ONLINE TICKET SALES ARE CLOSED. HOWEVER YOU ARE ABLE TO PURCHASE TICKETS AT THE EVENT TOMORROW MORNING. WE LOOK FORWARD TO SEEING YOU THERE!
Join the McCauley Family, EB advocates, and supporters for the 4th Annual Butterfly Breakfast at Applebees in Miller Place, NY on Saturday, October 13, 2018.
This event is a great way to support debra of America and those
with Epidermolysis Bullosa (EB) while enjoying a wonderful pancake breakfast!
Breakfast Tickets are:
$10 for Adults
$7 for Children
Seating is from 8:00 am - 9:00 am.
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 2017 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.