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National Transport Authority – Accessibility of Public Transport Survey

September 23rd, 2020

The National Transport Authority are looking for your feedback on how accessible you find the public transport system in your area.

You can do so by completing the survey below before 29 October.

The NTA operate the public transport system by contracts with Dublin Bus, Bus Eireann, Irish Rail, Luas, Go Ahead and Local Link. They also provide licences to taxis, private buses and coaches.

The Survey can be completed Online through the following link:

https://www.transportforireland.ie/getting-around/accessible-travel-information/

 

If you would like someone to call you and assist you with the survey please leave your contact details on accessibility@nationaltransport.ie and someone will call you back.

Completed surveys can be returned by email to accessibility@nationaltransport.ie or by post to: Transport Accessibility Manager, Dún Scéine, Iveagh Court, Harcourt Lane, Dublin 2, D02 WT20.

Accessibility of Public Transport Survey – PDF version

Accessibility on Public Transport Survey – Word Version

 

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Categories: Information

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