Welcome

This year is the Emerald Anniversary of Prader-Willi Syndrome!  That means it's 55 years since Drs Prader, Willi and Labhardt first described what we now call PWS.  Our International PWS Organisation helps over 90 countries in the world; it's a major task and we try to do this all for free.  But right now we really need your support for our Emerald Anniversary.   

Please, visit our "Light a Candle" page....

IPWSO supports over 90 countries with information, resources, and networking.

PARENTS

Early diagnosis of PWS can mean better management with informed decisions.  If your child has just been diagnosed with PWS, click on the picture to take you to our What is PWS? page for information.

 

  

 MEDICAL

Characteristics of PWS, medical diagnosis, medical support, good behavioural management and a strong knowledge of dietary and exercise needs for those with PWS is essential.  To know more about this, click on the picture.

 

  

CAREGIVERS

For Caregivers, support agencies, providers, educationalists and those supporting people with PWS, click on the picture to take you to further information.

  

 

 CONTACT

Click on the image to contact IPWSO