In this episode, I speak with Lisa Moane on sharing my journey of navigating life after my child’s epilepsy and intellectual disability diagnoses. We talk about the emotional weight of receiving medical news and the strength it takes to advocate for your child.
In this episode, we explore:
- My journey that led me to specialise in natural epilepsy management
- Parenting a child with a disability
- Advocating for our children’s health
- Processing the rollercoaster of emotions when you receive medical news
- What my everyday family life looks like
- Common misconceptions about epilepsy
- Social impacts of invisible disabilities
- Using Facebook support groups