The Urgo Foundation commits to 11 EB associations in Brazil! Since its creation, the URGO Foundation has committed to fight Epidermolysis bullosa (EB*), a rare genetic skin disorder affecting many children around the world. A…
read moreA summer camp in Poland for kids with EB! From 15th to 22th of July, the Debra association organized in Poland its annual Epidermolysis Bullosa Summer Camp, with the support of the Urgo Foundation. Taking…
read moreA university postgraduate course for a better care of venous ulcers! In collaboration with the Alfonso X El Sabio University, the Urgo Foundation proposed a university postgraduate course in Madrid, Spain. From January to June…
read morePUPS: the program that trains pharmacists in first aid! Rugby World Cup in 2023, Olympic Games in 2024… Over the next few months, crowd gatherings could generate a surge in requests for treatment in…
read moreZoom on the National Epidermolysis Bullosa Patient Conference in China On April 28th, the national EB* Patient Conference was held in Shanghai Children’s Medical Center. This conference was hosted by Debra (the EB care center…
read moreEndometriosis: the URGO Foundation commits! In February, the Urgo Foundation organized the first “endometriosis evening” in Nîmes, in partnership with the EndoFrance association. Bringing together members of the pharmacy profession, midwives and URGO employees, this…
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