The Noxx Foundation was created to bring awareness, provide direct support to families, and fund research for encephalocele, a rare neural tube defect that affects newborns worldwide. This foundation is deeply personal—it started with my own son’s diagnosis, but it has grown into a movement to help others facing the same battle.
Most people have never heard of encephalocele. We’re committed to changing that through education, advocacy, and outreach.
Families facing this diagnosis often struggle with medical costs, access to specialists, and emotional support. We aim to provide financial assistance, resources, and community-driven support.
Medical advancements are critical. The Noxx Foundation is working to fund research initiatives focused on early detection, improved treatment options, and long-term care solutions for children born with encephalocele.
Using Web3 and blockchain technology (via the Noxx Foundation Token on Solana) to transparently allocate funds. • Direct Assistance – Helping families with medical costs, travel expenses, and essential support during their journey.
Helping families with medical costs, travel expenses, and essential support during their journey.
Working with hospitals, medical researchers, and institutions to advance medical understanding and treatment.
Ensuring encephalocele gets the attention it deserves from the medical community and policymakers.
The goal is to make a permanent difference in the way encephalocele is treated, understood, and supported—so no family has to face it alone.
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