Support group news
News from national endometriosis organisations from around the world.
The ERC is pleased to announce that it has centralised and revamped its various awareness campaigns under one programme, in order to streamline and revitalise its efforts.
Ailsa Irving, founder of the National Endometriosis Society in the UK, shares memories on the 25th anniversary of the charity (now Endometriosis UK).
The very first meeting of Endometriosis de Puerto Rico was held on 26 March 2006 with Senator Lucy Arce presenting Dr Idhaliz Flores with a declaration for endometriosis awareness!
Endometriosis Awareness Week was kicked off ouside the UK Parliament at noon on Monday 6 March with a communal SCREAM, symbolic of he pain each woman with endometriosis has to endure and demonstrating their frustration at a lack of funding and action from the government.
Jacqueline Veit (co-founder/president of Associazione Italiana Endometriosi was received at the Senate for an audience as part of the investigation currently underway on the issue of endometriosis as a social disease.
First ever conference to address endometriosis as a social disease takes place in Rome in June 2005. Giorgio Vittori, Jacqueline Veit, and Lone Hummelshoj make their case for investment into the disease.
Endometriosis Support Groups in Europe simultaneous arranged awareness and informational events across Europe.
Ros Wood celebrates 21 years of achievements for the Endometriosis Association Victoria (Australia), including helplines, research, information, first ever endometriosis clinic, and the book Explaining Endometriosis.
The European Endometriosis Alliance (EEA) was founded in October 2004 and is an umbrella organistion for national endometriosis support organisations in Europe.