We know parenting a young person with complex needs is exhausting. That’s why our support comes from people who have been there.
We understand that the journey after a brain injury can feel overwhelming, unpredictable, and isolating. That’s why we take a holistic approach—looking not only at the medical or practical challenges, but also the emotional, social, and everyday realities that families face.
Contact an advisor today, we’re here to help.
Our team of in-house advisors and trusted professionals bring together expert knowledge and lived experience. Whether navigating care systems, finding practical solutions for daily life or simply having someone for emotional support, we’re here to walk alongside you every step of the way.
Insights from parents who have navigated health, education, social care & home adaptations
Information & resources to help you advocate with confidence for your child’s needs
Support with next steps: education, employment, independent living and adult services
Introduction to Court of Protection, trusts & financial planning for the future & legal advice
Explore funding options, understand available support, and begin planning for the future with greater clarity.
Explore funding options, understand available support, and begin planning for the future with greater clarity.
In collaboration with the Brain Injury Group, Growing Minds explores the many sides of childhood brain conditions through real stories, expert interviews and honest conversations. Each episode offers practical insights to help families, professionals and young people feel more understood. Bringing together specialists and those with lived experience, Growing Minds creates a space for learning, reflection and connection.
BIG Stepping Stones is here with one aim- to help children with complex neurological needs live the best life they can. Whether you are a family member or carer, our team of advisors share lived experience and professional knowledge with practical guidance and emotional understanding. Together, we’ll navigate the journey ahead.
If you’re Special Needs School or a Children’s Centre, we’d love to hear from you. We can deliver welcoming information days to give families direct access to resources and specialist advice within their familiar environment. Find more about our Information Days today and get in touch
Our COO, Clare Harrison, is joined by Heledd Wyn, Solicitor and Partner at Rothley Law, to discuss care, mental capacity, and planning for the future.They explore key considerations for families, including long-term care planning, EHCPs, and the transition from childhood to legal adulthood, highlighting the protections and support that can help ensure young people continue to receive the right care as they grow older.
In this episode, Kate Dixon Children and Young Person Specialist at the Brain Injury Group and Big Stepping Stones is joined by the CEO and Founder of Gympanzees, Stephanie Wheen. Learn more about the UK’s first fully inclusive exercise, therapy, play and leisure centre, the fundraising efforts and challenges that with the opening of the UK’s first full inclusive exercise., play and leisure centre – opening later this year.
In this episode, Georgina Davies, Rehabilitation and Partnerships Lead at Brain Injury Group, is joined by Chloe Hughes, a National Cerebral Palsy footballer for Bristol City CP. Chloe shares her experience of playing football while living with cerebral palsy, discussing the challenges and misconceptions she has faced, the importance of accessibility and inclusion in sport, and her ambitions for the future.
In this episode, Kate Dixon, Welfare Benefits Advisor and Young Person Specialist at the Brain Injury Group, is joined by Sarah Edwards, a Cerebral Palsy Specialist at Scope. Sarah shares both her lived and professional experience of living with cerebral palsy and supporting individuals with the condition, as well as how Scope advocates and supports young families.
Featuring Clare Harrison, COO at Brain Injury Group, and Laxmi Patel, Partner and Head of Education at Boyes Turner, this episode explores how support for young people with SEND evolves as they transition into adulthood. Through expert insight, they unpack EHCPs, transition planning, and navigating education, health, and care at this pivotal stage.
In this episode, we’re joined by the founder and CEO of The Eden Dora Trust to discuss how the charity began and its mission to support children with encephalitis and acquired brain injury (ABI). We explore the condition, the challenges families face after diagnosis, and how the Trust offers practical and emotional support through its SPEAK mission.
Featuring Clare, our COO, alongside Helen O’Neill – Nash, Director at Billy’s Charity, this episode offers a powerful family perspective on the litigation journey. Through real experiences and compassionate discussion, it sheds light on the emotional, practical, and long-term impacts of navigating the legal process following a birth injury.
Featuring Jacob, Clinical Advisor, and Emma Trudgill, Clinical Advisor for Children, this episode explores the early signs to notice in both parents and infants during the perinatal period. Together, they share clinical expertise, lived experience, and compassionate advice designed to help families recognise needs early and access the right support.
Featuring Clare Harrison, our COO, and Kate Dixon, Children and Young Person Specialist, this episode shares both personal and professional reflections on the challenges, rewards, and meaningful moments of parenting a child with a brain injury. Through open discussion, they highlight resilience, growth, and the importance of tailored support for families.
Our team of in-house advisors and trusted professionals bring together expert knowledge and lived experience, so you can feel understood as well as supported.
It was reassuring to know you both actually got it, it felt easier to ask questions without feeling judged.
Great information session this morning, I am glad I came. I felt it was easier to ask questions without feeling judged. The information I got was so useful and I have a list of things to start tackling.
Our team is here to help you explore the support available. Many parents carry these worries in silence. Starting the conversation can be the first step towards finding a way forward. You can contact us to: