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This is an archive article published on November 13, 2015

Courteney Cox opens up about epidermolysis bullosa

For Courteney Cox, the fight against the debilitating skin disease epidermolysis bullosa is a personal one.

Courteney Cox, Courteney Cox movies, Courteney Cox news, Courteney Cox latest news, entertainment news Courteney Cox said: “I’ve been a part of it since then. He’s 11 now. There is no cure for this disease. It’s just such a horrible thing.”

For Courteney Cox, the fight against the debilitating skin disease epidermolysis bullosa is a personal one.

“My friend’s son was born with EB,” the actress said.

“I’ve been a part of it since then. He’s 11 now. There is no cure for this disease. It’s just such a horrible thing.”

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The condition, which usually strikes babies and children, causes painful skin blisters; there is little hope for those affected beyond the age of 30, reported People magazine.

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“You have no choice to feel for these kids,” said Cox, 51, who has an 11-year-old daughter, Coco.

“The disease is very rare so need to bring awareness.”

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