LaSpes Onlus is a non-profit association that finances scholarships for young researchers. 100% of the money raised is devolved to the cause. The association was set up in memory of Francesco, a young man suffering from WAS, one of many rare genetic diseases.

WAS (Wiskott Aldrich Syndrom) is characterized by an immune deficiency belonging to the large category of primitive immunodeficiencies. It begins in childhood with eczema and recurrent infections, coagulation disorders and abnormalities in the number and function of platelets.

Understanding whether a child is affected by WAS means being able to intervene immediately: this is why early diagnosis is essential.

LaSpes Onlus therefore supports research that is not carried out by pharmaceutical companies. It focuses on young people and the future of science in the hope of give those affected by WAS and other rare diseases the longest possible future.

Italian actor and director Alessandro Preziosi is ambassador for the association.