Since the AIE was founded in 1999, it has filled a huge
gap: before 1999 nothing was available for women with
endometriosis in Italy. No support, education or awareness
whatsoever. The AIE has spent the last eight years working
hard at raising awareness about endometriosis and providing
education, research facilitation, and patient support
to the Italian endometriosis community.
Jacqueline Veit, AIE co-founder and
president, said: “No one with this disease should
ever feel alone, and one of our goals has always been
to ensure that women never have to feel that way again.”
Veit, who has been working closely
with the Italian Senate and MPs went on to say: “We
are very proud of the results that we have achieved
so far, and especially the part our Association has
played in getting politicians to listen and take action.
After collaborating with the Italian Senate for the
investigation into endometriosis as a social disease,
we are now working on a proposal of law.”
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