Prader-Willi Syndrome (PWS) is a rare genetic disorder that affects many aspects of a person’s life, including their physical health, behaviour, and metabolism. Finding effective… Read More »Can AI help us find new treatments for PWS? 

Prader-Willi Syndrome (PWS) is a complex, genetic disorder that affects many aspects of a person’s health and development. Scientists are exploring new ways to treat… Read More »What are ER Chaperones and Could they Improve Treatment for Prader-Willi Syndrome  

Prader-Willi Syndrome (PWS) affects many aspects of a person’s life, including their physical health and development. One of the challenges faced by adults with PWS… Read More »Can Growth Hormone slow down premature ageing in adults with PWS?   

Prader-Willi Syndrome (PWS) and Congenital Myasthenic Syndrome-22 (CMS22) are two rare genetic disorders that, at first glance, might seem unrelated. However, recent research has uncovered… Read More »Exploring the Connection Between PWS and CMS22 

FPWR UK is a volunteer led charity whose mission is to eliminate the challenges of Prader Willi Syndrome (PWS) through the advancement of research and… Read More »Volunteers wanted!

MindSight Research are looking to invite people to participate in a research study which is focused on an injection device to administer medication to people… Read More »PWS Stronger Together have been informed of a new research opportunity!!