The 29th February, 2016 marks the ninth international Rare Disease Day coordinated by EURORDIS and preparations are already getting underway in many areas. The main objective of Rare Disease Day is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients’ lives. The campaign targets primarily the general public and also seeks to raise awareness amongst policy makers, public authorities, industry representatives, researchers, health professionals and anyone who has a genuine interest in rare diseases.
Since Rare Disease Day was first launched by EURORDIS and its Council of National Alliances in 2008, thousands of events have taken place throughout the world reaching hundreds of thousands of people and resulting in a great deal of media coverage. The political momentum resulting from Rare Disease Day also serves advocacy purposes. It has notably contributed to the advancement of national plans and policies for rare diseases in a number of countries. Even though the campaign started as a European event, it has progressively become a world phenomenon, with the USA joining in 2009, and with the participation of a record-breaking 85 countries and regions around the world in 2015.
The theme of Rare Disease Day 2016 “Patient Voice” – paying tribute to the millions of people whose lives are affected by a rare disease and also to their families, friends and loved ones, who stand by them and support them every step of the way – recognizes the crucial role that patients play in voicing their needs and in instigating change that improves their lives and the lives of their families and carers. A call to solidarity and to the acknowledgement of rare diseases as a real problem, not to be dismissed under the veil of indifference. In particular, the Rare Disease Day 2016 slogan “Join us in making the voice of rare diseases heard” appeals to a wider audience, those that are not living with or directly affected by a rare disease, to join the rare disease community in making known the impact of rare diseases.
TEDDY Network welcomes this initiative and is pleased to contribute to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients’ lives. Due to the fragmentation of knowledge that makes difficult to perform research, it can take years before a patient affected by rare diseases get diagnosed and cured with appropriate medication. TEDDY is an International Network supporting Paediatric Research for innovative drugs with special attention to the constraints affecting rare diseases patients. Since Rare diseases affect children in more than 80% of cases, this is a huge priority of the Network.
TEDDY considers the promotion and the coordination of research extremely important for the health care system, and particularly for rare diseases, since they represent the tools with which to speed up the achievements in research and benefits for patients. This year Rare Disease Day encourages us to continue finding ways to work together to provide the different kinds of care that people living with a rare disease need.
TEDDY joins this event by becoming a friend of Rare Disease Day, showing its support on its official website and social networks.
For more info about the rare disease day, please visit http://www.rarediseaseday.org/