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Rare Disease Day takes place on the last day of February each year. 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.
WHAT?
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.
WHY?
Building awareness of rare diseases is so important because 1 in 20 people will live with a rare disease at some point in their life. Despite this, there is no cure for the majority of rare diseases and many go undiagnosed. Rare Disease Day improves knowledge amongst the general public of rare diseases while encouraging researchers and decision makers to address the needs of those living with rare diseases.
WHERE?
The campaign started as a European event and has progressively become a world phenomenon, with the USA joining in 2009 and participation in over 100 countries all over the world. We hope even more will join in 2024.
WHEN?
The first Rare Disease Day was celebrated in 2008 on February 29th, a ‘rare’ date that happens only once every four years. Ever since then, Rare Disease Day has taken place on the last day of February, a month known for having a ‘rare’ number of days.
On rarediseaseday.org you can find information about the thousands of events happening around the world on the last day of February.
By increasing awareness for people living with Cold Agglutinin Disease, your gift will help mobilize individuals and communities around the world to work towards more equitable access to diagnosis, treatment, care and social opportunity.
When: February 21th at 1:00 pm EST, Dr. Richard Furman with Weill Cornell will be doing our kick-off presentation for the 2024 CAD Foundation Webinar series.
One out of every 10 Americans is living with a rare disease. Worldwide, there are more than 300 million people with rare diseases. Too often, these individuals and families are left isolated and without answers to their medical questions. It doesn't have to be that way.
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Contact Us: info@cadfadvocacy.org