News

“Our son is home, alive, the same child we’ve always known and loved. I don’t know whether I believe in miracles, but I do know that without Sheffield Children’s, that wouldn’t be the case.” A family of a Sheffield...

Patients at Sheffield Children’s will soon have a bigger brighter space for their treatment for cancer, leukaemia and blood disorders, as work gets underway to transform their ward. The ward is being funded through generous donations to The Children’s...

Here at Sheffield Children’s the Clinical Research Facility Team in the Directorate of Research & Innovation are busy working across a number of clinical trials year round. Whether it is a drug trial exploring new therapies for diabetes patients...

Sheffield Children’s has opened nominations for new governors to represent staff and public members. Those elected will influence how the Trust makes plans to improve and develop services. Members of the public, aged 16 and above, from Sheffield can...

Sheffield Children’s is collaborating with four other UK specialist children’s hospitals to reduce time to treatment and decrease delays in children’s care caused by the pandemic. A collaborative which includes Sheffield Children’s, Birmingham Women and Children’s Hospital Trust, Alder...

Babies staying on the Neonatal Surgical Unit (NSU) at Sheffield Children’s will have momentous occasions captured for all the family to see, no matter where they are, thanks to a charity-funded secure messaging service. The Children’s Hospital Charity, which...

Hello Rúben! Two year old Rúben is no stranger to Sheffield Children’s. He first visited as a baby after being born ten weeks prematurely in Lincolnshire. Originally Rúben was brought in by ambulance because of a suspected retinopathy of...

The Children’s Hospital Charity Bears of Sheffield are coming this summer, featuring different designs, unique names and colourful patterns. One bear who has an extra special name is the Bear sponsored by Twinkl, named after a patient Rory, who...

Meet five year old Elijah, he lives in Leicestershire and travels up to Sheffield Children’s every 16 weeks for treatment. In 2019, Elijah was diagnosed with Spinal Muscular Atrophy (SMA) Type 2 after a genetics investigation, following an earlier...