Global cooperation is key in improving the quality of life of patients with rare diseases. This applies not only to the cooperation between experts, but also between patients and patient organizations. Therefore, since its establishment, HAE Junior patient organization has been regularly involved in international projects, conferences and campaigns to raise awareness of HAE.

Therefore, we regularly need to translate various materials for communication campaigns, to prepare presentations in English for foreign conferences or to actively participate in European patient working groups, such as ERN-RITA RIPAG. Moreover, our patient stories help us raise awareness about HAE Junior abroad, thanks their publication in English on Patient Worthy website, our US media partner.

Due to so many international activities, we very much welcome the partnership with Memsource, which has granted us a pro bono license to its translation platform, which supports 500+ languages, 50+ file types, and 30+ machine translation engines.

"Memsource is proud to partner with HAE Junior and support the organization's greatly beneficial mission. Their goals are to improve the quality of life of young people with hereditary angioedema and further cooperation with health care professionals, which are initiatives we are happy we can support." comments the benefits of the partnership Brittany Nelson, Community Specialist, Memsource.

HAE Junior team is happy to welcome Memsource as a new partner!