MDI Annual Reports and Audited Accounts

MDI Annual Report 2022

Click on the image above to download the 2022 Annual Report

 

Previous MDI Annual Reports

MDI Annual Report 2021
MDI Annual Report 2020
MDI Annual Report 2019
MDI Annual Report 2018
MDI Annual Report 2017
MDI Annual Report 2016
MDI Annual Report 2015
MDI Annual Report 2014
MDI Annual Report 2013
MDI Annual Report 2012
MDI Annual Report 2011
MDI Annual Report 2010
MDI Annual Report 2009
MDI Annual Report 2008
MDI Annual Report 2007
MDI Annual Report 2006
MDI Annual Report 2005
MDI Annual Report 2004

MDI Audited Accounts

Audited Accounts 2022
Audited Accounts 2021
Audited Accounts 2020
Audited Accounts 2019
Audited Accounts 2018
Audited Accounts 2017
Audited Accounts 2016
Audited Accounts 2015
Audited Accounts 2014
Audited Accounts 2013
Audited Accounts 2012
Audited Accounts 2011
Audited Accounts 2010
Audited Accounts 2009
Audited Accounts 2008
Audited Accounts 2007

Muscular Dystrophy Ireland CLG
75 Lucan Road, Chapelizod, Dublin D20 DR77
Telephone: 1800 245 300

Registered Charity Number: 20012038
CHY Charity Number: 6849
Company Number: 60460
Country of registration: Ireland

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
  • 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

2. Myotonic Disorders

  • Congenital Myotonic Dystrophy
  • Myotonia
  • Myotonic Dystrophy

3. Congenital Myopathies

  • Central Core Myopathy
  • Congenital Fibre-type Disproportion 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 Myositis

  • 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

  • Friedreich’s Ataxia

12. Other (Please Specify)

13. Unspecified