My CP Guide Blog
CP Spotlight


NDIS changes and cerebral palsy: your questions answered

Cytomegalovirus (CMV) Awareness Month
Read more of our blog posts
Filter by
Click on the filter options below to further refine your search results.

As NDIS reforms create uncertainty for Australians with a disability, Laura reflects on the guilt of using support, the fear of losing it, and why people with disability deserve the same opportunities, holidays and good experiences as everyone else.

When Erin's daughter Eve was diagnosed with grade 4 bilateral intraventricular haemorrhage shortly after birth, her family faced an uncertain future. In this story, Erin shares Eve's journey with cerebral palsy, the role of therapy and play in her development, and the strength, resilience and determination Eve shows every day.

In partnership with Mycpguide, CPSN hosted a webinar exploring ableism through both research and lived experience.

June is Cytomegalovirus (CMV) Awareness Month: a common virus which is a leading cause of cerebral palsy.

This blog by Margaret Wallen explores how AAC users can be meaningfully included in cerebral palsy research by adapting methods, allowing time, and supporting different communication styles.

In this blog, we explore what an exercise physiologist does, how exercise can support long-term health and wellbeing for people with cerebral palsy, and why finding the right balance with movement and energy is so important.

This Mother’s Day, we celebrate the mothers in the cerebral palsy community who share their stories, support others, and advocate for change.

Is Japan wheelchair-friendly? Our family shares real experiences, challenges and wins from travelling across five cities.

Brenton Ponza shares how volunteering gives him a sense of purpose, connection and belonging in his community.