The Israeli Wiskott Aldrich Syndrome association (R.A)
העמותה הישראלית לתסמונת וויסקוט אולדריץ' (ע"ר)
Who we are?
The Israeli Wiskott Aldrich Syndrome Association (IWASA) is a nonprofit organization established on May 2011 by Odeia and Amir Kedar, parents of Jonathan who was born with Wiskott Aldrich Syndrome (WAS). Our objectives are:
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To encourage clinical and basic research on WAS;
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To create an international medical registry in order to provide data for research;
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To educate physicians about WAS
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Encourage awareness to the syndrome among healthcare professionals and the public.
This website is informative and give most of the data in Hebrew. If you want to explore the hebrew part you should ask your web browser to translate into English.
about WAS
?What is WAS
Wiskott-Aldrich Syndrome (WAS) is a very rare life-threatening genetic disorder th...
WAS research project
The Israeli WAS Association launched an ambitious research project in 2011, aiming to find a...
HOW CAN YOU HELP?
Our projects are made possible with your involvement and generous support. Please sup...