WWOX Foundation of America

WWOX Foundation of America Funding research, and advocating for families affected by WWOX diseases

03/01/2026

🌍💜 Today we stand with the 300 million people living with a rare disease. We are united with their families, friends, caregivers, advocates, and the medical professionals, researchers and organisations that working tirelessly to build a more equitable future for our community.

Together, we’re showing our colours, raising awareness, and inspiring change by talking about what equity means to us.

Thank you to everyone who’s taken part, whether you’ve lit up your home, shared your story, joined an event, or supported someone you love. By standing together we’re proving that our community is strong, united, and truly more than anyone can imagine. ✨

👉 Learn more and discover ways you can still get involved: https://go.rarediseaseday.org/NEWS

02/16/2026

Today is International WWOX Awareness Day 🧡

12/01/2025

🚨 Dec 1-7 is Infantile Spasms Awareness Week! Infantile spasms are a medical emergency that can cause lasting brain damage if not treated fast. Know the signs! Learn more at infantilespasms.org

Address

P. O. Box 703
Maple Valley, WA
98038

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