dyskinesia Syndromes --- Etat Marbre --- Lingual-Facial-Buccal Dyskinesia --- Orofacial Dyskinesia --- Status Marmoratus --- Dyskinesia Syndrome --- Dyskinesia, Lingual-Facial-Buccal --- Dyskinesia, Linguofacial --- Dyskinesia, Oral --- Dyskinesia, Oral-facial --- Dyskinesia, Orofacial --- Dyskinesia, Tardive --- Dyskinesias, Lingual-Facial-Buccal --- Dyskinesias, Linguofacial --- Dyskinesias, Oral --- Dyskinesias, Oral-facial --- Dyskinesias, Orofacial --- Dyskinesias, Tardive --- Dystonia, Tardive --- Dystonias, Tardive --- Lingual Facial Buccal Dyskinesia --- Lingual-Facial-Buccal Dyskinesias --- Linguofacial Dyskinesias --- Movement Disorder --- Movement Disorder Syndrome --- Oral Dyskinesias --- Oral facial Dyskinesia --- Oral-facial Dyskinesias --- Orofacial Dyskinesias --- Tardive Dyskinesias --- Tardive Dystonias --- Tardive Oral Dyskinesias --- Psychomotor Disorders --- Diseases --- Movement disorders --- Movement Disorders --- Muscular Atrophy, Spinal --- Neuromuscular Diseases
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