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Premiering in celebration of Batman Day this year we are presenting a walkthrough webathon of the largest Batman collection in the world, over 16,400 items. It’s not just a walk through, there will be interviews as well as funny sketches. It is for the benefit of debra of America in support of families suffering from EB.
What is EB?
Epidermolysis Bullosa (ep-i-der-mo-lie-sis bu-low-suh), or EB, is a rare connective tissue disorder with many genetic and symptomatic variations. All types of EB share the major symptom of extremely fragile skin that blisters and tears from the slightest friction or trauma. Internal organs and bodily systems can also be seriously affected by the disease. EB is always painful, often pervasive and debilitating, and is in some cases lethal before the age of 30. There is currently no cure or treatment for EB. Pain management, wound care, and preventative bandaging are the only options available. Those born with Epidermolysis Bullosa are often called “Butterfly Children” because as the analogy goes, their skin is as fragile as the wings of a butterfly.
There are about 25,000 people living with EB in the US. It occurs in every racial and ethnic group and affects both genders equally. For a more in-depth and comprehensive understanding of Epidermolysis Bullosa, please also check out debra of America’s explanation by clicking here.
What is debra of America?
Because the cost of doing nothing is too great. This axiom defines debra of America's mission and directs all that we do. We are dedicated to improving the quality of life for those living with EB. To achieve our mission, we do two things in parallel: we provide free programs and services to the EB Community in the US, and fund the most innovative research directed at symptom relief and a systemic cure.
In 2019 alone, our largest program, the Wound Care Distribution Program, sent over $1 Million worth of specialized bandages. That translates to over 108,000 pieces of wound care sent to families across the US. Our research funding identified the genetic basis of EB and supports the science, which is at the forefront of gene and stem cell therapy, RNA repair, protein replacement, and inhibition of squamous cell carcinoma.
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Premiering in celebration of Batman Day this year we are presenting a walkthrough webathon of the largest Batman collection in the world, over 16,400 items. It’s not just a walk through, there will be interviews as well as funny sketches. It is for the benefit of debra of America in support of families suffering from EB. The webathon begins on (on the Batman Statue Collector channel/The Channel/Here) on Batman Day, 9/18/21.
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Thank You!
Thank you for your generous donation. Please share my fundraiser with your friends, and come back to this page to see updates on my progress.
Fundraiser First Name Fundraiser Last Name
Premiering in celebration of Batman Day this year we are presenting a walkthrough webathon of the largest Batman collection in the world, over 16,400 items. It’s not just a walk through, there will be interviews as well as funny sketches. It is for the benefit of debra of America in support of families suffering from EB. The webathon begins on (on the Batman Statue Collector channel/The Channel/Here) on Batman Day, 9/18/21.
Organization Name
Org Address Line 1 Org Address Line 2
Org City, Org State Org Zip
Need help? Org Email