Grants to Individuals
We are able to provide grants to support travel to conferences and funding for other items required to progress the knowledge of PWS in your country and support your association and experts to develop their skills and reach. We can also provide financial support and speakers if you are working to organise a conference or workshop.
Travel Scholarship Awards – ASPAE 2026
With the generous support of Friends of IPWSO (USA), IPWSO was delighted to award travel scholarships to 4 doctors from Nigeria to enable attendance at the 17th Annual Conference of the African Society for Paediatric and Adolescent Endocrinology, held in Dakar, Senegal, from 16-18 July 2026.
We are grateful to these physicians for all their efforts to rasie awareness of PWS in their country:
Dr Chioma Ahumaraeze,
Dr Theresa Nnaj
Dr Stella Oji-Onuoha
Dr Oluwadamilola Oladipo,
Picture shows left to right: Dr Chioma Ahumareze, Karin Clarke, IPWSO Vice President, Dr Oluwadamilola Oladipo and Dr Stella Oji-Onuoha.
Recipients from previous years
2025
2026
Dr Oluwadamilola Oladipo
Dr Chioma Ahumaraeze
Dr Stella Oji-Onuoha
Dr Theresa Nnaji
2023
2024
2019
Parent
2022
Student
2018
Scholarship to the PPCB Conference, Munich, Germany, August 2018
Do Thuy Lan (Vietnam), Professional
Scholarship to the PPCB Conference, Munich, Germany, August 2018
Registration to the PPCB Conference, Munich, Germany, August 2018
2016
Do you want to find out more?
If you have a particular project in mind or know of a conference you would love to attend get in touch with us and we can talk about how to take this forward.
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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.
Information for Medical Professionals
The latest medical and scientific research and information, plus guides into common medical issues affecting people with PWS.
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 Genetic Screening
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 genetic screening.



