This Australian disability knowledge guide explains Multiple System Atrophy, how it may affect daily living and what people should understand about the National Disability Insurance Scheme. Access to the NDIS is based on the person's individual circumstances and permanent impairment, not just the name of a condition.

Understanding Multiple System Atrophy

Multiple system atrophy (MSA) is a progressive neurological disorder affecting movement and automatic body functions. It may cause unsteady or slow movement, muscle stiffness, dizziness on standing and changes in bladder control. Some people also develop swallowing or speech difficulties.

Every person has different strengths, preferences and needs. A diagnosis can explain the cause of an impairment, but meaningful supports should be guided by what the person wants to achieve and what they need help doing day to day.

Recognising possible symptoms and impairments

Features that may be relevant include the following, although the mix and severity vary from person to person.

• Poor balance, slowing and difficulty walking
• Dizziness or fainting when standing due to blood pressure changes
• Bladder problems or other autonomic symptoms
• Muscle stiffness and tremor in some people
• Speech, swallowing or breathing-related changes needing medical review
• Variable rate of progression and disability support requirements

How daily living and participation can be affected

A person may need assistance with personal care, safe transfers, accessible home environments and community activities, while working with their treating clinicians on medical symptoms.

The NDIS considers functional capacity in areas including communication, social interaction, learning, mobility, self-care and self-management. A useful description of needs considers what happens in the home and community, how often assistance is required and what the person can do with equipment or accessible information.

Practical person-centred approaches

• Recognise that dizziness and falls may need urgent medical review, not simply exercise advice.
• Arrange appropriate assessment for mobility and safe transfers.
• Respect continence needs and privacy.
• Refer swallowing, breathing and blood pressure management to qualified clinicians.

Effective support involves consent, safeguarding the person's rights, and working with their chosen family members or representatives. Changes in medical status should be referred to qualified clinicians rather than managed through assumptions.

Multiple System Atrophy and NDIS eligibility

The historical List B identifies multiple system atrophy, including names such as Shy–Drager syndrome. That suggests a likely permanent impairment; all other NDIS conditions, including the age-at-application rule, still apply.

Generally, the NDIS requires applicants to meet age and residence rules, and either disability or early intervention criteria. Disability criteria concern impairments that are or are likely to be permanent, substantially reduce functional capacity, affect social or economic participation, and are likely to require NDIS supports throughout life. Early intervention requirements are different and may be relevant for some children and adults.

The NDIA's historical List A and List B guidance indicates conditions likely to satisfy particular elements of the requirements. List A concerns conditions likely to meet the disability requirements, while List B concerns conditions likely to involve permanent impairment. See the current NDIS eligibility guidance for the applicable rules. A listed condition is not an automatic promise of a funded plan.

What evidence is useful when applying?

The NDIA needs to understand functional impacts and any relevant ongoing impairments. Examples of useful evidence, depending on the person, include:

1. A diagnosis and any qualifying subtype from an appropriately qualified specialist.
2. Information about impairment permanence, health treatments considered and remaining functional limitations.
3. Occupational therapy, speech pathology, physiotherapy or other relevant functional assessments.
4. Examples of where disability-specific equipment, supervision, prompting or hands-on help is needed.
5. Evidence about work, study, relationships, social participation and expected long-term disability support needs.

If the person's condition changes over time, explain both their current needs and periods of increased difficulty. Describe real tasks and situations rather than relying only on general phrases such as 'requires assistance'.

NDIS supports that might be appropriate

Where someone is an eligible participant and the supports match their plan, disability funding might assist with daily living tasks, community participation, assistive technology, mobility or communication needs, disability-related allied health and support coordination. Specific supports are not guaranteed. Funding must be used for approved purposes and comply with the current NDIS support rules.

Medical diagnosis, prescribed medicines, disease-specific therapies, operations, hospital care and routine health treatment are primarily healthcare responsibilities. The NDIS can fund certain disability-related health supports in defined situations, but staff must have appropriate instructions, authorisation and competency for complex tasks.

Support from Beyond Health Services

Our team welcomes conversations about a participant's daily routines, goals, communication preferences, personal care requirements and participation in community life. Depending on the individual's circumstances, we can discuss support workers, relevant therapy services, disability-related nursing, support coordination and other suitable disability supports. Before services are arranged we work through the referral process and discuss relevant plan funding and staff requirements.