Progressive Supranuclear Palsy (PSP) — NDIS Support
Yes — Progressive Supranuclear Palsy (PSP) can qualify for NDIS support. PSP is on the NDIA’s List B — permanence is recognised, and you evidence the functional impact on daily life. Funding covers reasonable and necessary supports across daily living, therapy, social participation and capacity building.
Progressive supranuclear palsy (PSP) is a rare, degenerative brain condition caused by the build-up of a protein called tau in areas that control movement, balance, eye movement and thinking. It is one of a group of conditions known as atypical parkinsonism. Symptoms usually begin after the age of…
PSP & the NDIS FAQs
- Is PSP eligible for the NDIS?
- PSP is a permanent, degenerative neurological condition, so it can meet the NDIS disability requirements based on the substantial functional impact it causes. It is not listed on List A, so access is assessed on evidence — a neurologist's report confirming the diagnosis and permanence, plus functional assessments…
- How is PSP different from Parkinson's disease?
- Both cause slowed movement and stiffness, but PSP typically brings early, backward falls, difficulty moving the eyes (especially looking down), and faster progression. It also responds poorly to the levodopa medication that helps Parkinson's. These differences matter for planning, because PSP's needs change more…
- What supports can the NDIS fund for PSP?
- The NDIS funds disability supports rather than medical treatment — including physiotherapy, occupational therapy, speech pathology, support workers, assistive technology and home modifications. Because PSP progresses, plans focus on maintaining safety, communication and independence, and are reviewed regularly so…
- How quickly should I plan for changing needs?
- PSP tends to progress faster than Parkinson's, so it helps to plan proactively. Early falls-prevention, communication planning and home modifications can prevent injury and maintain independence for longer. Working with an occupational therapist and support coordinator to anticipate the next stage means equipment and…
- Can families and carers get support too?
- Caring for someone with PSP is demanding, and support workers funded through the participant's plan can provide respite and share daily care. Carers can also access counselling and carer supports through the broader health and community system. Coordinated care reduces carer burnout and helps keep the person with PSP…
PSP & the NDIS — practical guides
- Applying for the NDIS with Progressive Supranuclear Palsy (PSP)
- Assistive Technology for Progressive Supranuclear Palsy (PSP)
- Day Programs & Community Participation for Progressive Supranuclear Palsy (PSP)
- NDIS Funding & Budget for Progressive Supranuclear Palsy (PSP)
- Therapy & Allied Health for Progressive Supranuclear Palsy (PSP)
- Finding & Managing Support Workers for Progressive Supranuclear Palsy (PSP)
Related conditions
- Scleroderma (Systemic Sclerosis) and the NDIS
- Scoliosis (Severe / Neuromuscular) and the NDIS
- Sotos Syndrome and the NDIS
- Spinocerebellar Ataxia and the NDIS
- Sturge-Weber Syndrome and the NDIS
- SYNGAP1-Related Disorder and the NDIS
- Transverse Myelitis and the NDIS
- Younger Onset Dementia and the NDIS
- Autism Spectrum Disorder and the NDIS
- Intellectual Disability and the NDIS
Sources
Reviewed by the Novida editorial team · last reviewed 2026-07-12. General information only — not medical advice.