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Cerebra Lived Experience Advisory Group – Join Us

10 July 2026

We are looking for people to join our Lived Experience Advisory Group to help shape the work that directly affects families with children with neurodevelopmental conditions.

Cerebra Lived Experience Advisory Group – Join Us

10 July 2026

We are looking for people to join our Lived Experience Advisory Group to help shape the work that directly affects families with children with neurodevelopmental conditions.

Mum and happy young boy making sounds with sticks, sitting on a sofa

Who we are

Cerebra is the national charity dedicated to improving the lives of children with neurodevelopmental conditions and their families. We do this through research, practical support, and innovative services that help families navigate everyday challenges.

Why join

Your lived experience matters. By joining the Lived Experience Advisory Group, you’ll help shape the work that directly affects families like yours. Your insight will influence Cerebra’s strategy, research priorities, services and policy work, ensuring everything we do is relevant, accessible and genuinely helpful.

Who we’re looking for

We welcome parents, carers, siblings and young people aged 16–25 who have lived experience of neurological conditions. You don’t need any formal qualifications, just a willingness to share your perspective and work alongside others.

You might be a good fit if you:

  • Can listen to and learn from different experiences.
  • Care about improving support for families of children with neurological conditions.
  • Want to use your insight to help shape services, research and policy.

We value a wide range of experiences, whether that’s navigating health or social care systems, using assistive equipment, supporting a child with sleep difficulties, or finding creative ways to adapt everyday life. If your experience connects to Cerebra’s mission, we’d love to hear from you.

What you’ll do

  • Review and shape strategy and services, research priorities and public-facing materials.
  • Join 2–4 meetings a year (mainly online) and contribute by email between meetings.
  • Take part in workshops, consultations and occasional grant or publication reviews.
  • Provide occasional support for public communications, including offering commentary, reviewing key messages, or participating in interviews when appropriate.

Commitment and rewards

This voluntary role involves up to 25 hours per year. Meetings are mainly held by video call, with one possible in‑person meeting. Members will receive a fixed annual honorarium of £687.50, paid either twice yearly or as a single annual payment. All reasonable expenses are reimbursed.

How to apply

Please complete our short online application form (approx. 10–15 minutes). The form asks for basic contact details, information about your lived experience, and a few short answers so we can understand what you would bring to the group. If you need the form in an alternative format (Easy Read, Word, large print, audio) or help to complete it, contact us by email: [email protected].

Deadline

Applications close 5pm on 31 July 2026.

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Please donate

We rely on your generous donations to fund our vital research and services that improve the lives of children with brain conditions and their families.

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Your amazing donations could pay for a set of light-weight crutches for a child to move around more freely.

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Your kind donation could pay for a new library book to help parents understand their child’s condition.

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Your generous donation could pay for a new sensory toy for our toy library so a child can play and find joy.

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