Talk:Rare Disease Day
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[edit]For anyone else reading this...just so you know, towards the bottom of the AfD discussion is quite a large collection of links to foreign-language coverage of this topic, which might be useful for article expansion. The article right now already has a very high number of footnotes in proportion to the amount of prose (that happened mostly in response to the AfD) so I'm not in a rush right now to bombard it with more refs, but they might be useful for future work. (I can deal with the French and Spanish ones, but unfortunately I can't read Danish, so I might not be able to look at those as quickly.) rʨanaɢ talk/contribs 05:45, 19 February 2009 (UTC)
Rare Disease Day gets its own article in Huffington_Post CostelloDc (talk • contribs) 18:08, 19 February 2009 (CET)
Rare Disease Day 2011 took place on February 28th. Theme for 2011 is "Rare Diseases and Health Inequalities", to focus on differences for rare disease patients between and within countries, and compared to other segments of society, in order to ensure equal access for patients to health care, social services and rights, and to orphan drugs and treatments. The following countries have joined in 2011:
* ARGENTINA * ARMENIA * AUSTRALIA * AUSTRIA * BELGIUM * BRAZIL * BULGARIA * BURKINA FASO * CAMEROON * CANADA * CHINA * COLOMBIA * CROATIA * CYPRUS * DENMARK * EUROPE * FINLAND * FRANCE * GEORGIA * GERMANY * GREECE * HONG KONG * HUNGARY * INDIA * IRELAND * ITALY * JAPAN * LATVIA * LUXEMBOURG * MALAYSIA * MEXICO * MOROCCO * NEPAL * NEW ZEALAND * NORWAY * PANAMA * PHILIPPINES * POLAND * PORTUGAL * ROMANIA * RUSSIAN FEDERATION * SERBIA * SLOVENIA * SOUTH AFRICA * SPAIN * SWEDEN * SWITZERLAND * TAIWAN * THAILAND * UKRAINE * UNITED ARAB EMIRATES * UNITED KINGDOM * URUGUAY * USA
[1] — Preceding unsigned comment added by RobP46 (talk • contribs) 15:58, 8 March 2011 (UTC)
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