2026 IQSEC2 Strollathon Fundraiser to support gene replacement clinical trials

We’re fundraising to help bring hope, answers, and future treatments to children and families affected by IQSEC2. 💙 IQSEC2 is a rare genetic disorder that can cause significant developmental delays, intellectual disability, seizures, limited or absent speech, and challenges with mobility and everyday life. Because it is so rare, continued research and funding are critical. Our son, Yadi, is one of the children living with IQSEC2, which makes this mission incredibly personal to our family. Every milestone he reaches reminds us why we continue to fight for more research, better treatments, and a brighter future. Every donation, every share, and every step brings us closer. For Yadi and every child with IQSEC2. 💙🧬