Foundation for Prader Willi Research UK (FPWR UK) is the only UK charity dedicated to furthering research into the genetic condition Prader Willi Syndrome (PWS). PWS involves missing information on chromosome 15 and causes many symptoms including an insatiable appetite, sleep disturbances, orthopaedic issues, behavioural and emotional problems, development and speech delays and learning disability.
Our mission is to eliminate the challenges of Prader-Willi Syndrome (PWS) through the advancement of research. We believe research is the key to a brighter and more independent future for everyone with PWS.
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