Episode 2 explores 'Day One' - the moment a parent first suspects something may be different about their child.
Joined by community paediatrician and parent Dr Karen Russell, Carrie and Sam unpack the shock, grief cycles and uncertainty that so many families face. A compassionate, validating episode for anyone navigating those early signs and unanswered questions.
Cerebra – support, guides and resources for families of children with brain conditions (www.cerebra.org.uk)
The episode covers:
- The challenges of waiting for a diagnosis, or living without one
- System’s Generated Trauma
- Navigating autism, neurological conditions, and rare disorders
- Advocating for your child within the healthcare system
- Why protecting your own mental health is essential from day one
You’ll also hear real experiences from families, alongside practical advice on finding support. Helpful organisations mentioned include:
- Cerebra – support, guides and resources for families of children with brain conditions (www.cerebra.org.uk)
- https://cerebra.org.uk/download/after-diagnosis-what-now/
- https://cerebra.org.uk/download/information-and-support-for-parents-of-a-child-recently-diagnosed-with-a-genetic-condition/
- https://cerebra.org.uk/download/systems-generated-trauma-report/
- SWAN UK – support for families without a confirmed diagnosis (www.swanuk.org.uk)
- National Autistic Society – advice, support and local groups (www.autism.org.uk)
Contact has a comprehensive library (https://contact.org.uk/conditions/) of condition specific information and associated support groups.
Unique - support for families affected by rare chromosome and gene disorders (www.rarechrome.org)