Showing posts with label World Rare Disease Day 2013. Show all posts
Showing posts with label World Rare Disease Day 2013. Show all posts

Thursday, February 28, 2013

1 person in 20 is affected by a rare disease

1 person in 20 is affected by a rare disease! 
Today is a World Rare Disease Day 2013!
Life-threatening or chronically debilitating diseases – mostly inherited – that affect so few people that combined efforts are needed to:
  • reduce the number of people contracting the diseases
  • prevent newborns and young children dying from them
  • preserve sufferers' quality of life and socio-economic potential.
In EU countries, any disease affecting fewer than 5 people in 10 000 is considered rare. That number may seem small, but it translates into approximately 246 000 people throughout the EU's 27 member countries. Most patients suffer from even rarer diseases affecting 1 person in 100 000 or more.
It is estimated that today in the EU, 5-8000 distinct rare diseases affect 6-8% of the population – between 27 and 36 million people.
 
 

Wednesday, February 20, 2013

World Rare Disease Day 2013

Yann le Cam, Chief Executive Officer EURORDIS - European Rare Diseases Organisation, has this message for Rare Disease Day 2013 highlighting the need to work together internationally: "Rare Disorders without Borders".

Tuesday, February 19, 2013

Rare Disorders without Border: 28 February 2013

Dear Respiratory Friends we are happy to support World Rare Diseases 2013!
The sixth Rare Disease Day takes place on 28 February 2013. This year's slogan "Rare Disorders without Borders" emphasises the need for international cooperation. Join an activity taking place near you to demonstrate global solidarity. Let's go beyond borders for rare disorders. Show your solidarity today!

This video clip has been directed by Carlo S. Hintermann and produced by Citrullo International and Digital Room with financial support from EURORDIS and the Health Programme of the European Union.
The patients featured are members of: Associazione Italiana Sindrome di Noonan, Duchenne Parent Project and Xeroderma Pigmentosum Society
We thank them and Simona Bellagambi from the Federazione Italiana per le Malattie Rare (UNIAMO) for their invaluable contribution.
More than 20 people gave their time to this project that involved stop motion animation and live action cinematography. We also thank Mario Salvucci for the original music composed for this video. 


We are inviting you on Italian event, organized by our friend Rosalba Mele: