Noah’s Ark Children’s Hospice in Barnet features in new film that aims to increase public understanding of children’s palliative care

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A new, short film released today, featuring care provided by Noah’s Ark Children’s Hospice, is aiming to dramatically change the way people understand children’s palliative care.

Noah’s Ark Children’s Hospice’s Dr Su Laurent appears 38 seconds into the new film which can be seen here https://www.youtube.com/watch?v=fX3clFVZFa4

Dr Su Laurent is one of Noah’s Ark Children’s Hospice’s Associate Medical Directors. She was a Consultant Paediatrician at Barnet Hospital from 1993 to 2021. She has a keen interest in training and support and is the Director of Medical Education for the Hospital. Su has a special interest in managing children with complex medical problems. She has been involved with the charity Child Bereavement UK since its inception, inspired by their focus on learning from parents. She runs courses on bereavement support across the UK.

Dr Su Laurent said of her involvement in the film: ‘I was delighted to be asked to be part of Together for Short Lives’ Childhood Needs Magic Campaign. It’s so important to raise highlight that children with life-limiting and life-threatening conditions have the same needs as other children and that they deserve as much joy, fun and magic in their lives.’

Childhood Needs Magic is narrated by Dr Ranj Singh, a BAFTA award-winning TV and radio presenter, Sunday Times best-selling author, columnist and doctor. Through the eyes of four children, supported by NHS and children’s hospice professionals, it shows that every childhood needs magic, no matter how short it might be.

Children who are very unwell still need the same things all children do: friendship, games and relaxation. Sometimes more than the adults around them, children are brilliant at living in the moment and finding joy and wonder everywhere they go.

However, not enough people understand what children’s palliative care is and what it can achieve. This film beautifully illustrates how children’s palliative supports children and families, provides a team of experts around them and helps children to be children no matter how long or short that childhood may be. We hope this film will help to increase the public’s understanding of this essential service as inaccurate perceptions of children’s palliative care are compounding the challenges families experience, leading to further isolation and hindering access to services.

At its heart this film shows that children’s palliative care provides expert support to children who are likely to have short lives, when and where they need it – making magic moments possible. Using animation, the film brings to life their interior worlds and capacity for finding magic everywhere they go.

Childhood Needs Magic begins by showing some of the children becoming immersed in magical worlds as they read a book or pretend to a be in space. As the narrative unfolds, we see little moments of magic surrounding everyday scenes, with colours and shapes reflecting how the child feels in a more abstract way. The film shows that it is the children’s palliative care provided by professionals and services that make these experiences possible.

Childhood Needs Magic has been created by UK children’s palliative care charity Together for Short Lives, alongside Heard, a charity working with people, organisations and the media to inspire content and communication that changes hearts and minds. It has been produced by Catsnake: The Story Agency and has been funded by the True Colours Trust, an independent funder which focusses on improving access to palliative care for babies, children and young people in the UK.

Andy Fletcher, Chief Executive of Together for Short Lives said: “With the right support, seriously ill children can experience the joy, fun, and magic that every childhood needs. It’s really important that we improve understanding of what children’s palliative care is and what it can achieve I urge as many people as possible to watch Childhood Needs Magic and to share it as widely as possible so that more families can access the lifeline support that children’s palliative care provides.”