Celebrated on the Tuesday after Thanksgiving (and after the widely recognized shopping events, Black Friday and Cyber Monday), #GivingTuesday is a global day of giving, fueled by the power of social media and collaboration, that aims to inspire people across the globe to give back to causes and issues that matter to them.
Since its launch in 2012, #GivingTuesday has grown into the biggest generosity movement in history! Learn more about #GivingTuesday
Get involved on #GivingTuesday by giving the generous gift of your time, voice, or dollars.
Learn about EB
Epidermolysis Bullosa (EB) is a complex rare genetic connective tissue disorder. There are many genetic and symptomatic variations, but all share the prominent symptom of extremely fragile skin that blisters and tears with any friction. Take some time to learn about EB and pass your new knowledge along to others.
Learn about EB
Read our EB Stories
The EB Community is filled with inspiring individuals and families, each with a story to share. These stories strengthen the community and create a feeling of unity, especially when those with EB have often been searching for a story that resembles their own. If you’d like to share your own experience, please email us at email@example.com.
Read our Personal Stories
Give Your Voice
Spread the Word on your Social Media
Make your voice heard! Tell your friends, family and followers why you are passionate about helping the Epidermolysis Bullosa (EB) Community. Inform them about what EB is and what they can do to make an impact. Be sure to tag debra of America and use the hashtags #GivingTuesday and #WeFightEB!
Support our Wound Care Distribution Program
This #GivingTuesday, we are focusing our fundraising efforts towards our Wound Care Distribution Program, a key program that supports thousands of families across the United States.
Host a Facebook Fundraiser
Are you on Facebook? You can start a Facebook Fundraiser to raise funds in support of the EB Community. Your friends and followers can donate with just a few clicks, without leaving Facebook. 100% of proceeds go towards our mission.
Host a (Virtual!) Supporter Led Event
In the face of the pandemic, many of our supporters have pivoted to Virtual Supporter Led Events! Think: Zoom Happy Hour, Virtual Painting Class or Run! Email Jason at firstname.lastname@example.org to get started.
EB is a rare connective tissue disorder with many genetic & symptomatic variations. All forms share the prominent symptom of extremely fragile skin that blisters & tears with any friction.
“Because the cost of doing nothing is too great” is an axiom that defines our mission and directs all of debra of America’s actions as an organization.Learn More Other ways to get involved
There are many ways that you can join the fight against EB. Start an event, host a fundraiser, volunteer, and more!Learn More