Job Vacancies


Current employment opportunities with Muscular Dystrophy Ireland (MDI)

Community Support Worker [Western and Midlands Region]

Muscular Dystrophy Ireland (MDI) offers a range of support services nationally to persons affected by neuromuscular conditions and their families. The holder of this position will deliver a Youth Respite Service and coordinate summer camps provided by MDI to its members in the Western Health Service Executive Area and deliver a Family Support Service providing support to families in the Western and the Midlands Health Service Executive Area.

The ideal candidate will have a good understanding of health and social services and the needs of people living with disabilities. The candidate will have experience of outcome driven advocacy work and experience in the provision of practical support to adults/young people with disabilities and their families. A full clean driving licence is essential to this post.

Click here for more details and to apply

Information Officer

Reporting to the CEO, the Information Officer provides information to MDI members and their families, medical personnel, employees and all stakeholders. The role requires the job holder to keep abreast of research in the field of neuromuscular conditions, current treatment, standards of care & entitlements and disseminate relevant information to stakeholders in a timely manner. The job holder will act as an advocate on behalf of MDI.

Location: MDI National Office, 75 Lucan Road, Chapelizod, Dublin D20 DR77

Reporting to: CEO

Click here for more details and to apply

Personal Assistant (Careworker)

This role is centred around the Personal Assistant Programme, Successful applicants will be required to work closely with people with muscular dystrophy, provide personal assistance and support where needed and work as part of a team to provide the best possible service to our members.

Click here for more details and to apply

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1. Muscular Dystrophies

  • Becker muscular dystrophy
  • Duchenne muscular dystrophy
  • Manifesting carrier of Duchenne
  • Congenital muscular dystrophy - General
  • • MDC1A (merosin-deficient congenital muscular dystrophy)
  • • Rigid spine syndrome (RSS)
  • • Ullrich congenital muscular dystrophies
  • • Bethlem myopathy
  • Emery-Dreifuss muscular dystrophy

2. Myotonic Disorders

  • Congenital Myotonic Dystrophy
  • Myotonia
  • Myotonic Dystrophy

3. Congenital Myopathies

  • Central Core Myopathy
  • Minicore (Multicore) myopathy
  • Myotubular or Centronuclear myopathy
  • Nemaline myopathy

4. Mitochondrial Myopathies

  • Mitochondrial Myopathies

5. Metabolic Disorders

  • Metabolic disorders (general)
  • McArdle’s Disease
  • Pompe’s Disease

6. Periodic Paralyses

  • Periodic Paralyses

7. Autoimmune Myositides

  • Polymyositis, Dermatomyositis and Sarcoid myopathy
  • Juvenile dermatomyositis
  • Inclusion body myositis

8. Spinal Muscular Atrophies

  • Severe (Type I)
  • Intermediate (Type II)
  • Mild (Type III)
  • Adult spinal muscular atrophy

9. Hereditary Motor and Sensory Neuropathies

  • (Also known as Charcot-Marie-Tooth or Peroneal muscular atrophy)

10. Disorders of the Neuromuscular Junction

  • Congenital myasthenic syndromes
  • Myasthenia Gravis

11. Friedreich’s Ataxia

  • Facioscapulohumeral muscular dystrophy
  • Limb-girdle types of muscular dystrophy (LGMD) - General
  • • LGMD 1B (also known as Laminopathy)
  • • LGMD 1C (also known as Caveolinopathy)
  • • LGMD 2A (also known as Calpainopathy)
  • • LGMD 2B (also known as Dysferlinopathy)
  • • LGMD 2I
  • Ocular myopathies including ocularopharangeal muscular dystrophy

12. Other (Please Specify)

13. Unspecified