by IPWSO | Jun 24, 2024 | News
Things never stay the same, and that’s no different for IPWSO! Next year, we’ll see some of our Trustees complete their tenure of office and we’ll welcome new officers to the IPWSO Board. Thankfully, ex-officers never stray too far from our PWS community and remain...
by Nora McNairney | May 8, 2024 | News
We have launched a new round of funding for families and professionals to organise PWS projects in countries where they are needed most. IPWSO is offering microgrants for small projects to support the efforts of individuals and groups who are working to improve the...
by Nora McNairney | May 8, 2024 | News
Applications are now welcome for funding for PWS Conference and Workshops! Thanks to the support of Friends of IPWSO (USA), the IPWSO Grants Committee is able to offer funding to individuals and groups who are interested in planning and hosting a PWS event to promote...
by IPWSO | Dec 13, 2023 | News
We are looking for a Fundraising and Communications Manager to join our team. Remote working (must be UK based) £31,000 per annum pro rata (£16,534) Part-time (20 hours per week) Contract (12 months) Closing date is 12 January 2024 at 23:30 (UK time) We’re looking for...
by Nora McNairney | Nov 30, 2023 | News
Opportunities to attend the fifteenth African Society of Paediatric and Adolescent Endocrinology Congress on 7 & 8 March 2024, Algiers, Algeria. In order to share knowledge about Prader-Willi syndrome (PWS) around the world, IPWSO is delighted to offer a limited...
by IPWSO | Nov 15, 2023 | News
Please support our Advice Line Appeal Help us be there for people with PWS in parts of the world with little support. This month we’re raising funds to help people with PWS access our vital advice line. Your donations will provide essential life-saving advice for...
