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DonateWith help from supporters like you, Debra of America continues to provide programs and services to people with Epidermolysis Bullosa and their families, and to support EB research.Thank You. |
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The mounting cost of bandages is most often not covered by an EB family's health insurance. |  |
89.4¢ of every dollar donated goes directly to EB patients, families, and research. |
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Epidermolysis Bullosa (EB) is a rare genetic skin disease that causes the skin to be so fragile that the slightest friction can cause severe blistering–inside and outside the body. Today there is no cure. Severe forms of EB cause patients to live with constant pain and scarring. The worst forms of EB lead to eventual disfigurement, disability, and often early death. |
 Epidermolysis Bullosa (EB is a rare genetic disease characterized by blistering skin. Hear about it now |
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 Many have already joined the cause to help treat EB and pursue a cure. Will you? How you can make a difference |
 You're not alone. Debra of America has been helping families like yours for over 25 years. Get support from Debra now |
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The 12th Annual |
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Please Don’t Come to Our Sixth Annual Butterfly PicnicBecause Life with EB is No Picnic |
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Debra Faraone |
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Click here to make your gift online |
Instead, take a moment this summer to consider the struggles people with EB face in the warmer months and throughout the year. Read more |
Click here to read the excerpt from the magazine. |
Learn More about the bracelet or Purchase Online. To see an up to the minute list of important Debra news and announcements, please visit the
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