Founded by a Johns Hopkins–trained physician who witnessed EB's devastating reality firsthand — we exist because every child deserves a life free from pain.
To save the sickest, most medically neglected children suffering in severe pain with terminal diseases. Their lives depend on your loving, compassionate donations.
A world where no baby suffers from Epidermolysis Bullosa — where an affordable, full-body systemic cure is accessible to every child regardless of geography or economic status.
Compassion, transparency, urgency, innovation, and unwavering commitment to the forgotten children who need our voices the most.
Dr. Tabor received his MD from the prestigious Johns Hopkins School of Medicine and became a member of the American Society for Gene and Cell Therapy. But it was his encounter with children suffering from EB that changed the direction of his career forever.
Witnessing babies whose skin blistered and peeled at the lightest touch — unable to receive a hug from their own parents without suffering — Dr. Tabor knew he had to act. He assembled a world-class medical team of pioneering researchers, FDA experts, and scientific innovators to develop what he calls the Fast Cure Plan: an affordable, full-body systemic cure for EB that no child will be left without.
"These children are medically neglected. Big pharma ignores orphan diseases because they aren't profitable enough. That's exactly why we exist — to fill that gap with love, science, and compassion." — Dr. Aaron Tabor, MD, Founder
Over half a million people worldwide live with EB, yet it remains a largely unknown and underfunded disease.
No full-body systemic cure exists for EB. Only topical treatments and pain management — not a cure.
Life expectancy in severe forms is often less than 30 years, filled with constant pain and medical complications.
As an orphan disease, EB receives minimal government or pharmaceutical funding — making our work critical.
From a heartbreaking discovery to a global mission — here is how No Babies Blister grew from compassion into action.
See Our ResearchDr. Aaron Tabor MD establishes No Babies Blister after witnessing firsthand the devastating impact of EB on children and families. The 501(c)(3) status is obtained.
The organization begins directly funding medical supplies — bandages, antibiotics, and pain medication — for EB children in need. Ashley and Joyce are among the first.
A world-class medical team is assembled including researchers with patents in genetic skin therapy, FDA experts, and pioneering scientists to develop an affordable EB cure.
Phase I of our gene therapy research commences, targeting the root genetic mutation causing EB. Early results show promising pathways for stopping blistering at the cellular level.
No Babies Blister surpasses 1,000 children supported across 30+ countries. Our awareness campaigns reach millions on social media. Gene therapy enters Phase II trials.
Gene therapy and molecular research both show breakthrough results. We continue our mission with renewed urgency as our donor community grows past 2,400 monthly supporters.
Every decision we make begins with the question: how does this help the children? We are driven by love, not bureaucracy.
Every donation is tracked and reported. We believe you deserve to know exactly how your generosity changes lives.
Children are suffering right now. We act with urgency — not waiting for perfect conditions but meeting critical needs immediately.
We pursue affordable cures that work for all EB patients globally — not just those who can access expensive experimental treatments.
We build partnerships with families, churches, corporations, and researchers who share our commitment to ending EB suffering.
Any cure we develop must be affordable worldwide. No child's access to treatment should depend on their family's income or country.
Whether you donate $5 or $5,000, volunteer your time, or simply share our story — you become part of the solution.