In this issue
Welcome
Celebrating Florence Nightingale
Royal Patron gets creative
Trust is Living Wage employer
Grandfather thanks pioneer for saving sight
Applications for Summer School open
Review our mealtime menus
Two minutes with…our LGBT+ network
Opportunities to get involved
Be a hero
Friends and Family Test
Trust rated highly by patients
Funding for community services
Recognition for outstanding contribution
Diabetes teams scoop award
Leading edge research
Cancer patient lands record deal
Life-changing treatment
17 February – Science Museum
26 February – LGBT History Month
4 March – performing arts
2 June – free ophthalmology seminar
Donate
Life-changing treatment

The Sunday Express covered the story of Anastasia Buturin who was locked in her body. She is now able to talk and take steps after receiving life-changing care at Evelina London Children’s Hospital.

 

Anastasia was diagnosed with a rare genetic condition called Tyrosine Hydroxylase deficiency.

 

Her father Valentin says: “We are extremely grateful for the care Anastasia has received at Evelina London. Everyone involved in Anastasia’s care has gone out of their way to ensure that she got a diagnosis and was able to get the treatment she needed.”