Real Story

In 2020, Luca Evans, at just 15 weeks old was diagnosed with an inoperable Spinal Cord Tumour that would change his and his families lives forever.

Alys Prosser was has returned to Rainbow Ward 20 years after her own treatment to bring joy to the patients through song and dance

When the Witchell family take on this year’s Cardiff Marathon, it will mark a moment more than sixteen years in the making

Latch Ambassador Paula reflects on the journey her son, daughter-in-law and granddaughter have gone through since their world stopping diagnosis

After 30 years of support, Helen shares her story, how things have changed, and her hopes for the future

Advanced Nurse Practitioner, Julie shares the how Latch has helped improve treatment for children and families in peadiatric oncology

Jo shares how the family have been supported by Latch throughout Sharelle’s treatment, including with bereavement support. 

Ambassador Bec Pugh shares the story of her daughter Martha's treatment, and how her life inspired support for Latch

"I'm a Latch Ambassador because they helped us so much. I want to help them support more families and children, like Latch helped us."

More than a decade later, one family looks back on the journey through treatment

Two stories from one family about their journey from diagnosis to treatment.

Fundraising for Latch has changed the narrative of the past two years