Wiskott-Aldrich Foundation

Research, Education and Family support for WAS families worldwide

Connect with a family who has already gone through the challenges you face.

Provide guidance, support and inspiration to other families so they know they are not alone.

Find a trusting physician with active clinical experience in diagnosing and treating patients with Wiskott-Aldrich Syndrome.

You CAN make a difference. Find out how you can help us in the fight against Wiskott-Aldrich Syndrome.

Ask our community of doctors and families your questions, or answer questions with your own experience and expertise.

Search emerging treatments for WAS such as Gene Therapy, learn about the criteria for eligibility, and find out how to apply.

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Registration open for free monthly Educational Webinar, March 25, 2026: Hematopoietic Stem Cell Transplantation (Bone Marrow Transplant) for individuals affected by Wiskott-Aldrich Syndrome
- February Webinar Recording avaialable: Clinical Spectrum of WAS Carriers: Recording
WAF spearheads the First International Study on WAS Carriers: Clinical Spectrum of WAS Carriers, Self Reported Survey of 193 Carriers.
Introducing Wes, the Wiskott Warrior: An educational video introduction
The third round of the Delphi Consensus on the clinical Management of Wiskott-Aldrich Syndrome for patients living with WAS has been completed. Publication anticipated in third quarter of 2026.
We are proud to be a sponsor for the IDF National Conference, 2026.
You can now donate using Paypal
Michael Albert, M.D Talk on "Time to stop using XLT and mild-WAS to label patients" on May 10, 2024 . Read the Q&A Report based on audience questions.
EL-PFDD Voice of the Patient report approved. Read the report here.
EL-PFDD Meeting Feb 3, 2023 event successful broadcast with participation of Physicians, Researchers, FDA WAS families and board members.

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