Eligibility

CAPS Eligibility Criteria

 

For the purpose of CAPS, you are eligible for CAPS if you are five years of age or older and meet  requirements A, B or C below and meet the criteria on the CAPS Application Form:

A.  Eligible neurological conditions

You have permanent and severe loss of bladder and/or bowel function (incontinence) due directly to an eligible neurological condition. A list of eligible neurological conditions is provided below.

Or

B. Other conditions

You have permanent and severe loss of bladder and/or bowel function (incontinence) caused by an eligible "other" condition (for example, bladder prolapse). A list of eligible other conditions is provided below.

And

You have a Centrelink Pensioner Concession Card, or if you are under 16 years of age, your parent/guardian has a Centrelink Pensioner Concession Card.

Or

C. Other conditions

 

You have permanent and severe loss of bladder and/or bowel function (incontinence) caused by an eligible "other" condition (for example, bladder prolapse). A list of eligible other conditions is provided below.

And

You have a Department of Veterans Affairs Pensioner Concession Card, or if you are under 16 years of age, your parent/guardian has a Department of Veterans Affairs Pensioner Concession Card.

Applicants will need to complete a CAPS Application Form which includes a Health Report from a health professional.

 

Useful Links


CAPS Eligible Neurological Conditions

 

 

Category 1: Spina Bifida and Syringomyelia

  • Arnold-Chiari Syndrome 
  • Arthrogryposis 
  • Caudal Regression Syndrome 
  • Developmental Cord Disorder 
  • Holoprosencephaly 
  • Malformation of Spinal Cord 
  • Sacral Agenesis 
  • Spinal Agenesis 
  • Spinal Cord Congenital Abnormality 
  • Spinal Dysraphism 
  • Spinal Hemangioma 
  • Vater Syndrome/Vacterl Syndrome

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Category 2: Cerebral Palsy

  • Dystonic Cerebral Palsy 
  • Hereditary Spastic Paralysis 
  • Spastic Quadriplegia

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Category 3: Intellectual Disability

  • 2-Hydroxyglutaric Aciduria 
  • Agenesis of Corpus Callosum 
  • Alpers Disease 
  • Angelman Syndrome 
  • Apert Syndrome 
  • ATRX Syndrome 
  • Bardot Biedl Syndrome 
  • Batten Disease 
  • Beare-Stevenson Syndrome 
  • Cats Cry Syndrome/Cri Du Chat Syndrome 
  • CDKL5 Gene Mutation 
  • Cerebral Migration Disorders 
  • Charge Syndrome 
  • Chime Syndrome 
  • Chromosomal Abnormalities/Disorders 
  • Chromosome 1 Deletion 
  • Chromosome 13q Deletion Syndrome 
  • Chromosome 15q Duplication Syndrome 
  • Chromosome 18q Deletion Syndrome 
  • Chromosome 1p36 Deletion Syndrome/Mono 1p36 
  • Chromosome 22 Ring 
  • Chromosome 2q Deletion Syndrome 
  • Chromosome 6 Ring Syndrome 
  • Chromosome 8 Abnormality 
  • Chromosome 9p Deletion Syndrome 
  • Chromosome 9q Deletion Syndrome 
  • Chromosome Xp Duplication 
  • Cockayne Syndrome 
  • Coffin-Lowry Syndrome 
  • Cognitive Impairment 
  • Cohen Syndrome
  • Congenital Hydrocephalus 
  • Congenital Neurological Infections 
  • Cornelia de Lange Syndrome 
  • Costello Syndrome 
  • Cowden Disease 
  • Developmental Delay  
  • Developmental Delay associated with Autism and Autism Spectrum Disorder
  • Developmental Delay associated with Aspergers Syndrome 
  • Down Syndrome/Trisomy 21 
  • Dravet Syndrome 
  • Edwards Syndrome/Trisomy 18 
  • Fragile X Syndrome 
  • Fumarase Deficiency 
  • GLUT1-DS Condition 
  • Glutaric Aciduria Type 1 
  • Goldenhar’s Syndrome 
  • Hunter Syndrome 
  • Hurler-Scheie Syndrome 
  • Hypomyelination 
  • Incomplete Corpus Callosum/Aicardi Syndrome 
  • Inversion Duplication of Chromosome 8 
  • Jacobsen Syndrome/11q Chromosome Deletion 
  • Joubert Syndrome 
  • Kabuki Syndrome 
  • Langer-Gideon Syndrome 
  • Lawrence Moon Biedel Syndrome 
  • Lennox-Gastaut Syndrome 
  • Lesch-Nyhan Syndrome 
  • Lissencephaly 
  • Lowe Syndrome 
  • Mannosidosis 
  • Maple Syrup Urine Disease 
  • Meningitis 
  • Menkes Syndrome 
  • Microcephaly 
  • Mitochondrial Deficiency 
  • Molybdenum Cofactor Deficiency 
  • Mowat-Wilson Syndrome 
  • Mucolipidosis IV 
  • Myotonic Dystrophy (Type 1) 
  • Neonatal Hypoxia 
  • Neonatal Onset Multisystem Inflammatory Disease 
  • Normal Pressure Hydrocephalus 
  • OHDO Syndrome 
  • Opitz Trigonocephaly Syndrome 
  • Ohtahara Syndrome 
  • Ouvrier Syndrome 
  • Pallister-Killian Mosaic Syndrome 
  • Periventricular Leukomalacia 
  • Peroxisome Biogenesis Disorder 
  • Phelan McDermid Syndrome/22q 13 Deletion Syndrome 
  • Phenylketonuria 
  • Polymicrogyria 
  • Pontocerebellar Hypoplasia
  • Prader-Willi Syndrome 
  • Pyruvate Dehydrogenase Deficiency/Leigh's Disease 
  • Rare Congenital Neurological Syndromes and Conditions 
  • Rasmussen's Disease 
  • Rett Syndrome 
  • Rubinstein-Taybi Syndrome 
  • Schizencephaly 
  • Sensory Integration Disorder/Dysfunction 
  • Smith-Lemli-Opitz Syndrome 
  • Smith-Magenis Syndrome 
  • Sotos Syndrome 
  • Sturge-Weber Syndrome 
  • Subcortical Band Heterotopia 
  • Translocation of Chromosome 2 
  • Translocation Trisomy 5/18 
  • Trichothiodystrophy 
  • Trisomy 10 
  • Trisomy 13  
  • Trisomy 20p 
  • Trisomy 47 
  • Trisomy 4p 
  • Trisomy 9 
  • Tuberous Sclerosis 
  • Turner Syndrome 
  • Urea Cycle Defect 
  • Valproate Embryopathy 
  • Velocardiofacial Syndrome 
  • West Syndrome 
  • Williams Syndrome 
  • Wolf-Hirschhorn Syndrome 
  • X-Linked Adrenoleukodystrophy 
  • Young-Simpson Syndrome

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Category 4: Paraplegia and Quadriplegia

  • Paraparesis 
  • Spinal Cord Compression  
  • Spinal Cord Infarction 
  • Spinal Damage 
  • Syringomyelia 
  • Tetraplegia 
  • Transverse Myelitis

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Category 5: Acquired Neurological Conditions

  • Acquired Brain Injury 
  • Adhesive Arachnoiditis 
  • Alcoholic Encephalopathy 
  • Alzheimer's Disease 
  • Arachnoiditis 
  • Ascending Polyneuropathy 
  • Astrocytoma 
  • Autonomic Neuropathy Disease 
  • Basal Ganglia Infarction 
  • Benign Meningioma 
  • Brown-Sequard Syndrome
  • Cauda Equina Lesion 
  • Cerebral Abscess (Cryptococcus) 
  • Cerebral Aneurysm 
  • Cerebral Anoxia 
  • Cerebral Toxoplasmosis 
  • Cerebral Tumour 
  • Cerebrovascular Disease 
  • Chronic Hypoxia 
  • Chronic Inflammatory Demyelination Polyneuropathy (CIDP) 
  • Cortical-Basal Ganglionic Degeneration 
  • Dementia 
  • Developmental/Motor Dyspraxia 
  • Diabetic Autonomic Neuropathy 
  • Diabetic Neuropathic Bladder 
  • Dorsal Pontine Band Syndrome 
  • Encephalitis 
  • Ependymoma  
  • Epilepsy 
  • Focal Cerebral Degeneration 
  • Glioblastoma Multiforme 
  • Glioblastoma of Spine 
  • Hepatic Encephalopathy 
  • Hydrocephalus 
  • Hypoxic Brain Damage 
  • Inoperable Neurogenic Incontinence 
  • Intracerebral Haemorrhage 
  • Korsakoff’s Syndrome  
  • Leuco Posterior Encephalopathy 
  • Lewi Body Disease 
  • Macroencephaly 
  • Malignant Meningioma 
  • Metastatic Carcinoma with Neurological Syndrome 
  • Multiple Systems Atrophy 
  • Myopathy 
  • Nemaline Myopathy 
  • Oligodendroglioma 
  • Pachymeningitis 
  • Picks Disease 
  • Pilocytic Astrocytoma 
  • Poliomyelitis 
  • Polymyoneuropathy 
  • Primary Dystonia (case by case) 
  • Progressive Systemic Sclerosis 
  • Sacral Neuroplexy 
  • Sacral Plexopathy 
  • Schizophrenia (Catatonic) 
  • Spinal Canal Disease 
  • Spinal Chordoma 
  • Spinal Ependymoma 
  • Spinal Sacral Chordoma 
  • Spinal Tumour 
  • Stroke/Cerebrovascular Accident (CVA) 
  • Subarachnoid Haemorrhage 
  • Subdural Haematoma
  •  Vascular Dementi

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Category 6: Degenerative Neurological Diseases

  • Alexander Disease 
  • Amyotrophic Lateral Sclerosis 
  • Ataxia Telangiectasia 
  • Cauda Equina Syndrome 
  • Cervical Canal Stenosis 
  • Cervical Myelopathy 
  • Creutzfeldt-Jakob Disease (CJD) 
  • Cytochrome C Oxidase Deficiency 
  • Dejerine-Sottas Disease 
  • Demyelinating Neuropathy 
  • Demyelination of White Matter 
  • Fahr's Disease 
  • Friedreich’s Ataxia 
  • Guillain Barre Syndrome 
  • Huntington Chorea/Disease 
  • Hypoxic Ischaemic Encephalopathy 
  • Idiopathic Axonal Neuropathy 
  • Kugelberg-Welander Syndrome 
  • Machado Joseph Disease 
  • Metachromatic Leukodystrophy 
  • Mitochondrial Myopathy with Encephalopathy 
  • Morquio Syndrome 
  • Motor Neurone Disease 
  • Multiple Sclerosis 
  • Muscular Dystrophy 
  • Myoneural Disorders 
  • Neuroaxonal Dystrophy 
  • Neurofibromatosis NF 
  • Neurogenic Bowel 
  • Niemann-Pick Disease Type C 
  • Pallister-Hall Syndrome 
  • Parkinson Disease 
  • Parkinsonism 
  • PEHO Syndrome (Progressive encephalopathy with oedema, 
  • hypsarrhythmia and optic atrophy) 
  • Pelizaeus Merzbacher Disease 
  • Primary Lateral Sclerosis 
  • Progressive Supranuclear Palsy/Steele Richardson Syndrome 
  • Sanfilippo Syndrome 
  • Sarcoidosis of the Brain 
  • Shy-Drager Syndrome 
  • Spinal Cord Syndrome 
  • Spinal Degeneration 
  • Spinal Muscular Atrophy Type 1 
  • Spinal Muscular Atrophy Type 2 
  • Spinocerebellar Degeneration 
  • Stiff-Mans Syndrome 
  • Striato-Nigral Degeneration 
  • Vascular Myelopathy 
  • Wallerian Degeneration of White Matter 
  • Wilson's Disease

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Category 7: Bladder (Bowel) Innervation Disorders

  • Atonic Bladder/Hypotonic Bladder 
  • Bladder Exstrophy 
  • Bladder Innervation Urgency 
  • Cloacal Exstrophy 
  • Cystocele (not suitable for surgery) 
  • Dysfunctional Voiding 
  • Dystonic Bladder 
  • Ectopia Vesica 
  • Hirschsprung's Disease 
  • Linear Sebaceous Nevus Genetic 
  • Myasthenia Gravis 
  • Neurogenic Bladder 
  • Neuronal Intestinal Dysplasia 
  • Neuropathic Bladder 
  • Post Bladder Surgery 
  • Prostatectomy with nerve removal 
  • Prune Belly Syndrome 
  • Pudendal Nerve Palsy 
  • Radical Prostatectomy 
  • Schmidli Autonomic Neuropathy 
  • Slow Transit Constipation 
  • Smooth Muscle Myopathy 
  • Sphincter Deficiency  
  • Spinal Stenosis

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CAPS Other Eligible Conditions

 

Category 8: Other - Pensioners Concesion Card Required

  • Anal Carcinoma 
  • Anal Fistula 
  • Anorectal Malformation 
  • Anterior Prolapse 
  • Bilateral Nephrostomy Tubes 
  • Bladder Cancer 
  • Bladder Instability 
  • Bladder Muscle Dysfunction 
  • Bladder Neck Dysfunction 
  • Bladder Neck Fibrosis 
  • Bladder Prolapse 
  • Bowel Cancer 
  • Bowel Prolapse 
  • Cervical Cancer 
  • Chronic Urinary Retention 
  • Congenital Epispadias 
  • Detrusor Instability 
  • Detrusor Overactivity 
  • Enterocutaneous Fistula 
  • Faecal Incontinence Post-Colectomy 
  • Hypertonic Bladder 
  • Imperforate Anus 
  • Irradiated Rectum/Radiation Proctitis 
  • Metastatic Ovarian Carcinoma 
  • Post Ileorectal Anastomosis 
  • Post Ileal J Pouch Anastomosis 
  • Posterior Urethral Valve Syndrome 
  • Prostate Cancer 
  • Prostate Disease 
  • Rectal Prolapse 
  • Rectal Ulcer Syndrome 
  • Severe Ulcerative Proctitis 
  • Spastic Bladder 
  • Transurethral Resection of the Prostate (TURP) 
  • Urethral Stenosis 
  • Urinary Fistula 
  • Uterine Cancer 
  • Uterine Prolapse 
  • Vaginal Prolapse 
  • Vesico-Vaginal Fistula 
  • Vulva Cancer

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Not Eligible for CAPS

 

Applicants must complete the Eligibility Guide questions E1 to E5 in the CAPS application form to test their eligibility for CAPS.
 
An applicant is not eligible for CAPS if:
  • The applicant is not an Australian citizen or a permanent Australian resident.
  • The applicant is a high care resident in an Australian Government funded aged care home.
  • The applicant is receiving an Extended Aged Care at Home (EACH) or an EACH Dementia (EACHD) package and continence products are negotiated as part of the applicant’s care plan.
  • The applicant is eligible for assistance with continence products under the Rehabilitation Appliances Program (RAP) which is available through the Department of Veteran’s Affairs.
  • The applicant’s incontinence is one of the following types:
    • Transient incontinence (not permanent);
    • Incontinence that can be treated with an existing conservative treatment regime (eg pelvic floor exercises or bladder re-training), medication or surgery;
    • Confined to night time bed wetting (enuresis).
  • The applicant’s incontinence results from a condition other than an eligible neurological condition AND the applicant does not have Centrelink or DVA Pensioner Concession Card entitlement. 

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