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Epidermolysis Bullosa

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Scientists Grew a Full Body Skin Replacement for Boy with EB
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Scientists Grew a Full Body Skin Replacement for Boy with EB

  • Post author:Patient Worthy Contributor
  • Post published:November 9, 2017
  • Post category:Epidermolysis Bullosa/Rare Disease

Two years ago, a seven-year-old boy from Syria was in dire condition. 80% of his skin was gone; his entire body covered in wounds and abrasions. He still had some…

Continue Reading Scientists Grew a Full Body Skin Replacement for Boy with EB
Time is Running Out for Epidermolysis Bullosa Clinical Trial
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Time is Running Out for Epidermolysis Bullosa Clinical Trial

  • Post author:Sabina Kennedy
  • Post published:July 31, 2017
  • Post category:Epidermolysis Bullosa/Rare Disease/Timely

Let’s talk clinical trials. Clinical trials are part of clinical research and at the heart of all medical advances. Clinical trials look at new ways to prevent, detect, or treat…

Continue Reading Time is Running Out for Epidermolysis Bullosa Clinical Trial
Epidermolysis Bullosa (EB) Circle Hits Back Hard
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Epidermolysis Bullosa (EB) Circle Hits Back Hard

  • Post author:Sabina Kennedy
  • Post published:April 26, 2017
  • Post category:Epidermolysis Bullosa/Rare Disease

A health crisis—just like epidermolysis bullosa (EB)—is different for everyone. But, most have one thing in common: Bad news blindsides us. We take a hit—a hard one at that. When…

Continue Reading Epidermolysis Bullosa (EB) Circle Hits Back Hard
Tomorrow’s Epidermolysis Bullosa Treatment is All in the Genes
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Tomorrow’s Epidermolysis Bullosa Treatment is All in the Genes

  • Post author:Ronald Ledsen
  • Post published:January 26, 2017
  • Post category:Epidermolysis Bullosa/Rare Disease/Timely

It’s always heartening to see scientists take up research in therapeutic areas that are under served and poorly understood. And when their research yields positive results, it’s downright amazing. Honestly,…

Continue Reading Tomorrow’s Epidermolysis Bullosa Treatment is All in the Genes
Editor’s Choice: Our Mind is a Drug and the Dangers of Superbugs

Editor’s Choice: Our Mind is a Drug and the Dangers of Superbugs

  • Post author:Patient Worthy Contributor
  • Post published:January 13, 2017
  • Post category:Cystic Fibrosis/Cystinosis/Dystonia/Epidermolysis Bullosa/Rare Disease

Who is excited for another long weekend coming up this Monday?! To kick off your three-day weekend, take a look at these intriguing stories... Researchers have identified a superbug that…

Continue Reading Editor’s Choice: Our Mind is a Drug and the Dangers of Superbugs
How One Little EB Super Cutie is Changing Her World
[Source: pixabay.com]

How One Little EB Super Cutie is Changing Her World

  • Post author:Sabina Kennedy
  • Post published:January 11, 2017
  • Post category:Epidermolysis Bullosa/Rare Disease

When we need it most, stories can inspire, encourage, and quite frankly, make us feel good. Especially if the story is about a super cute little eight-year-old girl who was…

Continue Reading How One Little EB Super Cutie is Changing Her World
What You Need to Know About Epidermolysis Bullosa
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What You Need to Know About Epidermolysis Bullosa

  • Post author:Erica Zahn
  • Post published:December 26, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Epidermolysis bullosa (EB) is a disorder characterized by blistering of the skin. It also affects all the body's mucous membranes, so while the blisters may be visible, the person's lips, tongue, mouth,…

Continue Reading What You Need to Know About Epidermolysis Bullosa
If Epidermolysis Bullosa is So Terrible, How is One Mom So Happy?
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If Epidermolysis Bullosa is So Terrible, How is One Mom So Happy?

  • Post author:Sabina Kennedy
  • Post published:November 9, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Life is one wild ride, isn’t it? The greatest surprises of life may be just around the corner. My life was changed by one little red radio flyer wagon. An…

Continue Reading If Epidermolysis Bullosa is So Terrible, How is One Mom So Happy?
The Astonishing and Sad Reality of Butterfly Children
[Source: pixabay.com]

The Astonishing and Sad Reality of Butterfly Children

  • Post author:Erica Zahn
  • Post published:November 3, 2016
  • Post category:Epidermolysis Bullosa

I always have a knee-jerk reaction that borders on anger when I read about babies who are dealt an unfair hand in the rare disease world. It seems incredibly unfair…

Continue Reading The Astonishing and Sad Reality of Butterfly Children
EB and the Butterfly Children of America
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EB and the Butterfly Children of America

  • Post author:Octavia Walker
  • Post published:October 24, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

  They are called, "butterfly children." These butterfly children earned their names for their fragile skin---said to be as delicate as the wings of a butterfly. The official name of…

Continue Reading EB and the Butterfly Children of America
Urgent: Why You Need to Know About This Pharma Company
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Urgent: Why You Need to Know About This Pharma Company

  • Post author:Farrah Fontaine
  • Post published:October 11, 2016
  • Post category:Acromegaly/Epidermolysis Bullosa/Rare Disease

Here's a riddle to start your day: What do acromegaly, Cushing's disease, and epidermolysis bullosa have in common? If you guessed that they all have treatments owned by a small pharma…

Continue Reading Urgent: Why You Need to Know About This Pharma Company
Why EB is the Worst Disease You’ve Never Heard Of
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Why EB is the Worst Disease You’ve Never Heard Of

  • Post author:Erica Zahn
  • Post published:September 12, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Epidermolysis Bullosa, or EB, is a connective tissue disorder that approximately 200 babies are born with each year. The most serious symptom is the extreme fragility of skin. People with EB suffer…

Continue Reading Why EB is the Worst Disease You’ve Never Heard Of
EB Tips and Tricks from the Debra CARE Conference

EB Tips and Tricks from the Debra CARE Conference

  • Post author:Rebekah
  • Post published:August 19, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Pictured: Dr. Jakub Tolar EB can make a lot of daily activities difficult and painful. Check out some tips and tricks compiled from presentations at the 2016 Debra CARE Conference.…

Continue Reading EB Tips and Tricks from the Debra CARE Conference
How to Support EB in the Most Youthful Way Possible
Source: www.pixabay.com

How to Support EB in the Most Youthful Way Possible

  • Post author:Kiki Jones
  • Post published:August 16, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Can I just tell you how I tired I am of all the millennial hate out there? People are beyond harsh to the younger generations, and this article on Heritage High…

Continue Reading How to Support EB in the Most Youthful Way Possible
All Aboard! This is What Living with a Rare Disease Should Look Like
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All Aboard! This is What Living with a Rare Disease Should Look Like

  • Post author:Lady Kehveen Abernathy
  • Post published:August 12, 2016
  • Post category:Epidermolysis Bullosa/Rare Disease

Imagine being 16 years old, and instead of meeting cute girls, going out with friends, and going to parties that get busted, you have to manage a rare, chronic condition…

Continue Reading All Aboard! This is What Living with a Rare Disease Should Look Like
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Finding Light Through Story-The Power of Ambassadorship in the Endometrial Cancer Community
*cancer that cannot be removed with surgery or has spread to other parts of the body. GEJ= gastroesophageal junction (where the esophagus joins the stomach)
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