Rare Disease Day 2018!

The last day of February is Rare Disease Day. This is the day of the year above all others that as a community we try to raise awareness amongst the general public, policy makers, public authorities, industry representatives, researchers, health professionals and anyone who has a genuine interest in rare diseases.

Here in Newcastle some of the staff at the John Walton Muscular Dystrophy Research Centre tried to do just that by participating in a ‘Genetics Matters’ afternoon. Attendees benefitted from a series of talks followed by round table lightning talks. Below are a few photos from the day.

The ERNs are co-funded by the
European Union (Health Programme and CEF)

EU Commission


“EURO-NMD is one of the 24 European Reference Networks (ERNs) approved by the ERN Board of Member States. The ERNs are co-funded by the European Union (Health Programme and CEF).
For more information about the ERNs and the EU health strategy,
please visit ec.europa.eu/health/ern