The URGO Foundation was in Portugal on October 28th (Lisbon), and November 25th (Porto) to lead Mission Compression days, a global initiative aiming to raise awareness and educate healthcare professionals on the critical role of compression therapy in treating venous leg ulcers (VLUs). A major public health issueCompression…
read moreWithin the framework of the 48th National AISD (Italian Association for the Study of Pain) Congress, held in Turin from 25 to 27 September 2025, a dedicated workshop shed light on the innovative applications of…
read moreFor the third consecutive year, the URGO Foundation is joining forces with the EndoMIND association as a partner of the ENDOrun. The aim is to support research and raise public awareness of this inflammatory gynaecological…
read moreIn early October, the URGO Foundation and the DEBRA Piel de Mariposa charity welcomed nearly 400 people directly or indirectly affected by epidermolysis bullosa (EB) to the Sol de Marbella hotel in Spain. Three days…
read moreOn October 11, the URGO Foundation met with 70 healthcare professionals in Martinique who are involved in wound care. The aim was to provide healthcare professionals of the island with practical tools to improve the…
read moreMenopause represents one of the most significant—and often underestimated—milestones in a woman’s life. It is not a one-size-fits-all phenomenon, but rather a transition that can take many different forms. Each woman’s experience is unique, bringing…
read moreOn September 28, in Sichuan province, the URGO Foundation and the Debra patient association brought together children with epidermolysis bullosa, their families, and healthcare professionals for a day dedicated to this rare disease. It was…
read moreThe SAWC Fall 2025 session, held in early September in the United States, provided the perfect venue for the demonstration of the commitment of Urgo Foundation towards the training to the clinical community in advanced…
read moreAs for many years now, the URGO Foundation has been supporting Debra Poland in August to allow EB patients and their families to gather for a summer camp. This year, 40 families enjoyed a week…
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