News

A newborn baby whose rare form of eye cancer was detected at birth thanks to world-leading research is receiving vital early treatment by Birmingham Children’s Hospital medics.

A doctor who went above and beyond in the care of a patient expecting high risk twins has been picked by the public for a prestigious gong at an NHS awards ceremony.

Families across England will benefit from enhanced early detection of Hereditary Tyrosinemia Type 1 (HT1), a rare but treatable genetic disorder.

Birmingham Women’s and Children's Hospital and Charity is delighted to announce much-loved TV presenter Emma Willis as its newest Patron.

But despite suffering a brain injury, Jaden has overcome the odds to launch his own business inspired by the care he receives.

After our fantastic Team BCH enjoyed a hugely successful British Transplant Games this summer, some of our superstars went on to proudly represent Great Britain joining competitors from across the globe in Germany just a couple of weeks later.

Sarah, aged 49, stepped in to save the teenager despite having Multiple Sclerosis (MS) after he was diagnosed with a rare genetic condition called Nephronophthisis NPHP 1 .    

Young diabetic patients were treated to a fun packed activity weekend thanks to Birmingham Children’s Hospital staff. 

A Birmingham mum is raising awareness about the warning signs of a rare type of blood cancer after her son was diagnosed with the disease.