#52 2011 - Rain
I donated this painting to a raffle for
Prader-Willi Syndrome research
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#PraderWilliSyndrome
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Further information, by country:
https://ipwso.org/
https://pwsai.ie/
https://prader-willi.de/
https://www.pwsa.co.uk/
https://www.pwsausa.org/
https://prader-willi.de/
https://www.praderwilli.org.za/
http://prader-willi.se/
http://www.pws.org.au/
https://www.pwsamalaysia.org.my/
http://www.xpwilli.org/m/
http://www.ipwsa.com/
https://www.spwbrasil.com.br/
http://www.prader-willi.cl/
https://www.fpwr.ca/
https://www.prader-willi.fr/
https://www.praderwilli.it/
A personal post: Here is some information about Prader-Willi syndrome.
https://ipwso.org/pws-information/what-is-pws/
PWS is a rare genetic disorder characterised by physical, behavioural, neurocognitive, and other dysfunctions.
Folks with PWS require 24-hour care supervision for life. For obvious reasons therefore, their families & carers require corresponding ongoing supports.
PWS affects c. 1 in 20,000 births. As such, while rare, there are many cases in every country every year.