Meet some of the patients benefiting from rare disease research

Read stories from some of our families involved in the pioneering research that will take place in the Zayed Centre for Research. 

 

Meet Katie

Katie and her mum

Katie has a rare movement disorder called dystonia, which causes uncontrollable muscle spasms due to incorrect signals from the brain.Katie’s problems began at the age of two, but it wasn’t until she was referred to GOSH at the age of seven that she finally got a diagnosis. Since then, her condition has played a key role in advancing related scientific research.

Read Katie's story


Meet Nina

Nina and her dad

One of the main areas of research within the Zayed Centre for Research will be to develop new gene therapy approaches to offer transformative and curative therapies for a wide range of genetic diseases. ince 2001, more than 70 children have been treated with gene therapy for immune system disorders at GOSH including Nina, aged 7.

Read Nina's story


Meet Mela

The Zayed Centre for Research has a dedicated Craniofacial research team of clinicians and engineers, focused on using 3D technology to improve the outcome and safety of craniofacial surgery for children born with conditions affecting their head and/or face. Mela, 9, was born with a rare craniofacial condition called Apert syndrome. 

Read Mela's story


Meet Kai

Kai was one of the first patients to be treated at the Zayed Centre for Research. Kai has hypertrophic cardiomyopathy, a rare cardiac condition. Learn about Kai's story and how he is taking part in a research project at the Centre, which is aiming to discover new biological markers of inherited cardiac conditions.

Read Kai's story