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News

Follow the latest news from around the world and the international PWS family.

Use our Media Guide for information about how to write and report about Prader-Willi syndrome.

Could your country host IPWSO 2025?

The General Assembly of IPWSO has agreed to extend the bidding period for potential hosts to submit proposals to hold the 12th International Prader-Willi Syndrome Organisation conference in 2025. This is an exciting opportunity to bring international speakers and...

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IPWSO Support for the People of Ukraine

IPWSO Support for the People of Ukraine The continuing suffering of the people of Ukraine is a cause of great sadness to IPWSO.  We have watched from afar as the horror of this war unfolded and are conscious of the tremendous injustice, hardship, and anxiety that...

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XI Conferencia Internacional IPWSO 2022

XI Conferencia Internacional IPWSO 2022 (*) University of Limerick - Irlanda 6 al 10 de julio Ya es tiempo que volvamos a reunirnos presencialmente como comunidad global, después de estos difíciles tiempos de pandemia en que hemos estado aislados. IPWSO 2022 ha...

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Could you help guide our work?

We are looking for people interested in joining the IPWSO Board from July 2022. Could you get involved and help guide and support our vital work? Trustees play a crucial role in the work of IPWSO. We are lucky to work with a fantastic group of people on our current...

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Asia Pacific PWS conference – October 2021!

The PWS associations of Australia, New Zealand, Malaysia and Thailand have come together to present the 5th Asia Pacific Prader-Willi syndrome conference! The event will be hosted online from 29th to 31st October 2021. We are delighted to be involved in what promises...

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PWSA USA conference goes online and open to all!

The PWSA USA's national convention is going online from 22nd to 26th June, 2021. Over the course of five days, attendees will share ideas and experiences while learning from leaders in the field of PWS. The virtual format makes it possible for more families than ever...

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IPWSO calls for use of Growth Hormone treatment in adults

IPWSO argues that Growth Hormone treatment should be universally available not just to children but also to adults with PWS. Our Clinical and Scientific Advisory Board has written to the Editor of the Orphanet Journal of Rare Diseases calling for the use of Growth...

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Semaglutide trial results

A study published in the New England Journal of Medicine has shown exciting results from trials of a drug called semaglutide on people with severe obesity. The trial showed that people lost an average of 15kg when receiving semaglutide compared with only 2.6kg in...

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Prader-Willi research

Our Clinical and Scientific Advisory Board has published a collated list of all PWS research papers published from October to December 2020.

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International Community

IPWSO was established so that PWS associations, families, clinicians and caregivers around the world could exchange information and support and have a united global voice under one umbrella.

three adults and a child smiling

Information for
Families

Find useful guides, research and information to help families manage PWS.

One man one lady at conference

Information for Medical Professionals

The latest medical and scientific research and information, plus guides into common medical issues affecting people with PWS.

Information for
Professional Caregivers

Sharing international knowledge among professional service providers throughout the world.

What is PWS?

Prader-Willi syndrome is a complex genetic condition. Various studies have shown that between 1 in 15,000 to 25,000 children are born with Prader-Willi syndrome and it affects all races and both sexes equally.  

Free Diagnosis

If you suspect your patient has Prader-Willi syndrome, based on the clinical signs and symptoms, but are unable to access testing in your country, then you may be able to access free testing.

Find support in my country

We have contacts in many countries and regions around the world.