Our Story & Mission

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.

Our Mission

To save the sickest, most medically neglected children suffering in severe pain with terminal diseases. Their lives depend on your loving, compassionate donations.

Our Vision

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.

Our Values

Compassion, transparency, urgency, innovation, and unwavering commitment to the forgotten children who need our voices the most.

Dr. Aaron Tabor MD
Johns Hopkins, MD
American Society for Gene & Cell Therapy

Dr. Aaron Tabor, MD & His Heartbreaking Discovery

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

Johns Hopkins School of Medicine
Gene & Cell Therapy Expert
FDA Pathway Navigator
American Medical Association
Anti-Aging Medicine Specialist
American Heart Association

Why No Babies Blister Exists

500K+
Worldwide Sufferers

Over half a million people worldwide live with EB, yet it remains a largely unknown and underfunded disease.

0
Full-Body Cures

No full-body systemic cure exists for EB. Only topical treatments and pain management — not a cure.

30yr
Average Life Expectancy

Life expectancy in severe forms is often less than 30 years, filled with constant pain and medical complications.

Low
Government Funding

As an orphan disease, EB receives minimal government or pharmaceutical funding — making our work critical.

Our History & Milestones

From a heartbreaking discovery to a global mission — here is how No Babies Blister grew from compassion into action.

See Our Research
2017

Organization Founded

Dr. 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.

2018

First Children Supported

The organization begins directly funding medical supplies — bandages, antibiotics, and pain medication — for EB children in need. Ashley and Joyce are among the first.

2019

Fast Cure Plan Launched

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.

2021

Gene Therapy Research Begins

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.

2023

1,000+ Children Reached

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.

2025

Fast Cure Plan — Phase II Progress

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.

Our Core Values

Radical Compassion

Every decision we make begins with the question: how does this help the children? We are driven by love, not bureaucracy.

Complete Transparency

Every donation is tracked and reported. We believe you deserve to know exactly how your generosity changes lives.

Urgent Action

Children are suffering right now. We act with urgency — not waiting for perfect conditions but meeting critical needs immediately.

Scientific Innovation

We pursue affordable cures that work for all EB patients globally — not just those who can access expensive experimental treatments.

Community First

We build partnerships with families, churches, corporations, and researchers who share our commitment to ending EB suffering.

Global Equity

Any cure we develop must be affordable worldwide. No child's access to treatment should depend on their family's income or country.

Join Our Mission

Whether you donate $5 or $5,000, volunteer your time, or simply share our story — you become part of the solution.