Medics4RareDiseases is thrilled to partner with Medscape Education, a global education website for medics, to produce a film with ITN. The programme, that will be released on Rare Disease Day […]
It may be impossible for all doctors to have knowledge of more than 7,000 recognised rare diseases. However, it is feasible for all future and current medical professionals to learn […]
On Tuesday Lucy was invited to present alongside Sioned Preece at the UK Astrazeneca conference held at the Intercontinental right next to the O2 in North Greenwich! Astrazeneca has recently […]
Rare disease day highlights the impact of rare disease on millions of people all around the world. There’s loads of ways you can get involved to support this incredible day, […]
by Dr Alexandra Downes, Paediatric Registrar My Rare Disease journey began in the second year of my Human Genetics degree at University College London. I still remember to this day […]
Rare Diseases affect 3.5 million people in the UK. People with rare conditions take an average of FIVE years to reach a diagnosis. They often experience diagnostic delay because healthcare […]
Say hello to our newest team member!! Eleanor Churchill has joined us in the newly created role of Digital Projects Officer. We are so excited to welcome her to the […]
Are you a young person interested in finding out more about genomics and health, or affected by a rare or genetic condition? Chromosomes! Dr Andrew Fry, Clinical Senior Lecturer in […]
We are M4RD and we #daretothinkrare Medics4RareDiseases is a registered charity started by medics, for medics! In fact, M4RD started out as a university society at Barts & The London. […]
Medics4RareDiseases has been accredited as a Living Wage Employer. Our Living Wage commitment will see everyone working at M4RD receive a minimum hourly wage of £9.90 in the UK or […]